Many

skin condition A skin condition, also known as cutaneous condition, is any medical condition that affects the integumentary system—the organ system that encloses the body and includes skin, nails, and related muscle and glands. The major function of this s ...

s affect the human integumentary system—the

organ system An organ system is a biological system consisting of a group of organs that work together to perform one or more functions. Each organ has a specialized role in a plant or animal body, and is made up of distinct tissues. Plants Plants have ...

covering the entire surface of the

body Body may refer to: In science * Physical body, an object in physics that represents a large amount, has mass or takes up space * Body (biology), the physical material of an organism * Body plan, the physical features shared by a group of anima ...

and composed of

skin Skin is the layer of usually soft, flexible outer tissue covering the body of a vertebrate animal, with three main functions: protection, regulation, and sensation. Other animal coverings, such as the arthropod exoskeleton, have different de ...

, hair, nails, and related muscle and

glands In animals, a gland is a group of cells in an animal's body that synthesizes substances (such as hormones) for release into the bloodstream (endocrine gland) or into cavities inside the body or its outer surface (exocrine gland). Structure De ...

. The major function of this system is as a barrier against the external environment. The skin weighs an average of four kilograms, covers an area of two square metres, and is made of three distinct layers: the epidermis, dermis, and subcutaneous tissue. The two main types of human skin are: glabrous skin, the hairless skin on the palms and soles (also referred to as the "palmoplantar" surfaces), and hair-bearing skin.Burns, Tony; ''et al''. (2006) ''Rook's Textbook of Dermatology CD-ROM''. Wiley-Blackwell. . Within the latter type, the hairs occur in structures called pilosebaceous units, each with hair follicle,

sebaceous gland A sebaceous gland is a microscopic exocrine gland in the skin that opens into a hair follicle to secrete an oily or waxy matter, called sebum, which lubricates the hair and skin of mammals. In humans, sebaceous glands occur in the greatest nu ...

, and associated arrector pili muscle. In the embryo, the epidermis, hair, and glands form from the ectoderm, which is chemically influenced by the underlying mesoderm that forms the dermis and subcutaneous tissues. The epidermis is the most superficial layer of skin, a

squamous epithelium Epithelium or epithelial tissue is one of the four basic types of animal tissue, along with connective tissue, muscle tissue and nervous tissue. It is a thin, continuous, protective layer of compactly packed cells with a little intercellula ...

with several strata: the stratum corneum,

stratum lucidum The stratum lucidum (Latin, 'clear layer') is a thin, clear layer of dead skin cells in the epidermis named for its translucent appearance under a microscope. It is readily visible by light microscopy only in areas of thick skin, which are found ...

stratum granulosum The stratum granulosum (or granular layer) is a thin layer of cells in the epidermis lying above the stratum spinosum and below the stratum corneum ( stratum lucidum on the soles and palms).James, William; Berger, Timothy; Elston, Dirk (2005) '' ...

stratum spinosum The stratum spinosum (or spinous layer/prickle cell layer) is a layer of the epidermis found between the stratum granulosum and stratum basale. This layer is composed of polyhedral keratinocytes. These are joined with desmosomes. Their spiny (La ...

, and

stratum basale The ''stratum basale'' (basal layer, sometimes referred to as ''stratum germinativum'') is the deepest layer of the five layers of the epidermis, the external covering of skin in mammals. The ''stratum basale'' is a single layer of columnar or ...

. Nourishment is provided to these layers by

diffusion Diffusion is the net movement of anything (for example, atoms, ions, molecules, energy) generally from a region of higher concentration to a region of lower concentration. Diffusion is driven by a gradient in Gibbs free energy or chemica ...

from the dermis since the epidermis is without direct blood supply. The epidermis contains four cell types:

keratinocyte Keratinocytes are the primary type of cell found in the epidermis, the outermost layer of the skin. In humans, they constitute 90% of epidermal skin cells. Basal cells in the basal layer (''stratum basale'') of the skin are sometimes referre ...

s, melanocytes,

Langerhans cell A Langerhans cell (LC) is a tissue-resident macrophage of the skin. These cells contain organelles called Birbeck granules. They are present in all layers of the epidermis and are most prominent in the stratum spinosum. They also occur in the ...

s, and

Merkel cell Merkel cells, also known as Merkel-Ranvier cells or tactile epithelial cells, are oval-shaped mechanoreceptors essential for light touch sensation and found in the skin of vertebrates. They are abundant in highly sensitive skin like that of the f ...

s. Of these, keratinocytes are the major component, constituting roughly 95 percent of the epidermis. This stratified squamous epithelium is maintained by cell division within the stratum basale, in which differentiating cells slowly displace outwards through the stratum spinosum to the stratum corneum, where cells are continually shed from the surface. In normal skin, the rate of production equals the rate of loss; about two weeks are needed for a cell to migrate from the basal cell layer to the top of the granular cell layer, and an additional two weeks to cross the stratum corneum. The dermis is the layer of skin between the epidermis and subcutaneous tissue, and comprises two sections, the

papillary dermis The dermis or corium is a layer of skin between the epidermis (with which it makes up the cutis) and subcutaneous tissues, that primarily consists of dense irregular connective tissue and cushions the body from stress and strain. It is divided in ...

and the

reticular dermis The dermis or corium is a layer of skin between the epidermis (with which it makes up the cutis) and subcutaneous tissues, that primarily consists of dense irregular connective tissue and cushions the body from stress and strain. It is divided in ...

. The superficial papillary dermis interdigitates with the overlying

rete ridge The epidermis is the outermost of the three layers that comprise the skin, the inner layers being the dermis and hypodermis. The epidermis layer provides a barrier to infection from environmental pathogens and regulates the amount of water relea ...

s of the epidermis, between which the two layers interact through the basement membrane zone. Structural components of the dermis are collagen, elastic fibers, and

ground substance Ground substance is an amorphous gel-like substance in the extracellular space that contains all components of the extracellular matrix (ECM) except for fibrous materials such as collagen and elastin. Ground substance is active in the development, m ...

. Within these components are the pilosebaceous units, arrector pili muscles, and the

eccrine Merocrine (or eccrine) is a term used to classify exocrine glands and their secretions in the study of histology. A cell is classified as merocrine if the secretions of that cell are excreted via exocytosis from secretory cells into an epithelia ...

and

apocrine gland Apocrine () glands are a type of exocrine gland, which are themselves a type of gland, i.e. a group of cells specialized for the release of secretions. Exocrine glands secrete by one of three means: holocrine, merocrine and apocrine. In apocrine ...

s. The dermis contains two vascular networks that run parallel to the skin surface—one superficial and one deep plexus—which are connected by vertical communicating vessels. The function of blood vessels within the dermis is fourfold: to supply nutrition, to regulate temperature, to modulate inflammation, and to participate in wound healing. The subcutaneous tissue is a layer of fat between the dermis and underlying fascia. This tissue may be further divided into two components, the actual fatty layer, or panniculus adiposus, and a deeper vestigial layer of muscle, the

panniculus carnosus The panniculus carnosus is a part of the subcutaneous tissues in vertebrates. It is a layer of striated muscle deep to the panniculus adiposus.McGrath, J.A.; Eady, R.A.; Pope, F.M. (2004). ''Rook's Textbook of Dermatology'' (Seventh Edition). Black ...

. The main cellular component of this tissue is the adipocyte, or fat cell. The structure of this tissue is composed of septal (i.e. linear strands) and lobular compartments, which differ in microscopic appearance. Functionally, the subcutaneous fat insulates the body, absorbs trauma, and serves as a reserve energy source. Conditions of the human integumentary system constitute a broad spectrum of diseases, also known as

dermatoses A skin condition, also known as cutaneous condition, is any medical condition that affects the integumentary system—the organ system that encloses the body and includes skin, nails, and related muscle and glands. The major function of this s ...

, as well as many nonpathologic states (like, in certain circumstances,

melanonychia Melanonychia is a black or brown pigmentation of the normal nail plate, and may be present as a normal finding on many digits in Afro-Caribbeans, as a result of trauma, systemic disease, or medications, or as a postinflammatory event from such local ...

and

racquet nails A racket, or racquet, is a sports implement used for striking a ball or shuttlecock in games such as squash, tennis, racquetball, badminton and padel. In the strictest sense a racket consists of a handled frame with an open hoop across which a n ...

). While only a small number of skin diseases account for most visits to the

physician A physician (American English), medical practitioner (Commonwealth English), medical doctor, or simply doctor, is a health professional who practices medicine, which is concerned with promoting, maintaining or restoring health through th ...

, thousands of skin conditions have been described. Classification of these conditions often presents many

nosological Nosology () is the branch of medical science that deals with the classification of diseases. Fully classifying a medical condition requires knowing its cause (and that there is only one cause), the effects it has on the body, the symptoms that ...

challenges, since underlying etiologies and pathogenetics are often not known. Therefore, most current textbooks present a classification based on location (for example, conditions of the mucous membrane), morphology ( chronic blistering conditions), etiology (

skin conditions resulting from physical factors Skin is the layer of usually soft, flexible outer tissue covering the body of a vertebrate animal, with three main functions: protection, regulation, and sensation. Other animal coverings, such as the arthropod exoskeleton, have different de ...

), and so on. Clinically, the diagnosis of any particular skin condition is made by gathering pertinent information regarding the presenting

skin lesion A skin condition, also known as cutaneous condition, is any medical condition that affects the integumentary system—the organ system that encloses the body and includes skin, nails, and related muscle and glands. The major function of th ...

(s), including the location (such as arms, head, legs), symptoms (

pruritus Itch (also known as pruritus) is a sensation that causes the desire or reflex to scratch. Itch has resisted many attempts to be classified as any one type of sensory experience. Itch has many similarities to pain, and while both are unpleasant ...

, pain), duration (acute or chronic), arrangement (solitary, generalized, annular, linear), morphology (

macule A skin condition, also known as cutaneous condition, is any medical condition that affects the integumentary system—the organ system that encloses the body and includes skin, nails, and related muscle and glands. The major function of this s ...

papule A papule is a small, well-defined bump in the skin. It may have a rounded, pointed or flat top, and may have a dip. It can appear with a stalk, be thread-like or look warty. It can be soft or firm and its surface may be rough or smooth. Some h ...

vesicle Vesicle may refer to: ; In cellular biology or chemistry * Vesicle (biology and chemistry) In cell biology, a vesicle is a structure within or outside a cell, consisting of liquid or cytoplasm enclosed by a lipid bilayer. Vesicles form nat ...

s), and

color Color (American English) or colour (British English) is the visual perceptual property deriving from the spectrum of light interacting with the photoreceptor cells of the eyes. Color categories and physical specifications of color are assoc ...

(red, blue, brown, black, white, yellow). Diagnosis of many conditions often also requires a

skin biopsy Skin biopsy is a biopsy technique in which a skin lesion is removed to be sent to a pathologist to render a microscopic diagnosis. It is usually done under local anesthetic in a physician's office, and results are often available in 4 to 10 days. ...

which yields

histologic Histology, also known as microscopic anatomy or microanatomy, is the branch of biology which studies the microscopic anatomy of biological tissues. Histology is the microscopic counterpart to gross anatomy, which looks at larger structures vis ...

information that can be correlated with the clinical presentation and any laboratory data.

Acneiform eruptions

Acneiform eruption Acneiform eruptions are a group of dermatoses including acne vulgaris, rosacea, folliculitis, and perioral dermatitis. Restated, acneiform eruptions are follicular eruptions characterized by papules and pustules resembling acne.James, William; Be ...

s are caused by changes in the pilosebaceous unit. *

Acne aestivalis Acne aestivalis also called as acne mallorca, is a special kind of polymorphous light eruption induced by ultra violet A radiation. This condition is said to be seasonal, usually affecting people in springtime and goes away in autumn when there i ...

(Mallorca acne)Any given cutaneous condition is only included once within this list. Parentheticals are used to indicate other names by which a condition is known. If there are multiple alternative names for a condition, they are separated by commas within the parenthetical.Citations for any given condition name and/or alternative name(s) may be found within the condition's respective article. *

Acne conglobata Acne conglobata is a highly inflammatory disease presenting with comedones, nodules, abscesses, and draining sinus tracts. This condition generally begins between the ages of 18 and 30. It usually persists for a very long time, and often until t ...

Acne cosmetica The term acne cosmetica refers to acne caused by or aggravated by cosmetics. The mechanism is thought to be chemically induced plugging of the pilosebaceous orifice. This became a significant problem for dermatologists in the 1970s and 1980s, bu ...

(cosmetic acne) *

Acne fulminans Acne fulminans (also known as "acute febrile ulcerative acne"Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. .) is a severe form of the skin disease, acne, which can occur after unsuccessful tre ...

(acute febrile ulcerative acne) * Acne keloidalis nuchae (acne keloidalis, dermatitis papillaris capillitii, folliculitis keloidalis, folliculitis keloidis nuchae, nuchal keloid acne) *

Acne mechanica Acne mechanica is an acneiform eruption that has been observed after repetitive physical trauma to the skin such as rubbing, occurring from clothing (belts and straps) or sports equipment (football helmets and shoulder pads).Freedberg, et al. ( ...

Acne medicamentosa Acne medicamentosa is acne that is caused or aggravated by medication. Because acne is generally a disorder of the pilosebaceous units caused by hormones, the medications that trigger acne medicamentosa most frequently are hormone analogs. It is a ...

Acne miliaris necrotica Acne miliaris necrotica is a rare condition consisting of follicular vesicopustules, sometimes occurring as solitary lesions that are usually very itchy.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinic ...

(acne varioliformis) * Acne vulgaris (acne simplex) *

Acne with facial edema Acne with facial edema occurs uncommonly, and is associated with a peculiar inflammatory edema of the mid-third of the face.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). Page 685. McGraw-Hill. . See al ...

(solid facial edema)This list uses American English; therefore, the symbols æ and œ, which are common to British English, are not used, but, rather, simplified to a single e. For example, the spelling of

nevus Nevus (plural nevi) is a nonspecific medical term for a visible, circumscribed, chronic lesion of the skin or mucosa. The term originates from ''nævus'', which is Latin for "birthmark"; however, a nevus can be either congenital (present at bir ...

is favored over nævus, edema over œdema, and so forth. For more information, see

American and British English differences The English language was introduced to the Americas by British colonisation, beginning in the late 16th and early 17th centuries. The language also spread to numerous other parts of the world as a result of British trade and colonisation an ...

. * Blepharophyma * Erythrotelangiectatic rosacea (erythematotelangiectatic rosacea, vascular rosacea) *

Excoriated acne Excoriated acne is a mild acne accompanied by extensive excoriations caused by the person picking at the pimples (that is, scratching or squeezing them).Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw ...

(''acne excoriée des jeunes filles'', Picker's acne)Non-

English English usually refers to: * English language * English people English may also refer to: Peoples, culture, and language * ''English'', an adjective for something of, from, or related to England ** English national ide ...

names are included within this list when those terms are found in English

medical literature Medical literature is the scientific literature of medicine: articles in journals and texts in books devoted to the field of medicine. Many references to the medical literature include the health care literature generally, including that of denti ...

. Inclusion of '' acne excoriée des jeunes filles'' ( French), '' Frambösie'' (

German German(s) may refer to: * Germany (of or related to) ** Germania (historical use) * Germans, citizens of Germany, people of German ancestry, or native speakers of the German language ** For citizens of Germany, see also German nationality law **Ge ...

), and '' parangi'' (

Malay Malay may refer to: Languages * Malay language or Bahasa Melayu, a major Austronesian language spoken in Indonesia, Malaysia, Brunei and Singapore ** History of the Malay language, the Malay language from the 4th to the 14th century ** Indonesi ...

) represent examples of this convention. * Glandular rosacea * Gnathophyma * Gram-negative rosacea *

Granulomatous facial dermatitis Granulomatous facial dermatitis is found in patients with persistent facial erythema involving one or more convex surfaces of the face, with lesions that show granulomatous reaction histologically.James, William; Berger, Timothy; Elston, Dirk (2005 ...

* Granulomatous perioral dermatitis *

Halogen acne Halogen acne is caused by iodides, bromides and fluorides (halogens) that induce an acneiform eruption similar to that observed with steroids.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). Page 684. McGraw-H ...

Hidradenitis suppurativa Hidradenitis suppurativa (HS), sometimes known as acne inversa or Verneuil's disease, is a long-term dermatological condition characterized by the occurrence of inflamed and swollen lumps. These are typically painful and break open, releasing ...

(acne inversa, pyoderma fistulans significa, Verneuil's disease) *

Idiopathic facial aseptic granuloma Idiopathic facial aseptic granuloma is a cutaneous condition characterized by a chronic, painless, solitary nodule, reminiscent of an acne nodule, appearing on the cheeks of young children. It has a prolonged course, but spontaneously heals. See ...

* Infantile acne *

Lupoid rosacea Rosacea is a long-term skin condition that typically affects the face. It results in redness, pimples, swelling, and small and superficial dilated blood vessels. Often, the nose, cheeks, forehead, and chin are most involved. A red, enlarge ...

(granulomatous rosacea, micropapular tuberculid, rosacea-like tuberculid of Lewandowsky) * Lupus miliaris disseminatus faciei * Metophyma * Neonatal acne (acne infantum, acne neonatorum, neonatal cephalic pustulosis) * Occupational acne * Oil acne *

Ocular rosacea Ocular rosacea is a manifestation of rosacea that affects the eyes and eyelids. Signs and symptoms generally consist of redness, irritation or burning of the eyes. Affected individuals may also feel that there is something, such as an eyelash, i ...

(ophthalmic rosacea, ophthalmorosacea) * Otophyma *

Periorificial dermatitis Perioral dermatitis, also known as periorificial dermatitis, is a common type of skin rash. Symptoms include multiple small (1–2 mm) bumps and blisters sometimes with background redness and scale, localized to the skin around the mouth and ...

Persistent edema of rosacea Persistent edema of rosacea (also known as chronic upper facial erythematous edema, Morbihan's disease or rosaceous lymphedema) is a hard, nonpitting edema found on the areas involved, those mainly being the forehead, glabella, upper eyelids, nose, ...

(chronic upper facial erythematous edema, Morbihan's disease, rosaceous lymphedema) *

Phymatous rosacea Rosacea is a long-term skin condition that typically affects the face. It results in redness, pimples, swelling, and small and superficial dilated blood vessels. Often, the nose, cheeks, forehead, and chin are most involved. A red, enlarge ...

* Pomade acne *

Papulopustular rosacea Rosacea is a long-term skin condition that typically affects the face. It results in redness, pimples, swelling, and small and superficial dilated blood vessels. Often, the nose, cheeks, forehead, and chin are most involved. A red, enlarge ...

(inflammatory rosacea) *

Perifolliculitis capitis abscedens et suffodiens Dissecting cellulitis of the scalp, also known as dissecting folliculitis, perifolliculitis capitis abscedens et suffodiens of Hoffman, perifolliculitis abscedens et suffodiens, or folliculitis abscedens et suffodiens, is an inflammatory condition ...

(dissecting cellulitis of the scalp, dissecting folliculitis, perifolliculitis capitis abscedens et suffodiens of Hoffman) *

Perioral dermatitis Perioral dermatitis, also known as periorificial dermatitis, is a common type of skin rash. Symptoms include multiple small (1–2 mm) bumps and blisters sometimes with background redness and scale, localized to the skin around the mouth and ...

* Periorbital dermatitis (periocular dermatitis) *

Pyoderma faciale Rosacea is a long-term skin condition that typically affects the face. It results in redness, pimples, swelling, and small and superficial dilated blood vessels. Often, the nose, cheeks, forehead, and chin are most involved. A red, enlarge ...

(rosacea fulminans) *

Rhinophyma Rhinophyma is a condition causing development of a large, bulbous nose associated with granulomatous infiltration, commonly due to untreated rosacea. The condition is most common in older white males. Colloquial terms for the rhinophyma includ ...

Rosacea Rosacea is a long-term skin condition that typically affects the face. It results in redness, pimples, swelling, and small and superficial dilated blood vessels. Often, the nose, cheeks, forehead, and chin are most involved. A red, enlarg ...

(acne rosacea) *

Rosacea conglobata Rosacea is a long-term skin condition that typically affects the face. It results in redness, pimples, swelling, and small and superficial dilated blood vessels. Often, the nose, cheeks, forehead, and chin are most involved. A red, enlarge ...

* Synovitis–acne–pustulosis–hyperostosis–osteomyelitis syndrome (SAPHO syndrome)Abbreviations for condition names commonly described in medical literature with an acronym or initialism are included within this list. * Steroid rosacea * Tar acne * Tropical acne

Autoinflammatory syndromes

Autoinflammatory syndromes Periodic fever syndromes are a set of disorders characterized by recurrent episodes of systemic and organ-specific inflammation. Unlike autoimmune disorders such as systemic lupus erythematosus, in which the disease is caused by abnormalities of t ...

are a group of inherited disorders characterized by bouts of inflammatory

s and periodic

fevers Fever, also referred to as pyrexia, is defined as having a temperature above the normal range due to an increase in the body's temperature set point. There is not a single agreed-upon upper limit for normal temperature with sources using val ...

. *

Blau syndrome Blau syndrome is an autosomal dominant genetic inflammatory disorder which affects the skin, eyes, and joints. It is caused by a mutation in the ''NOD2'' (''CARD15'') gene. Symptoms usually begin before the age of four, and the disease manifests ...

* Chronic infantile neurologic cutaneous and articular syndrome *

Familial cold urticaria Cold urticaria (essentially meaning cold hives) is a disorder in large red welts called hives (''urticaria'') form on the skin after exposure to a cold stimulus. The hives are usually itchy and often the hands and feet will become itchy and swolle ...

(familial cold autoinflammatory syndrome) *

Familial Mediterranean fever Familial Mediterranean fever (FMF) is a hereditary inflammatory disorder. FMF is an autoinflammatory disease caused by mutations in Mediterranean fever gene, which encodes a 781–amino acid protein called pyrin. While all ethnic groups are sus ...

Hyper-IgD syndrome Mevalonate kinase deficiency (MKD) is an autosome, autosomal Dominance (genetics), recessive metabolic disorder that disrupts the biosynthesis of cholesterol and isoprenoids. It is a Rare genetic disease, very rare genetic disease. It is charact ...

Within this list, the term immunoglobulin is abbreviated to Ig when used as a prefix to a specific antibody isotype (i.e. IgA, IgD,

IgE Immunoglobulin E (IgE) is a type of antibody (or immunoglobulin (Ig) " isotype") that has been found only in mammals. IgE is synthesised by plasma cells. Monomers of IgE consist of two heavy chains (ε chain) and two light chains, with the ε c ...

IgG Immunoglobulin G (Ig G) is a type of antibody. Representing approximately 75% of serum antibodies in humans, IgG is the most common type of antibody found in blood circulation. IgG molecules are created and released by plasma B cells. Each IgG ...

, and

IgM Immunoglobulin M (IgM) is one of several isotypes of antibody (also known as immunoglobulin) that are produced by vertebrates. IgM is the largest antibody, and it is the first antibody to appear in the response to initial exposure to an antig ...

). *

Majeed syndrome Majeed syndrome is an inherited skin disorder characterized by chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and a neutrophilic dermatosis. It is classified as an autoinflammatory bone disorder. The condition i ...

Muckle–Wells syndrome Muckle–Wells syndrome (MWS) is a rare autosomal dominant disease which causes sensorineural deafness and recurrent hives, and can lead to amyloidosis. Individuals with MWS often have episodic fever, chills, and joint pain. As a result, MWS is ...

TNF receptor associated periodic syndrome TNF receptor associated periodic syndrome (TRAPSsubscription needed) is a periodic fever syndrome associated with mutations in a receptor for the molecule tumor necrosis factor (TNF) that is inheritable in an autosomal dominant manner. Individua ...

(familial Hibernian fever, TRAPS, tumor necrosis factor receptor associated periodic syndrome)

Chronic blistering

Chronic blistering cutaneous conditions have a prolonged course and present with

vesicles Vesicle may refer to: ; In cellular biology or chemistry * Vesicle (biology and chemistry), a supramolecular assembly of lipid molecules, like a cell membrane * Synaptic vesicle ; In human embryology * Vesicle (embryology), bulge-like features o ...

and bullae. *

Adult linear IgA disease Linear IgA bullous dermatosis is a rare immune-mediated blistering skin disease frequently associated with medication exposure, especially vancomycin, with men and women being equally affected.James, William; Berger, Timothy; Elston, Dirk (2005). ' ...

Bullous pemphigoid Bullous pemphigoid (type of pemphigoid) is an autoimmune pruritic skin disease which typically occurs in people aged over 60, that may involve the formation of blisters ( bullae) in the space between the epidermal and dermal skin layers. It i ...

Bullous lupus erythematosus Lupus erythematosus is a collection of autoimmune diseases in which the human immune system becomes hyperactive and attacks healthy tissues. Symptoms of these diseases can affect many different body systems, including joints, skin, kidneys, bl ...

* Childhood linear IgA disease (chronic bullous disease of childhood) *

Cicatricial pemphigoid Mucous membrane pemphigoid is a rare chronic autoimmune subepithelial blistering disease characterized by erosive lesions of the mucous membranes and skin. It is one of the pemphigoid diseases that can result in scarring. Signs and symptoms Th ...

(benign mucosal pemphigoid, benign mucous membrane pemphigoid, ocular pemphigus, scarring pemphigoid) *

Dermatitis herpetiformis Dermatitis herpetiformis (DH) is a chronic autoimmune blistering skin condition, characterised by intensely itchy blisters filled with a watery fluid. DH is a cutaneous manifestation of coeliac disease, although the exact causal mechanism is not k ...

(Duhring disease) *

Endemic pemphigus Pemphigus foliaceus is an autoimmune blistering disease ( bullous disorder) of the skin. Pemphigus foliaceus causes a characteristic inflammatory attack at the subcorneal layer of epidermis, which results in skin lesions that are scaly or crusted ...

(endemic pemphigus foliaceus, fogo selvagem) *

Epidermolysis bullosa acquisita Epidermolysis bullosa acquisita, also known as acquired epidermolysis bullosa, is a longterm autoimmune blistering skin disease. It generally presents with fragile skin that blisters and becomes red with or without trauma. Marked scarring is left w ...

Grover's disease Grover's disease (GD) is a polymorphic, pruritic, papulovesicular dermatosis characterized histologically by acantholysisFreedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. . with or without dyskera ...

(benign papular acantholytic dermatosis, persistent acantholytic dermatosis, transient acantholytic dermatosis) Grover's disease, advanced case

IgA pemphigus IgA pemphigus is a subtype of pemphigus with two distinct forms: * ''Subcorneal pustular dermatosis'' (also known as Sneddon–Wilkinson disease and pustulosis subcornealis) is skin condition that is a rare, chronic, recurrent, pustular eruption ...

* Intraepidermal neutrophilic IgA dermatosis *

Localized cicatricial pemphigoid Mucous membrane pemphigoid is a rare chronic autoimmune subepithelial blistering disease characterized by erosive lesions of the mucous membranes and skin. It is one of the pemphigoid diseases that can result in scarring. Signs and symptoms The ...

(Brunsting–Perry cicatricial pemphigoid) *

Paraneoplastic pemphigus Paraneoplastic pemphigus (PNP) is an autoimmune disorder stemming from an underlying tumor. It is hypothesized that antigens associated with the tumor trigger an immune response resulting in blistering of the skin and mucous membranes. While pati ...

* Pemphigus erythematosus (Senear–Usher syndrome) *

Pemphigus foliaceus Pemphigus foliaceus is an autoimmune blistering disease ( bullous disorder) of the skin. Pemphigus foliaceus causes a characteristic inflammatory attack at the subcorneal layer of epidermis, which results in skin lesions that are scaly or cruste ...

Pemphigus herpetiformis Pemphigus herpetiformis is a cutaneous condition, a clinical variant of pemphigus that combines the clinical features of dermatitis herpetiformis with the immunopathologic features of pemphigus. Pathophysiology Pemphigus Herpetiformis is an IGg ...

