MarketList of skin conditions
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List of skin conditions

Many skin conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscles and glands. 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, and hair-bearing skin. Within the latter type, the hairs occur in structures called pilosebaceous units, each with hair follicle, sebaceous gland, 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.

Acneiform eruptions
|alt=Adult forehead with scattered red pimples|alt=Boggy, suppurative nodule with patchy hair loss typical of dissecting cellulitis of the scalp|alt=Adult male with a large, red, bulbous noseAcneiform eruptions are caused by changes in the pilosebaceous unit. • Acne aestivalis (Mallorca acne) • Acne conglobataAcne cosmetica (cosmetic acne) • Acne fulminans (acute febrile ulcerative acne) • Acne keloidalis nuchae (acne keloidalis, dermatitis papillaris capillitii, folliculitis keloidalis, folliculitis keloidis nuchae, nuchal keloid acne) • Acne mechanicaAcne medicamentosaAcne miliaris necrotica (acne varioliformis) • Acne vulgaris (acne simplex) • Acne with facial edema (solid facial edema) • BlepharophymaChloracneErythrotelangiectatic rosacea (erythematotelangiectatic rosacea, vascular rosacea) • Excoriated acne (acne excoriée des jeunes filles, Picker's acne) • Glandular rosaceaGnathophymaGram-negative rosaceaGranulomatous facial dermatitisGranulomatous perioral dermatitisHalogen acneHidradenitis suppurativa (acne inversa, pyoderma fistulans significa, Verneuil's disease) • Idiopathic facial aseptic granulomaInfantile acneLupoid rosacea (granulomatous rosacea, micropapular tuberculid, rosacea-like tuberculid of Lewandowsky) • Lupus miliaris disseminatus facieiMetophymaNeonatal acne (acne infantum, acne neonatorum, neonatal cephalic pustulosis) • Occupational acneOil acneOcular rosacea (ophthalmic rosacea, ophthalmorosacea) • OtophymaPeriorificial dermatitisPersistent edema of rosacea (chronic upper facial erythematous edema, Morbihan's disease, rosaceous lymphedema) • Phymatous rosaceaPomade acnePapulopustular rosacea (inflammatory rosacea) • Perifolliculitis capitis abscedens et suffodiens (dissecting cellulitis of the scalp, dissecting folliculitis, perifolliculitis capitis abscedens et suffodiens of Hoffman) • Perioral dermatitisPeriorbital dermatitis (periocular dermatitis) • Pyoderma faciale (rosacea fulminans) • RhinophymaRosacea (acne rosacea) • Rosacea conglobataSynovitis–acne–pustulosis–hyperostosis–osteomyelitis syndrome (SAPHO syndrome) • Steroid rosaceaTar acneTropical acne == Autoinflammatory syndromes ==
Autoinflammatory syndromes
Autoinflammatory syndromes are a group of inherited disorders characterized by bouts of inflammatory skin lesions and periodic fevers. • Blau syndrome |alt=Multiple reddish-brown papules coalescing over the right arm of a boy • Chronic infantile neurologic cutaneous and articular syndromeFamilial cold urticaria (familial cold autoinflammatory syndrome) • Familial Mediterranean feverHyper-IgD syndromeMajeed syndromeMuckle–Wells syndromeTNF receptor associated periodic syndrome (familial Hibernian fever, TRAPS, tumor necrosis factor receptor associated periodic syndrome) == Chronic blistering ==
Chronic blistering
Chronic blistering cutaneous conditions have a prolonged course and present with vesicles and bullae. • Adult linear IgA diseaseBullous pemphigoidBullous lupus erythematosusChildhood linear IgA disease (chronic bullous disease of childhood) • Cicatricial pemphigoid (benign mucosal pemphigoid, benign mucous membrane pemphigoid, ocular pemphigus, scarring pemphigoid) • Dermatitis herpetiformis (Duhring disease) • Dyshidrosis (recurrent vesicular palmoplantar dermatitis, acute vesiculobullous hand eczema, dyshidrotic dermatitis, pompholyx) • Endemic pemphigus (endemic pemphigus foliaceus, fogo selvagem) • Epidermolysis bullosa acquisitaGrover's disease (benign papular acantholytic dermatosis, persistent acantholytic dermatosis, transient acantholytic dermatosis) |alt=Adult chest