(acantholytic herpetiform dermatitis, herpetiform pemphigus, mixed bullous disease, pemphigus controlled by sulfapyridine) * Pemphigoid nodularis * Pemphigus vegetans * Pemphigus vegetans of Hallopeau * Pemphigus vegetans of Neumann * Pemphigus vulgaris * Vesicular pemphigoid *

Vulvar childhood pemphigoid Vulvar childhood pemphigoid is a cutaneous condition, a childhood form of bullous pemphigoid, peculiar variant with involvement of the genital area and perineum. See also * Vesicular pemphigoid * List of cutaneous conditions Many skin con ...

Conditions of the mucous membranes

Conditions of the

mucous membranes A mucous membrane or mucosa is a membrane that lines various cavities in the body of an organism and covers the surface of internal organs. It consists of one or more layers of epithelial cells overlying a layer of loose connective tissue. It is ...

involve the moist linings of the eyes, nose, mouth, genitals, and anus. * Acatalasia (acatalasemia, Takahara's disease) *

Acquired dyskeratotic leukoplakia Oral leukoplakia is a ''potentially malignant disorder'' affecting the oral mucosa. It is defined as "essentially an oral mucosal white lesion that cannot be considered as any other definable lesion." Oral leukoplakia is a white patch or plaque th ...

* Actinic cheilitis (actinic cheilosis) *

Acute necrotizing ulcerative gingivitis Acute necrotizing ulcerative gingivitis (ANUG) is a common, non-contagious infection of the gums with sudden onset. The main features are painful, bleeding gums, and ulceration of inter-dental papillae (the sections of gum between adjacent teeth ...

(acute membranous gingivitis, acute necrotizing ulcerative gingivostomatitis, fusospirillary gingivitis, fusospirillosis, fusospirochetal gingivitis, necrotizing gingivitis, phagedenic gingivitis, trench mouth, ulcerative gingivitis, Vincent gingivitis, Vincent infection, Vincent stomatitis, Vincent's disease) *

Allergic contact cheilitis Cheilitis is a medical condition characterized by inflammation of the lips. The inflammation may include the perioral skin (the skin around the mouth), the vermilion border, or the labial mucosa. The skin and the vermilion border are more commo ...

Angina bullosa haemorrhagica Angina bullosa haemorrhagica is a condition of the mucous membranes characterized by the sudden appearance of one or more blood blisters within the oral cavity. The lesions, which may be caused by mild trauma to the mouth tissues such as hot food ...

Angular cheilitis Angular cheilitis (AC) is inflammation of one or both corners of the mouth. Often the corners are red with skin breakdown and crusting. It can also be itchy or painful. The condition can last for days to years. Angular cheilitis is a type of ch ...

(''perlèche'') *

Behçet's disease Behçet's disease (BD) is a type of inflammatory disorder which affects multiple parts of the body. The most common symptoms include painful sores on the mucous membranes of the mouth and other parts of the body, inflammation of parts of the ey ...

(Behçet's syndrome, oculo-oral-genital syndrome) *

Black hairy tongue Black hairy tongue syndrome (BHT) is a condition of the tongue in which the small bumps on the tongue elongate with black or brown discoloration, giving a black and hairy appearance. The appearance may be alarming, but it is a harmless condit ...

(hairy tongue, lingua villosa nigra) Black tongue

Caviar tongue Caviar tongue is a condition characterized by the purplish nodular swelling of veins found on the undersurface of the tongue. It is normal for there to be veins visible underneath the tongue, partly because the mucous membrane is so thin and ...

* Cheilitis exfoliativa *

Cheilitis glandularis Cheilitis is a medical condition characterized by inflammation of the lips. The inflammation may include the perioral skin (the skin around the mouth), the vermilion border, or the labial mucosa. The skin and the vermilion border are more commo ...

Cheilitis granulomatosa Orofacial granulomatosis (OFG) is a condition characterized by persistent enlargement of the soft tissues of the mouth, lips and the area around the mouth on the face, causing in most cases extreme pain. The mechanism of the enlargement is granulom ...

(granulomatous cheilitis, orofacial granulomatosis) *

Cutaneous sinus of dental origin A cutaneous sinus of dental origin is where a dental infection drains onto the surface of the skin of the face or neck. This is uncommon as usually dental infections drain into the mouth, typically forming a parulis ("gumboil"). Cutaneous sinuses ...

(dental sinus) *

Cyclic neutropenia Cyclic neutropenia (CyN) is a rare hematologic disorder and form of congenital neutropenia that tends to occur approximately every three weeks and lasting for few days at a time due to changing rates of neutrophil production by the bone marrow. It ...

Desquamative gingivitis Desquamative gingivitis is an erythematous (red), desquamatous (shedding) and ulcerated appearance of the gums. It is a descriptive term and can be caused by several different disorders. Signs and symptoms Desquamative gingivitis involves lesions ...

* Drug-induced ulcer of the lip * Epidermization of the lip *

Epulis Epulis ( gr, ἐπουλίς; plural ''epulides'') is any tumor like enlargement (i.e. lump) situated on the gingival or alveolar mucosa. The word literally means "(growth) on the gingiva", and describes only the location of the mass and has no fu ...

* Epulis fissuratum (granuloma fissuratum) * Eruptive lingual papillitis * Erythroplakia (erythroplasia) *

Fissured tongue Fissured tongue is a benign condition characterized by deep grooves (fissures) in the dorsum of the tongue. Although these grooves may look unsettling, the condition is usually painless. Some individuals may complain of an associated burning sen ...

(furrowed tongue, lingua plicata, plicated tongue, scrotal tongue) *

Geographic tongue Geographic tongue, also known by several other terms, is a condition of the mucous membrane of the tongue, usually on the dorsal surface. It is a common condition, affecting approximately 2–3% of the general population. It is characterized by a ...

(benign migratory glossitis, benign migratory stomatitis, glossitis areata exfoliativa, glossitis areata migrans, lingua geographica, stomatitis areata migrans, transitory benign plaques of the tongue) * Gingival fibroma *

Gingival hypertrophy Gingival enlargement is an increase in the size of the gingiva (gums). It is a common feature of gingival disease. Gingival enlargement can be caused by a number of factors, including inflammatory conditions and the side effects of certain medica ...

Hairy leukoplakia Hairy leukoplakia is a white patch on the side of the tongue with a corrugated or hairy appearance. It is caused by Epstein-Barr virus (EBV) and occurs usually in persons who are immunocompromised, especially those with human immunodeficiency v ...

(oral hairy leukoplakia) *

Intraoral dental sinus Intraoral dental sinus (also termed a parulis and commonly, a gumboil) is an oral lesion characterized by a soft erythematous papule (red spot) that develops on the alveolar process in association with a non-vital tooth and accompanying dental abs ...

* Linea alba *

Leukoplakia Oral leukoplakia is a ''potentially malignant disorder'' affecting the oral mucosa. It is defined as "essentially an oral mucosal white lesion that cannot be considered as any other definable lesion." Oral leukoplakia is a white patch or plaque th ...

Leukoplakia with tylosis and esophageal carcinoma Oral leukoplakia is a ''potentially malignant disorder'' affecting the oral mucosa. It is defined as "essentially an oral mucosal white lesion that cannot be considered as any other definable lesion." Oral leukoplakia is a white patch or plaque th ...

* Major aphthous ulcer (periadenitis mucosa necrotica recurrens) *

Median rhomboid glossitis Median rhomboid glossitis is a condition characterized by an area of redness and loss of lingual papillae on the central dorsum of the tongue, sometimes including lesions of the tongue and palate. It is seen in patients using inhaled steroids a ...

(central papillary atrophy) *

Melanocytic oral lesion Melanocytic oral lesions are an extremely uncommon condition characterized by pigmented lesions of the mucous membranes. See also * List of cutaneous conditions * Mucosal squamous cell carcinoma * Mucous membrane * Oral florid papillomatosis Or ...

Melkersson–Rosenthal syndrome Melkersson–Rosenthal syndrome is a rare neurological disorder characterized by recurring facial paralysis, swelling of the face and lips (usually the upper lip: cheilitis granulomatosis) and the development of folds and furrows in the tongue ( ...

Morsicatio buccarum Morsicatio buccarum is a condition characterized by chronic irritation or injury to the buccal mucosa (the lining of the inside of the cheek within the mouth), caused by repetitive chewing, biting or nibbling. Signs and symptoms The lesions are ...

(chronic cheek biting, chronic cheek chewing) * Mucosal squamous cell carcinoma *

Mucous cyst of the oral mucosa Oral mucocele (also mucous extravasation cyst, mucous cyst of the oral mucosa, and mucous retention and extravasation phenomena.) is a condition caused by two related phenomena - mucus extravasation phenomenon and mucous retention cyst. Mucous e ...

(mucocele) * Nagayama's spots * Oral Crohn's disease * Oral florid papillomatosis *

Oral melanosis Oral pigmentation is asymptomatic and does not usually cause any alteration to the texture or thickness of the affected area. The colour can be uniform or speckled and can appear solitary or as multiple lesions. Depending on the site, depth, and qua ...

* Osseous choristoma of the tongue * Peripheral ameloblastoma * Plasma cell cheilitis (plasma cell gingivitis, plasma cell orificial mucositi) *

Plasmoacanthoma Plasmoacanthoma is a condition of the oral mucosa characterized by a verrucous tumor with a plasma cell infiltrate. See also * Plasma cell cheilitis * Skin lesion A skin condition, also known as cutaneous condition, is any medical conditi ...

* Proliferative verrucous leukoplakia *

Pyogenic granuloma A pyogenic granuloma or lobular capillary hemangioma is a vascular tumor that occurs on both mucosa and skin, and appears as an overgrowth of tissue due to irritation, physical trauma, or hormonal factors. It is often found to involve the gums ...

(eruptive hemangioma, granulation tissue-type hemangioma, granuloma gravidarum, lobular capillary hemangioma, pregnancy tumor, tumor of pregnancy) Pyogenic granuloma on a finger-1

* Pyostomatitis vegetans *

Recurrent aphthous stomatitis Recurrence and recurrent may refer to: *''Disease recurrence'', also called relapse *''Eternal recurrence'', or eternal return, the concept that the universe has been recurring, and will continue to recur, in a self-similar form an infinite number ...

(aphthosis, canker sores, recurrent oral aphthae) *

Recurrent intraoral herpes simplex infection Recurrence and recurrent may refer to: *''Disease recurrence'', also called relapse *''Eternal recurrence'', or eternal return, the concept that the universe has been recurring, and will continue to recur, in a self-similar form an infinite number ...

Smooth tongue Glossitis can mean soreness of the tongue, or more usually inflammation with depapillation of the dorsal surface of the tongue (loss of the lingual papillae), leaving a smooth and erythematous (reddened) surface, (sometimes specifically termed atro ...

(atrophic glossitis, bald tongue, hunter glossitis, moeller) *

Stomatitis nicotina Stomatitis nicotina is a diffuse white patch on the hard palate, usually caused by tobacco smoking, usually pipe or cigar smoking. It is painless, and it is caused by a response of the palatal oral mucosa to chronic heat. A more pronounced appeara ...

(nicotine stomatitis, smoker's keratosis, smoker's patches) *

Torus palatinus A torus palatinus (pl. tori palatini), or palatal torus (pl. palatal tori), is a bony protrusion on the palate. Palatal tori are usually present on the midline of the hard palate.Neville, B.W., D. Damm, C. Allen, J. Bouquot. ''Oral & Maxillofaci ...

Trumpeter's wart A trumpeter's wart is a cutaneous Skin is the layer of usually soft, flexible outer tissue covering the body of a vertebrate animal, with three main functions: protection, regulation, and sensation. Other animal coverings, such as the arth ...

* Vestibular papillomatosis *

White sponge nevus White sponge nevus (WSN) is an autosomal dominant condition of the oral mucosa (the mucous membrane lining of the mouth). It is caused by a mutations in certain genes coding for keratin, which causes a defect in the normal process of keratinizati ...

(white sponge nevus of Cannon)

Conditions of the skin appendages

Conditions of the

skin appendages Skin appendages (or adnexa of skin) are anatomical skin-associated structures that serve a particular function including sensation, contractility, lubrication and heat loss in animals. In humans, some of the more common skin appendages are hairs ...

are those affecting the glands of the skin, hair, nails, and arrector pili muscles. * Acne necrotica * Acquired generalized hypertrichosis (acquired hypertrichosis lanuginosa, hypertrichosis lanuginosa acquisita) * Acquired perforating dermatosis (acquired perforating collagenosis) *

Acrokeratosis paraneoplastica of Bazex Paraneoplastic acrokeratosis, or Bazex syndrome is a cutaneous condition characterized by wikt:psoriasiform, psoriasiform changes of hands, feet, ears, and nose, with involvement of the nails and periungual tissues being characteristic and indis ...

(acrokeratosis neoplastica, Bazex syndrome) *

Acroosteolysis Acroosteolysis is resorption of the distal bony phalanges. Acroosteolysis has two patterns of resorption in adults: diffuse and bandlike. The diffuse pattern of resorption has a widely diverse differential diagnosis which includes: pyknod ...

Acute paronychia Paronychia is an inflammation of the skin around the nail, which can occur suddenly, when it is usually due to the bacterium '' Staphylococcus aureus'', or gradually when it is commonly caused by the fungus ''Candida albicans''. The term is fr ...

Alopecia areata Alopecia areata, also known as spot baldness, is a condition in which hair is lost from some or all areas of the body. Often, it results in a few bald spots on the scalp, each about the size of a coin. Psychological stress and illness are pos ...

Alopecia neoplastica Alopecia neoplastica may present as a scarring alopecia, appearing anywhere on the scalp, and it has been described with cutaneous metastasis from breast, gastric, lung, renal and pancreatic carcinomas. See also * Alopecia areata Alopecia ...

Anagen effluvium Anagen effluvium is the pathologic loss of anagen or growth-phase hairs. Classically, it is caused by radiation therapy to the head and systemic chemotherapy, especially with alkylating agents.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology ...

* Androgenic alopecia (androgenetic alopecia) *

Anhidrosis Hypohidrosis is a disorder in which a person exhibits diminished sweating in response to appropriate stimuli. In contrast with hyp''er''hidrosis, which is a socially troubling yet often benign condition, the consequences of untreated hypohidrosi ...

(hypohidrosis) * Anonychia *

Apparent leukonychia Apparent leukonychia is a cutaneous condition characterized by white discoloration of the nail that fades with pressure. See also * Nail anatomy A nail is a claw-like plate found at the tip of the Finger, fingers and Toe, toes on most primate ...

* Beau's lines * Blue nails * Bromidrosis (apocrine bromhidrosis, fetid sweat, malodorous sweating, osmidrosis) * Bubble hair deformity * Central centrifugal cicatricial alopecia (follicular degeneration syndrome, pseudopelade of the central scalp) * Chevron nail (herringbone nail) * Chromhidrosis (colored sweat) *

Chronic paronychia Paronychia is an inflammation of the skin around the nail, which can occur suddenly, when it is usually due to the bacterium '' Staphylococcus aureus'', or gradually when it is commonly caused by the fungus ''Candida albicans''. The term is fr ...

Cicatricial alopecia Scarring hair loss, also known as cicatricial alopecia, is the loss of hair which is accompanied with scarring. This is in contrast to non scarring hair loss. It can be caused by a diverse group of rare disorders that destroy the hair follicle, ...

* Clubbing (drumstick fingers, Hippocratic fingers, watch-glass nails) * Congenital onychodysplasia of the index fingers * Disseminate and recurrent infundibulofolliculitis *

Erosive pustular dermatitis of the scalp Erosive pustular dermatitis of the scalp presents with pustules, erosions, and crusts on the scalp of primarily older Caucasian females, and on biopsy, has a lymphoplasmacytic infiltrate with or without foreign body giant cells and pilosebaceous a ...

(erosive pustular dermatosis of the scalp) *

Erythromelanosis follicularis faciei et colli Erythromelanosis follicularis faciei et colli is an erythematous pigmentary disease involving the follicles, characterized by a reddish-brown, sharply demarcated, symmetrical discoloration involving the preauricular and maxillary regions.James, Wil ...

* Folliculitis decalvans * Folliculitis nares perforans * Fox–Fordyce disease *

Frontal fibrosing alopecia Frontal fibrosing alopecia is the frontotemporal hair loss, hairline recession and eyebrow loss in postmenopausal women that is associated with perifollicular erythema, especially along the hairline.Freedberg, et al. (2003). ''Fitzpatrick's Derma ...

* Generalized congenital hypertrichosis (congenital hypertrichosis lanuginosa) *

Generalized hyperhidrosis Hyperhidrosis is a condition characterized by abnormally increased sweating, in excess of that required for regulation of body temperature. Although primarily a benign physical burden, hyperhidrosis can deteriorate quality of life from a psychologi ...

Graham-Little syndrome Graham-Little syndrome is a cutaneous condition characterized by lichen planus-like skin lesion A skin condition, also known as cutaneous condition, is any medical condition that affects the integumentary system—the organ system that enclo ...

* Granulosis rubra nasi *

Green nails Green nails may be (1) due to a ''Pseudomonas aeruginosa'' infection causing a green nail syndrome or (2) the result of copper in tap water.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatolog ...

Gustatory hyperhidrosis Gustatory hyperhidrosis is excessive sweating classified under focal hyperhidrosis, that is, it is restricted to certain regions of the body. Affected people regularly experience this on the forehead (scalp), upper lip, perioral region, or sternum ...

* Hair casts (pseudonits) *

Hair follicle nevus Hair follicle nevus is a cutaneous condition that presents as a small papule from which fine hairs protrude evenly from the surface. Signs and symptoms Hair follicle nevus usually presents as a single, skin-colored papule or nodule on the face ...

(vellus hamartoma) *

Hairy palms and soles Hairy palms and soles are both a type of cutaneous condition characterized by a hereditary hypertrichosis affecting the palms and soles. This condition is inherited in an autosomal dominant fashion. See also * List of cutaneous conditions * ...

* Half and half nails (Lindsay's nails) *

Hangnail A hangnail is a tiny, torn piece of skin next to a fingernail or toenail, related to ingrown nails. The hangnail's other scientific names are: eponychium or paronychium. Hangnails are typically caused by having dry skin, or by trauma to the fin ...

* Hapalonychia *

Hematidrosis Hematidrosis, also called blood sweat, is a very rare condition in which a human sweats blood. The term is from Ancient Greek ''haîma/haímatos'' ( αἷμα/ αἵματος), meaning blood, and ''hīdrṓs'' ( ἱδρώς), meaning sweat. Sig ...

Hirsutism Hirsutism is excessive body hair on parts of the body where hair is normally absent or minimal. The word is from early 17th century: from Latin ''hirsutus'' meaning "hairy". It usually refers to a "male" pattern of hair growth in a female that ...

* Hook nail * Hot comb alopecia * Hypertrichosis cubiti (hairy elbow syndrome) *

Hypertrichosis simplex of the scalp Hypertrichosis simplex of the scalp is a cutaneous condition caused by defects in the corneodesmosin protein. See also * Hairy elbow syndrome * List of cutaneous conditions * List of conditions caused by problems with junctional proteins M ...

* Intermittent hair–follicle dystrophy *

Keratosis pilaris atrophicans Keratosis pilaris atropicans includes many forms of keratosis pilaris with cicatricial alopecia.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. . Variants include ...

* Kinking hair (acquired progressive kinking) *

Koenen's tumor Koenen's tumor (KT), also commonly termed periungual angiofibroma,Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. . is a subtype of the angiofibromas. Angiofibromas are benign papule, nodule, an ...

(Koenen's periungual fibroma, periungual fibroma) *

Koilonychia Koilonychia, also known as spoon nails,James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. . is a nail disease that can be a sign of hypochromic anemia, especially ...

(spoon nails) *

Kyrle disease Kyrle disease is identified as a form of an acquired perforating disease. Other major perforating diseases are elastosis perforans serpiginosa and reactive perforating collagenosis. Recently, however, there is a controversy on categorizing Kyrle d ...

Leukonychia Leukonychia (or leuconychia) is a medical term for white discoloration appearing on nails.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. pp. 658–59. . It is derived from the Greek words ''l ...

(white nails) *

Lichen planopilaris Lichen planus (LP) is a chronic inflammatory and immune-mediated disease that affects the skin, nails, hair, and mucous membranes. It is not an actual lichen, and is only named that because it looks like one. It is characterized by polygonal, fla ...

(acuminatus, follicular lichen planus, lichen planus follicularis, peripilaris) *

Lichen planus of the nails Lichen planus (LP) is a chronic inflammatory and immune-mediated disease that affects the skin, nails, hair, and mucous membranes. It is not an actual lichen, and is only named that because it looks like one. It is characterized by polygonal, fla ...

* Lichen spinulosus (keratosis spinulosa) * Lipedematous alopecia (lipedematous scalp) *

Localized acquired hypertrichosis Local may refer to: Geography and transportation * Local (train), a train serving local traffic demand * Local, Missouri, a community in the United States * Local government, a form of public administration, usually the lowest tier of administra ...

* Localized congenital hypertrichosis * Longitudinal erythronychia * Longitudinal melanonychia *

Loose anagen syndrome Loose anagen syndrome, also known as loose anagen hair syndrome, is a hair disorder related to dermatology. It is characterised by the easy and pain free detachment of anagen staged hairs from the scalp. This hair condition can be spontaneous or g ...

(loose anagen hair syndrome) *

Lupus erythematosus Lupus erythematosus is a collection of autoimmune diseases in which the human immune system becomes hyperactive and attacks healthy tissues. Symptoms of these diseases can affect many different body systems, including joints, skin, kidneys, blo ...

Madarosis Madarosis is a condition that results in the loss of eyelashes, and sometimes eyebrows. The term "madarosis" is derived from the ancient Greek "madaros", meaning "bald". It originally was a disease of only losing eyelashes but it currently is the ...

* Malalignment of the nail plate * Male-pattern baldness * Marie–Unna hereditary hypotrichosis (Marie–Unna hypotrichosis) * Median nail dystrophy (dystrophia unguis mediana canaliformis, median canaliform dystrophy of Heller, solenonychia) * Mees' lines *

Melanonychia Melanonychia is a black or brown pigmentation of the normal nail plate, and may be present as a normal finding on many digits in Afro-Caribbeans, as a result of trauma, systemic disease, or medications, or as a postinflammatory event from such local ...

Menkes kinky hair syndrome Menkes is a surname. Notable people with the surname include: *John Menkes (1928– 2008), Austrian-American pediatric neurologist and author of fictional novels and plays *Murray Menkes (died 2013), Canadian property developer *Nina Menkes (born ...

(kinky hair disease, Menkes disease) *

Monilethrix Monilethrix (also referred to as beaded hair) is a rare autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded. It comes from the Latin word for necklace (''monile'') and the Greek word for hair (''thrix'' ...

(beaded hair) * Muehrcke's nails (Muehrcke's lines) *

Nail–patella syndrome Nail–patella syndrome is a genetic disorder that results in small, poorly developed nails and kneecaps, but can also affect many other areas of the body, such as the elbows, chest, and hips. The name "nail–patella" can be very misleading bec ...

(Fong syndrome, hereditary osteoonychodysplasia, HOOD syndrome) * Neoplasms of the nailbed * Nevoid hypertrichosis *

Noncicatricial alopecia Non scarring hair loss, also known as noncicatricial alopecia is the loss of hair without any scarring being present.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders ...

Onychauxis Onychauxis presents with thickened nails without deformity, and this simple thickening may be the result of trauma, acromegaly, Darier's disease, psoriasis, or pityriasis rubra pilaris, or, in some cases, hereditary.James, William; Berger, Timothy ...

Onychoatrophy Onychoatrophy is a faulty underdevelopment of the nail that may be congenital A birth defect, also known as a congenital disorder, is an abnormal condition that is present at birth regardless of its cause. Birth defects may result in disabiliti ...

* Onychocryptosis (ingrown nail, unguis incarnatus) *

Onychogryphosis Onychogryphosis is a hypertrophy that may produce nails resembling claws or a ram's horn. Causes Onychogryphosis may be caused by trauma or peripheral vascular disease, but most often secondary to self-neglect and failure to cut the nails for ...

(ram's horn nails) *

Onycholysis Onycholysis is a common medical condition characterized by the painless detachment of the nail from the nail bed, usually starting at the tip and/or sides. On the hands, it occurs particularly on the ring finger but can occur on any of the fingern ...

* Onychomadesis * Onychomatricoma * Onychophagia (nail biting) * Onychophosis *

Onychoptosis defluvium Onychoptosis defluvium (also known as "Alopecia unguium") is casting off the nail seen in association with alopecia areata.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. . See also * Nail (anato ...

(alopecia unguium) *

Onychorrhexis Onychorrhexis (from the Greek words ὄνυχο- ''ónycho-'', "nail" and ῥῆξις ''rhexis'', "bursting"), is a brittleness with breakage of finger or toenails that may result from hypothyroidism, anemia, anorexia nervosa or bulimia, or aft ...

(brittle nails) *

Onychoschizia Onychoschizia, also known as nail splitting and brittle nails, is a splitting of the free-edged tip of the Nail (anatomy), nail. There is also often a longitudinal split in addition to the separation of keratin layers. Cause Frequent hand-washing ...

* Onychotillomania * Ophiasis *

Palmoplantar hyperhidrosis A palmoplantar hyperhidrosis is excessive sweating localized to the palms of the hands and soles of the feet. It is a form of focal hyperhidrosis in that the excessive sweating is limited to a specific region of the body. As with other types of foc ...

(emotional hyperhidrosis) * Parakeratosis pustulosa * Patterned acquired hypertrichosis * Perforating folliculitis * Pili annulati (ringed hair) *

Pili bifurcati Pili bifurcati is characterized by bifurcation found in short segments along the shafts of several hairs, with each branch of the bifurcation being covered with its own cuticle.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Disea ...

Pili multigemini Pili multigemini, also known as "compound hairs," is a malformation characterized by the presence of bifurcated or multiple divided hair matrices and Hair follicle, papillae, giving rise to the formation of multiple hair shafts within the individu ...

* Pili pseudoannulati (pseudo pili annulati) * Pili torti (twisted hairs) * Pincer nails (omega nails, trumpet nails) * Pityriasis amiantacea (tinea amiantacea) * Platonychia * Plica neuropathica (felted hair) * Plummer's nail *

Premature greying of hair Premature greying of hair (PGH), also known as canities, can have negative effects on appearance, self-confidence, self-esteem, and social acceptance of the affected individual. Hair is said to have greyed prematurely if it occurs before the age of ...

Prepubertal hypertrichosis Prepubertal hypertrichosis, also known as childhood hypertrichosis, is a cutaneous condition characterized by increased hair growth, found in otherwise healthy infants and children. Prepubertal hypertrichosis is a cosmetic condition and does not af ...

Pressure alopecia Pressure alopecia (also known as "Postoperative alopecia," and "Pressure-induced alopecia") occurs in adults after prolonged pressure on the scalp during general anesthesia, with the head fixed in one position, and may also occur in chronically ill ...

(postoperative alopecia, pressure-induced alopecia) *

Pseudofolliculitis barbae Pseudofolliculitis barbae (PFB) is a persistent irritation caused by shaving. It was first described in 1956. Signs and symptoms Related conditions Razor burn is a less serious condition caused by shaving, characterized by mild to moderate rednes ...

(barber's itch, folliculitis barbae traumatica, razor bumps, scarring pseudofolliculitis of the beard, shave bumps) * Pseudopelade of Brocq (alopecia cicatrisata) * Psoriatic nails * Pterygium inversum unguis (pterygium inversus unguis, ventral pterygium) * Pterygium unguis (dorsal pterygium) * Purpura of the nail bed * Racquet nail (brachyonychia, ''nail en raquette'', racquet thumb) * Recurrent palmoplantar hidradenitis (idiopathic palmoplantar hidradenitis, idiopathic plantar hidradenitis, painful plantar erythema, palmoplantar eccrine hidradenitis, plantar panniculitis) * Red lunulae *

Ross' syndrome Ross' syndrome consists of Adie's syndrome Adie syndrome, also known as Holmes-Adie syndrome, is a neurological disorder characterized by a tonically dilated pupil that reacts slowly to light but shows a more definite response to accommodati ...

Rubinstein–Taybi syndrome Rubinstein–Taybi syndrome (RTS) is a rare genetic condition characterized by short stature, moderate to severe learning difficulties, distinctive facial features, and broad thumbs and first toes. Other features of the disorder vary among affect ...

* Setleis syndrome * Shell nail syndrome * Short anagen syndrome * Splinter hemorrhage

Spotted lunulae Spotted lunulae is a distinctive change that occurs with alopecia areata Alopecia areata, also known as spot baldness, is a condition in which hair is lost from some or all areas of the body. Often, it results in a few bald spots on the scalp ...

* Staining of the nail plate * Stippled nails *

Subungual hematoma A subungual hematoma is a collection of blood (hematoma) underneath a toenail or fingernail. It can be extremely painful for an injury of its size, although otherwise it is not a serious medical condition. Nature A laceration of the nail bed c ...

Telogen effluvium Telogen effluvium is a scalp disorder characterized by the thinning or shedding of hair resulting from the early entry of hair in the telogen phase (the resting phase of the hair follicle).Marks, James G; Miller, Jeffery (2006). ''Lookingbill and ...

* Terry's nails *

Traction alopecia Traction alopecia is a type of alopecia or hair loss caused by a chronic pulling force being applied to the hair. It commonly results from a person frequently wearing their hair in a particularly tight ponytail, pigtails, or braids with increased ...

Traumatic alopecia Traumatic alopecia is a cutaneous condition that results from the forceful pulling out of the scalp hair. See also * Traction alopecia Traction alopecia is a type of alopecia or hair loss caused by a chronic pulling force being applied to the h ...

* Traumatic anserine folliculosis * Triangular alopecia (temporal alopecia, temporal triangular alopecia) *

Trichomegaly Trichomegaly is a congenital condition in which the eyelashes are abnormally long, greater than 12mm in the central area and 8mm in the peripheral. The term was first used by H. Gray in 1944 in a publication in the Stanford Medical Bulletin, though ...

* Trichomycosis axillaris *

Trichorrhexis invaginata Trichorrhexis invaginata is a distinctive hair shaft abnormality that may occur sporadically, either in normal hair or with other hair shaft abnormalities, or regularly as a marker for Netherton's syndrome.Freedberg, et al. (2003). ''Fitzpatrick' ...

(bamboo hair) * Trichorrhexis nodosa *

Trichostasis spinulosa Trichostasis spinulosa is a common but rarely diagnosed disorder of the hair follicles that clinically gives the impression of blackheads, but the follicles are filled with funnel-shaped, horny plugs that are bundles of vellus hairs.James, Willia ...

* Tufted folliculitis * Tumor alopecia * Twenty-nail dystrophy (sandpapered nails, trachyonychia) *

Uncombable hair syndrome Uncombable hair syndrome (UHS) is a rare structural anomaly of the hair with a variable degree of effect. It is characterized by hair that is silvery, dry, frizzy, wiry, and impossible to comb. It was first reported in the early 20th century. It ...

(''cheveux incoiffable'', pili trianguli et canaliculi, spun-glass hair) * Wooly hair nevus (woolly hair nevus) * X-linked hypertrichosis

Conditions of the subcutaneous fat

Conditions of the

subcutaneous fat The subcutaneous tissue (), also called the hypodermis, hypoderm (), subcutis, superficial fascia, is the lowermost layer of the integumentary system in vertebrates. The types of cells found in the layer are fibroblasts, adipose cells, and macro ...

are those affecting the layer of

adipose tissue Adipose tissue, body fat, or simply fat is a loose connective tissue composed mostly of adipocytes. In addition to adipocytes, adipose tissue contains the stromal vascular fraction (SVF) of cells including preadipocytes, fibroblasts, vascular ...

that lies between the dermis and underlying fascia. *

Acquired generalized lipodystrophy Acquired generalized lipodystrophy (also known as "Lawrence syndrome," and "Lawrence–Seip syndrome", abbreviation: AGL) is a rare skin condition that appears during childhood or adolescence, characterized by fat loss affecting large areas of the ...

(Lawrence syndrome, Lawrence–Seip syndrome) *

Adiposis dolorosa Adiposis dolorosa is an outdated term for many years used synonymously as Dercum's disease, lipedema Lipedema is a condition that is almost exclusively found in women and results in enlargement of both legs due to deposits of fat under the skin ...

(Dercum's disease) *

Alpha-1 antitrypsin deficiency panniculitis Panniculitis is a group of diseases whose hallmark is inflammation of subcutaneous adipose tissue (the fatty layer under the skin – panniculus adiposus). Symptoms include tender skin nodules, and systemic signs such as weight loss and fatigu ...

(alpha1-protease deficiency panniculitis, alpha1-proteinase deficiency panniculitis) *

Atrophic connective tissue panniculitis Atrophic connective tissue panniculitis is a rare condition, and often occurs on the upper or lower extremities. See also * Involutional lipoatrophy * List of cutaneous conditions References

Conditions of the subcutaneous fat {{Dermat ...

Barraquer–Simons syndrome Barraquer–Simons syndrome is a rare form of lipodystrophy, which usually first affects the head, and then spreads to the thorax. It is named for Luis Barraquer Roviralta (1855–1928), a Spanish physician, and Arthur Simons (1879–1942), a Germ ...

(acquired partial lipodystrophy, cephalothoracic lipodystrophy, progressive lipodystrophy) *

Benign symmetric lipomatosis Benign symmetric lipomatosis is a skin condition characterized by extensive symmetric fat deposits in the head, neck, and shoulder girdle area. The German surgeon Otto Wilhelm Madelung was the first to give a detailed description of the disorder. ...

(benign symmetric lipomatosis of Launois–Bensaude, Madelung's disease) *

Centrifugal abdominal lipodystrophy Centrifugal abdominal lipodystrophy is a skin condition characterized by areas of subcutaneous fat loss that slowly enlarge. See also * Lipodystrophy * List of cutaneous conditions * Skin lesion A skin condition, also known as cutaneous con ...

(centrifugal lipodystrophy, lipodystrophia centrifugalis abdominalis infantalis) *

Chronic erythema nodosum Erythema nodosum (EN) is an inflammation, inflammatory condition characterized by panniculitis, inflammation of the fat cells under the skin, resulting in tender red nodules or lumps that are usually seen on both shins. It can be caused by a varie ...

(erythema nodosum migrans, subacute migratory panniculitis of Vilanova and Piñol, subacute nodular migratory panniculitis) * Cold panniculitis (popsicle panniculitis) * Congenital generalized lipodystrophy (Berardinelli–Seip syndrome) *

Cytophagic histiocytic panniculitis Panniculitis is a group of diseases whose hallmark is inflammation of subcutaneous adipose tissue (the fatty layer under the skin – panniculus adiposus). Symptoms include tender skin nodules, and systemic signs such as weight loss and fatigue ...

* Drug-induced lipodystrophy *

Factitial panniculitis Panniculitis is a group of diseases whose hallmark is inflammation of subcutaneous adipose tissue (the fatty layer under the skin – panniculus adiposus). Symptoms include tender skin nodules, and systemic signs such as weight loss and fatigu ...

Familial partial lipodystrophy Familial partial lipodystrophy, also known as Köbberling–Dunnigan syndrome, is a rare genetic metabolic condition characterized by the loss of subcutaneous fat. FPL also refers to a rare metabolic condition in which there is a loss of subcutane ...

(Köbberling–Dunnigan syndrome) *

Gouty panniculitis Panniculitis is a group of diseases whose hallmark is inflammation of Subcutaneous tissue, subcutaneous adipose tissue (the fatty layer under the skin – panniculus adiposus). Symptoms include tender skin Nodule (dermatology), nodules, and system ...

Hemihyperplasia–multiple lipomatosis syndrome Hemihyperplasia–multiple lipomatosis syndrome is a cutaneous condition characterized by multiple lipomas in association with asymmetric (but non-progressive and non-distorting) overgrowth, cutaneous capillary malformations, and thickened plantar ...

HIV-associated lipodystrophy HIV-associated lipodystrophy is a condition characterized by loss of subcutaneous fat associated with infection with HIV. Presentation HIV-associated lipodystrophy commonly presents with fat loss in face, buttocks, arms and legs. There is also ...

Within this list, the terms human immunodeficiency virus and acquired immunodeficiency syndrome are abbreviated to

HIV The human immunodeficiency viruses (HIV) are two species of ''Lentivirus'' (a subgroup of retrovirus) that infect humans. Over time, they cause acquired immunodeficiency syndrome (AIDS), a condition in which progressive failure of the immune ...

and AIDS, respectively. *

Involutional lipoatrophy Involutional lipoatrophy is a cutaneous condition, and is an idiopathic lipoatrophy characterized clinically by non-inflammatory focal loss of fat. Idiopathic localized involutional lipoatrophy (ILIL) is a rare and nosologically imprecise conditi ...

Lipoatrophia annularis Lipoatrophia annularis is a skin condition affecting primarily women, characterized by the loss of subcutaneous fat in the upper extremity.Ferreira-Marques J. Lipoatrophia annularis. Arch Dermatol Syphilis 1953; 195: 479-91. It is a form of lipod ...

(Ferreira–Marques lipoatrophia) * Lipoatrophia semicircularis (semicircular lipoatrophy) *

Lipodermatosclerosis Lipodermatosclerosis is a skin and connective tissue disease. It is a form of lower extremity panniculitis,Bruce AJ. et al., Lipodermatosclerosis: Review of cases evaluated at Mayo Clinic. J Am Acad Dermatol. 2002. an inflammation of the layer of ...

(chronic panniculitis with lipomembranous changes, hypodermitis sclerodermiformis, sclerosing panniculitis, stasis panniculitis) *

Lipohypertrophy Lipohypertrophy is a lump under the skin caused by accumulation of extra fat at the site of many subcutaneous injections of insulin. It may be unsightly, mildly painful, and may change the timing or completeness of insulin action. It is a common, ...

* Localized lipodystrophy * Neutrophilic lobular panniculitis *

Nodular vasculitis Nodular vasculitis is a skin condition characterized by crops of small, tender, erythematous nodules on the legs, mostly on the calves and shins. Miroscopically there are epithelioid granulomas and vasculitis in the subcutaneous tissue, making it ...

Non-progressive late-onset linear hemifacial lipoatrophy Non-progressive late-onset linear hemifacial lipoatrophy is a cutaneous condition that occurs on the malar cheek, mostly in the elderly population. See also * Drug-induced lipodystrophy * List of cutaneous conditions Many skin conditions a ...

Pancreatic panniculitis Panniculitis is a group of diseases whose hallmark is inflammation of subcutaneous adipose tissue (the fatty layer under the skin – panniculus adiposus). Symptoms include tender skin nodules, and systemic signs such as weight loss and fatigue ...

(enzymatic panniculitis, pancreatic fat necrosis, subcutaneous fat necrosis) *

Poland's syndrome Poland syndrome is a birth defect characterized by an underdeveloped chest muscle and short webbed fingers on one side of the body. There may also be short ribs, less fat, and breast and nipple abnormalities on the same side of the body. Typical ...

* Post-steroid panniculitis * Sclerema neonatorum *

Sclerosing lipogranuloma Panniculitis is a group of diseases whose hallmark is inflammation of Subcutaneous tissue, subcutaneous adipose tissue (the fatty layer under the skin – panniculus adiposus). Symptoms include tender skin Nodule (dermatology), nodules, and system ...

(paraffinoma) *

Septal panniculitis Septal panniculitis is a condition of the subcutaneous tissue, subcutaneous fat affecting the layer of adipose tissue that lies between the dermis and underlying fascia, of which there are two forms: acute erythema nodosum and chronic erythema nodo ...

Subcutaneous fat necrosis of the newborn Subcutaneous fat necrosis of the newborn is a rare form of lobular panniculitis occurring in newborns that is usually self-remitting and non-recurring. Proposed causes include perinatal stress, local trauma, hypoxia and hypothermia, though the ex ...

* Traumatic panniculitis *

Tumor lysis syndrome Tumor lysis syndrome (TLS) is a group of metabolic abnormalities that can occur as a complication from the treatment of cancer, where large amounts of tumor cells are killed off ( lysed) from the treatment, releasing their contents into the blood ...

Weber–Christian disease Weber–Christian disease, is a cutaneous condition characterized by recurrent subcutaneous nodules that heal with depression of the overlying skin. It is a type of panniculitis. It is a rare disease seen in females 30–60 years of age. It is a ...

(relapsing febrile nonsuppurative panniculitis)

Congenital anomalies

Cutaneous congenital anomalies are a diverse group of disorders that result from faulty

morphogenesis Morphogenesis (from the Greek ''morphê'' shape and ''genesis'' creation, literally "the generation of form") is the biological process that causes a cell, tissue or organism to develop its shape. It is one of three fundamental aspects of deve ...

, the biological process that forms the shape of a human body. *

Accessory nail of the fifth toe The accessory nail of the fifth toe, also known as petaloid toenail, is a physical trait of the small toe, where a minuscule "sixth toenail" is present in the outer corner of the nail situated on the smallest toe. Trait The trait can be observed ...

Accessory tragus An accessory auricle is considered a developmental anomaly resulting from the persistence of a structure which variably recapitulates the normal external ear. Signs and symptoms The general presentation is of a skin-covered nodule, papule, or no ...

(ear tag, preauricular appendage, preauricular tag) *

Amniotic band syndrome Constriction ring syndrome (CRS) is a congenital disorder with unknown cause. Because of the unknown cause there are many different, and sometimes incorrect names. It is a malformation due to intrauterine bands or rings that give deep grooves in, ...

(ADAM complex, amniotic band sequence, congenital constriction bands, pseudoainhum) *

Aplasia cutis congenita Aplasia cutis congenita is a rare disorder characterized by congenital absence of skin. Ilona J. Frieden classified ACC in 1986 into 9 groups on the basis of location of the lesions and associated congenital anomalies.Moss C, Shahidulla H. Naevi a ...

(cutis aplasia, congenital absence of skin, congenital scars) *

Arteriovenous fistula An arteriovenous fistula is an abnormal connection or passageway between an artery and a vein. It may be congenital, surgically created for hemodialysis treatments, or acquired due to pathologic process, such as trauma or erosion of an arterial ...

* Benign neonatal hemangiomatosis * Branchial cyst (branchial cleft cyst) * Bronchogenic cyst *

Capillary hemangioma A capillary is a small blood vessel from 5 to 10 micrometres (μm) in diameter. Capillaries are composed of only the tunica intima, consisting of a thin wall of simple squamous endothelial cells. They are the smallest blood vessels in the body: ...

(infantile hemangioma, nevus maternus, strawberry hemangioma, strawberry nevus) * Cavernous venous malformation * Congenital cartilaginous rest of the neck (cervical accessory tragus, wattle) * Congenital erosive and vesicular dermatosis *

Congenital hypertrophy of the lateral fold of the hallux Congenital hypertrophy of the lateral fold of the hallux is a rare cutaneous condition of unknown pathology that present to newborns. The condition was "first described by Martinet et al. in 1984." This sometimes painful condition involves "an ove ...

Congenital lip pit A congenital lip pit or lip sinus is a congenital disorder characterized by the presence of pits and possibly associated fistulas in the lips. They are often hereditary, and may occur alone or in association with cleft lip and palate, termed Van d ...

(congenital sinus of the lower lip, lip sinus, midline sinus of the upper lip) *

Congenital malformations of the dermatoglyphs Congenital malformations of the dermatoglyphs are a cutaneous condition divided into four main categories based on the appearance of the dermal ridges of which they are composed: (1) ridge aplasia Aplasia (; from Greek ''a'', "not", "no" + ''pla ...

Congenital smooth muscle hamartoma Congenital smooth muscle hamartoma is typically a skin colored or lightly pigmented patch or plaque with hypertrichosis.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunde ...

* Cystic lymphatic malformation *

Dermoid cyst A dermoid cyst is a teratoma of a cystic nature that contains an array of developmentally mature, solid tissues. It frequently consists of skin, hair follicles, and sweat glands, while other commonly found components include clumps of long hair ...

Diffuse neonatal hemangiomatosis Diffusion is the net movement of anything (for example, atoms, ions, molecules, energy) generally from a region of higher concentration to a region of lower concentration. Diffusion is driven by a gradient in Gibbs free energy or chemical p ...

Encephalocele Encephalocele is a neural tube defect characterized by sac-like protrusions of the brain and the membranes that cover it through openings in the skull. These defects are caused by failure of the neural tube to close completely during fetal develop ...

* Familial disseminated comedones without dyskeratosis * Focal facial dermal dysplasia *

Hutchinson's teeth Hutchinson's teeth is a sign of congenital syphilis. Affected people have teeth that are smaller and more widely spaced than normal and which have notches on their biting surfaces. It is named after Sir Jonathan Hutchinson, an English surgeon an ...

* Hyperkeratotic cutaneous capillary-venous malformation * Intrauterine epidermal necrosis * Limb–mammary syndrome * Lowry–MacLean syndrome *

Macrocheilia Macrocheilia is a condition of permanent swelling of the lip that results from greatly distended lymphatic spaces. This causes an abnormal largeness of the lip The lips are the visible body part at the mouth of many animals, including human ...

Macrocystic lymphatic malformation A cystic hygroma is an abnormal growth that usually appears on a baby's neck or head. It consists of one or more cysts and tends to grow larger over time. The disorder usually develops while the fetus is still in the uterus, but can also appear a ...

* Malignant pilomatricoma (pilomatrical carcinoma, pilomatrix carcinoma) *

Maternal autoimmune bullous disease Maternal autoimmune bullous disease is a blistering skin condition that presents at birth. See also * Accessory nail of the fifth toe * List of cutaneous conditions References Cutaneous congenital anomalies {{Dermatology-stub ...

* Median raphe cyst *

Melanotic neuroectodermal tumor of infancy Melanotic neuroectodermal tumor of infancy is a very rare oral cavity tumor that is seen in patients usually at or around birth. It must be removed to be cured. Definitions: A rare, biphasic, neuroblastic, and pigmented epithelial neoplasm of cr ...

* Membranous aplasia cutis * Microcystic lymphatic malformation * Midline cervical cleft *

Mongolian spot A Mongolian spot, also known as slate grey nevus or congenital dermal melanocytosis, is a benign, flat, congenital birthmark with wavy borders and an irregular shape. In 1883, it was described and named after Mongolians by Erwin Bälz, a German a ...

(congenital dermal melanocytosis, dermal melanocytosis) * Mulberry molar * Nager acrofacial dysostosis * Nasal glioma (brain-like heterotopia, cephalic brain-like heterotopia, glial hamartoma, heterotopic neuroglial tissue, nasal cerebral heterotopia, nasal heterotopic brain tissue) * Nasolacrimal duct cyst *

Nevus psiloliparus Nevus psiloliparus is a cutaneous condition, a rare scalp anomaly characterized by a variable degree of alopecia and an excessive amount of adipose tissue. It is the main hallmark of encephalocraniocutaneous lipomatosis (ECCL), otherwise known as ...

Non-involuting congenital hemangioma A vascular tumor is a tumor of vascular origin; a soft tissue growth that can be either benign or malignant, formed from blood vessels or lymph vessels. Examples of vascular tumors include hemangiomas, lymphangiomas, hemangioendotheliomas, K ...

* Omphalomesenteric duct cyst (omphalomesenteric duct remnant, vitelline cyst) * PELVIS syndrome *

Pilomatricoma Pilomatricoma, is a benign skin tumor derived from the hair matrix. These neoplasms are relatively uncommon and typically occur on the scalp, face, and upper extremities. Clinically, pilomatricomas present as a subcutaneous nodule or cyst with un ...

(calcifying epithelioma of Malherbe, Malherbe calcifying epithelioma, pilomatrixoma) * Poland anomaly * Posterior fossa malformations–hemangiomas–arterial anomalies–cardiac defects–eye abnormalities–sternal cleft and supraumbilical raphe syndrome (PHACE association, PHACES syndrome) *

Preauricular sinus and cyst Preauricular sinuses and preauricular cysts are two common congenital malformation, congenital malformations. Each involves the external ear. The difference between them is that a cyst does not connect with the skin, but a sinus does. Frequency o ...

(ear pit, congenital auricular fistula, congenital preauricular fistula, preauricular cyst) *

Rapidly involuting congenital hemangioma A vascular tumor is a tumor of vascular origin; a soft tissue growth that can be either benign or malignant, formed from blood vessels or lymph vessels. Examples of vascular tumors include hemangiomas, lymphangiomas, hemangioendotheliomas, Kapo ...

(congenital nonprogressive hemangioma) * Rosenthal–Kloepfer syndrome *

Rudimentary supernumerary digit Polydactyly or polydactylism (), also known as hyperdactyly, is an anomaly in humans and animals resulting in supernumerary fingers and/or toes. Polydactyly is the opposite of oligodactyly (fewer fingers or toes). Signs and symptoms In humans ...

(rudimentary polydactyly) *

SACRAL syndrome SACRAL syndrome is a congenital condition characterized by spinal dysraphism, spinal dysraphism, anogenital, cutaneous, Kidney disease, renal and Urologic disease, urologic anomalies, associated with an angioma, angioma of lumbosacral localization. ...

Sinus pericranii Sinus pericranii (SP) is a rare disorder characterized by a congenital (or occasionally, acquired) epicranial venous malformation of the scalp. Sinus pericranii is an abnormal communication between the intracranial and extracranial venous drainag ...

Skin dimple Skin dimples (also known as "Skin fossa") are deep cutaneous depressions that are seen most commonly on the cheeks or chin, occurring in a familial pattern suggestive of autosomal dominant inheritance. See also * Sinus pericranii * List of cuta ...

(skin fossa) *

Superficial lymphatic malformation Superficial lymphatic malformation is a congenital malformation of the superficial lymphatics, presenting as groups of deep-seated, vesicle-like papules resembling frog spawn, at birth or shortly thereafter.James, William; Berger, Timothy; Elston, ...

(lymphangioma circumscriptum) * Supernumerary nipple (accessory nipple, pseudomamma) *

Thyroglossal duct cyst A thyroglossal cyst is a fibrous cyst that forms from a persistent thyroglossal duct. Thyroglossal cysts can be defined as an irregular neck mass or a lump which develops from cells and tissues left over after the formation of the thyroid gland d ...

* Verrucous vascular malformation (angiokeratoma circumscriptum naeviforme)

Connective tissue diseases

Connective tissue diseases are caused by a complex array of

autoimmune In immunology, autoimmunity is the system of immune responses of an organism against its own healthy cells, tissues and other normal body constituents. Any disease resulting from this type of immune response is termed an "autoimmune disease". ...

responses that target or affect collagen or

. * Acute cutaneous lupus erythematosus * Atrophoderma of Pasini and Pierini (dyschromic and atrophic variation of scleroderma, morphea plana atrophica, ''sclérodermie atrophique d'emblée'') * Calcinosis–Raynaud phenomenon–esophageal dysmotility–sclerodactyly–telangiectasia syndrome (CREST syndrome) * Chilblain lupus erythematosus (chilblain lupus erythematosus of Hutchinson) * Childhood dermatomyositis *

Childhood discoid lupus erythematosus Discoid lupus erythematosus is the most common type of chronic cutaneous lupus (CCLE), an autoimmune skin condition on the lupus erythematosus spectrum of illnesses. It presents with red, painful, inflamed and coin-shaped patches of skin with a sc ...

* Childhood systemic lupus erythematosus * Complement deficiency syndromes *

Dermatomyositis Dermatomyositis (DM) is a long-term inflammatory disorder which affects skin and the muscles. Its symptoms are generally a skin rash and worsening muscle weakness over time. These may occur suddenly or develop over months. Other symptoms may inc ...

* Ehlers–Danlos syndrome *

Eosinophilia–myalgia syndrome Eosinophilia–myalgia syndrome is a rare, sometimes fatal neurological condition linked to the ingestion of the dietary supplement L-tryptophan. The risk of developing EMS increases with larger doses of tryptophan and increasing age. Some rese ...

* Frontal linear scleroderma (''en coup de sabre'', morphea ''en coup de sabre'') Frontal linear scleroderma 2

Generalized discoid lupus erythematosus Discoid lupus erythematosus is the most common type of chronic cutaneous lupus (CCLE), an Autoimmune disease, autoimmune skin condition on the lupus erythematosus spectrum of illnesses. It presents with red, painful, inflamed and coin-shaped patch ...

* Generalized morphea *

Interstitial granulomatous dermatitis Interstitial granulomatous dermatitis with arthritis (IGDA) or Ackerman dermatitis syndrome is a skin condition that most commonly presents with symmetrical round-to-oval red or violet plaques on the flanks, armpits, inner thighs, and lower abdome ...

Juvenile rheumatoid arthritis Juvenile may refer to: *Juvenile status, or minor (law), prior to adulthood *Juvenile (organism) * Juvenile (rapper) (born 1975), American rapper * ''Juvenile'' (2000 film), Japanese film * ''Juvenile'' (2017 film) *Juvenile (greyhounds), a greyh ...

(juvenile idiopathic arthritis, Still's disease) * Keloid morphea * Linear atrophoderma of Moulin (Moulin atrophoderma linearis) *

Linear scleroderma Morphea is a form of scleroderma that involves isolated patches of hardened skin on the face, hands, and feet, or anywhere else on the body, with no internal organ involvement. Signs and symptoms Morphea most often presents as macules or pla ...

* Localized discoid lupus erythematosus * Localized morphea * Lupus erythematosus panniculitis (lupus erythematosus profundus, lupus panniculitis, lupus profundus, subcutaneous lupus erythematosus) * Lupus erythematosus–lichen planus overlap syndrome (lichen planus–lupus erythematosus overlap syndrome) * Methotrexate-induced papular eruption *

Mixed connective tissue disease Mixed connective tissue disease, commonly abbreviated as MCTD, is an autoimmune disease characterized by the presence of elevated blood levels of a specific autoantibody, now called anti-U1 ribonucleoprotein (RNP) together with a mix of symptoms of ...

(Sharp's syndrome, undifferentiated connective tissue disease) * Morphea profunda * Morphea–lichen sclerosus et atrophicus overlap *

Mouth and genital ulcers with inflamed cartilage syndrome Mouth and genital ulcers with inflamed cartilage syndrome (also known as "MAGIC syndrome") is a cutaneous condition with features of both Behçet's disease and relapsing polychondritis. Recently, it has been questioned whether these two conditions ...

(MAGIC syndrome) * Neonatal lupus erythematosus *

Nephrogenic systemic fibrosis Nephrogenic systemic fibrosis is a rare syndrome that involves fibrosis of skin, joints, eyes, and internal organs. NSF is caused by exposure to gadolinium in gadolinium-based MRI contrast agents (GBCAs) in patients with impaired kidney function ...

(nephrogenic fibrosing dermopathy) *

Nicolau–Balus syndrome Nicolau–Balus syndrome is a cutaneous condition characterized by syringomas and milia. See also * Parry–Romberg syndrome * List of cutaneous conditions Many skin conditions affect the human integumentary system—the organ system c ...

* Nodulosis–arthropathy–osteolysis syndrome *

Normophosphatemic familial tumoral calcinosis Normophosphatemic familial tumoral calcinosis is a cutaneous disorder characterized by cutaneous calcification or ossification. See also * Progressive systemic sclerosis * List of cutaneous conditions * List of genes mutated in cutaneous conditi ...