and abdomen with many red skin lesions • IgA pemphigusIntraepidermal neutrophilic IgA dermatosisLocalized cicatricial pemphigoid (Brunsting–Perry cicatricial pemphigoid) • Paraneoplastic pemphigusPemphigus erythematosus (Senear–Usher syndrome) • Pemphigus foliaceusPemphigus herpetiformis (acantholytic herpetiform dermatitis, herpetiform pemphigus, mixed bullous disease, pemphigus controlled by sulfapyridine) • Pemphigoid nodularisPemphigus vegetansPemphigus vegetans of HallopeauPemphigus vegetans of NeumannPemphigus vulgarisVesicular pemphigoidVulvar childhood pemphigoid == Conditions of the mucous membranes ==
Conditions of the mucous membranes
Conditions of the mucous membranes involve the moist linings of the eyes, nose, mouth, genitals, and anus. • Acatalasia (acatalasemia, Takahara's disease) • Acquired dyskeratotic leukoplakiaActinic cheilitis (actinic cheilosis) • Acute necrotizing ulcerative gingivitis (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 cheilitisAngina bullosa haemorrhagicaAngular cheilitis (perlèche) • Behçet's disease (Behçet's syndrome, oculo-oral-genital syndrome) • Black hairy tongue (hairy tongue, lingua villosa nigra) |alt=Adult tongue with a strikingly black top • Caviar tongueCheilitis exfoliativaCheilitis glandularisCheilitis granulomatosa (granulomatous cheilitis, orofacial granulomatosis) • Cutaneous sinus of dental origin (dental sinus) • Cyclic neutropeniaDesquamative gingivitisDrug-induced ulcer of the lipEpidermization of the lipEpulisEpulis fissuratum (granuloma fissuratum) • Eruptive lingual papillitisErythroplakia (erythroplasia) • Fissured tongue (furrowed tongue, lingua plicata, plicated tongue, scrotal tongue) • Geographic tongue (benign migratory glossitis, benign migratory stomatitis, glossitis areata exfoliativa, glossitis areata migrans, lingua geographica, stomatitis areata migrans, transitory benign plaques of the tongue) • Gingival fibromaGingival hypertrophyHairy leukoplakia (oral hairy leukoplakia) • Intraoral dental sinusLinea albaLeukoplakiaLeukoplakia with tylosis and esophageal carcinomaMajor aphthous ulcer (periadenitis mucosa necrotica recurrens) • Median rhomboid glossitis (central papillary atrophy) • Melanocytic oral lesionMelkersson–Rosenthal syndromeMorsicatio buccarum (chronic cheek biting, chronic cheek chewing) • Mucosal squamous cell carcinomaMucous cyst of the oral mucosa (mucocele) • Nagayama's spotsOral Crohn's diseaseOral florid papillomatosisOral melanosisOsseous choristoma of the tonguePeripheral ameloblastomaPlasma cell cheilitis (plasma cell gingivitis, plasma cell orificial mucositi) • PlasmoacanthomaProliferative verrucous leukoplakiaPyogenic granuloma (eruptive hemangioma, granulation tissue-type hemangioma, granuloma gravidarum, lobular capillary hemangioma, pregnancy tumor, tumor of pregnancy) |alt=A solitary papule of inflamed vascular granulation tissue on the index finger of an adult • Pyostomatitis vegetansRecurrent aphthous stomatitis (aphthosis, canker sores, recurrent oral aphthae) • Recurrent intraoral herpes simplex infectionSmooth tongue (atrophic glossitis, bald tongue, hunter glossitis, moeller) • Stomatitis nicotina (nicotine stomatitis, smoker's keratosis, smoker's patches) • Torus palatinusTrumpeter's wartVestibular papillomatosisWhite sponge nevus (white sponge nevus of Cannon) == Conditions of the skin appendages ==
Conditions of the skin appendages
Conditions of the skin appendages are those affecting the glands of the skin, hair, nails, and arrector pili muscles. • Acne necroticaAcquired generalized hypertrichosis (acquired hypertrichosis lanuginosa, hypertrichosis lanuginosa acquisita) • Acquired perforating dermatosis (acquired perforating collagenosis) • Acrokeratosis paraneoplastica of Bazex (acrokeratosis neoplastica, Bazex syndrome) • AcroosteolysisAcute paronychiaAlopecia areata |alt=Circular coin-sized bare patch on the back of a person's scalp • Alopecia neoplasticaAnagen effluviumAndrogenic alopecia (androgenetic alopecia) • Anhidrosis (hypohidrosis) • AnonychiaApparent