Palisaded neutrophilic and granulomatous dermatitis Palisaded neutrophilic and granulomatous dermaititis is usually associated with a well-defined connective tissue disease, lupus erythematosus or rheumatoid arthritis most commonly, and often presents with eroded or ulcerated symmetrically distribu ...

* Pansclerotic morphea *

Parry–Romberg syndrome Parry–Romberg syndrome (PRS) is a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of th ...

(progressive hemifacial atrophy) *

Progressive systemic sclerosis Systemic scleroderma, or systemic sclerosis, is an autoimmune rheumatic disease characterised by excessive production and accumulation of collagen, called fibrosis, in the skin and internal organs and by injuries to small arteries. There are two m ...

Relapsing polychondritis Relapsing polychondritis is a multi-systemic condition characterized by repeated episodes of inflammation and deterioration of cartilage. The often painful disease can cause joint deformity and be life-threatening if the respiratory tract, heart ...

(atrophic polychondritis, systemic chondromalacia) *

Rheumatoid arthritis Rheumatoid arthritis (RA) is a long-term autoimmune disorder that primarily affects joints. It typically results in warm, swollen, and painful joints. Pain and stiffness often worsen following rest. Most commonly, the wrist and hands are invol ...

Rheumatoid nodulosis Rheumatoid nodulosis is a cutaneous condition associated with rheumatoid arthritis, characterized by the appearance of multiple nodules, most often on the hands. See also * Rheumatoid neutrophilic dermatitis * Rheumatoid nodule * List of cutane ...

(accelerated rheumatoid nodulosis) * Rheumatoid vasculitis * Rowell's syndrome * Scleredema adultorum (Bushke disease, scleredema diabeticorum, scleredema adultorum of Buschke, scleredema of Buschke) * Silicosis * Sjögren's syndrome (Mikulicz disease, Sicca syndrome) * Subacute cutaneous lupus erythematosus * Systemic lupus erythematosus *

Toxic oil syndrome Toxic oil syndrome (TOS) or simply toxic syndrome (Spanish: ''síndrome del aceite tóxico'' or ''síndrome tóxico'') is a musculoskeletal disease. A 1981 outbreak in Spain which affected about 20,000 people, with over 300 dying within a few m ...

* Tumid lupus erythematosus (lupus erythematosus tumidus) * Tuzun syndrome *

Verrucous lupus erythematosus Verrucous lupus erythematosus presents with non-pruritic papulonodular lesions on the arms and hands, resembling keratoacanthoma or hypertropic lichen planus.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: ...

(hypertrophic lupus erythematosus) *

Winchester syndrome Winchester syndrome is a rare hereditary connective tissue disease described in 1969, of which the main characteristics are short stature, marked contractures of joints, opacities in the cornea, coarse facial features, dissolution of the carpal ...

Abnormalities of dermal fibrous and elastic tissue

Abnormalities of dermal fibrous and elastic tissue are caused by problems in the regulation of collagen synthesis or degradation. * Acrodermatitis chronica atrophicans (Herxheimer disease, primary diffuse atrophy) *

Actinic elastosis Actinic elastosis, also known as solar elastosis, is an accumulation of abnormal elastin (elastic tissue) in the dermis of the skin, or in the conjunctiva of the human eye, eye, which occurs as a result of the cumulative effects of prolonged and e ...

(solar elastosis) *

Anetoderma Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). Page 1027. McGraw-Hill. . Anetoderma ...

(anetoderma maculosa, anetoderma maculosa cutis, atrophia maculosa cutis, macular atrophy) *

Blepharochalasis Blepharochalasis is an inflammation of the eyelid that is characterized by exacerbations and remissions of eyelid edema, which results in a stretching and subsequent atrophy of the eyelid tissue, leading to the formation of redundant folds over ...

Cutis laxa Cutis laxa or pachydermatocele is a group of rare connective tissue disorders in which the skin becomes inelastic and hangs loosely in folds. Signs and symptoms It is characterised by skin that is loose, hanging, wrinkled, and lacking in elast ...

(chalazoderma, dermatochalasia, dermatolysis, dermatomegaly, generalized elastolysis, generalized elastorrhexis, pachydermatocele) *

Cutis rhomboidalis nuchae Cutis rhomboidalis nuchae is a skin condition of the posterior neck, characterized by deep furrowing of the skin. See also * List of cutaneous conditions Many skin conditions affect the human integumentary system—the organ system cover ...

* Ehlers–Danlos syndrome (cutis hyperelastica, elastic skin, India rubber skin) *

Elastosis perforans serpiginosa Elastosis perforans serpiginosa is a unique perforating disorder characterized by transepidermal elimination of elastic fibers and distinctive clinical lesions, which are serpiginous in distribution and can be associated with specific diseases.Free ...

Homocystinuria Homocystinuria or HCU is an inherited disorder of the metabolism of the amino acid methionine due to a deficiency of cystathionine beta synthase or methionine synthase. It is an inherited autosomal recessive trait, which means a child needs to i ...

* Jadassohn–Pellizzari anetoderma *

Linear focal elastosis Linear focal elastosis or elastotic striae is a skin condition that presents with asymptomatic, palpable or atrophic, yellow lines of the middle and lower back, thighs, arms and breasts.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andre ...

(elastotic striae) *

Loeys–Dietz syndrome Loeys–Dietz syndrome (LDS) is an autosomal dominant genetic connective tissue disorder. It has features similar to Marfan syndrome and Ehlers–Danlos syndrome. The disorder is marked by aneurysms in the aorta, often in children, and the aorta ...

* Marfan syndrome *

Occipital horn syndrome Occipital horn syndrome (OHS), formerly considered a variant of Ehlers–Danlos syndrome, is an X-linked recessive mitochondrial and connective tissue disorder. It is caused by a deficiency in the transport of the essential mineral copper, associ ...

Osteogenesis imperfecta Osteogenesis imperfecta (; OI), colloquially known as brittle bone disease, is a group of genetic disorders that all result in bones that break easily. The range of symptoms—on the skeleton as well as on the body's other organs—may b ...

(Lobstein syndrome) *

Perforating calcific elastosis Perforating calcific elastosis is an acquired, localized cutaneous disorder, most frequently found in obese, multiparous, middle-aged women, characterized by lax, well-circumscribed, reticulated or cobble-stoned plaques occurring in the periumbil ...

(localized acquired cutaneous pseudoxanthoma elasticum, perforating periumbilical calcific elastosis, periumbilical perforating pseudoxanthoma elasticum) *

Pseudoxanthoma elasticum Pseudoxanthoma elasticum (PXE) is a genetic disease that causes mineralization of elastic fibers in some tissues. The most common problems arise in the skin and eyes, and later in blood vessels in the form of premature atherosclerosis. PXE is cau ...

(Grönblad–Strandberg syndrome) *

Reactive perforating collagenosis Reactive perforating collagenosis is a rare, familial, nonpuritic skin disorder characterized by papules that grow in a diameter of 4 to 6mm and develop a central area of umbilication to which keratinous material is lodged.James, William; Berger, ...

Schweninger–Buzzi anetoderma Anetoderma is a localized laxity of the skin with herniation or outpouching resulting from abnormal dermal elastic tissue.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). Page 1027. McGraw-Hill. . Anetoderma c ...

* Sclerotic fibroma *

Striae atrophicans Striae atrophicans are a cutaneous condition characterized by usually multiple, symmetric, well-defined linear atrophic lesions that often follow the lines of cleavage. See also * Striae distensae * List of cutaneous conditions Many skin c ...

* Striae distensae * Ullrich disease * Verrucous perforating collagenoma *

Wrinkly skin syndrome Wrinkly skin syndrome (WSS) is a rare genetic condition characterized by sagging, wrinkled skin, low skin elasticity, and delayed fontanelle (soft spot) closure, along with a range of other symptoms. The disorder exhibits an autosomal recessive in ...

Dermal and subcutaneous growths

Dermal and subcutaneous growths result from (1) reactive or

neoplastic A neoplasm () is a type of abnormal and excessive growth of tissue. The process that occurs to form or produce a neoplasm is called neoplasia. The growth of a neoplasm is uncoordinated with that of the normal surrounding tissue, and persists ...

proliferation of cellular components of the dermis or subcutaneous tissue, or (2) neoplasms invading or aberrantly present in the dermis. *

Acquired progressive lymphangioma Acquired progressive lymphangioma is a group of lymphangiomas that occur anywhere in young individuals, grow slowly, and present as bruise-like lesions or erythematous macule A skin condition, also known as cutaneous condition, is any medical c ...

(benign lymphangioendothelioma) *

Acral arteriolar ectasia Acral arteriolar ectasia is characterized by purple serpiginous ectatic arterioles on the back of the fingers, presenting in the fifth decade of life.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical De ...

Acral fibrokeratoma Acral fibrokeratoma (also known as an "Acquired digital fibrokeratoma," and "Acquired periungual fibrokeratoma"Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. .) is a skin lesion characterized ...

(acquired digital fibrokeratoma, acquired periungual fibrokeratoma) *

Acrochordon A skin tag, or acrochordon (pl. acrochorda), is a small benign tumor that forms primarily in areas where the skin forms creases (or rubs together), such as the neck, armpit and groin. They may also occur on the face, usually on the eyelids. Tho ...

(cutaneous papilloma, cutaneous tag, fibroepithelial polyp, fibroma molluscum, fibroma pendulum, papilloma colli, skin tag, soft fibroma, Templeton skin tag) *

Adenoma sebaceum Adenoma sebaceum is a misnamed cutaneous disorder consisting of angiofibromas that begin in childhood (generally present between 2–5 years of age) and appear clinically as red papules on the face especially on the nasolabial folds, cheek and chi ...

* Adult type of generalized eruption of cutaneous mastocytosis *

African cutaneous Kaposi sarcoma Kaposi's sarcoma (KS) is a type of cancer that can form masses in the skin, in lymph nodes, in the mouth, or in other organs. The skin lesions are usually painless, purple and may be flat or raised. Lesions can occur singly, multiply in a limite ...

African lymphadenopathic Kaposi sarcoma Kaposi's sarcoma (KS) is a type of cancer that can form masses in the skin, in lymph nodes, in the mouth, or in other organs. The skin lesions are usually painless, purple and may be flat or raised. Lesions can occur singly, multiply in a limit ...

Aggressive infantile fibromatosis Aggressive infantile fibromatosis is a locally recurring, non-metastasizing lesion, presenting with a single or multiple fast-growing masses that are present at birth or occur within the first year of life.James, William; Berger, Timothy; Elston, Di ...

AIDS-associated Kaposi sarcoma Kaposi's sarcoma (KS) is a type of cancer that can form masses in the skin, in lymph nodes, in the mouth, or in other organs. The skin lesions are usually painless, purple and may be flat or raised. Lesions can occur singly, multiply in a limit ...

* Ainhum (''bankokerend'', dactylolysis spontanea, ''sukhapakla'') *

Angiofibroma Angiofibroma (AGF) is a descriptive term for a wide range of benign skin or mucous membrane (i.e. the outer membrane lining body cavities such as the mouth and nose) lesions in which individuals have: 1) benign papules, i.e. pinhead-sized elevation ...

Angiokeratoma Angiokeratoma is a benign cutaneous lesion of capillaries, resulting in small marks of red to blue color and characterized by hyperkeratosis. ''Angiokeratoma corporis diffusum'' refers to Fabry's disease, but this is usually considered a distinct c ...

Angiokeratoma of Fordyce Angiokeratoma is a benign cutaneous lesion of capillaries, resulting in small marks of red to blue color and characterized by hyperkeratosis. ''Angiokeratoma corporis diffusum'' refers to Fabry's disease, but this is usually considered a distinct c ...

(angiokeratoma of the scrotum and vulva) Angiokeratoma of the Scrotum 7

* Angiokeratoma of Mibelli (Mibelli's angiokeratoma, telangiectatic warts) *

Angioleiomyoma Angioleiomyoma (vascular leiomyoma, angiomyoma) of the skin is thought to arise from vascular smooth muscle, and is generally acquired.Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). Page 1033. McGraw-Hill. ...

(vascular leiomyoma) *

Angiolipoleiomyoma Angiolipoleiomyoma is an acquired, solitary, asymptomatic acral nodule, characterized histologically by well-circumscribed subcutaneous tumors composed of smooth muscle cells, blood vessels, connective tissue, and fat.James, William; Berger, Timo ...

Angiolipoma Angiolipoma is a subcutaneous nodule with vascular structure, having all other features of a typical lipoma. They are commonly painful.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. ( ...

* Angioma serpiginosum *

Angiosarcoma Angiosarcoma is a rare and aggressive cancer that starts in the endothelial cells that line the walls of blood vessels or lymphatic vessels. Since they are made from vascular lining, they can appear anywhere and at any age, but older people are ...

* Aponeurotic fibroma (calcifying aponeurotic fibroma, juvenile aponeurotic fibroma) *

Atypical fibroxanthoma Atypical fibroxanthoma of the skin is a low-grade malignancy related to malignant fibrous histiocytoma, which it resembles histologically.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology'' ...

* Benign lipoblastomatosis (embryonic lipoma) *

Buschke–Ollendorff syndrome Buschke–Ollendorff syndrome (BOS) is a rare genetic disorder associated with LEMD3. It is believed to be inherited in an autosomal dominant manner. It is named for Abraham Buschke and Helene Ollendorff Curth, who described it in a 45-year-old ...

(dermatofibrosis lenticularis disseminata) * Capillary aneurysms *

Carcinoid A carcinoid (also carcinoid tumor) is a slow-growing type of neuroendocrine tumor originating in the cells of the neuroendocrine system. In some cases, metastasis may occur. Carcinoid tumors of the midgut (jejunum, ileum, appendix, and cecum) ...

* Cellular angiofibroma * Cherry angioma (De Morgan spot, senile angioma) *

Chondrodermatitis nodularis chronica helicis Chondrodermatitis nodularis chronica helicis is a small, nodular, tender, chronic inflammatory lesion occurring on the helix A helix () is a shape like a corkscrew or spiral staircase. It is a type of smooth space curve with tangent lines ...

(chondrodermatitis nodularis helicis) Chondrodermatitis 02

Chondroid lipoma Chondroid lipomas are deep-seated, firm, yellow tumors that characteristically occur on the legs of women. They exhibit a characteristic genetic translocation t(11;16) with a resulting C11orf95-MKL2 fusion oncogene.James, William; Berger, Timot ...

Chordoma Chordoma is a rare slow-growing neoplasm thought to arise from cellular remnants of the notochord. The evidence for this is the location of the tumors (along the neuraxis), the similar immunohistochemical staining patterns, and the demonstration ...

* Classic Kaposi sarcoma *

Collagenous fibroma Collagenous fibroma (also known as "desmoplastic fibroblastoma") is a slow-growing, deep-set, benign fibrous tumor, usually located in the deep subcutis, fascia, aponeurosis, or skeletal muscle of the extremities, limb girdles, or head and neck reg ...

(desmoplastic fibroblastoma) * Composite hemangioendothelioma * Connective tissue nevus (collagenoma, elastoma, shagreen patch) *

Cutaneous endometriosis Cutaneous endometriosis is characterized by the appearance of papules at the umbilicus or in lower abdominal scars after gynecologic surgery in middle-aged women.James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: ...

* Cutaneous meningioma (heterotopic meningeal tissue, rudimentary meningocele) * Cutaneous myelofibrosis * Cutaneous myxoma * Cutis marmorata telangiectatica congenita (congenital generalized phlebectasia, Van Lohuizen syndrome) * Dermal dendrocyte hamartoma *

Dermatofibroma A dermatofibroma, or benign fibrous histiocytomas, is a benign nodule in the skin, typically on the legs, elbows or chest of an adult. It is usually painless. It usually ranges from 0.2cm to 2cm in size but larger examples have been reported. It ...

(benign fibrous histiocytoma, dermal dendrocytoma, fibrous dermatofibroma, fibrous histiocytoma, fibroma simplex, histiocytoma, nodular subepidermal fibrosis, sclerosing hemangioma) *

Dermatofibrosarcoma protuberans Dermatofibrosarcoma protuberans (DFSP) is a rare locally aggressive malignant cutaneous soft-tissue sarcoma. DFSP develops in the connective tissue cells in the middle layer of the skin (dermis). Estimates of the overall occurrence of DFSP in the ...

Desmoid tumor Aggressive fibromatosis or desmoid tumor is a rare condition. Desmoid tumors arise from cells called fibroblasts, which are found throughout the body and provide structural support, protection to the vital organs, and play a critical role in wou ...

Diffuse cutaneous mastocytosis Mastocytosis, a type of mast cell disease, is a rare disorder affecting both children and adults caused by the accumulation of functionally defective mast cells (also called ''mastocytes'') and CD34+ mast cell precursors. People affected by masto ...

Diffuse infantile fibromatosis Diffuse infantile fibromatosis is a rare condition affecting infants during the first 3 years of life. This condition is a multicentric infiltration of muscle fibers with fibroblasts resembling those seen in aponeurotic fibromas, presenting as lesi ...

Dupuytren's contracture Dupuytren's contracture (also called Dupuytren's disease, Morbus Dupuytren, Viking disease, palmar fibromatosis and Celtic hand) is a condition in which one or more fingers become progressively bent in a flexed position. It is named after Guill ...

(Dupuytren's diathesis, Dupuytren's disease, palmar fibromatosis) *

Eccrine angiomatous hamartoma Eccrine angiomatous hamartoma (EAH), first described by Lotzbeck in 1859, is a rare benign vascular hamartoma characterized histologically by a proliferation of eccrine and vascular components. EAH exists on a spectrum of cutaneous tumors that in ...

Elastofibroma dorsi Elastofibroma dorsi is an ill-defined fibroelastic tumor-like condition made up of enlarged and irregular elastic fibers. The World Health Organization, 2020, has classified elastofibroma tumors as one specific type of the fibroblastic and myofibr ...

Endovascular papillary angioendothelioma Hemangioendotheliomas are a family of vascular neoplasms of intermediate malignancy. Signs and symptoms They have been described as masses that fall between a hemangioma and angiosarcoma. They are vascular tumors that commonly present with an enl ...

(Dabska tumor, Dabska-type hemangioendothelioma, hobnail hemangioendothelioma, malignant endovascular papillary angioendothelioma, papillary intralymphatic angioendothelioma) * Epithelioid cell histiocytoma *

Epithelioid hemangioendothelioma Epithelioid hemangioendothelioma (eHAE) is a rare tumor, first characterized by Sharon Weiss and Franz Enzinger in 1982 that both clinically and histologically is intermediate between angiosarcoma and hemangioma. However, a distinct, disease-defin ...

Epithelioid sarcoma Epithelioid sarcoma is a rare soft tissue sarcoma arising from mesenchymal tissue and characterized by epithelioid-like features. It accounts for less than 1% of all soft tissue sarcomas. It was first clearly characterized by F.M. Enzinger in 197 ...

Erythrodermic mastocytosis Mastocytosis, a type of mast cell disease, is a Rare disease, rare disorder affecting both children and adults caused by the accumulation of functionally defective mast cells (also called ''mastocytes'') and CD34+ mast cell precursors. People affe ...

Extraskeletal chondroma Extraskeletal chondroma is a cutaneous condition, a rare benign tumor of mature cartilage. See also * List of cutaneous conditions Many skin conditions affect the human integumentary system—the organ system covering the entire surface ...

(chondroma of soft parts) *

Familial myxovascular fibromas Familial myxovascular fibromas present with multiple verrucous papules on the palms and fingers, which on biopsy show focal neovascularization and mucin-like changes in the papillary dermis.James, William; Berger, Timothy; Elston, Dirk (2005). ''A ...

* Fascial hernia *

Fibroma of tendon sheath Fibroma of tendon sheath is a benign tumor that presents as a small subcutaneous nodule that slowly increases in size. The tumors often have a multinodular growth pattern, with individual nodules being composed of bland, slender, spindle-shaped ce ...

Fibromatosis colli Fibromatosis colli (FMC), also termed sternocleidomastoid tumor of infancy, pseudotumor of infancy, and infancy sternocleidomastoid pseudotumor, is an uncommon (incidence: 0.4%–1.3% of live births), congenital tumor in one of the two sternocleid ...

(sternomastoid tumor of infancy) * Fibrous hamartoma of infancy *

Fibrous papule of the nose Fibrous papule of the nose is a harmless small bump on or near the nose. It is typically dome-shaped, skin-colored, white or reddish, smooth and firm. Less frequently it can occur elsewhere on the face. Sometimes there are a few. It may be shiny ...

(benign solitary fibrous papule, fibrous papule of the face) * Folded skin with scarring (Michelin tire baby syndrome) *

Fordyce's spot Fordyce spots (also termed Fordyce granules)James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. . are visible sebaceous glands that are present in most individuals ...

(Fordyce's disease) Fordyces spot closeup

* Ganglion cyst *

Ganglioneuroma Ganglioneuroma is a rare and benign tumor of the autonomic nerve fibers arising from neural crest sympathogonia, which are completely undifferentiated cells of the sympathetic nervous system. However, ganglioneuromas themselves are fully differ ...

* Gardner fibroma * Genital leiomyoma (dartoic leiomyoma) * Giant cell fibroblastoma *

Giant cell tumor of the tendon sheath Tenosynovial giant cell tumor (TGCT) is a group of rare, typically non-malignant tumors of the joints. TGCT tumors often develop from the lining of joints (also known as synovial tissue). Common symptoms of TGCT include swelling, pain, stiffne ...

(giant cell synovioma, localized nodular tenosynovitis, pigmented villonodular synovitis) * Glomeruloid hemangioma *

Glomus tumor :''Glomus tumor was also the name formerly (and incorrectly) used for a tumor now called a paraganglioma.'' A glomus tumor (also known as a "solitary glomus tumor," "solid glomus tumor,") is a rare neoplasm arising from the glomus body and mainl ...

(glomangioma, solid glomus tumor, solitary glomus tumor) *

Granular cell tumor Granular cell tumor is a tumor that can develop on any skin or mucosal surface, but occurs on the tongue 40% of the time. It is also known as Abrikossoff's tumor, granular cell myoblastoma, granular cell nerve sheath tumor, and granular cell schw ...

(Abrikossoff's tumor, Abrikossov's tumor, granular cell myoblastoma, granular cell nerve sheath tumor, granular cell schwannoma) *

Hamartoma A hamartoma is a mostly benign, local malformation of cells that resembles a neoplasm of local tissue but is usually due to an overgrowth of multiple aberrant cells, with a basis in a systemic genetic condition, rather than a growth descended fr ...

Hemangiopericytoma A hemangiopericytoma is a type of soft-tissue sarcoma that originates in the pericytes in the walls of capillaries. When inside the nervous system, although not strictly a meningioma tumor, it is a meningeal tumor with a special aggressive behavior ...

Hemangiosarcoma Hemangiosarcoma is a rapidly growing, highly invasive variety of cancer that occurs almost exclusively in dogs, and only rarely in cats, horses, mice, or humans (vinyl chloride toxicity). It is a sarcoma arising from the lining of blood vessels; ...

Hibernoma A hibernoma is a benign neoplasm of vestigial brown fat. The term was originally used by the French anatomist Louis Gery in 1914. Signs and symptoms Patients present with a slow-growing, painless, solitary mass, usually of the subcutaneous tiss ...

(fetal lipoma, lipoma of embryonic fat, lipoma of immature adipose tissue) *

Hypertrophic scar A hypertrophic scar is a cutaneous condition characterized by deposits of excessive amounts of collagen which gives rise to a raised scar, but not to the degree observed with keloids. Like keloids, they form most often at the sites of pimples, b ...

* Immunosuppression-associated Kaposi sarcoma *

Infantile digital fibromatosis Infantile digital fibromatosis (IDF), also termed inclusion body fibromatosis, Reye tumor, or Reye's tumor, usually occurs as a single, small, asymptomatic, nodule in the dermis on a finger or toeFreedberg, et al. (2003). ''Fitzpatrick's Dermatol ...

(inclusion body fibromatosis, infantile digital myofibroblastoma, Reye tumor) *

Infantile hemangiopericytoma Infantile hemangiopericytoma is a cutaneous condition characterized by single or multiple dermal and subcutaneous nodules that may be alarmingly large at birth or grow rapidly. See also * Hemangiopericytoma A hemangiopericytoma is a type of sof ...

(congenital hemangiopericytoma) * Infantile myofibromatosis (congenital generalized fibromatosis, congenital multicentric fibromatosis) *

Infantile systemic hyalinosis Infantile systemic hyalinosis is an allelic autosomal-recessive condition characterized by multiple skin nodules, hyaline deposition, gingival hypertrophy, osteolytic bone lesions and joint contractures.James, William; Berger, Timothy; Elston, Di ...

(juvenile systemic hyalinosis) * Intradermal spindle cell lipoma * Intravascular papillary endothelial hyperplasia (Masson's ''hemangio-endotheliome vegetant intravasculaire'', Masson's lesion, Masson's pseudoangiosarcoma, Masson's tumor, papillary endothelial hyperplasia) * Juvenile hyaline fibromatosis (fibromatosis hyalinica multiplex juvenilis, Murray–Puretic–Drescher syndrome) *

Kaposiform hemangioendothelioma A vascular tumor is a tumor of vascular system, vascular origin; a soft tissue growth that can be either Benign tumor, benign or malignant, formed from blood vessels or lymph vessels. Examples of vascular tumors include hemangiomas, lymphangiomas, ...

(infantile kaposiform hemangioendothelioma) *

Kasabach–Merritt syndrome Kasabach–Merritt syndrome, also known as hemangioma with thrombocytopenia, is a rare disease, usually of infants, in which a vascular tumor leads to decreased platelet counts and sometimes other bleeding problems, which can be life-threatening. ...

(hemangioma with thrombocytopenia) * Keloid (Keloidal scar) Verbrennungsnarbe keloid1

* Keratinizing metaplasia * Keratocyst * Klippel–Trenaunay syndrome (angioosteohypertrophy syndrome, hemangiectatic hypertrophy) *

Knuckle pads Knuckle pads (also known as " Heloderma", meaning similar to the skin of the Gila monster lizard for which it is named) are circumscribed, keratotic, fibrous growths over the dorsa of the interphalangeal joints. They are described as well-define ...

(heloderma) *

Leiomyosarcoma Leiomyosarcoma is a malignant (cancerous) smooth muscle tumor. A benign tumor originating from the same tissue is termed leiomyoma. While leiomyosarcomas are not thought to arise from leiomyomas, some leiomyoma variants' classification is evolv ...

Lipoma A lipoma is a benign tumor made of fat tissue. They are generally soft to the touch, movable, and painless. They usually occur just under the skin, but occasionally may be deeper. Most are less than in size. Common locations include upper back, ...

Liposarcoma Liposarcomas are the most common subtype of soft tissue sarcomas, accounting for at least 20% of all sarcomas in adults. Soft tissue sarcomas are rare neoplasms with over 150 different histological subtypes or forms. Liposarcomas arise from the pr ...

(atypical lipoma, atypical lipomatous tumor) *

Lymphangiectasis Lymphangiectasia, also known as "lymphangiectasis", is a pathologic dilation of lymph vessels.McGavin/ Zachary (2007), Pathologic Basis of Veterinary Disease When it occurs in the intestines of dogs, and more rarely humans, it causes a disease kno ...

(lymphangioma) *

Lymphangiomatosis Lymphangiomatosis is a condition where a lymphangioma is not present in a single localised mass, but in a widespread or multifocal manner. It is a rare type of tumor which results from an abnormal development of the lymphatic system. It is though ...

Malignant fibrous histiocytoma Undifferentiated pleomorphic sarcoma (UPS), also termed pleomorphic myofibrosarcoma, high-grade myofibroblastic sarcoma, and high-grade myofibrosarcoma, is characterized by the World Health Organization (WHO), 2020, as a rare, poorly differentiate ...

Malignant peripheral nerve sheath tumor A malignant peripheral nerve sheath tumor (MPNST) is a form of cancer of the connective tissue surrounding nerves. Given its origin and behavior it is classified as a sarcoma. About half the cases are diagnosed in people with neurofibromatosis; t ...

(malignant schwannoma, neurofibrosarcoma, neurosarcoma) *

Mast cell sarcoma Mast cell sarcoma is an extremely aggressive form of sarcoma made up of neoplastic mast cells. A sarcoma is a tumor made of cells from connective tissue. Mast cell sarcoma is an extremely rare tumor. Only three cases have been are reported so far. ...

Meningocele Spina bifida (Latin for 'split spine'; SB) is a birth defect in which there is incomplete closing of the spine and the membranes around the spinal cord during early development in pregnancy. There are three main types: spina bifida occulta, men ...

Metastatic carcinoma Metastatic carcinoma is cancer that is able to grow at sites distant from the primary site of origin; thus, dissemination to the skin may occur with any malignant neoplasm, and these infiltrates may result from direct invasion of the skin from under ...

* Microvenular hemangioma (microcapillary hemangioma) * Midline nevus flammeus (angel's kiss, salmon patch) *

Multifocal lymphangioendotheliomatosis Multifocal lymphangioendotheliomatosis, also known as congenital cutaneovisceral angiomatosis with thrombocytopenia and multifocal lymphangioendotheliomatosis with thrombocytopenia, is a skin condition that presents at birth with hundreds of red-br ...

(congenital cutaneovisceral angiomatosis with thrombocytopenia, multifocal lymphangioendotheliomatosis with thrombocytopenia) * Multinucleate cell angiohistocytoma *

Multiple cutaneous and uterine leiomyomatosis syndrome Reed's syndrome is a rare inherited condition characterised by multiple cutaneous leiomyomas and, in women, uterine leiomyomas. It predisposes for renal cell cancer, an association denominated hereditary leiomyomatosis and renal cell cancer, an ...

(leiomyomatosis cutis et uteri, multiple leiomyomatosis, Reed's syndrome) *

Multiple cutaneous leiomyoma Multiple cutaneous leiomyomas, also known as Pilar leiomyomas, arise from the arrectores pilorum muscles, and are made up of a poorly circumscribed proliferation of haphazardly arranged smooth muscle fibers located in the dermis that appear to infi ...

(pilar leiomyoma) * Neural fibrolipoma *

Neuroblastoma Neuroblastoma (NB) is a type of cancer that forms in certain types of nerve tissue. It most frequently starts from one of the adrenal glands but can also develop in the neck, chest, abdomen, or spine. Symptoms may include bone pain, a lump in th ...

(infantile neuroblastoma, neuroepithelioma) * Neuroma cutis * Neurothekeoma (bizarre cutaneous neurofibroma, cutaneous lobular neuromyxoma, myxoma of the nerve sheath, myxomatous perineurioma, nerve sheath myxoma) * Nevus flammeus (capillary malformation, port-wine stain) * Nevus flammeus nuchae (stork bite) * Nevus lipomatosus superficialis (nevus lipomatosis of Hoffman and Zurhelle) * Nevus oligemicus *

Nodular fasciitis Nodular fasciitis (NF) is a benign, soft tissue tumor composed of myofibroblasts (i.e. immature cells that contain features of myocytes and fibroblasts) that typically occurs in subcutaneous tissue (i.e. lowermost layer of the skin), fascia (i. ...

(nodular pseudosarcomatous fasciits, pseudosarcomatous fasciitis, subcutaneous pseudosarcomatous fibromatosis) *Oral submucous fibrosis *Pachydermodactyly *Palisaded encapsulated neuroma *Paraneoplastic syndrome *Pearly penile papules (hirsuties coronae glandis, hirsutoid papillomas) *Peyronie's disease (induratio penis plastica) *Phakomatosis pigmentovascularis *Piloleiomyoma *Plantar fibromatosis (Ledderhose's disease) *Pleomorphic fibroma *Pleomorphic lipoma *Plexiform fibrohistiocytic tumor *Porokeratotic eccrine ostial and dermal duct nevus *Progressive nodular histiocytoma *Proliferating angioendotheliomatosis *Prominent inferior labial artery *Pseudo-ainhum *: *: Venous lake 1

*Retiform hemangioendothelioma (hobnail hemangioendothelioma) *Schwannoma (acoustic neuroma, neurilemmoma, neurinoma, neurolemmoma, Schwann cell tumor) *Solitary angiokeratoma *Solitary cutaneous leiomyoma *Solitary mastocytoma *Solitary neurofibroma (plexiform neurofibroma, solitary nerve sheath tumor, sporadic neurofibroma) *Spider angioma (nevus araneus, spider telangiectasia, spider nevus, vascular spider) *Spindle cell hemangioendothelioma (spindle cell hemangioma) *Spindle cell lipoma *Sternal cleft *Subungual exostosis *Superficial acral fibromyxoma *Systemic mastocytosis *Targetoid hemosiderotic hemangioma (hobnail hemangioma) *Telangiectasia *Telangiectasia macularis eruptiva perstans *Teratoma *Tufted angioma (acquired tufted angioma, angioblastoma, angioblastoma of Nakagawa, hypertrophic hemangioma, progressive capillary hemangioma, tufted hemangioma) *Umbilical granuloma *Universal angiomatosis (generalized telangiectasia) *Urticaria pigmentosa (childhood type of generalized eruption of cutaneous mastocytosis) *Venous lake (phlebectasis) *Wildervanck syndrome *Xanthelasmoidal mastocytosis *Zosteriform metastasis

Dermatitis

Dermatitis is a general term for "inflammation of the skin". *Childhood granulomatous periorificial dermatitis *Essential dermatitis

Atopic

Atopic dermatitis is a Chronic (medicine), chronic dermatitis associated with a hereditary tendency to develop allergy, allergies to food and inhalant substances. *Atopic dermatitis (atopic eczema, disseminated neurodermatitis, flexural eczema, infantile eczema, prurigo diathsique)

Contact

Contact dermatitis is caused by certain substances coming in contact with the skin. *Abietic acid dermatitis *Acid-induced contact dermatitis, Acid-induced *Acrylic monomer dermatitis *Adhesive dermatitis *African blackwood dermatitis *Airbag dermatitis (airbag burn) *Alkali-induced contact dermatitis, Alkali-induced *Allergic contact dermatitis, Allergic *Antifungal agent-induced contact dermatitis, Antifungal agent-induced *Antimicrobial agent-induced contact dermatitis, Antimicrobial agent-induced *Arsenic dermatitis *Artificial nail-induced contact dermatitis, Artificial nail-induced *Axillary antiperspirant-induced contact dermatitis, Axillary antiperspirant-induced *Axillary deodorant-induced contact dermatitis, Axillary deodorant-induced *Baboon syndrome *Black dermatographism *Bleaching cream-induced contact dermatitis, Bleaching cream-induced *Capsaisin-induced contact dermatitis, Capsaisin-induced *Chemical burn Sodium hydroxide burn

*Chloracne *Chrome dermatitis *Clothing-induced contact dermatitis, Clothing-induced *Cobalt dermatitis *Contact stomatitis (contact lichenoid reaction, lichenoid amalgam reaction, oral mucosal cinnamon reaction) *Contact urticaria *Corticosteroid-induced contact dermatitis, Corticosteroid-induced *Cosmetic dermatitis *Cosmetic intolerance syndrome *Dentifrice-induced contact dermatitis, Dentifrice-induced *Dermatitis from metals and metal salts *Dust-induced contact dermatitis, Dust-induced *Epoxy resin dermatitis *Ethylenediamine-induced contact dermatitis, Ethylenediamine-induced *Eye makeup-induced contact dermatitis, Eye makeup-induced *Fiberglass dermatitis *Flower-induced contact dermatitis, Flower-induced *Formaldehyde-induced contact dermatitis, Formaldehyde-induced *Formaldehyde-releasing agent-induced contact dermatitis, Formaldehyde-releasing agent-induced *Fragrance-induced contact dermatitis, Fragrance-induced *Gold dermatitis *Hair bleach-induced contact dermatitis, Hair bleach-induced *Hair dye-induced contact dermatitis, Hair dye-induced *Hair lotion-induced contact dermatitis, Hair lotion-induced *Hair spray-induced contact dermatitis, Hair spray-induced *Hair straightener-induced contact dermatitis, Hair straightener-induced *Hair tonic-induced contact dermatitis, Hair tonic-induced *Houseplant-induced contact dermatitis, Houseplant-induced *Hydrocarbon-induced contact dermatitis, Hydrocarbon-induced *Irritant folliculitis *Lacquer dermatitis (lacquer sensitivity) *Lanolin-induced contact dermatitis, Lanolin-induced *Lipstick-induced contact dermatitis, Lipstick-induced *Local anesthetic-induced contact dermatitis, Local anesthetic-induced *Makassar ebony dermatitis *Marine plant-induced contact dermatitis, Marine plant-induced *Mechanical irritant dermatitis *Mercury dermatitis *Mouthwash-induced contact dermatitis, Mouthwash-induced *Nail lacquer-induced contact dermatitis, Nail lacquer-induced *Nail polish remover-induced contact dermatitis, Nail polish remover-induced *Nickel dermatitis *Occupation-induced contact dermatitis, Occupation-induced *p-Chloro-Meta-Xylenol-induced contact dermatitis, p-Chloro-meta-xylenol-induced *Paraben-induced contact dermatitis, Paraben-induced *Paraphenylenediamine dermatitis *Permanent wave preparation-induced contact dermatitis, Permanent wave preparation-induced *Phenothiazine drug-induced contact dermatitis, Phenothiazine drug-induced *Photoallergic contact dermatitis, Photoallergic *Photoirritant contact dermatitis, Photoirritant *Plant derivative-induced contact dermatitis, Plant derivative-induced *Pollen-induced contact dermatitis, Pollen-induced *Polyester resin dermatitis *Propylene glycol-induced contact dermatitis, Propylene glycol-induced URUSHIOL BLISTERING

*Protein contact dermatitis *Quaternium-15 hypersensitivity *Reed dermatitis *Rosewood dermatitis *Rosin dermatitis *Rubber dermatitis *Seed-induced contact dermatitis, Seed-induced *Shoe dermatitis *Solvent-induced contact dermatitis, Solvent-induced *Sorbic acid-induced contact dermatitis, Sorbic acid-induced *Subjective irritant contact dermatitis (sensory irritant contact dermatitis) *Sunscreen-induced contact dermatitis, Sunscreen-induced *Systemic contact dermatitis *Tear gas dermatitis *Textile dermatitis *Traumatic irritant contact dermatitis *Tree-associated plant-induced contact dermatitis, Tree-associated plant-induced *Tree-induced contact dermatitis, Tree-induced *Tulip fingers *Urushiol-induced contact dermatitis, Urshiol-induced *Vegetable-induced contact dermatitis, Vegetable-induced

Eczema

Eczema refers to a broad range of conditions that begin as Spongiosis, spongiotic dermatitis and may progress to a Lichenification, lichenified stage. *Autoimmune estrogen dermatitis *Autoimmune progesterone dermatitis *Autosensitization dermatitis *Breast eczema (nipple eczema) *Chronic vesiculobullous hand eczema *Circumostomy eczema *Dyshidrosis (acute vesiculobullous hand eczema, cheiropompholyx, dyshidrotic eczema, pompholyx, podopompholyx) *Ear eczema *Eyelid dermatitis *Hand eczema *Hyperkeratotic hand dermatitis *Id reaction (disseminated eczema, generalized eczema) *Irritant diaper dermatitis (diaper dermatitis, napkin dermatitis) *Juvenile plantar dermatosis (atopic winter feet, dermatitis plantaris sicca, forefoot dermatitis, moon-boot foot syndrome, sweaty sock dermatitis) *Molluscum dermatitis *Nummular dermatitis (discoid eczema, microbial eczema, nummular eczema, nummular neurodermatitis) *Nutritional deficiency eczema *Sulzberger–Garbe syndrome (oid-oid disease) *Xerotic eczema (asteatotic eczema, desiccation dermatitis, ''eczema craquelé'', pruritus hiemalis, winter eczema, winter itch)

Pustular

Pustular dermatitis is an inflammation of the skin that presents with pustular skin lesion, lesions. *Eosinophilic pustular folliculitis (Ofuji's disease, sterile eosinophilic pustulosis) *Reactive arthritis *Subcorneal pustular dermatosis (Sneddon–Wilkinson disease)

Seborrheic

Seborrheic dermatitis is a chronic (medicine), chronic, superficial, inflammatory disease characterized by Scale (dermatology), scaling on an erythematous base. *Infantile seborrheic dermatitis *Leiner's disease *Pityriasis simplex capillitii (dandruff) *Seborrheic dermatitis (seborrheic eczema)

Disturbances of pigmentation

Disturbances of human pigmentation, either loss or reduction, may be related to loss of melanocytes or the inability of melanocytes to produce melanin or transport melanosomes correctly. *Albinism–black lock–cell migration disorder of the neurocytes of the gut–deafness syndrome (ABCD syndrome) *Albinism–deafness syndrome (Woolf syndrome, Ziprkowski–Margolis syndrome) *Alezzandrini syndrome *Argyria *Arsenic poisoning *Berlin syndrome *Pigmentation changes caused by the bioaccumulation of pigments, e.g. Canthaxanthin *Chédiak–Higashi syndrome *Chrysiasis *Cross–McKusick–Breen syndrome (Cross syndrome, oculocerebral-hypopigmentation syndrome) *Dermatopathia pigmentosa reticularis (dermatopathia pigmentosa reticularis hyperkeratotica et mutilans, dermatopathia pigmentosa reticularis hypohidotica et atrophica, dermatopathic pigmentosa reticularis) *Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi, symmetrical dyschromatosis of the extremities) *Dyschromatosis universalis hereditaria *Elejalde syndrome (Griscelli syndrome type 1) *Eruptive hypomelanosis *Familial progressive hyperpigmentation *Galli–Galli disease *Griscelli syndrome type 2 (partial albinism with immunodeficiency) *Griscelli syndrome type 3 *Hemochromatosis (bronze diabetes) *Hemosiderin hyperpigmentation *Hermansky–Pudlak syndrome *Idiopathic guttate hypomelanosis (leukopathia symmetrica progressiva) *Iron metallic discoloration *Klein–Waardenburg syndrome *Lead poisoning *Leukoderma *Melanoma-associated leukoderma *Melasma (chloasma faciei, mask of pregnancy) *Mukamel syndrome *Necklace of Venus *Nevus anemicus

*Nevus depigmentosus (nevus achromicus) *Ocular albinism *Oculocutaneous albinism *Pallister–Killian syndrome *Periorbital hyperpigmentation *Photoleukomelanodermatitis of Kobori *Phylloid hypomelanosis *Piebaldism *Pigmentatio reticularis faciei et colli *Pityriasis alba *Poikiloderma of Civatte *Poikiloderma vasculare atrophicans *Postinflammatory hyperpigmentation (postinflammatory hypermelanosis) *Postinflammatory hypopigmentation *Progressive macular hypomelanosis *Quadrichrome vitiligo *Reticular pigmented anomaly of the flexures (dark dot disease, Dowling–Degos' disease) *Reticulate acropigmentation of Kitamura *Revesz syndrome *Riehl melanosis *Scratch dermatitis (flagellate pigmentation from bleomycin) *Segmental vitiligo *Shah–Waardenburg syndrome *Shiitake mushroom dermatitis (flagellate mushroom dermatitis, mushroom worker's disease, shiitake-induced toxicoderma) *Tar melanosis (melanodermatitis toxica lichenoides) *Tietz syndrome *Titanium metallic discoloration *Transient neonatal pustular melanosis (transient neonatal pustulosis, lentigines neonatorum) *Trichrome vitiligo *Vagabond's leukomelanoderma *Vasospastic macule *Vitiligo *Vitiligo ponctué *Vogt–Koyanagi–Harada syndrome *Waardenburg syndrome *Wende–Bauckus syndrome (Pegum syndrome) *Woronoff's ring *X-linked reticulate pigmentary disorder (familial cutaneous amyloidosis, Partington amyloidosis, Partington cutaneous amyloidosis, Partington syndrome type II, reticulate pigmentary disorder, X-linked reticulate pigmentary disorder with systemic manifestations) *Yemenite deaf-blind hypopigmentation syndrome

Drug eruptions

Drug eruptions are adverse drug reactions that present with cutaneous manifestations. *Acrodynia (calomel disease, erythredemic polyneuropathy, pink disease) *Acute generalized exanthematous pustulosis (pustular drug eruption, toxic pustuloderma)

Acute generalized exanthematous pustulosis

*Adverse reaction to biologic agents *Adverse reaction to cytokines *Allopurinol hypersensitivity syndrome *Anticoagulant-induced skin necrosis *Anticonvulsant hypersensitivity syndrome *Bromoderma *Bullous drug reaction (bullous drug eruption, generalized bullous fixed drug eruption, multilocular bullous fixed drug eruption) *Chemotherapy-induced acral erythema (palmoplantar erythrodysesthesia syndrome) *Chemotherapy-induced hyperpigmentation *Drug-induced acne *Drug-induced angioedema *Drug-related gingival hyperplasia *Drug-induced lichenoid reaction (drug-induced lichen planus, lichenoid drug eruption) *Drug-induced lupus erythematosus *Drug-induced nail changes *Drug-induced pigmentation *Drug-induced pseudolymphoma *Drug-induced urticaria *Erythema multiforme major (erythema multiforme minor–erythema multiforme von Hebra) *Exudative hyponychial dermatitis *Fixed drug reaction *Halogenoderma *Heparin necrosis *HIV disease-related drug reaction *Hydroxyurea dermopathy *Injection site reaction *Iododerma *Leukotriene receptor antagonist-associated Churg–Strauss syndrome *Linear IgA bullous dermatosis (linear IgA dermatosis) *Photosensitive drug reaction *Red man syndrome (Drug eruption), Red man syndrome *Severe cutaneous adverse reactions (includes DRESS syndrome, Steven Johnson syndrome, Toxic epidermal necrolysis, Stevens–Johnson syndrome#Classification, Stevens-Johnson/toxic epidermal necrolysis overlap syndrome, and Acute generalized exanthematous pustulosis) *Scleroderma-like reaction to taxanes *Serum sickness-like reaction *Steroid acne *Steroid folliculitis *Stevens–Johnson syndrome *Sulfonamide hypersensitivity syndrome *Texier's disease *Toxic epidermal necrolysis (Lyell's syndrome) *Urticarial erythema multiforme *Vitamin K reaction *Warfarin necrosis

Endocrine-related

Endocrine conditions often present with cutaneous findings as the

interacts with the endocrine system in many ways. *Acanthosis nigricans associated with malignancy (acanthosis nigricans type I) *Acanthosis nigricans associated with obesity, insulin-resistant states, and endocrinopathy (acanthosis nigricans type III) *Acral acanthosis nigricans (acral acanthotic anomaly) *Acral dry gangrene *Acromegaly *Addison's disease *Adrenal adenoma *Adrenal carcinoma *Adrenal hyperplasia *Alopecia–nail dystrophy–ophthalmic complications–thyroid dysfunction–hypohidrosis–ephelides and enteropathy–respiratory tract infections syndrome (ANOTHER syndrome) *Arrhenoblastoma *Cretinism *Cushing's syndrome *Excess ovarian androgen release syndrome (ovarian SAHA syndrome) *Familial acanthosis nigricans (acanthosis nigricans type II) *Growth hormone deficiency *Hyperandrogenism–insulin resistance–acanthosis nigricans syndrome (HAIR-AN syndrome) *Hyperparathyroidism *Hyperprolactinemic SAHA syndrome *Hyperthyroidism *Hypoparathyroidism *Hypothyroidism *Leydig cell tumor *Multiple endocrine neoplasia type 1 (Wermer syndrome) *Multiple endocrine neoplasia type 2 (multiple endocrine neoplasia type 2A, pheochromocytoma and amyloid-producing medullary thyroid carcinoma, PTC syndrome, Sipple syndrome) *Multiple endocrine neoplasia type 3 (mucosal neuromata with endocrine tumors, multiple endocrine neoplasia type 2B, multiple mucosal neuroma syndrome, Wagenmann–Froboese syndrome) *Myxedema *Panhypopituitarism *Persistent adrenarche syndrome (adrenal SAHA syndrome) *Polycystic ovarian syndrome *Seborrhoea–acne–hirsutism–alopecia (SAHA syndrome) *Thyroid acropachy

Eosinophilic

Eosinophilic cutaneous conditions encompass a wide variety of diseases that are characterized histologically by the presence of eosinophils in the inflammatory infiltrate, or evidence of eosinophil degranulation. *Angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma, histiocytoid hemangioma, inflammatory angiomatous nodule, inflammatory arteriovenous hemangioma, intravenous atypical vascular proliferation, papular angioplasia, pseudopyogenic granuloma) *Annular erythema of infancy *Arthropod assault *Eosinophilic cellulitis (Wells' syndrome) *Eosinophilic fasciitis (Shulman's syndrome) *Eosinophilic granuloma *Eosinophilic granulomatosis with polyangiitis *Eosinophilic pustular folliculitis of infancy (eosinophilic pustular folliculitis in infancy, infantile eosinophilic pustular folliculitis, neonatal eosinophilic pustular folliculitis) *Eosinophilic ulcer of the oral mucosa (eosinophilic ulcer of the tongue, Riga–Fede disease, traumatic eosinophilic granuloma) *Eosinophilic vasculitis *Erythema toxicum neonatorum (erythema toxicum, toxic erythema of the newborn) *Granuloma faciale *Hypereosinophilia *Hypereosinophilic syndrome *Incontinentia pigmenti (Bloch–Siemens syndrome, Bloch–Sulzberger disease, Bloch–Sulzberger syndrome) *Itchy red bump disease (papular dermatitis) *Juvenile xanthogranuloma *Kimura's disease *Nodules–eosinophilia–rheumatism–dermatitis–swelling syndrome *Pachydermatous eosinophilic dermatitis *Papular eruption of blacks *Papuloerythroderma of Ofuji *Pruritic papular eruption of HIV disease

Epidermal nevi, neoplasms, and cysts

Epidermal nevus, nevi, neoplasms, and cysts are

s that develop from the Epidermis (skin), epidermal layer of the skin. *Aberrant basal cell carcinoma *Acanthoma fissuratum (granuloma fissuratum, spectacle frame acanthoma) *Acrospiroma (clear cell hidradenoma, dermal duct tumor, hidroacanthoma simplex, nodular hidradenoma, poroma) *Actinic keratosis (senile keratosis, solar keratosis) *Adenoid squamous cell carcinoma (pseudoglandular squamous cell carcinoma) *Aggressive digital papillary adenocarcinoma (digital papillary adenocarcinoma, papillary adenoma) Basal cell carcinoma2

*Apocrine gland carcinoma *Apocrine nevus *Arsenical keratosis *Atrophic actinic keratosis *Balanitis plasmacellularis (balanoposthitis chronica circumscripta plasmacellularis, balanitis circumscripta plasmacellularis, plasma cell balanitis, plasma cell vulvitis, vulvitis circumscripta plasmacellularis, Zoon's balanitis, Zoon's erythroplasia, Zoon's vulvitis) *Basal cell carcinoma *Basaloid follicular hamartoma *Basaloid squamous cell carcinoma *Birt–Hogg–Dubé syndrome *Bowen's disease (squamous cell carcinoma ''in situ'') *Brooke–Fordyce syndrome *Ceruminoma *Cicatricial basal cell carcinoma (morpheaform basal cell carcinoma, morphoeic basal cell carcinoma) *Ciliated cyst of the vulva (cutaneous Müllerian cyst, paramesonephric mucinous cyst of the vulva) *Clear cell acanthoma (acanthome cellules claires of Degos and Civatte, Degos acanthoma, pale cell acanthoma) *Clear cell squamous cell carcinoma (clear cell carcinoma of the skin) *Chronic scar keratosis (chronic cicatrix keratosis) *Clonal seborrheic keratosis *Common seborrheic keratosis (basal cell papilloma, solid seborrheic keratosis) *Cowden syndrome (Cowden's disease, multiple hamartoma syndrome) *Cutaneous ciliated cyst *Cutaneous columnar cyst *Cutaneous horn (Cornu cutaneum) *Cystic basal cell carcinoma *Dermal eccrine cylindroma (cylindroma) *Dermatosis papulosa nigra *Desmoplastic trichoepithelioma *Dilated pore (dilated pore of Winer) *Eccrine carcinoma (syringoid carcinoma) *Eccrine nevus *Epidermal cyst (epidermal inclusion cyst, epidermoid cyst, infundibular cyst, keratin cyst) *Epidermal nevus syndrome (Feuerstein and Mims syndrome, Solomon's syndrome) *Epidermolytic acanthoma *Epithelioma cuniculatum (Ackerman tumor, carcinoma cuniculatum) *Eruptive vellus hair cyst *Erythroplasia of Queyrat *Extramammary Paget's disease *Fibroepithelioma *Fibroepithelioma of Pinkus *Fibrofolliculoma *Follicular hybrid cyst (Hybrid cyst) *Folliculosebaceous-apocrine hamartoma (follicular-apocrine hamartoma) *Folliculosebaceous cystic hamartoma *Generalized eruptive keratoacanthoma (generalized eruptive keratoacanthoma of Grzybowski) *Giant solitary trichoepithelioma *Hidradenoma *Hidradenocarcinoma *Hidrocystoma (cystadenoma, Moll's gland cyst, sudoriferous cyst) *Hydrocarbon keratosis (pitch keratosis, tar keratosis, tar wart) *Hyperkeratosis lenticularis perstans (Flegel's disease) *Hyperkeratosis of the nipple and areola *Hyperkeratotic actinic keratosis *Ichthyosis hystrix (ichthyosis hystrix gravior type Lambert, porcupine man, systematized verrucous nevus) *Ichthyosis hystrix of Curth–Macklin *Infiltrative basal cell carcinoma *Inflammatory linear verrucous epidermal nevus *Inverted follicular keratosis *Irritated seborrheic keratosis (basosquamous cell acanthoma, inflamed seborrheic keratosis) *Isthmicoma (infundibuloma, tumor of the follicular infundibulum) *Juvenile myelomonocytic leukemia *Keratin implantation cyst *Keratoacanthoma *Keratoacanthoma centrifugum marginatum *Large cell acanthoma *Lichenoid actinic keratosis *Lichenoid keratosis (benign lichenoid keratosis, lichen planus-like keratosis, solitary lichen planus, solitary lichenoid keratosis) *Linear verrucous epidermal nevus (linear epidermal nevus, verrucous epidermal nevus) *Malignant acrospiroma (spiradenocarcinoma) *Malignant mixed tumor (malignant chondroid syringoma) *Malignant trichilemmal cyst *Mantleoma *Marjolin's ulcer *Melanoacanthoma (pigmented seborrheic keratosis) *Merkel cell carcinoma (cutaneous apudoma, primary neuroendocrine carcinoma of the skin, primary small cell carcinoma of the skin, trabecular carcinoma of the skin) *Microcystic adnexal carcinoma (sclerosing sweat duct carcinoma) *Micronodular basal cell carcinoma *Milia en plaque *Milium (disease), Milium Milia big