leukonychiaBeau's linesBlue nailsBromidrosis (apocrine bromhidrosis, fetid sweat, malodorous sweating, osmidrosis) • Bubble hair deformityCentral centrifugal cicatricial alopecia (follicular degeneration syndrome, pseudopelade of the central scalp) • Chevron nail (herringbone nail) • Chromhidrosis (colored sweat) • Chronic paronychiaCicatricial alopeciaClubbing (drumstick fingers, Hippocratic fingers, watch-glass nails) • Congenital onychodysplasia of the index fingersDisseminate and recurrent infundibulofolliculitisErosive pustular dermatitis of the scalp (erosive pustular dermatosis of the scalp) • Erythromelanosis follicularis faciei et colliFolliculitis decalvansFolliculitis nares perforansFox–Fordyce diseaseFrontal fibrosing alopeciaGeneralized congenital hypertrichosis (congenital hypertrichosis lanuginosa) • Generalized hyperhidrosisGraham-Little syndromeGranulosis rubra nasiGreen nailsGustatory hyperhidrosisHair casts (pseudonits) • Hair follicle nevus (vellus hamartoma) • Hairy palms and solesHalf and half nails (Lindsay's nails) • HangnailHapalonychiaHematidrosisHirsutismHook nailHot comb alopeciaHypertrichosis cubiti (hairy elbow syndrome) • Hypertrichosis simplex of the scalp • Intermittent hair–follicle dystrophy • Keratosis pilaris atrophicansKinking hair (acquired progressive kinking) • Koenen's tumor (Koenen's periungual fibroma, periungual fibroma) • Koilonychia (spoon nails) • Kyrle diseaseLeukonychia (white nails) • Lichen planopilaris (acuminatus, follicular lichen planus, lichen planus follicularis, peripilaris) • Lichen planus of the nailsLichen spinulosus (keratosis spinulosa) • Lipedematous alopecia (lipedematous scalp) • Localized acquired hypertrichosisLocalized congenital hypertrichosisLongitudinal erythronychiaLongitudinal melanonychiaLoose anagen syndrome (loose anagen hair syndrome) • Lupus erythematosusMadarosisMalalignment of the nail plateMale-pattern baldnessMarie–Unna hereditary hypotrichosis (Marie–Unna hypotrichosis) • Median nail dystrophy (dystrophia unguis mediana canaliformis, median canaliform dystrophy of Heller, solenonychia) • Mees' linesMelanonychiaMenkes kinky hair syndrome (kinky hair disease, Menkes disease) • Monilethrix (beaded hair) • Muehrcke's nails (Muehrcke's lines) • Nail–patella syndrome (Fong syndrome, hereditary osteoonychodysplasia, HOOD syndrome) |alt=Big toe with most of the toenail missing; only the nail's root is present • Neoplasms of the nailbedNevoid hypertrichosisNoncicatricial alopeciaOnychauxisOnychoatrophyOnychocryptosis (ingrown nail, unguis incarnatus) • Onychogryphosis (ram's horn nails) • OnycholysisOnychomadesisOnychomatricomaOnychophagia (nail biting) • OnychophosisOnychoptosis defluvium (alopecia unguium) • Onychorrhexis (brittle nails) • OnychoschiziaOnychotillomania|alt=Multiple, dystrophic, irregular, shortened fingernails • OphiasisPalmoplantar hyperhidrosis (emotional hyperhidrosis) • Parakeratosis pustulosaPatterned acquired hypertrichosisPerforating folliculitisPili annulati (ringed hair) • Pili bifurcatiPili multigeminiPili pseudoannulati (pseudo pili annulati) • Pili torti (twisted hairs) • Pincer nails (omega nails, trumpet nails) • Pityriasis amiantacea (tinea amiantacea) • PlatonychiaPlica neuropathica (felted hair) • Plummer's nailPremature greying of hairPrepubertal hypertrichosisPressure alopecia (postoperative alopecia, pressure-induced alopecia) • Pseudofolliculitis barbae (barber's itch, folliculitis barbae traumatica, razor bumps, scarring pseudofolliculitis of the beard, shave bumps) • Pseudopelade of Brocq (alopecia cicatrisata) • Psoriatic nailsPterygium inversum unguis (pterygium inversus unguis, ventral pterygium) • Pterygium unguis (dorsal pterygium) • Purpura of the nail bedRacquet 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 lunulaeRoss' syndromeRubinstein–Taybi syndromeSetleis syndromeShell nail syndromeShort anagen syndromeSplinter hemorrhage |alt=Small, linear, blue-black areas of discoloration beneath the nail plate of an adult finger • Spotted lunulaeStaining of the nail plateSubungual hematomaTelogen effluviumTerry's nailsTraction alopeciaTraumatic alopeciaTraumatic anserine folliculosisTriangular alopecia (temporal alopecia, temporal triangular alopecia) • TrichomegalyTrichomycosis axillarisTrichorrhexis invaginata (bamboo hair) • Trichorrhexis nodosaTrichostasis spinulosaTufted folliculitisTumor alopeciaTwenty-nail dystrophy (sandpapered nails, trachyonychia) • Uncombable hair syndrome (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