*Mixed tumor (chondroid syringoma) *Mucinous carcinoma *Mucinous nevus (nevus mucinosus) *Muir–Torre syndrome *Multiple familial trichoepithelioma (Brooke–Spiegler syndrome, epithelioma adenoides cysticum) *Multiple keratoacanthomas (Ferguson–Smith syndrome, Ferguson-Smith type of multiple self-healing keratoacanthomas, multiple keratoacanthomas of the Ferguson–Smith type) *Multiple minute digitate hyperkeratosis (digitate keratoses, disseminated spiked hyperkeratosis, familial disseminated piliform hyperkeratosis, minute aggregate keratosis) *Nevoid basal cell carcinoma syndrome (basal cell nevus syndrome, Gorlin syndrome, Gorlin–Goltz syndrome) *Nevus comedonicus (comedo nevus) *Nevus comedonicus syndrome *Nevus sebaceous (nevus sebaceous of Jadassohn, organoid nevus) *Nevus unius lateris *Nodular basal cell carcinoma (classic basal cell carcinoma) *Paget's disease of the breast *Papillary eccrine adenoma (tubular apocrine adenoma) *Papillary hidradenoma (hidradenoma papilliferum) *Papillomatosis cutis carcinoides (Gottron's carcinoid papillomatosis, papillomatosis cutis carcinoides of Gottron–Eisenlohr) *Patch blue nevus (acquired dermal melanocytosis, dermal melanocyte hamartoma) *Perifollicular fibroma *Phakomatosis pigmentokeratotica *Pigmented actinic keratosis *Pigmented basal cell carcinoma *Pigmented hairy epidermal nevus syndrome *Pilar sheath acanthoma *Pilonidal sinus (Barber's interdigital pilonidal sinus, pilonidal cyst, pilonidal disease) *Porocarcinoma (malignant poroma, eccrine porocarcinoma) *Polypoid basal cell carcinoma *Pore-like basal cell carcinoma *Primary cutaneous adenoid cystic carcinoma *Proliferating epidermoid cyst (proliferating epithelial cyst) *Proliferating trichilemmal cyst (pilar tumor, proliferating follicular cystic neoplasm, proliferating pilar tumor, proliferating trichilemmal tumor) *Pseudocyst of the auricle (auricular endochondrial pseudocyst, cystic chondromalacia, endochondral pseudocyst, intracartilaginous cyst) *Pseudoepitheliomatous keratotic and micaceous balanitis *PUVA keratosis *Rasmussen syndrome *Reactional keratosis *Reticulated seborrheic keratosis (adenoid seborrheic keratosis) *Rodent ulcer (Jacobi ulcer) *Schimmelpenning syndrome (Schimmelpenning–Feuerstein–Mims syndrome) *Sebaceoma (sebaceous epithelioma) *Sebaceous adenoma *Sebaceous carcinoma *Sebaceous hyperplasia *Sebaceous nevus syndrome *Seboacanthoma *Seborrheic keratosis (seborrheic verruca, senile wart) *Seborrheic keratosis with squamous atypia *Signet-ring cell squamous cell carcinoma *Solitary keratoacanthoma (subungual keratoacanthoma) *Solitary trichoepithelioma *Spindle cell squamous cell carcinoma (spindle cell carcinoma) *Spiradenoma *Squamous cell carcinoma

*Steatocystoma multiplex (epidermal polycystic disease, sebocystomatosis) *Steatocystoma simplex (simple sebaceous duct cyst, solitary steatocystoma) *Stucco keratosis (digitate seborrheic keratosis, hyperkeratotic seborrheic keratosis, keratosis alba, serrated seborrheic keratosis, verrucous seborrheic keratosis) *Superficial basal cell carcinoma (superficial multicentric basal cell carcinoma) *Syringadenoma papilliferum (syringocystadenoma papilliferum) *Syringofibroadenoma (acrosyringeal nevus of Weedon and Lewis) *Syringoma *Systematized epidermal nevus *Thermal keratosis *Trichilemmal carcinoma *Trichilemmal cyst (isthmus-catagen cyst, pilar cyst) *Trichilemmoma *Trichoadenoma (trichoadenoma of Nikolowski) *Trichoblastoma *Trichoblastic fibroma *Trichodiscoma *Trichofolliculoma *Unilateral palmoplantar verrucous nevus *Urethral caruncle *Verrucous carcinoma *Verrucous cyst (cystic papilloma) *Viral keratosis *Warty dyskeratoma (isolated dyskeratosis follicularis) *Waxy keratosis of childhood (kerinokeratosis papulosa) *Zoon's vulvitis *Zosteriform speckled lentiginous nevus

Erythemas

Erythema migrans - erythematous rash in Lyme disease - PHIL 9875

Erythemas are reactive skin conditions in which there is Blanch (medical), blanchable redness. *Erythema annulare centrifugum (deep gyrate erythema, erythema perstans, palpable migrating erythema, superficial gyrate erythema) *Erythema gyratum repens (Gammel's disease) *Erythema migrans (erythema chronicum migrans) *Erythema multiforme *Erythema multiforme minor (herpes simplex-associated erythema multiforme) *Erythema palmare *Generalized erythema *Necrolytic acral erythema *Necrolytic migratory erythema (glucagonoma syndrome)

Genodermatoses

Genodermatoses are Heredity, inherited genetic skin conditions often grouped into three categories: chromosome, chromosomal, single gene, and polygenesis (genetics), polygenetic. *18q deletion syndrome *Acrodermatitis enteropathica *Acrogeria (Gottron syndrome) *Acrokeratosis verruciformis (acrokeratosis verruciformis of Hopf) *Adams–Oliver syndrome *Adducted thumbs syndrome *Albright's hereditary osteodystrophy *Angelman syndrome *Apert syndrome (acrocephalosyndactyly) *Arthrogryposis–renal dysfunction–cholestasis syndrome *Ataxia telangiectasia (Louis–Bar syndrome) *Atrichia with papular lesions (papular atrichia) *Atrophodermia vermiculata (acne vermoulante, acne vermoulanti, atrophoderma reticulata symmetrica faciei, atrophoderma reticulatum, atrophoderma vermiculata, atrophoderma vermiculatum, atrophodermia reticulata symmetrica faciei, atrophodermia ulerythematosa, ''atrophodermie vermiculée des joues avec kératoses folliculaires'', folliculitis ulerythema reticulata, folliculitis ulerythematous reticulata, folliculitis ulerythemosa, honeycomb atrophy, ulerythema acneforme, ulerythema acneiforme) *Autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome *Bart syndrome *Bazex–Dupré–Christol syndrome (Bazex syndrome, follicular atrophoderma and basal cell carcinomas) *Beare–Stevenson cutis gyrata syndrome *Bloom syndrome (Bloom–Torre–Machacek syndrome) *Blue rubber bleb nevus syndrome *Brittle hair–intellectual impairment–decreased fertility–short stature syndrome *Cantú syndrome *Cardio-facio-cutaneous syndrome (cardiofaciocutaneous syndrome) *Cartilage–hair hypoplasia (McKusick type metaphyseal chondrodysplasia) *Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome *Childhood tumor syndrome *Chondrodysplasia punctata *Junctional epidermolysis bullosa (medicine), Cicatricial junctional epidermolysis bullosa *Craniosynostosis–anal anomalies–porokeratosis syndrome *Cockayne syndrome *Colobomas of the eye–heart defects–ichthyosiform dermatosis–mental retardation–ear defects syndrome (CHIME syndrome, Zunich neuroectodermal syndrome, Zunich–Kaye syndrome) *Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (CHILD syndrome) *Conradi–Hünermann syndrome (Conradi–Hünermann–Happle syndrome, Happle syndrome, X-linked dominant chondrodysplasia punctata) *Costello syndrome *Cronkhite–Canada syndrome *Crouzon syndrome *Cutis verticis gyrata *Darier's disease (Darier–White disease, dyskeratosis follicularis, keratosis follicularis)

*DeSanctis–Cacchione syndrome *Disseminated superficial actinic porokeratosis *Disseminated superficial porokeratosis *Dolichol kinase deficiency *Dominant dystrophic epidermolysis bullosa *Dyskeratosis congenita (Zinsser–Cole–Engman syndrome) *Dystrophic epidermolysis bullosa *Ectodermal dysplasia *Ectodermal dysplasia with corkscrew hairs *Ectrodactyly–ectodermal dysplasia–cleft syndrome (EEC syndrome, split hand–split foot–ectodermal dysplasia–cleft syndrome) *Epidermolysis bullosa herpetiformis (Dowling–Meara epidermolysis bullosa simplex) *Epidermolysis bullosa simplex *Epidermolysis bullosa simplex of Ogna *Epidermolysis bullosa simplex with mottled pigmentation *Epidermolysis bullosa simplex with muscular dystrophy *Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma, bullous ichthyosiform erythroderma) *Erythrokeratodermia with ataxia (Giroux–Barbeau syndrome) *Familial benign chronic pemphigus (familial benign pemphigus, Hailey–Hailey disease) *Fanconi syndrome (familial pancytopenia, familial panmyelophthisis) *Fibrodysplasia ossificans progressiva *Focal dermal hypoplasia (Goltz syndrome) *Follicular atrophoderma *Franceschetti–Klein syndrome (mandibulofacial dysostosis) *Gardner's syndrome (familial colorectal polyposis) *Gastrocutaneous syndrome *Junctional epidermolysis bullosa (medicine), Generalized atrophic benign epidermolysis bullosa *Generalized epidermolysis bullosa simplex (Koebner variant of generalized epidermolysis bullosa simplex) *Generalized trichoepithelioma *Giant axonal neuropathy with curly hair *Gingival fibromatosis with hypertrichosis *Haber syndrome *Hallerman–Streiff syndrome *Harlequin-type ichthyosis (harlequin baby, harlequin fetus, harlequin ichthyosis, ichthyosis congenita, ichthyosis congenita gravior) *Hay–Wells syndrome (AEC syndrome, ankyloblepharon filiforme adnatum–ectodermal dysplasia–cleft palate syndrome, ankyloblepharon–ectodermal defects–cleft lip and palate syndrome, ankyloblepharon–ectodermal dysplasia–clefting syndrome) *Hereditary sclerosing poikiloderma Keratosis pilaris arm

*Heterochromia iridum *Holocarboxylase synthetase deficiency *Hypohidrotic ectodermal dysplasia (anhidrotic ectodermal dysplasia, Christ–Siemens–Touraine syndrome) *Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome *Hypotrichosis–lymphedema–telangiectasia syndrome *Ichthyosis–brittle hair–impaired intelligence–decreased fertility–short stature syndrome (IBIDS syndrome, sulfur-deficient brittle hair syndrome, Tay's syndrome, trichothiodystrophy, trichothiodystrophy with ichthyosis) *Ichthyosis bullosa of Siemens (ichthyosis exfoliativa) *Ichthyosis follicularis (ichthyosis follicularis with alopecia and photophobia syndrome) *Ichthyosis linearis circumflexa *Ichthyosis prematurity syndrome *Ichthyosis vulgaris (autosomal dominant ichthyosis, ichthyosis simplex) *Ichthyosis with confetti *Neonatal ichthyosis–sclerosing cholangitis syndrome (ichthyosis–sclerosing cholangitis syndrome, NISCH syndrome) *Incontinentia pigmenti achromians (hypomelanosis of Ito) *Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndrome *Jaffe–Campanacci syndrome *Johanson–Blizzard syndrome *Johnson–McMillin syndrome *Joubert syndrome *Junctional epidermolysis bullosa (medicine), Junctional epidermolysis bullosa *Junctional epidermolysis bullosa gravis (epidermolysis bullosa letalis, Herlitz disease, Herlitz epidermolysis bullosa, Herlitz syndrome, lethal junctional epidermolysis bullosa) *Junctional epidermolysis bullosa with pyloric atresia *Kabuki syndrome (Kabuki makeup syndrome, Niikawa–Kuroki syndrome) *Keratolytic winter erythema (erythrokeratolysis hiemalis, Oudtshoorn disease, Oudtshoorn skin) *Keratosis follicularis spinulosa decalvans (Siemens-1 syndrome) *Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome *Keratosis pilaris atrophicans faciei (folliculitis rubra, keratosis pilaris rubra atrophicans faciei, lichen pilare, ''lichen pilaire ou xerodermie pilaire symmetrique de la face'', ulerythema ophryogenes, ''xerodermi pilaire symmetrique de la face'') *Keratosis pilaris *Kindler syndrome (acrokeratotic poikiloderma, bullous acrokeratotic poikiloderma of Kindler and Weary, congenital poikiloderma with blisters and keratoses, congenital poikiloderma with bullae and progressive cutaneous atrophy, hereditary acrokeratotic poikiloderma, hyperkeratosis–hyperpigmentation syndrome, Weary–Kindler syndrome) *Klinefelter syndrome *Klippel–Feil syndrome *Lamellar ichthyosis (collodion baby) *Legius syndrome (neurofibromatosis type 1-like syndrome) *Lelis syndrome *Lenz–Majewski syndrome *Leschke syndrome *Lethal acantholytic epidermolysis bullosa *Lhermitte–Duclos disease *Linear and whorled nevoid hypermelanosis (linear nevoid hyperpigmentation, progressive cribriform and zosteriform hyperpigmentation, reticulate and zosteriform hyperpigmentation, reticulate hyperpigmentation of Iijima and Naito and Uyeno, zebra-like hyperpigmentation in whorls and streaks, zebra-line hyperpigmentation) *Linear Darier disease (acantholytic dyskeratotic epidermal nevus) *Linear porokeratosis *Localized epidermolysis bullosa simplex (Weber–Cockayne syndrome, Weber–Cockayne variant of generalized epidermolysis bullosa simplex) *Mandibuloacral dysplasia *Marinesco–Sjögren syndrome *McCune–Albright syndrome *McCusick syndrome *Metageria *Microphthalmia–dermal aplasia–sclerocornea syndrome *Junctional epidermolysis bullosa (medicine), Mitis junctional epidermolysis bullosa (nonlethal junctional epidermolysis bullosa) *Mitochondrial myopathy–encephalopathy–lactic acidosis–stroke syndrome *Multiple lentigines syndrome (cardiocutaneous syndrome, Gorlin syndrome II, lentiginosis profusa syndrome, LEOPARD syndrome, progressive cardiomyopathic lentiginosis) *Multiple pterygium syndrome *Multiple sulfatase deficiency (Austin disease, mucosulfatidosis) *Naegeli–Franceschetti–Jadassohn syndrome (chromatophore nevus of Naegeli) *Netherton syndrome *Neurofibromatosis type 1 (von Recklinghausen's disease) *Neurofibromatosis type 3 (neurofibromatosis mixed type) *Neurofibromatosis type 4 (neurofibromatosis variant type) *Neutral lipid storage disease (Dorfman–Chanarin syndrome) *Nonbullous congenital ichthyosiform erythroderma (congenital ichthyosiform erythroderma) *Noonan syndrome *Oculocerebrocutaneous syndrome (Delleman–Oorthuys syndrome) *Oculodentodigital dysplasia *Odonto–Tricho–Ungual–Digital–Palmar syndrome *Oliver–McFarlane syndrome *Orofaciodigital syndrome *Pachydermoperiostosis (idiopathic hypertrophic osteoathorpathy, Touraine–Solente–Gole syndrome) *Peeling skin syndrome (acral peeling skin syndrome, continual peeling skin syndrome, familial continual skin peeling, idiopathic deciduous skin, keratolysis exfoliativa congenita) *Pfeiffer syndrome *Photosensitivity–ichthyosis–brittle sulfur-deficient hair–impaired intelligence–decreased fertility–short stature syndrome *Pityriasis rotunda (pityriasis circinata, tinea circinata) *Plate-like osteoma cutis *Plaque-type porokeratosis (classic porokeratosis, porokeratosis of Mibelli) *Polyneuropathy–organomegaly–endocrinopathy–monoclonal gammopathy–skin changes syndrome (Crow–Fukase syndrome) *Polyostotic fibrous dysplasia (Albright's disease) *Popliteal pterygium syndrome *Porokeratosis *Porokeratosis palmaris et plantaris disseminata *Prader–Willi syndrome *Progeria (Hutchinson–Gilford progeria syndrome, Hutchinson–Gilford syndrome, progeria syndrome) *Progressive osseous heteroplasia *Progressive symmetric erythrokeratodermia (erythrokeratodermia progressiva symmetrica) *Proteus syndrome *Proteus-like syndrome *Punctate porokeratosis *Rapp–Hodgkin syndrome (Rapp–Hodgkin ectodermal dysplasia syndrome) *Recessive dystrophic epidermolysis bullosa (Hallopeau–Siemens variant of epidermolysis bullosa, Hallopeau–Siemens disease) *Refsum's disease (heredopathia atactica polyneuritiformis, phytanic acid storage disease) *Relapsing linear acantholytic dermatosis *Restrictive dermopathy *Rhizomelic chondrodysplasia punctata (autosomal recessive chondrodysplasia punctata type 1, chondrodystrophia calcificans punctata, peroxisomal biogenesis disorder complementation group 11) *Rombo syndrome *Rothmund–Thomson syndrome (poikiloderma congenitale) *Rud syndrome *Say syndrome *Scalp–ear–nipple syndrome (Finlay–Marks syndrome) *Schindler disease (Kanzaki disease, alpha-N-acetylgalactosaminidase deficiency) *Schinzel–Giedion syndrome *Scleroatrophic syndrome of Huriez (Huriez syndrome, palmoplantar keratoderma with scleroatrophy, palmoplantar keratoderma with sclerodactyly, scleroatrophic and keratotic dermatosis of the limbs, sclerotylosis) *Segmental neurofibromatosis *Senter syndrome (Desmons' syndrome) *Shabbir syndrome (laryngo–onycho–cutaneous syndrome) *Silver–Russell syndrome *Sjögren–Larsson syndrome *Skin fragility syndrome (plakophilin 1 deficiency) *Smith–Lemli–Opitz syndrome *Sturge–Weber syndrome *Supernumerary nipples–uropathies–Becker's nevus syndrome *Terminal osseous dysplasia with pigmentary defects *Tooth and nail syndrome (hypodontia with nail dysgenesis, Witkop syndrome) *Townes–Brocks syndrome *Transient bullous dermolysis of the newborn Xeroderma pigmentosum 02

*Treacher Collins syndrome (Treacher Collins–Franceschetti syndrome) *Tricho–dento–osseous syndrome *Tricho–rhino–phalangeal syndrome *Tuberous sclerosis (Bourneville disease, epiloia) *Turner syndrome *Ulnar–mammary syndrome *Van Der Woude syndrome *Von Hippel–Lindau syndrome *Watson syndrome *Werner syndrome (adult progeria) *Westerhof syndrome *Whistling syndrome (craniocarpotarsal syndrome, distal arthrogryposis type 2, Freeman–Sheldon syndrome, Windmill–Vane–Hand syndrome) *Wilson–Turner syndrome *Wolf–Hirschhorn syndrome (4p- syndrome) *X-linked ichthyosis (steroid sulfatase deficiency, X-linked recessive ichthyosis) *X-linked recessive chondrodysplasia punctata *Xeroderma pigmentosum (Cockayne syndrome complex) *XXYY genotype *Zimmermann–Laband syndrome

Infection-related

Infection-related cutaneous conditions may be caused by bacteria, fungi, yeast, viruses, or parasitism, parasites.

Bacterium-related

Bacterium-related cutaneous conditions often have distinct Morphology (biology), morphologic characteristics that may be an indication of a generalized systemic process or simply an isolated superficial infection. *Aeromonas infection, ''Aeromonas'' infection *African tick bite fever *American tick bite fever (''Rickettsia parkeri'' infection) *Arcanobacterium haemolyticum infection, ''Arcanobacterium haemolyticum'' infection *Bacillary angiomatosis *Bejel (endemic syphilis) *Blastomycosis-like pyoderma (pyoderma vegetans) *Blistering distal dactylitis *Botryomycosis *Brill–Zinsser disease *Brucellosis (Bang's disease, Malta fever, undulant fever) *Bubonic plague *Bullous impetigo *Cat scratch disease (cat scratch fever, English–Wear infection, inoculation lymphoreticulosis, subacute regional lymphadenitis) *Cellulitis Cellulitis1

*Chancre *Chancroid (soft chancre, ulcus molle) *Chlamydial infection *Chronic lymphangitis *Chronic recurrent erysipelas *Chronic undermining burrowing ulcers (Meleney gangrene) *Chromobacteriosis infection *Condylomata lata *Cutaneous actinomycosis *Cutaneous anthrax infection *Cutaneous diphtheria infection, Cutaneous ''C. diphtheriae'' infection (Barcoo rot, diphtheric desert sore, septic sore, Veldt sore) *Cutaneous group B streptococcal infection *Cutaneous Pasteurella hemolytica infection, Cutaneous ''Pasteurella hemolytica'' infection *Cutaneous Streptococcus iniae infection, Cutaneous ''Streptococcus iniae'' infection *Dermatitis gangrenosa (gangrene of the skin) *Ecthyma *Ecthyma gangrenosum *Ehrlichiosis ewingii infection, ''Ehrlichiosis ewingii'' infection *Elephantiasis nostras *Endemic typhus (murine typhus) *Epidemic typhus (epidemic louse-borne typhus) *Erysipelas (ignis sacer, Saint Anthony's fire) *Erysipeloid of Rosenbach *Erythema marginatum *Erythrasma *External otitis (otitis externa, swimmer's ear)

*Felon (skin), Felon *Flea-borne spotted fever *Flinders Island spotted fever *Flying squirrel typhus *Folliculitis *Fournier gangrene (Fournier gangrene of the penis or scrotum) *Furunculosis (boil) *Gas gangrene (clostridial myonecrosis, myonecrosis) *Glanders (equinia, farcy, malleus) *Gonococcemia (arthritis–dermatosis syndrome, disseminated gonococcal infection) *Gonorrhea (clap) *Gram-negative folliculitis *Gram-negative toe web infection *Granuloma inguinale (Donovanosis, granuloma genitoinguinale, granuloma inguinale tropicum, granuloma venereum, granuloma venereum genitoinguinale, lupoid form of groin ulceration, serpiginous ulceration of the groin, ulcerating granuloma of the pudendum, ulcerating sclerosing granuloma) *Green nail syndrome *Group JK corynebacterium sepsis, Group JK ''Corynebacterium'' sepsis *Haemophilus influenzae cellulitis, ''Haemophilus influenzae'' cellulitis *Helicobacter cellulitis, ''Helicobacter'' cellulitis *Hospital furunculosis *Hot tub folliculitis (''Pseudomonas aeruginosa'' folliculitis) *Human granulocytotropic anaplasmosis *Human monocytotropic ehrlichiosis *Impetigo contagiosa *Japanese spotted fever *Leptospirosis (Fort Bragg fever, pretibial fever, Weil's disease) *Listeriosis *Ludwig's angina *Lupoid sycosis *Lyme disease (Afzelius' disease, Lyme borreliosis) *Lymphogranuloma venereum (climatic bubo, Durand–Nicolas–Favre disease, lymphogranuloma inguinale, poradenitis inguinale, strumous bubo) *Malakoplakia (malacoplakia) *Mediterranean spotted fever (Boutonneuse fever) *Melioidosis (Whitmore's disease) *Meningococcemia *Missouri Lyme disease *Mycoplasma infection *Necrotizing fasciitis (flesh-eating bacteria syndrome) *Neonatal toxic shock-like exanthematous disease *Nocardiosis *Noma neonatorum *North Asian tick typhus *Ophthalmia neonatorum Erysipel2

*Oroya fever (Carrion's disease) *Pasteurellosis *Perianal cellulitis (perineal dermatitis, streptococcal perianal disease) *Periapical abscess *Pinta (disease), Pinta *Pitted keratolysis (keratolysis plantare sulcatum, keratoma plantare sulcatum, ringed keratolysis) *Plague (disease), Plague *Primary gonococcal dermatitis *Pseudomonal pyoderma *Pseudomonas hot-foot syndrome *Pyogenic paronychia *Pyomyositis *Q fever *Queensland tick typhus *Rat-bite fever *Recurrent toxin-mediated perineal erythema *Rhinoscleroma *Rickettsia aeschlimannii infection, ''Rickettsia aeschlimannii'' infection *Rickettsialpox *Rocky Mountain spotted fever *Saber shin (anterior tibial bowing) *Saddle nose *Salmonellosis *Scarlet fever *Scrub typhus (Tsutsugamushi fever) *Shigellosis *Staphylococcal scalded skin syndrome (pemphigus neonatorum, Ritter's disease) *Streptococcal intertrigo *Superficial pustular folliculitis (impetigo of Bockhart, superficial folliculitis) *Sycosis vulgaris (barber's itch, sycosis barbae) *Syphilid *Syphilis (lues) *Tick-borne lymphadenopathy *Toxic shock syndrome (streptococcal toxic shock syndrome, streptococcal toxic shock-like syndrome, toxic streptococcal syndrome) *Trench fever (five-day fever, quintan fever, urban trench fever) *Tropical ulcer (Aden ulcer, jungle rot, Malabar ulcer, tropical phagedena) *Tularemia (deer fly fever, Ohara's disease, Pahvant Valley plague, rabbit fever) *Verruga peruana *Vibrio vulnificus infection, ''Vibrio vulnificus'' infection *Yaws (bouba, ''frambösie'', ''parangi, pian'')

''Mycobacterium''-related

''Mycobacterium''-related cutaneous conditions are caused by ''Mycobacterium'' infections. *Aquarium granuloma (fish-tank granuloma, swimming-pool granuloma) *Borderline lepromatous leprosy *Borderline leprosy *Borderline tuberculoid leprosy *Buruli ulcer (Bairnsdale ulcer, Searl ulcer, Searle's ulcer) Buruli ulcer hand Nigeria

*Erythema induratum (Bazin disease) *Histoid leprosy *Lepromatous leprosy *Leprosy (Hansen's disease) *Lichen scrofulosorum (tuberculosis cutis lichenoides) *Lupus vulgaris (tuberculosis luposa) *Miliary tuberculosis (disseminated tuberculosis, tuberculosis cutis acuta generalisata, tuberculosis cutis disseminata) *Mycobacterium avium-intracellulare complex infection, ''Mycobacterium avium-intracellulare'' complex infection *Mycobacterium haemophilum infection, ''Mycobacterium haemophilum'' infection *Mycobacterium kansasii infection, ''Mycobacterium kansasii'' infection *Papulonecrotic tuberculid *Primary inoculation tuberculosis (cutaneous primary complex, primary tuberculous complex, tuberculous chancre) *Rapid growing mycobacterium infection, Rapid-growing ''Mycobacterium'' infection *Scrofuloderma (tuberculosis cutis colliquativa) *Tuberculosis cutis orificialis (acute tuberculous ulcer, orificial tuberculosis) *Tuberculosis verrucosa cutis (lupus verrucosus, prosector's wart, warty tuberculosis) *Tuberculous cellulitis *Tuberculous gumma (metastatic tuberculous abscess, metastatic tuberculous ulcer) *Tuberculoid leprosy

Mycosis-related

Mycosis-related cutaneous conditions are caused by fungi or yeasts, and may present as either a superficial or deep infection of the skin, hair, or nails. *African histoplasmosis *Alternariosis *Antibiotic candidiasis (iatrogenic candidiasis) *Black piedra *Candidal intertrigo *Candidal onychomycosis *Candidal paronychia *Candidal vulvovaginitis *Candidid *Chromoblastomycosis (chromomycosis, cladosporiosis, Fonseca's disease, Pedroso's disease, phaeosporotrichosis, verrucous dermatitis) *Chronic mucocutaneous candidiasis *Coccidioidomycosis (California disease, desert rheumatism, San Joaquin Valley fever, valley fever) *Congenital cutaneous candidiasis *Cryptococcosis *Dermatophytid *Diaper candidiasis *Disseminated coccidioidomycosis (coccidioidal granuloma) *Distal subungual onychomycosis *Entomophthoromycosis *Erosio interdigitalis blastomycetica *Favus *Fungal folliculitis (majocchi granuloma) *Fusariosis *Geotrichosis *Granuloma gluteale infantum *Histoplasmosis (cave disease, Darling's disease, Ohio Valley disease, reticuloendotheliosis) *Hyalohyphomycosis *Kerion *Lobomycosis (keloidal blastomycosis, lacaziosis, Lobo's disease) *Mucormycosis *Eumycetoma, Mycetoma (Madura foot, maduromycosis) *North American blastomycosis (blastomycetic dermatitis, blastomycosis, Gilchrist's disease) *Onychomycosis (dermatophytic onychomycosis, ringworm of the nail, tinea unguium) *Oral candidiasis (thrush) *Otomycosis *Perianal candidiasis *''Perlèche'' (angular cheilitis) *Phaeohyphomycosis *Piedra (trichosporosis) *Pityrosporum folliculitis *Primary cutaneous aspergillosis *Primary cutaneous coccidioidomycosis *Primary cutaneous histoplasmosis *Primary pulmonary coccidioidomycosis *Primary pulmonary histoplasmosis *Progressive disseminated histoplasmosis *Proximal subungual onychomycosis *Rhinosporidiosis *South American blastomycosis (Brazilian blastomycosis, paracoccidioidal granuloma, paracoccidioidomycosis) *Sporotrichosis (rose-gardener's disease) *Systemic candidiasis *Tinea barbae (barber's itch, ringworm of the beard, tinea sycosis) Tinea barbae 4807 lores