Conditions of the subcutaneous fat are those affecting the layer of adipose tissue that lies between the dermis and underlying fascia. • Acquired generalized lipodystrophy (Lawrence syndrome, Lawrence–Seip syndrome) • Adiposis dolorosa (Dercum's disease) • Alpha-1 antitrypsin deficiency panniculitis (alpha1-protease deficiency panniculitis, alpha1-proteinase deficiency panniculitis) • Atrophic connective tissue panniculitisBarraquer–Simons syndrome (acquired partial lipodystrophy, cephalothoracic lipodystrophy, progressive lipodystrophy) • Benign symmetric lipomatosis (benign symmetric lipomatosis of Launois–Bensaude, Madelung's disease) • Centrifugal abdominal lipodystrophy (centrifugal lipodystrophy, lipodystrophia centrifugalis abdominalis infantalis) • Chronic erythema nodosum (erythema nodosum migrans, subacute migratory panniculitis of Vilanova and Piñol, subacute nodular migratory panniculitis) |alt=Dark area of skin, reminiscent of a bruise, on the inner ankle of an adult • Cold panniculitis (popsicle panniculitis) • Congenital generalized lipodystrophy (Berardinelli–Seip syndrome) • Cytophagic histiocytic panniculitisDrug-induced lipodystrophyFactitial panniculitisFamilial partial lipodystrophy (Köbberling–Dunnigan syndrome) • Gouty panniculitisHemihyperplasia–multiple lipomatosis syndromeHIV-associated lipodystrophyInvolutional lipoatrophyLipoatrophia annularis (Ferreira–Marques lipoatrophia) • Lipoatrophia semicircularis (semicircular lipoatrophy) • Lipodermatosclerosis (chronic panniculitis with lipomembranous changes, hypodermitis sclerodermiformis, sclerosing panniculitis, stasis panniculitis) • LipohypertrophyLocalized lipodystrophyNeutrophilic lobular panniculitisNodular vasculitisNon-progressive late-onset linear hemifacial lipoatrophyPancreatic panniculitis (enzymatic panniculitis, pancreatic fat necrosis, subcutaneous fat necrosis) • Poland's syndromePost-steroid panniculitisSclerema neonatorumSclerosing lipogranuloma (paraffinoma) • Septal panniculitisSubcutaneous fat necrosis of the newbornTraumatic panniculitisTumor lysis syndromeWeber–Christian disease (relapsing febrile nonsuppurative panniculitis) == Congenital anomalies ==
Congenital anomalies
Cutaneous congenital anomalies are a diverse group of disorders that result from faulty morphogenesis, the biological process that forms the shape of a human body. • Accessory nail of the fifth toeAccessory tragus (ear tag, preauricular appendage, preauricular tag) • Amniotic band syndrome (ADAM complex, amniotic band sequence, congenital constriction bands, pseudoainhum) • Aplasia cutis congenita (cutis aplasia, congenital absence of skin, congenital scars) • Arteriovenous fistulaBenign neonatal hemangiomatosisBranchial cyst (branchial cleft cyst) • Bronchogenic cystCapillary hemangioma (infantile hemangioma, nevus maternus, strawberry hemangioma, strawberry nevus) • Cavernous venous malformationCongenital cartilaginous rest of the neck (cervical accessory tragus, wattle) • Congenital erosive and vesicular dermatosisCongenital hypertrophy of the lateral fold of the halluxCongenital lip pit (congenital sinus of the lower lip, lip sinus, midline sinus of the upper lip) • Congenital malformations of the dermatoglyphsCongenital smooth muscle hamartomaCystic lymphatic malformationDermoid cystDiffuse neonatal hemangiomatosisEncephaloceleFamilial disseminated comedones without dyskeratosisFocal facial dermal dysplasiaHutchinson's teethHyperkeratotic cutaneous capillary-venous malformationIntrauterine epidermal necrosisLimb–mammary syndromeLowry–MacLean