*Tinea capitis (herpes tonsurans, ringworm of the hair, ringworm of the scalp, scalp ringworm, tinea tonsurans) *Tinea corporis (ringworm, tinea circinata, tinea glabrosa) *Tinea corporis gladiatorum *Tinea cruris (crotch itch, eczema marginatum, gym itch, jock itch, ringworm of the groin) *Tinea faciei *Tinea imbricata (''tokelau'') *Tinea incognito *Tinea manuum *Tinea nigra (superficial phaeohyphomycosis, tinea nigra palmaris et plantaris) *Tinea pedis (athlete's foot, ringworm of the foot) *Tinea versicolor (dermatomycosis furfuracea, pityriasis versicolor, tinea flava) *White piedra *White superficial onychomycosis *Zygomycosis (phycomycosis)

Parasitic infestations, stings, and bites

Parasitic infestations, stings, and bites in humans are caused by several groups of organisms belonging to the following Phylum, phyla: Annelida, Arthropoda, Bryozoa, Chordata, Cnidaria, Cyanobacteria, Echinodermata, Nematode, Nemathelminthes, Platyhelminthes, and Protozoa. *Acanthamoeba infection, ''Acanthamoeba'' infection *Amebiasis cutis *Ant sting *Arachnidism *Baker's itch *Balamuthia infection, ''Balamuthia'' infection *Bedbug infestation (bedbug bite, cimicosis) *Bee and wasp stings *Blister beetle dermatitis *Bombardier beetle burn *Bristleworm sting Larva Migrans Cutanea

*Centipede bite *Cheyletiella dermatitis *Chigger bite *Coolie itch *Copra itch *Coral dermatitis *Creeping eruption (cutaneous larva migrans) *Cutaneous leishmaniasis (Aleppo boil, Baghdad boil, bay sore, Biskra button, Chiclero ulcer, Delhi boil, Kandahar sore, Lahore sore, leishmaniasis tropica, oriental sore, ''pian bois, uta'') *Cysticercosis cutis, ''Cysticercosis'' cutis *Demodex folliculitis, usually caused by the ''Demodex folliculorum'' mite *Dogger Bank itch *Dracunculiasis (dracontiasis, guinea worm disease, Medina worm) *Echinococcosis (hydatid disease) *Elephantiasis tropica (elephantiasis arabum) *Elephant skin *Enterobiasis (oxyuriasis, pinworm infection, seatworm infection) *''Erisipela de la costa'' *Feather pillow dermatitis *Funnel web spider bite *Gamasoidosis *Gnathostomiasis (larva migrans profundus) *Grain itch (barley itch, mattress itch, prairie itch, straw itch) *Grocer's itch *Head lice infestation (cooties, pediculosis capitis) *Hookworm disease (ancylostomiasis, ground itch, necatoriasis, uncinariasis) *Human trypanosomiasis *Hydroid dermatitis *Irukandji syndrome *Jellyfish dermatitis *Ked itch *Larva currens *Latrodectism (widow spider bite) *Leech bite *Leopard skin *Lepidopterism (Caripito itch, caterpillar dermatitis, moth dermatitis) *Lizard skin *Loaiasis (Calabar swelling, fugitive swelling, ''loa loa'', tropical swelling) *Loxoscelism (brown recluse spider bite, necrotic cutaneous loxoscelism) *''Mal morando'' *Millipede burn *Mosquito bite *Mucocutaneous leishmaniasis (espundia, leishmaniasis americana) *Myiasis *Nairobi fly dermatitis (Kenya fly dermatitis, Nairobi eye) *Nematode dermatitis *Norwegian scabies (crusted scabies) Norwegian Scabies in Homeless AIDS Patient

Norwegian Scabies in Homeless AIDS Patient

*Onchocerciasis *Ophthalmia nodosa *Paederus dermatitis *Pediculosis corporis (pediculosis vestimenti, Vagabond's disease) *Pediculosis pubis (crabs, phthirus pubis, phthirus pubis, pubic lice) *Pneumocystosis (often classified as fungal) *Portuguese man-of-war dermatitis *Post-kala-azar dermal leishmaniasis (post-kala-azar dermatosis) *Protothecosis *Pulicosis (flea bites) *Reduviid bite *Scabies (itch mite infestation, seven-year itch) *Scorpion sting *Sea anemone dermatitis *Seabather's eruption (sea lice) *Sea urchin injury *Seaweed dermatitis *Snake bite *Sowda *Sparganosis *Spider bite *Stingray injury *Swimmer's itch (cercarial dermatitis, schistosome cercarial dermatitis) Cercarial dermatitis lower legs

*Tarantula bite *Tick bite *Toxoplasmosis *Trichinosis *Trichomoniasis *Tungiasis (''bicho de pie'', chigoe flea bite, jigger bite, ''nigua, pique'') *Visceral leishmaniasis (dumdum fever, ''kala-azar'') *Visceral schistosomiasis (bilharziasis) *Viscerotropic leishmaniasis *Wheat warehouse itch

Virus-related

Virus-related cutaneous conditions are caused by two main groups of viruses–DNA virus, DNA and RNA virus, RNA types–both of which are Obligation, obligatory intracellular parasites. *Alphavirus infection *Asymmetric periflexural exanthem of childhood (unilateral laterothoracic exanthem) *B virus infection *Boston exanthem disease *Bovine papular stomatitis *Bowenoid papulosis *Buffalopox *Butcher's wart *Chikungunya fever *Condylomata acuminata *Congenital rubella syndrome *Cowpox *Cytomegalic inclusion disease *Dengue (Break-bone fever) *Disseminated herpes zoster *Eczema herpeticum (Kaposi's varicelliform eruption) Eczema vaccinatum infant

*Eczema vaccinatum *Epidermodysplasia verruciformis *Eruptive pseudoangiomatosis *Erythema infectiosum (fifth disease, slapped cheek disease) *Exanthem of primary HIV infection (acute retroviral syndrome) *Farmyard pox *Generalized vaccinia *Genital herpes (herpes genitalis, herpes progenitalis) *Gianotti–Crosti syndrome (infantile papular acrodermatitis, papular acrodermatitis of childhood, papulovesicular acrolocated syndrome) *Giant condyloma acuminatum (Buschke–Löwenstein tumor, giant condyloma of Buschke–Löwenstein tumor) *Hand-foot-and-mouth disease *Heck's disease (focal epithelial hyperplasia) *Hemorrhagic fever with renal syndrome *Hepatitis B *Hepatitis C *Herpangina *Herpes gladiatorum (scrum pox) *Herpes simplex *Herpes zoster oticus (Ramsay–Hunt syndrome) *Herpetic keratoconjunctivitis *Herpetic sycosis *Herpetic whitlow *HIV-associated pruritus *Human monkeypox *Human T-lymphotropic virus 1 infection *Human tanapox *Immune reconstitution inflammatory syndrome (immune recovery syndrome) *Infectious mononucleosis (glandular fever) *Inflammatory skin lesions following zoster infection (isotopic response) *Intrauterine herpes simplex Kaposi's Sarcoma

*Kaposi sarcoma *Lassa fever *Lipschütz ulcer (ulcus vulvae acutum) *Measles (rubeola, morbilli) *Milker's nodule *Modified varicella-like syndrome *Molluscum contagiosum *Myrmecia (skin), Myrmecia *Neonatal herpes simplex *Ophthalmic zoster *Orf (disease), Orf (contagious pustular dermatosis, ecthyma contagiosum, infectious labial dermatitis, sheep pox) *Orf-induced immunobullous disease *Orolabial herpes (herpes labialis) *Papular purpuric gloves and socks syndrome *Pigmented wart *Postherpetic neuralgia (zoster-associated pain) *Post-vaccination follicular eruption *Progressive vaccinia (vaccinia gangrenosum, vaccinia necrosum) *Pseudocowpox *Recurrent respiratory papillomatosis (laryngeal papillomatosis) *Rift Valley fever *Roseola infantum (exanthem subitum, exanthema subitum, sixth disease) *Roseola vaccinia *Rubella (German measles) *Pappataci fever, Sandfly fever (Pappataci fever, phlebotomus fever) *Sealpox *Varicella (chickenpox) *Variola major (smallpox) *Verruca plana (flat wart) *Verruca plantaris (plantar wart) *Verruca vulgaris (wart) *Verrucae palmares et plantares *Viral-associated trichodysplasia (ciclosporin-induced folliculodystrophy) *Wasting syndrome *West Nile virus infection *Zoster (herpes zoster, shingles) *Zoster sine herpete

Lichenoid eruptions

Lichenoid eruptions are

related to the unique, common inflammatory disorder lichen planus, which affects the skin, mucous membranes, nails, and hair. *Annular lichen planus

*Atrophic lichen planus *Bullous lichen planus (vesiculobullous lichen planus) *Erosive lichen planus *Erythema dyschromicum perstans (ashy dermatosis, dermatosis cinecienta) *Giant cell lichenoid dermatitis *Hepatitis-associated lichen planus *Hypertrophic lichen planus (lichen planus verrucosus) *Idiopathic eruptive macular pigmentation *Inverse lichen planus *Keratosis lichenoides chronica (Nékam's disease) *Kraurosis vulvae *Lichen nitidus *Lichen planus actinicus (actinic lichen niditus, actinic lichen planus, lichen planus atrophicus annularis, lichen planus subtropicus, lichen planus tropicus, lichenoid melanodermatitis, lichenoid melanodermatosis, summertime actinic lichenoid eruption) *Lichen planus pemphigoides *Lichen planus pigmentosus *Lichen planus–lichen sclerosus overlap syndrome *Lichen ruber moniliformis *Lichen sclerosus (lichen sclerosus et atrophicus) *Lichen striatus (Blaschko linear acquired inflammatory skin eruption, linear lichenoid dermatosis) *Lichen verrucosus et reticularis *Lichenoid trikeratosis *Lichenoid dermatitis *Lichenoid reaction of graft-versus-host disease *Linear lichen planus *Mucosal lichen planus *Peno-gingival syndrome *Ulcerative lichen planus *Vulvovaginal gingival syndrome *Vulvovaginal lichen planus

Lymphoid-related

Lymphoid-related cutaneous conditions are a group of disorders characterized by collections of lymphocyte cells within the skin. *Adult T-cell leukemia/lymphoma *Angiocentric lymphoma (extranodal natural killer cell lymphoma, nasal-type NK lymphoma, NK/T-cell lymphoma, polymorphic/malignant midline reticulosis) *Angioimmunoblastic T-cell lymphoma (angioimmunoblastic lymphadenopathy with dysproteinemia) *Blastic NK-cell lymphoma *CD30+ cutaneous T-cell lymphoma (primary cutaneous anaplastic large cell lymphoma) *Cutaneous lymphoid hyperplasia (borrelial lymphocytoma, lymphadenosis benigna cutis, lymphocytoma cutis, pseudolymphoma, pseudolymphoma of Spiegler and Fendt, sarcoidosis of Spiegler and Fendt, Spiegler–Fendt lymphoid hyperplasia, Spiegler–Fendt sarcoid)

*Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns *Cutaneous lymphoid hyperplasia with nodular pattern (nodular pattern of cutaneous lymphoid hyperplasia) *Diffuse large B-cell lymphoma (primary cutaneous large B-cell lymphoma) *Granulocytic sarcoma (chloroma, myeloid sarcoma) *Granulomatous slack skin *Hairy-cell leukemia *Hodgkin's disease *Ichthyosis acquisita (acquired ichthyosis) *IgG4-related skin disease, IgG₄-related skin disease *Intravascular large B-cell lymphoma (angiotropic large cell lymphoma, intralymphatic lymphomatosis, intravascular lymphomatosis, malignant angioendotheliomatosis) *Jessner lymphocytic infiltrate of the skin (benign lymphocytic infiltration of the skin, Jessner lymphocytic infiltration of the skin, Jessner–Kanof lymphocytic infiltration of the skin, lymphocytic infiltrate of Jessner) *Kikuchi's disease (histiocytic necrotizing lymphadenitis) *Large plaque parapsoriasis (parapsoriasis en plaques) *Lennert lymphoma (lymphoepitheliod lymphoma) *Leukemia cutis *Lymphoma cutis *Lymphomatoid granulomatosis *Lymphomatoid papulosis *Malignant histiocytosis (histiocytic medullary reticulosis) *Marginal zone B-cell lymphoma *Mucosa-associated lymphoid tissue lymphoma *Mycosis fungoides *Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma *Nonspecific cutaneous conditions associated with leukemia (leukemid) *Pagetoid reticulosis (acral mycoses fungoides, localized epidermotropic reticulosis, mycosis fungoides palmaris et plantaris, unilesional mycosis fungoides, Woringer–Kolopp disease) *Pityriasis lichenoides chronica (chronic guttate parapsoriasis, chronic pityriasis lichenoides, dermatitis psoriasiformis nodularis, parapsoriasis chronica, parapsoriasis lichenoides chronica) *Pityriasis lichenoides et varioliformis acuta (acute guttate parapsoriasis, acute parapsoriasis, acute pityriasis lichenoides, Mucha–Habermann disease, parapsoriasis acuta, parapsoriasis lichenoides et varioliformis acuta, parapsoriasis varioliformis) *Plasmacytoma Plaque of mycosis fungoides 2

*Plasmacytosis *Pleomorphic T-cell lymphoma (non-mycosis fungoides CD30− pleomorphic small/medium-sized cutaneous T-cell lymphoma) *Polycythemia vera (erythremia) *Primary cutaneous follicular lymphoma (follicular center cell lymphoma, follicular center lymphoma) *Primary cutaneous immunocytoma *Primary cutaneous marginal zone lymphoma *Retiform parapsoriasis *Secondary cutaneous CD30+ large cell lymphoma *Sézary syndrome *Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) *Subcutaneous T-cell lymphoma (panniculitis-like T-cell lymphoma) *Vesiculopustular eruption and leukemoid reaction in Down syndrome

Melanocytic nevi and neoplasms

Melanocytic nevi and neoplasms are caused by either a proliferation of (1) melanocytes, or (2) nevus cells, a form of melanocyte that lack dendritic processes. *Acral nevus (melanocytic nevus of acral skin, melanocytic nevus with intraepidermal ascent of cells) *Amelanotic blue nevus (hypomelanotic blue nevus) *Balloon cell nevus *Bannayan–Riley–Ruvalcaba syndrome *Becker's nevus (Becker's melanosis, Becker's pigmentary hamartoma, nevoid melanosis, pigmented hairy epidermal nevus) *Benign melanocytic nevus (banal nevus, common acquired melanocytic nevus, mole, nevocellular nevus, nevocytic nevus) *Blue nevus (blue neuronevus, dermal melanocytoma, nevus bleu) *Blue nevus of Jadassohn–Tièche (common blue nevus, nevus ceruleus) *Carney complex (LAMB syndrome, NAME syndrome) *Cellular blue nevus *Centrofacial lentiginosis *Congenital melanocytic nevus *Deep penetrating nevus *Dysplastic nevus (atypical mole, atypical nevus, B-K mole, Clark's nevus, dysplastic melanocytic nevus, nevus with architectural disorder) *Dysplastic nevus syndrome (B-K mole syndrome, familial atypical multiple mole–melanoma syndrome, familial melanoma syndrome) *Ephelis (freckle) *Epithelioid blue nevus *Generalized lentiginosis *Giant pigmented nevus (bathing trunk nevus, congenital nevomelanocytic nevus, garment nevus, giant hairy nevus, nevus pigmentosus et pilosus) *Halo nevus (leukoderma acquisitum centrifugum, perinevoid vitiligo, Sutton nevus) *Hori's nevus (acquired bilateral nevus of Ota-like macules) *Inherited patterned lentiginosis in black persons *Ink spot lentigo (sunburn lentigo) *Laugier–Hunziker syndrome *Lentigo simplex (simple lentigo) *Malignant blue nevus *Medium-sized congenital nevocytic nevus *Melanoacanthoma *Melanocytic tumors of uncertain malignant potential *Moynahan syndrome *Mucosal lentigines (labial and penile and vulvar melanosis, melanotic macules) *Nevus of Ito (nevus fuscoceruleus acromiodeltoideus) *Nevus of Ota (congenital melanosis bulbi, melanosis bulborum and aberrant dermal melanocytosis, nevus fuscoceruleus ophthalmomaxillaris, oculodermal melanocytosis, oculomucodermal melanocytosis) *Nevus spilus (speckled lentiginous nevus, zosteriform lentiginous nevus) *Partial unilateral lentiginosis (segmental lentiginosis) *Peutz–Jeghers syndrome *Pigmented spindle cell nevus (pigmented spindle cell tumor of Reed, pigmented variant of Spitz nevus) *Pseudomelanoma (recurrent melanocytic nevus, recurrent nevus) *PUVA lentigines *Small-sized congenital nevocytic nevus *Spitz nevus (benign juvenile melanoma, epithelioid and spindle cell nevus, Spitz's juvenile melanoma) *Solar lentigo (lentigo senilis, liver spot, old age spot, senile freckle)

Melanoma

Melanoma is a malignant proliferation of melanocytes and the most aggressive type of skin cancer. *Acral lentiginous melanoma *Amelanotic melanoma *Animal-type melanoma *Desmoplastic melanoma (neurotropic melanoma, spindled melanoma) *Lentigo maligna (lentiginous melanoma on sun-damaged skin) *Lentigo maligna melanoma *Melanoma with features of a Spitz nevus (Spitzoid melanoma) *Melanoma with small nevus-like cells (small cell melanoma) *Mucosal melanoma *Nevoid melanoma *Nodular melanoma *Polypoid melanoma *Seborrheic keratosis-like melanoma *Soft-tissue melanoma (clear-cell sarcoma, melanoma of the soft parts) *Superficial spreading melanoma (superficially spreading melanoma) *Uveal melanoma

Monocyte- and macrophage-related

Monocyte- and macrophage-related cutaneous conditions are characterized Histology, histologically by Infiltration (medical), infiltration of the skin by monocyte or macrophage cells, often divided into several categories, including granulomatous disease, histiocytoses, and sarcoidosis. *Actinic granuloma (O'Brien granuloma) *Annular elastolytic giant cell granuloma (giant cell elastophagocytosis, Meischer's granuloma, Miescher's granuloma of the face) *Annular sarcoidosis

*Benign cephalic histiocytosis (histiocytosis with intracytoplasmic worm-like bodies) *Congenital self-healing reticulohistiocytosis (Hashimoto–Pritzker disease, Hashimoto–Pritzker syndrome) *Erythrodermic sarcoidosis *Generalized eruptive histiocytoma (eruptive histiocytoma, generalized eruptive histiocytosis) *Generalized granuloma annulare *Giant cell reticulohistiocytoma (solitary reticulohistiocytoma, solitary reticulohistiocytosis) *Granuloma annulare in HIV disease *Granuloma multiforme (Mkar disease, granuloma multiforme (Leiker)) *Hand–Schüller–Christian disease *Heerfordt's syndrome *Hereditary progressive mucinous histiocytosis *Hypopigmented sarcoidosis *Ichthyosiform sarcoidosis *Indeterminate cell histiocytosis *Interstitial granulomatous drug reaction *Langerhans cell histiocytosis (histiocytosis X) *Letterer–Siwe disease *Localized granuloma annulare *Löfgren syndrome *Lupus pernio *Morpheaform sarcoidosis *Mucosal sarcoidosis *Multicentric reticulohistiocytosis *Necrobiotic xanthogranuloma (necrobiotic xanthogranuloma with paraproteinemia) *Non-X histiocytosis *Papular sarcoid *Papular xanthoma *Patch-type granuloma annulare (macular granuloma annulare) *Perforating granuloma annulare Cutaneous findings in systemic sarcoidosis

Cutaneous findings in systemic sarcoidosis

*Progressive nodular histiocytosis *Reticulohistiocytoma *Scar sarcoid (sarcoidosis in scars) *Sea-blue histiocytosis *Subcutaneous granuloma annulare (deep granuloma annulare, pseudorheumatoid nodule) *Subcutaneous sarcoidosis (Darier–Roussy disease, Darier–Roussy sarcoid) *Systemic sarcoidosis *Ulcerative sarcoidosis *Xanthoma disseminatum (disseminated xanthosiderohistiocytosis, Montgomery syndrome)

Mucinoses

Mucinoses are a group of conditions caused by dermis, dermal fibroblasts producing abnormally large amounts of mucopolysaccharides. *Acral persistent papular mucinosis *Atypical lichen myxedematosus (intermediate lichen myxedematosus) *Atypical tuberous myxedema (Jadassohn–Dosseker syndrome) *Cutaneous focal mucinosis *Cutaneous lupus mucinosis (papular and nodular mucinosis in lupus erythematosus, papular and nodular mucinosis of Gold, papulonodular mucinosis in lupus erythematosus) *Discrete papular lichen myxedematosus *Eccrine mucinosis *Follicular mucinosis (alopecia mucinosa, mucinosis follicularis, Pinkus' follicular mucinosis, Pinkus' follicular mucinosis–benign primary form) *Localized lichen myxedematosus *Myxoid cyst (digital mucous cyst, mucous cyst) *Myxoid lipoblastoma *Neuropathia mucinosa cutanea *Nodular lichen myxedematosus *Papular mucinosis (generalized lichen myxedematosus, sclerodermoid lichen myxedematosus, scleromyxedema) *Papular mucinosis of infancy (cutaneous mucinosis of infancy) *Perifollicular mucinosis *Reticular erythematous mucinosis (midline mucinosis, plaque-like cutaneous mucinosis, REM syndrome) *Scleroderma *Self-healing juvenile cutaneous mucinosis *Self-healing papular mucinosis *Stiff skin syndrome (congenital fascial dystrophy)

Neurocutaneous

Neurocutaneous conditions are due Organ (anatomy), organic nervous system disease or are psychiatric in etiology. *Atypical chronic pain syndrome *Body dysmorphic disorder (dysmorphic syndrome, dysmorphophobia) *Brachioradial pruritus *Bromidrosiphobia *Complex regional pain syndrome (reflex sympathetic dystrophy) *Congenital insensitivity to pain with anhidrosis *Delusional parasitosis (delusions of parasitosis, Ekbom syndrome, monosymptomatic hypochondriacal psychosis) *Dermatothlasia *Factitious dermatitis (dermatitis artefacta, factitial dermatitis)

*Glossodynia (burning mouth syndrome, burning tongue, orodynia) *Levator ani syndrome *Malum perforans pedis (neurotrophic ulcer, perforating ulcer of the foot) *Meralgia paresthetica (Roth–Bernhardt disease) *Neurotic excoriations *Notalgia paresthetica (hereditary localized pruritus, posterior pigmented pruritic patch, subscapular pruritus) *Postencephalitic trophic ulcer *Psychogenic pruritus *Riley–Day syndrome (familial dysautonomia) *Scalp dysesthesia *Sciatic nerve injury *Scrotodynia *Syringomyelia (Morvan's disease) *Traumatic neuroma (amputation neuroma) *Trichotillomania (trichotillosis) *Trigeminal neuralgia (tic douloureux) *Trigeminal trophic lesion (trigeminal trophic syndrome) *Vulvodynia (vestibulodynia)

Noninfectious immunodeficiency-related

Noninfectious immunodeficiency-related cutaneous conditions are caused by T-cell or B-cell dysfunction. *Bare lymphocyte syndrome *Chronic granulomatous disease (Bridges–Good syndrome, chronic granulomatous disorder, Quie syndrome) *Common variable immunodeficiency (acquired hypogammaglobulinemia) *Complement deficiency *DiGeorge syndrome (DiGeorge anomaly, thymic hypoplasia) *Graft-versus-host disease *Griscelli syndrome *Hyper-IgE syndrome (Buckley syndrome, Job syndrome) *Immunodeficiency with hyper-IgM *Immunodeficiency–centromeric instability–facial anomalies syndrome (ICF syndrome) *Isolated IgA deficiency *Isolated primary IgM deficiency *Janus kinase 3 deficiency *Leukocyte adhesion molecule deficiency *LIG4 syndrome *Myeloperoxidase deficiency *Neutrophil immunodeficiency syndrome *Nezelof syndrome (thymic dysplasia with normal immunoglobulins) *Omenn syndrome

*Purine nucleoside phosphorylase deficiency *Severe combined immunodeficiency (alymphocytosis, Glanzmann–Riniker syndrome, severe mixed immunodeficiency syndrome, thymic alymphoplasia) *Shwachman–Bodian–Diamond syndrome *Thymoma with immunodeficiency (Good syndrome) *Transient hypogammaglobulinemia of infancy *Warts–hypogammaglobulinemia–infections–myelokathexis syndrome (WHIM syndrome) *Wiskott–Aldrich syndrome *X-linked agammaglobulinemia (Bruton syndrome, sex-linked agammaglobulinemia) *X-linked hyper-IgM syndrome *X-linked hypogammaglobulinemia *X-linked lymphoproliferative disease (Duncan's disease) *X-linked neutropenia

Nutrition-related

Nutrition-related cutaneous conditions are caused by malnutrition due to an improper or inadequate Diet (nutrition), diet. *Biotin deficiency *Carotenemia *Essential fatty acid deficiency *Folic acid deficiency *Hypervitaminosis A *Hypovitaminosis A (phrynoderma) *Iron deficiency (medicine), Iron deficiency Kwashiorkor dermatosis

*Kwashiorkor *Lycopenemia *Maple syrup urine disease *Marasmus *Niacin deficiency (pellagra, vitamin B₃ deficiency) *Selenium deficiency *Vitamin B1 deficiency, Vitamin B₁ deficiency (beriberi, thiamine deficiency) *Vitamin B12 deficiency, Vitamin B₁₂ deficiency (cyanocobalamin deficiency) *Vitamin B2 deficiency, Vitamin B₂ deficiency (ariboflavinosis, riboflavin deficiency) *Vitamin B6 deficiency, Vitamin B₆ deficiency (pyridoxine deficiency) *Vitamin B6 excess, Vitamin B₆ excess (pyridoxine excess) *Vitamin C deficiency (scurvy) *Vitamin K deficiency *Zinc deficiency

Papulosquamous hyperkeratotic

Papulosquamous Hyperkeratosis, hyperkeratotic cutaneous conditions are those that present with

s and Scale (dermatology), scales caused by a thickening of the stratum corneum. Pityriasis rosea-3

*Confluent and reticulated papillomatosis (confluent and reticulated papillomatosis of Gougerot and Carteaud, familial cutaneous papillomatosis, familial occurrence of confluent and reticulated papillomatosis) *Digitate dermatosis *Drug-induced keratoderma *Exfoliative dermatitis (dermatitis exfoliativa, erythroderma, red man syndrome) *Florid cutaneous papillomatosis *Granular parakeratosis (axillary granular parakeratosis, intertriginous granular parakeratosis) *Keratolysis exfoliativa (lamellar dyshidrosis, recurrent focal palmar peeling, recurrent palmar peeling) *Keratosis punctata of the palmar creases (hyperkeratosis penetrans, hyperkeratosis punctata, keratodermia punctata, keratosis punctata, keratotic pits of the palmar creases, lenticular atrophia of the palmar creases, punctate keratosis of the palmar creases) *Meesmann corneal dystrophy *Paraneoplastic keratoderma *Pityriasis rosea (pityriasis rosea Gibert) *Pityriasis rubra pilaris (Devergie's disease, lichen ruber acuminatus, lichen ruber pilaris) *Pure hair-nail type ectodermal dysplasia *Small plaque parapsoriasis (chronic superficial dermatitis) *Tripe palms *Xanthoerythrodermia perstans