syndromeMacrocheiliaMacrocystic lymphatic malformationMalignant pilomatricoma (pilomatrical carcinoma, pilomatrix carcinoma) • Maternal autoimmune bullous diseaseMedian raphe cystMelanotic neuroectodermal tumor of infancyMembranous aplasia cutisMicrocystic lymphatic malformationMidline cervical cleftMongolian spot (congenital dermal melanocytosis, dermal melanocytosis) |alt=Several light blue patches of skin distributed over a child's lower back and buttock • Mulberry molarNager acrofacial dysostosisNasal glioma (brain-like heterotopia, cephalic brain-like heterotopia, glial hamartoma, heterotopic neuroglial tissue, nasal cerebral heterotopia, nasal heterotopic brain tissue) • Nasolacrimal duct cystNevus psiloliparusNon-involuting congenital hemangiomaOmphalomesenteric duct cyst (omphalomesenteric duct remnant, vitelline cyst) • PELVIS syndromePilomatricoma (calcifying epithelioma of Malherbe, Malherbe calcifying epithelioma, pilomatrixoma) • Poland anomalyPosterior fossa malformations–hemangiomas–arterial anomalies–cardiac defects–eye abnormalities–sternal cleft and supraumbilical raphe syndrome (PHACE association, PHACES syndrome) • Preauricular sinus and cyst (ear pit, congenital auricular fistula, congenital preauricular fistula, preauricular cyst) • Rapidly involuting congenital hemangioma (congenital nonprogressive hemangioma) • Rosenthal–Kloepfer syndromeRudimentary supernumerary digit (rudimentary polydactyly) • SACRAL syndromeSinus pericraniiSkin dimple (skin fossa) • Superficial lymphatic malformation (lymphangioma circumscriptum) • Supernumerary nipple (accessory nipple, pseudomamma) • Thyroglossal duct cystVerrucous vascular malformation (angiokeratoma circumscriptum naeviforme) == Connective tissue diseases ==
Connective tissue diseases
Connective tissue diseases are caused by a complex array of autoimmune responses that target or affect collagen or ground substance. • Acute cutaneous lupus erythematosusAtrophoderma 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 dermatomyositisChildhood discoid lupus erythematosusChildhood systemic lupus erythematosusComplement deficiency syndromesDermatomyositisEhlers–Danlos syndromeEosinophilia–myalgia syndromeFrontal linear scleroderma (en coup de sabre, morphea en coup de sabre) |alt=A young girl with facial palsy, complete ptosis, and marked atrophy of subcutaneous and bony structures on the left upper side of the face • Generalized discoid lupus erythematosusGeneralized morpheaInterstitial granulomatous dermatitisJuvenile rheumatoid arthritis (juvenile idiopathic arthritis, Still's disease) • Keloid morpheaLinear atrophoderma of Moulin (Moulin atrophoderma linearis) • Linear sclerodermaLocalized discoid lupus erythematosusLocalized morphea |alt=The lower back of an adult with thickened, indurated patches of skin • 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 eruptionMixed connective tissue disease (Sharp's syndrome, undifferentiated connective tissue disease) • Morphea profundaMorphea–lichen sclerosus et atrophicus overlapMouth and genital ulcers with inflamed cartilage syndrome (MAGIC syndrome) • Neonatal lupus erythematosusNephrogenic systemic fibrosis (nephrogenic fibrosing dermopathy) • Nicolau–Balus syndromeNodulosis–arthropathy–osteolysis syndromeNormophosphatemic familial tumoral calcinosisPalisaded neutrophilic and granulomatous dermatitisPansclerotic morpheaParry–Romberg syndrome (progressive hemifacial atrophy) • Progressive systemic sclerosisRelapsing polychondritis (atrophic polychondritis, systemic chondromalacia) • Rheumatoid arthritisRheumatoid nodulosis (accelerated rheumatoid nodulosis) • Rheumatoid vasculitisRowell's syndromeScleredema adultorum (Bushke disease, scleredema diabeticorum, scleredema adultorum of Buschke, scleredema of Buschke) • SilicosisSjögren's syndrome (Mikulicz disease, Sicca syndrome) • Subacute cutaneous lupus erythematosusSystemic lupus erythematosusToxic oil syndromeTumid lupus erythematosus (lupus erythematosus tumidus) • Tuzun syndromeVerrucous lupus erythematosus (hypertrophic lupus erythematosus) • Winchester syndrome Abnormalities of dermal fibrous and elastic tissue |alt=Fuzzy red lines on an abdomen 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 (solar elastosis) • Anetoderma (anetoderma maculosa, anetoderma maculosa cutis, atrophia maculosa cutis, macular atrophy) • BlepharochalasisCutis laxa (chalazoderma, dermatochalasia, dermatolysis, dermatomegaly, generalized elastolysis, generalized elastorrhexis, pachydermatocele) • Cutis rhomboidalis nuchaeEhlers–Danlos syndrome (cutis hyperelastica, elastic skin, India rubber skin) • Elastosis perforans serpiginosaHomocystinuriaJadassohn–Pellizzari anetodermaLinear focal elastosis (elastotic striae) • Loeys–Dietz syndromeMarfan syndromeOccipital horn syndromeOsteogenesis imperfecta (Lobstein syndrome) • Perforating calcific elastosis (localized acquired cutaneous pseudoxanthoma elasticum, perforating periumbilical calcific elastosis, periumbilical perforating pseudoxanthoma elasticum) • Pseudoxanthoma elasticum (Grönblad–Strandberg syndrome) • Reactive perforating collagenosisSchweninger–Buzzi anetodermaSclerotic fibromaStriae atrophicansStriae distensaeUllrich diseaseVerrucous perforating collagenomaWrinkly skin syndrome == Dermal and subcutaneous growths ==
Dermal and subcutaneous growths
Dermal and subcutaneous growths result from (1) reactive or neoplastic proliferation of cellular components of the dermis or subcutaneous tissue, or (2) neoplasms invading or aberrantly present in the dermis. • Acquired progressive lymphangioma (benign lymphangioendothelioma) • Acral fibrokeratoma (acquired digital fibrokeratoma, acquired periungual fibrokeratoma) • Acrochordon (cutaneous papilloma, cutaneous tag, fibroepithelial polyp, fibroma molluscum, fibroma pendulum, papilloma colli, skin tag, soft fibroma, Templeton skin tag) • Adenoma sebaceumAdult type of generalized eruption of cutaneous mastocytosisAfrican cutaneous Kaposi sarcomaAfrican lymphadenopathic Kaposi sarcomaAggressive infantile fibromatosisAIDS-associated Kaposi sarcomaAinhum (bankokerend, dactylolysis spontanea, sukhapakla) • AngiofibromaAngiokeratomaAngiokeratoma of Fordyce (angiokeratoma of the scrotum and vulva) |alt=Multiple, small, blue to red papules on the scrotum • Angiokeratoma of Mibelli (Mibelli's angiokeratoma, telangiectatic warts) • Angioleiomyoma (vascular leiomyoma) • AngiolipoleiomyomaAngiolipomaAngioma serpiginosumAngiosarcomaAponeurotic fibroma (calcifying aponeurotic fibroma, juvenile aponeurotic fibroma) • Atypical fibroxanthomaBenign lipoblastomatosis (embryonic lipoma) • Buschke–Ollendorff syndrome (dermatofibrosis lenticularis disseminata) • Capillary aneurysmsCarcinoidCellular angiofibromaCherry angioma (De Morgan spot, senile angioma) • Chondrodermatitis nodularis chronica helicis (chondrodermatitis nodularis helicis) |alt=Solitary, pink, dome-shaped papule on the superior helix of an adult • Chondroid lipomaChordomaClassic Kaposi sarcomaCollagenous fibroma (desmoplastic fibroblastoma) • Composite hemangioendotheliomaConnective tissue nevus (collagenoma, elastoma, shagreen patch) • Cutaneous endometriosisCutaneous meningioma (heterotopic meningeal tissue, rudimentary meningocele) • Cutaneous myelofibrosisCutaneous myxomaCutis marmorata telangiectatica congenita (congenital generalized phlebectasia, Van Lohuizen syndrome) • Dermal dendrocyte hamartomaDermatofibroma (benign fibrous histiocytoma, dermal dendrocytoma, fibrous dermatofibroma, fibrous histiocytoma, fibroma simplex, histiocytoma, nodular subepidermal fibrosis, sclerosing hemangioma) • Dermatofibrosarcoma protuberansDesmoid tumorDiffuse cutaneous mastocytosisDiffuse infantile fibromatosisDupuytren's contracture (Dupuytren's diathesis, Dupuytren's disease, palmar fibromatosis) • Eccrine angiomatous hamartomaElastofibroma dorsiEndovascular papillary angioendothelioma (Dabska tumor, Dabska-type hemangioendothelioma, hobnail hemangioendothelioma, malignant endovascular papillary angioendothelioma, papillary intralymphatic angioendothelioma) • Epithelioid cell