Palmoplantar keratodermas

Palmoplantar keratodermas are a diverse group of hereditary and acquired keratodermas in which there is hyperkeratosis of the skin of the palms and soles. *Acrokeratoelastoidosis of Costa (keratoelastoidosis marginalis) *Aquagenic keratoderma (acquired aquagenic palmoplantar keratoderma, aquagenic syringeal acrokeratoderma, aquagenic wrinkling of the palms, transient reactive papulotranslucent acrokeratoderma) *Bart–Pumphrey syndrome (palmoplantar keratoderma with knuckle pads and leukonychia and deafness) *Camisa disease *Carvajal syndrome (striate palmoplantar keratoderma with woolly hair and cardiomyopathy, striate palmoplantar keratoderma with woolly hair and left ventricular dilated cardiomyopathy) *Corneodermatoosseous syndrome (CDO syndrome) *Diffuse epidermolytic palmoplantar keratoderma (palmoplantar keratoderma cum degeneratione granulosa Vörner, Vörner's epidermolytic palmoplantar keratoderma, Vörner keratoderma) *Diffuse nonepidermolytic palmoplantar keratoderma (diffuse orthohyperkeratotic keratoderma, hereditary palmoplantar keratoderma, keratosis extremitatum progrediens, keratosis palmoplantaris diffusa circumscripta, tylosis, Unna–Thost disease, Unna–Thost keratoderma) *Erythrokeratodermia variabilis (erythrokeratodermia figurata variabilis, keratosis extremitatum progrediens, keratosis palmoplantaris transgrediens et progrediens, Mendes da Costa syndrome, Mendes da Costa type erythrokeratodermia, progressive symmetric erythrokeratoderma) *Focal acral hyperkeratosis (acrokeratoelastoidosis lichenoides, degenerative collagenous plaques of the hand) *Focal palmoplantar and gingival keratosis *Focal palmoplantar keratoderma with oral mucosal hyperkeratosis (focal epidermolytic palmoplantar keratoderma, hereditary painful callosities, hereditary painful callosity syndrome, keratosis follicularis, keratosis palmoplantaris nummularis, nummular epidermolytic palmoplantar keratoderma) *Haim–Munk syndrome (palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis) *Hidrotic ectodermal dysplasia (alopecia congenita with keratosis palmoplantaris, Clouston syndrome, Clouston's hidrotic ectodermal dysplasia, Fischer–Jacobsen–Clouston syndrome, keratosis palmaris with drumstick fingers, palmoplantar keratoderma and clubbing) *Howel–Evans syndrome (familial keratoderma with carcinoma of the esophagus, focal non-epidermolytic palmoplantar keratoderma with carcinoma of the esophagus, palmoplantar ectodermal dysplasia type III, palmoplantar keratoderma associated with esophageal cancer, tylosis, tylosis–esophageal carcinoma) *Hystrix-like ichthyosis–deafness syndrome (HID syndrome) *Keratoderma climactericum (acquired plantar keratoderma, climacteric keratoderma, Haxthausen's disease) *Keratosis punctata palmaris et plantaris (Buschke–Fischer–Brauer disease, Davis Colley disease, keratoderma disseminatum palmaris et plantaris, keratosis papulosa, keratoderma punctatum, keratodermia punctata, keratoma hereditarium dissipatum palmare et plantare, palmar and plantar seed dermatoses, palmar keratoses, papulotranslucent acrokeratoderma, punctate keratoderma, punctate keratoses of the palms and soles, maculosa disseminata) *Keratitis–ichthyosis–deafness syndrome (erythrokeratodermia progressiva Burns, ichthyosiform erythroderma with corneal involvement and deafness, KID syndrome) *Mal de Meleda (acral keratoderma, Gamborg–Nielsen keratoderma, mutilating palmoplantar keratoderma of the Gamborg–Nielsen type, palmoplantar ectodermal dysplasia type VIII, palmoplantar keratoderma of the Norrbotten type) *Naxos syndrome (diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy, diffuse palmoplantar keratoderma with woolly hair and arrythmogenic right ventricular cardiomyopathy of Naxos, Naxos disease) *Olmsted syndrome (mutilating palmoplantar keratoderma with periorificial keratotic plaques, mutilating palmoplantar keratoderma with periorificial plaques, polykeratosis of Touraine) *Pachyonychia congenita type I (Jadassohn–Lewandowsky syndrome) *Pachyonychia congenita type II (Jackson–Lawler pachyonychia congenita, Jackson–Sertoli syndrome) *Palmoplantar keratoderma and spastic paraplegia (Charcot–Marie–Tooth disease with palmoplantar keratoderma and nail dystrophy) *Palmoplantar keratoderma of Sybert (Greither palmoplantar keratoderma, Greither syndrome, keratosis extremitatum hereditaria progrediens, keratosis palmoplantaris transgrediens et progrediens, Sybert keratoderma, transgrediens and progrediens palmoplantar keratoderma) *Papillon–Lefèvre syndrome (palmoplantar keratoderma with periodontitis) *Porokeratosis plantaris discreta *Punctate palmoplantar keratoderma *Schöpf–Schulz–Passarge syndrome (eyelid cysts with palmoplantar keratoderma and hypodontia and hypotrichosis) *Scleroatrophic syndrome of Huriez (Huriez syndrome, palmoplantar keratoderma with scleroatrophy, palmoplantar keratoderma with sclerodactyly, scleroatrophic and keratotic dermatosis of the limbs, sclerotylosis) *Striate palmoplantar keratoderma (acral keratoderma, Brünauer–Fuhs–Siemens type of palmoplantar keratoderma, focal non-epidermolytic palmoplantar keratoderma, keratosis palmoplantaris varians, palmoplantar keratoderma areata, palmoplantar keratoderma striata, Wachter keratoderma, Wachters palmoplantar keratoderma) *Spiny keratoderma (porokeratosis punctata palmaris et plantaris, punctate keratoderma, punctate porokeratosis of the palms and soles) *Tyrosinemia type II (oculocutaneous tyrosinemia, Richner–Hanhart syndrome) *Vohwinkel syndrome (keratoderma hereditaria mutilans, keratoma hereditaria mutilans, mutilating keratoderma of Vohwinkel, mutilating palmoplantar keratoderma)

Pregnancy-related

Pregnancy-related cutaneous conditions are a group of skin changes observed during pregnancy. *Impetigo herpetiformis *Intrahepatic cholestasis of pregnancy (cholestasis of pregnancy, jaundice of pregnancy, obstetric cholestasis, prurigo gravidarum) *Linea nigra *Pemphigoid gestationis (gestational pemphigoid, herpes gestationis) *Prurigo gestationis (Besnier prurigo, early-onset prurigo of pregnancy, linear IgM dermatosis of pregnancy, papular dermatitis of pregnancy, prurigo of pregnancy, Spangler's papular dermatitis of pregnancy) *Pruritic folliculitis of pregnancy *Pruritic urticarial papules and plaques of pregnancy (late-onset prurigo of pregnancy, polymorphic eruption of pregnancy, PUPPP syndrome, toxemic rash of pregnancy, toxic erythema of pregnancy) *Striae gravidarum

Pruritic

Pruritus, commonly known as itchiness, is a sensation exclusive to the skin, and characteristic of many skin conditions. *Adult blaschkitis *Aquadynia *Aquagenic pruritus *Biliary pruritus *Cholestatic pruritus *Drug-induced pruritus *Hydroxyethyl starch-induced pruritus *Lichen simplex chronicus (neurodermatitis) Lichen simplex chronicus 2

*Prion pruritus *Prurigo nodularis *Prurigo pigmentosa *Prurigo simplex *Pruritus ani *Pruritus scroti *Pruritus vulvae *Puncta pruritica (itchy points) *Scalp pruritus *Senile pruritus *Uremic pruritus (renal pruritus)

Psoriasis

Psoriasis is a common, chronic, and recurrent inflammatory disease of the skin characterized by circumscribed, erythematous, dry, scaling Plaque (dermatology), plaques. *Annular pustular psoriasis *Drug-induced psoriasis *Exanthematic pustular psoriasis *Generalized pustular psoriasis (pustular psoriasis of von Zumbusch) *Guttate psoriasis (eruptive psoriasis) *Inverse psoriasis *Keratoderma blennorrhagica (keratoderma blennorrhagicum) *Localized pustular psoriasis *Napkin psoriasis *Psoriasis vulgaris (chronic stationary psoriasis, plaque-like psoriasis) *Psoriatic arthritis *Psoriatic erythroderma (erythrodermic psoriasis) *Seborrheic-like psoriasis (sebopsoriasis, seborrhiasis)

Reactive neutrophilic

Reactive neutrophilic dermatoses, Reactive neutrophilic cutaneous conditions constitute a spectrum of disease mediated by neutrophils, and typically associated with underlying diseases, such as inflammatory bowel disease and hematology, hematologic malignancy. Pyoderma gangrenosum 01

*Acute erythema nodosum *Bowel-associated dermatosis–arthritis syndrome (bowel bypass syndrome, bowel bypass syndrome without bowel bypass, intestinal bypass arthritis–dermatitis syndrome) *Marshall syndrome *Neutrophilic dermatosis of the dorsal hands (pustular vasculitis of the dorsal hands) *Neutrophilic eccrine hidradenitis *Pyoderma gangrenosum *Pyogenic arthritis–pyoderma gangrenosum–acne syndrome (PAPA syndrome) *Rheumatoid neutrophilic dermatitis (rheumatoid neutrophilic dermatosis) *Superficial granulomatous pyoderma *Sweet's syndrome (acute febrile neutrophilic dermatosis) *Sweet's syndrome-like dermatosis *Vesicopustular dermatosis

Recalcitrant palmoplantar eruptions

Recalcitrant palmoplantar eruptions are skin conditions of the Hand, palms and Sole (foot), soles which are resistant to treatment. *Dermatitis repens (acrodermatitis continua, acrodermatitis continua of Hallopeau, acrodermatitis continua suppurativa Hallopeau, acrodermatitis perstans, dermatitis repens Crocker, Hallopeau's acrodermatitis, Hallopeau's acrodermatitis continua, pustular acrodermatitis) *Infantile acropustulosis (acropustulosis of infancy) *Palmoplantar pustulosis (persistent palmoplantar pustulosis, pustular psoriasis of the Barber type, pustular psoriasis of the extremities, pustulosis of palms and soles, pustulosis palmaris et plantaris) *Pustular bacterid

Resulting from errors in metabolism

Skin conditions resulting from errors in metabolism are caused by enzyme, enzymatic defects that lead to an accumulation or deficiency of various cellular components, including, but not limited to, amino acids, carbohydrates, and lipids. *Acute intermittent porphyria *Adrenoleukodystrophy (Schilder's disease) *Alkaptonuria *Aminolevulinic acid dehydratase deficiency porphyria (Doss porphyria, plumboporphyria) *B-mannosidase deficiency *Carotenosis *Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome (CADASIL syndrome) *Cerebrotendinous xanthomatosis *Citrullinemia *Congenital erythropoietic porphyria (Gunther's disease) *Diabetic bulla (bullosis diabeticorum, bullous eruption of diabetes mellitus) *Diabetic cheiroarthropathy *Diabetic dermopathy (shin spots) *Dystrophic calcinosis cutis *Eruptive xanthoma *Erythropoietic protoporphyria Chronic skin lesions of EPP

*Fabry disease (Anderson–Fabry disease, angiokeratoma corporis diffusum) *Familial alpha-lipoprotein deficiency (Tangier disease) *Familial amyloid polyneuropathy *Familial apoprotein CII deficiency *Familial combined hyperlipidemia (multiple-type hyperlipoproteinemia) *Familial defective apolipoprotein B-100 *Familial dysbetalipoproteinemia (broad beta disease, remnant removal disease) *Familial hypertriglyceridemia *Farber disease (fibrocytic dysmucopolysaccharidosis, lipogranulomatosis) *Fucosidosis *Gaucher's disease *Gout (podagra, urate crystal arthropathy, urate deposition disease) *Hartnup disease (pellagra-like dermatosis) *Hemodialysis-associated amyloidosis *Hepatoerythropoietic porphyria *Hereditary coproporphyria *Hereditary gelsolin amyloidosis *Heredofamilial amyloidosis *Hunter syndrome *Hurler syndrome (gargoylism, mucopolysaccharidosis type I) *Hurler–Scheie syndrome (mucopolysaccharidosis type I H-S) *Hyaluronidase deficiency (mucopolysaccharidosis type IX) *Iatrogenic calcinosis cutis *Idiopathic scrotal calcinosis (idiopathic calcified nodules of the scrotum) *Lafora disease *Lesch–Nyhan syndrome (juvenile gout) *Lichen amyloidosis *Limited joint mobility *Lipoid proteinosis (hyalinosis cutis et mucosae, Urbach–Wiethe disease) *Lipoprotein lipase deficiency (chylomicronemia, chylomicronemia syndrome) *Macular amyloidosis Multiple hand xanthomas 18 yo case report

Multiple hand xanthomas 18 yo case report

*Maroteaux–Lamy syndrome (mucopolysaccharidosis type VI) *Medication-induced hyperlipoproteinemia *Metastatic calcinosis cutis *Milia-like calcinosis *Morquio's disease (mucopolysaccharidosis type IV) *Necrobiosis lipoidica (necrobiosis lipoidica diabeticorum) *Niemann–Pick disease *Nodular amyloidosis *Nodular xanthoma *Normolipoproteinemic xanthomatosis *Obstructive liver disease (xanthomatous biliary cirrhosis) *Ochronosis *Osteoma cutis *Palmar xanthoma *Phenylketonuria *Phytosterolemia (sitosterolemia) *Porphyria cutanea tarda *Primary cutaneous amyloidosis *Primary systemic amyloidosis *Prolidase deficiency *Pseudoporphyria (pseudoporphyria cutanea tarda) *Sanfilippo syndrome *Scheie syndrome (mucopolysaccharidosis type I S) *Secondary cutaneous amyloidosis *Secondary systemic amyloidosis *Sialidosis *Sly syndrome (mucopolysaccharidosis type VII) *Subepidermal calcified nodule (solitary congenital nodular calcification, Winer's nodular calcinosis) *Transient erythroporphyria of infancy (purpuric phototherapy-induced eruption) *Traumatic calcinosis cutis *Tuberoeruptive xanthoma (tuberous xanthoma) *Tumoral calcinosis *Variegate porphyria (mixed hepatic porphyria, mixed porphyria, South African genetic porphyria, South African porphyria) *Verruciform xanthoma *Waxy skin *Wilson's disease (hepatolenticular degeneration) *Xanthelasma palpebrarum (xanthelasma) *Xanthoma diabeticorum *Xanthoma planum (plane xanthoma) *Xanthoma striatum palmare *Xanthoma tendinosum (tendinous xanthoma) *Xanthoma tuberosum

Resulting from physical factors

Skin conditions resulting from physical factors occur from a number of causes, including, but not limited to, hot and cold temperatures, friction, and moisture. *Abrasion (medical), Abrasion *Acrocyanosis *Actinic prurigo (familial polymorphous light eruption of American Indians, hereditary polymorphous light eruption of American Indians, Hutchinson's summer prurigo, hydroa aestivale) *Aerosol burn *Benign summer light eruption *Beryllium granuloma *Black heel and palm (black heel, calcaneal petechiae, chromidrose plantaire, post-traumatic punctate intraepidermal hemorrhage, tache noir, talon noir) *Callus (callosity, clavus, corn, heloma, heloma durum, heloma molle, intractable plantar keratosis, tyloma) *Carbon stain *Chilblains (pernio, perniosis) *Chronic actinic dermatitis (actinic reticuloid, chronic photosensitivity dermatitis, persistent light reactivity, photosensitive eczema) *Colloid milium *Coma blister *Coral cut *Delayed blister *Dermatosis neglecta *Edema blister (edema bulla, hydrostatic bulla, stasis blister) *Electrical burn *Equestrian perniosis *Erythema ab igne (fire stains, toasted skin syndrome) *Erythrocyanosis crurum *Favre–Racouchot syndrome (Favre–Racouchot disease, nodular cutaneous elastosis with cysts and comedones) *Foreign body reaction *Fracture blister *Friction blister *Frostbite *Garrod's pad (violinist's viola pad) *Harpist's finger *Heel stick wound *Heat edema *Hot tar burn *Hunan hand syndrome (chili burn) *Hydroa vacciniforme (Bazin's hydroa vacciniforme) *Jogger's nipple *Juvenile spring eruption *Kairo cancer *Kang cancer *Kangri ulcer *Lightning burn *Loop mark *Magnetic resonance imaging burn (MRI burn) *Mercury granuloma *Miliaria crystallina (miliaria crystalline, sudamina) *Miliaria profunda (mammillaria) *Miliaria pustulosa *Miliaria rubra (heat rash, prickly heat) *Narcotic dermopathy *Occlusion miliaria *Painful fat herniation (painful piezogenic pedal papules, piezogenic papules) *Peat fire cancer *Photoaging (dermatoheliosis) *Photosensitivity with HIV infection *Phototoxic tar dermatitis *Photosenitization *Phytophotodermatitis (Berloque dermatitis) *Pinch mark *Polymorphous light eruption (polymorphic light eruption) *Postmiliarial hypohidrosis Escarre Stade 4 détail

*Postoperative hematoma *Pressure ulcer (decubitus ulcer) *Pseudoacanthosis nigricans *Pseudoverrucous papules and nodules *Pulling boat hands *PUVA-induced acrobullous dermatosis *Runner's rump *Sclerosing lymphangiitis *Silica granuloma *Silicone granuloma *Skin pop scar *Skin track *Slap mark *Solar erythema *Soot tattoo *Subcutaneous emphysema *Sucking blister *Sunburn *Surfer's knots *Tattoo *Tennis toe *Thermal burn *Traumatic asphyxia *Trench foot *Tropical anhidrotic asthenia *Tropical immersion foot (paddy foot, paddy-field foot) *Turf toe *Uranium dermatosis *UV-sensitive syndrome *Vibration white finger (dead finger, hand–arm vibration syndrome) *Warm water immersion foot *Weathering nodule of ear *Wrestler's ear (cauliflower ear, traumatic auricular hematoma) *Zirconium granuloma

Ionizing radiation-induced

Ionizing radiation-induced cutaneous conditions result from exposure to ionizing radiation. *Acute radiodermatitis

*Chronic radiation keratosis *Chronic radiodermatitis *Eosinophilic, polymorphic, and pruritic eruption associated with radiotherapy *Fluoroscopy burn *Radiation acne *Radiation cancer *Radiation dermatitis (radiodermatitis) *Radiation recall reaction *Radiation-induced erythema multiforme *Radiation-induced hypertrophic scar *Radiation-induced keloid *Radiation-induced morphea

Urticaria and angioedema

Urticaria is a vascular reaction of the skin characterized by the appearance of Wheal response, wheals, which are firm, elevated swellings of the skin. Angioedema, which can occur alone or with urticaria, is characterized by a well-defined, edematous swelling that involves subcutaneous tissues, abdominal organs, or upper airway. *Acquired C1 esterase inhibitor deficiency *Acute urticaria *Adrenergic urticaria *Anaphylaxis *Aquagenic urticaria *Cholinergic urticaria *Chronic urticaria (ordinary urticaria) *Cold urticaria *Dermatographism (dermographism) *Episodic angioedema with eosinophilia (Gleich's syndrome) *Exercise urticaria (exercise-induced urticaria) *Galvanic urticaria *Heat urticaria *Hereditary angioedema (Quincke's edema) *Localized heat contact urticaria *Mast cell-independent urticaria *Physical urticaria *Primary cold contact urticaria *Pressure urticaria (delayed pressure urticaria) *Reflex cold urticaria *Schnitzler syndrome *Secondary cold contact urticaria *Solar urticaria *Systemic capillary leak syndrome *Urticarial allergic eruption *Urticaria-like follicular mucinosis *Vibratory angioedema

Vascular-related

Vascular-related cutaneous conditions result from dysfunction of the blood or blood vessels in the dermis, or lymphatics in the subcutaneous tissues. *Aagenaes syndrome *Acroangiodermatitis (acroangiodermatitis of Mali, Mali acroangiodermatitis, Pseudo-Kaposi's sarcoma) *Acrocyanosis *Acute hemorrhagic edema of infancy (acute hemorrhagic edema of childhood, Finkelstein's disease, infantile postinfectious iris-like purpura and edema, medallion-like purpura, purpura en cocarde avec oedema, Seidlmayer syndrome) *Arterial insufficiency ulcer (ischemic ulcer) *Arteriosclerosis obliterans *Bier spots *Blueberry muffin baby *Bonnet–Dechaume–Blanc syndrome (Wyburn–Mason syndrome) *Bullous lymphedema *Bullous small vessel vasculitis (bullous variant of small vessel vasculitis) *Calciphylaxis *Caput succedaneum *Cholesterol embolus (warfarin blue toe syndrome) *Cobb syndrome *Corona phlebectatica *Cryofibrinogenemic purpura *Cryoglobulinemic purpura *Cryoglobulinemic vasculitis *Cutaneous small-vessel vasculitis (cutaneous leukocytoclastic angiitis, cutaneous leukocytoclastic vasculitis, cutaneous necrotizing venulitis, hypersensitivity angiitis) *Deep venous thrombosis *Disseminated intravascular coagulation *Doucas and Kapetanakis pigmented purpura *Drug-induced purpura *Drug-induced thrombocytopenic purpura *Eczematid-like purpura of Doucas and Kapetanakis *Epidemic dropsy *Erythema elevatum diutinum *Erythromelalgia (acromelalgia, erythermalgia) *Factitial lymphedema (hysterical edema) *Fibrinolysis syndrome (defibrinating syndrome, hypofibrinogenemia) *Food-induced purpura *Generalized essential telangiectasia (general essential telangiectasia) *Giant-cell arteritis *Gougerot–Blum syndrome (pigmented purpuric lichenoid dermatitis, pigmented purpuric lichenoid dermatitis of Gougerot and Blum) * Granulomatosis with polyangiitis *Harlequin color change *Hematopoietic ulcer *Hennekam syndrome (Hennekam lymphangiectasia-lymphedema syndrome, intestinal lymphagiectasia-lymphedema-mental retardation syndrome) *Henoch–Schönlein purpura (anaphylactoid purpura, purpura rheumatica, Schönlein–Henoch purpura) *Hereditary hemorrhagic telangiectasia (Osler's disease, Osler–Weber–Rendu disease) *Idiopathic thrombocytopenic purpura (autoimmune thrombocytopenic purpura, Werlhof's disease) *IgA vasculitis *Kawasaki's disease (mucocutaneous lymph node syndrome) *Levamisole-induced vasculitis *Lichen aureus (lichen purpuricus) *Livedo racemosa *Livedo reticularis *Livedoid dermatitis (embolia cutis medicamentosa, Nicolau syndrome) *Livedoid vasculopathy (atrophie blanche, livedo reticularis with summer ulceration, livedoid vasculitis, PURPLE syndrome, segmental hyalinizing vasculitis) *Lymphedema praecox *Lymphedema–distichiasis syndrome *Maffucci syndrome *Majocchi's disease (purpura annularis telangiectodes, purpura annularis telangiectodes of Majocchi) *Malignant atrophic papulosis (Degos' disease) *Marshall–White syndrome *Meige lymphedema *Microscopic polyangiitis (microscopic polyarteritis, microscopic polyarteritis nodosa) *Mondor's disease (Mondor's syndrome of superficial thrombophlebitis) *Neuropathic ulcer (mal perforans) *Njolstad syndrome *Nonne–Milroy–Meige syndrome (hereditary lymphedema, Milroy disease) *Obstructive purpura *Orthostatic purpura (stasis purpura) *Painful bruising syndrome (autoerythrocyte sensitization, Gardner–Diamond syndrome, psychogenic purpura) *Parkes Weber syndrome *Paroxysmal hand hematoma (Achenbach syndrome) *Paroxysmal nocturnal hemoglobinuria *Polyarteritis nodosa (panarteritis nodosa, periarteritis nodosa) *Postcardiotomy syndrome *Perinatal gangrene of the buttock *Pigmentary purpuric eruptions (progressive pigmentary dermatosis, progressive pigmenting purpura, purpura pigmentosa chronica) *Postinflammatory lymphedema *Postmastectomy lymphangiosarcoma (Stewart–Treves syndrome) *Purpura fulminans (purpura gangrenosa) *Purpura secondary to clotting disorders *Purpuric agave dermatitis *Raynaud phenomenon *Raynaud's disease (primary Raynaud's phenomenon) *Reactive angioendotheliomatosis *Schamberg's disease (progressive pigmentary dermatosis of Schamberg, purpura pigmentosa progressiva, Schamberg's purpura) *Secondary lymphedema *Septic thrombophlebitis *Sinusoidal hemangioma *Sneddon's syndrome (idiopathic livedo reticularis with cerebrovascular accidents) *Solar purpura (actinic purpura, senile purpura) *Stasis dermatitis (congestion eczema, gravitational dermatitis, gravitational eczema, stasis eczema, varicose eczema) *Superficial thrombophlebitis *Takayasu arteritis (aortic arch syndrome, pulseless disease) *Temporal arteritis (cranial arteritis, Horton's disease) *Thromboangiitis obliterans (Buerger's disease) *Thrombotic thrombocytopenic purpura (Moschcowitz syndrome) *Traumatic purpura *Trousseau's syndrome *Unilateral nevoid telangiectasia (nevoid telangiectasia) *Urticarial vasculitis (chronic urticaria as a manifestation of venulitis, hypocomplementemic urticarial vasculitis syndrome, hypocomplementemic vasculitis, unusual lupus-like syndrome) *Venous insufficiency ulceration *Waldenström hyperglobulinemic purpura (purpura hyperglobulinemica) *Waldenström macroglobulinemia *Yellow nail syndrome (primary lymphedema associated with yellow nails and pleural effusion)

Footnotes

References

External links

*
All the Internet - Directory - Main/Health/Conditions_and_Diseases/Skin_Disorders

Images in Clinical Dermatology
at the New England Journal of Medicine {{DEFAULTSORT:Cutaneous conditions Cutaneous conditions, Dermatology-related lists Lists of diseases

Acneiform eruptions

Autoinflammatory syndromes

Chronic blistering

Conditions of the mucous membranes

Conditions of the skin appendages

Conditions of the subcutaneous fat

Congenital anomalies

Connective tissue diseases

Abnormalities of dermal fibrous and elastic tissue

Dermal and subcutaneous growths

Dermatitis

Atopic

Contact

Eczema

Pustular

Seborrheic

Disturbances of pigmentation

Drug eruptions

Endocrine-related

Eosinophilic

Epidermal nevi, neoplasms, and cysts

Erythemas

Genodermatoses

Infection-related

Bacterium-related

''Mycobacterium''-related

Mycosis-related

Parasitic infestations, stings, and bites

Virus-related

Lichenoid eruptions

Lymphoid-related

Melanocytic nevi and neoplasms

Melanoma

Monocyte- and macrophage-related

Mucinoses

Neurocutaneous

Noninfectious immunodeficiency-related

Nutrition-related

Papulosquamous hyperkeratotic

Palmoplantar keratodermas

Pregnancy-related

Pruritic

Psoriasis

Reactive neutrophilic

Recalcitrant palmoplantar eruptions

Resulting from errors in metabolism

Resulting from physical factors

Ionizing radiation-induced

Urticaria and angioedema

Vascular-related

See also

Footnotes

References

Further reading

External links