histiocytomaEpithelioid hemangioendotheliomaEpithelioid sarcomaErythrodermic mastocytosisExtraskeletal chondroma (chondroma of soft parts) • Familial myxovascular fibromas • Fascial herniaFibroma of tendon sheathFibromatosis colli (sternomastoid tumor of infancy) • Fibrous hamartoma of infancyFibrous papule of the nose (benign solitary fibrous papule, fibrous papule of the face) • Folded skin with scarring (Michelin tire baby syndrome) • Fordyce's spot (Fordyce's disease) |alt=Small, raised, skin-colored lesions • Ganglion cystGanglioneuromaGardner fibromaGenital leiomyoma (dartoic leiomyoma) • Giant cell fibroblastomaGiant cell tumor of the tendon sheath (giant cell synovioma, localized nodular tenosynovitis, pigmented villonodular synovitis) • Glomeruloid hemangiomaGlomus tumor (glomangioma, solid glomus tumor, solitary glomus tumor) • Granular cell tumor (Abrikossoff's tumor, Abrikossov's tumor, granular cell myoblastoma, granular cell nerve sheath tumor, granular cell schwannoma) • HamartomaHemangiopericytomaHemangiosarcomaHibernoma (fetal lipoma, lipoma of embryonic fat, lipoma of immature adipose tissue) • Hypertrophic scarImmunosuppression-associated Kaposi sarcomaInfantile digital fibromatosis (inclusion body fibromatosis, infantile digital myofibroblastoma, Reye tumor) • Infantile hemangiopericytoma (congenital hemangiopericytoma) • Infantile myofibromatosis (congenital generalized fibromatosis, congenital multicentric fibromatosis) • Infantile systemic hyalinosis (juvenile systemic hyalinosis) • Intradermal spindle cell lipomaIntravascular 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 (infantile kaposiform hemangioendothelioma) • Kasabach–Merritt syndrome (hemangioma with thrombocytopenia) • Keloid (Keloidal scar) |alt=Excessive scar tissue along an adult jawline • Keratinizing metaplasiaKeratocystKlippel–Trenaunay syndrome (angioosteohypertrophy syndrome, hemangiectatic hypertrophy) • Knuckle pads (heloderma) • LeiomyosarcomaLipomaLiposarcoma (atypical lipoma, atypical lipomatous tumor) • Lymphangiectasis (lymphangioma) • LymphangiomatosisMalignant fibrous histiocytomaMalignant peripheral nerve sheath tumor (malignant schwannoma, neurofibrosarcoma, neurosarcoma) • Mast cell sarcomaMeningoceleMetastatic carcinomaMicrovenular hemangioma (microcapillary hemangioma) • Midline nevus flammeus (angel's kiss, salmon patch) • Multifocal lymphangioendotheliomatosis (congenital cutaneovisceral angiomatosis with thrombocytopenia, multifocal lymphangioendotheliomatosis with thrombocytopenia) • Multinucleate cell angiohistocytomaMultiple cutaneous and uterine leiomyomatosis syndrome (leiomyomatosis cutis et uteri, multiple leiomyomatosis, Reed's syndrome) • Multiple cutaneous leiomyoma (pilar leiomyoma) • Neural fibrolipomaNeuroblastoma (infantile neuroblastoma, neuroepithelioma) • Neuroma cutisNeurothekeoma (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 oligemicusNodular fasciitis (nodular pseudosarcomatous fasciits, pseudosarcomatous fasciitis, subcutaneous pseudosarcomatous fibromatosis) • Oral submucous fibrosisPachydermodactylyPalisaded encapsulated neuromaParaneoplastic syndromePearly penile papules (hirsuties coronae glandis, hirsutoid papillomas) • Peyronie's disease (induratio penis plastica) • Phakomatosis pigmentovascularisPiloleiomyomaPlantar fibromatosis (Ledderhose's disease) • Pleomorphic fibromaPleomorphic lipomaPlexiform fibrohistiocytic tumorPorokeratotic eccrine ostial and dermal duct nevusProgressive nodular histiocytomaProliferating angioendotheliomatosisProminent inferior labial arteryPseudo-ainhum • :|alt=Multiple tan patches scattered over the back of a young child • :|alt=A small blue- to purple-colored lesion on the lower lip of an adult • Retiform hemangioendothelioma (hobnail hemangioendothelioma) • Schwannoma (acoustic neuroma, neurilemmoma, neurinoma, neurolemmoma, Schwann cell tumor) • Solitary angiokeratomaSolitary cutaneous leiomyomaSolitary mastocytomaSolitary 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 lipomaSternal cleftSubungual exostosisSuperficial acral fibromyxomaSystemic mastocytosisTargetoid hemosiderotic hemangioma (hobnail hemangioma) • TelangiectasiaTelangiectasia macularis eruptiva perstansTeratomaTufted 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 syndromeXanthelasmoidal mastocytosisZosteriform metastasis == Dermatitis ==
Dermatitis
Dermatitis is a general term for "inflammation of the skin". • Childhood granulomatous periorificial dermatitisEssential dermatitis Atopic Atopic dermatitis is a chronic dermatitis associated with a hereditary tendency to develop 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 dermatitisAcid-inducedAcrylic monomer dermatitisAdhesive dermatitisAfrican blackwood dermatitisAirbag dermatitis (airbag burn) • Alkali-inducedAllergicAntifungal agent-inducedAntimicrobial agent-inducedArsenic dermatitisArtificial nail-inducedAxillary antiperspirant-inducedAxillary deodorant-inducedBaboon syndromeBlack dermatographismBleaching cream-inducedCapsaisin-inducedChemical burn |alt=Red erosions, some with crusting, all on the back of an adult hand • ChloracneChrome dermatitisClothing-inducedCobalt dermatitisContact stomatitis (contact lichenoid reaction, lichenoid amalgam reaction, oral mucosal cinnamon reaction) • Contact urticariaCorticosteroid-inducedCosmetic dermatitisCosmetic intolerance syndromeDentifrice-inducedDermatitis from metals and metal saltsDust-inducedEpoxy resin dermatitisEthylenediamine-inducedEye makeup-inducedFiberglass dermatitisFlower-inducedFormaldehyde-inducedFormaldehyde-releasing agent-inducedFragrance-inducedGold dermatitisHair bleach-inducedHair dye-inducedHair lotion-inducedHair spray-inducedHair straightener-inducedHair tonic-inducedHouseplant-inducedHydrocarbon-inducedIrritant folliculitisLacquer dermatitis (lacquer sensitivity) • Lanolin-inducedLipstick-inducedLocal anesthetic-inducedMakassar ebony dermatitisMarine plant-inducedMechanical irritant dermatitisMercury dermatitisMouthwash-inducedNail lacquer-inducedNail polish remover-inducedNickel dermatitisOccupation-inducedp-Chloro-meta-xylenol-inducedParaben-inducedParaphenylenediamine dermatitisPermanent wave preparation-inducedPhenothiazine drug-inducedPhotoallergicPhotoirritantPlant derivative-inducedPollen-inducedPolyester resin dermatitisPropylene glycol-induced |alt=Blisters distributed over an adult forearm • Protein contact dermatitisQuaternium-15 hypersensitivityReed dermatitisRosewood dermatitisRosin dermatitisRubber dermatitisSeed-inducedShoe dermatitisSolvent-inducedSorbic acid-inducedSubjective irritant contact dermatitis (sensory irritant contact dermatitis) • Sunscreen-inducedSystemic contact dermatitisTear gas dermatitisTextile dermatitisTraumatic irritant contact dermatitisTree-associated plant-inducedTree-inducedTulip fingersUrushiol-inducedVegetable-induced Eczema Eczema refers to a broad range of conditions that begin as spongiotic dermatitis and may progress to a lichenified stage. |alt=Small blisters and crusting on the distal fingertips • Autoimmune estrogen dermatitisAutoimmune progesterone dermatitisAutosensitization dermatitisBreast eczema (nipple eczema) • Chronic vesiculobullous hand eczemaCircumostomy eczemaDyshidrosis (acute vesiculobullous hand eczema, cheiropompholyx, dyshidrotic eczema, pompholyx, podopompholyx) • Ear eczemaEyelid dermatitisHand eczemaHyperkeratotic hand dermatitisId 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 dermatitisNummular dermatitis (discoid eczema, microbial eczema, nummular eczema, nummular neurodermatitis) • Nutritional deficiency eczemaSulzberger–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 lesions. • Eosinophilic pustular folliculitis (Ofuji's disease, sterile eosinophilic pustulosis) • Reactive arthritisSubcorneal pustular dermatosis (Sneddon–Wilkinson disease) Seborrheic Seborrheic dermatitis is a chronic, superficial, inflammatory disease characterized by scaling on an erythematous base. • Infantile seborrheic dermatitisLeiner's diseasePityriasis simplex capillitii (dandruff) • Seborrheic dermatitis (seborrheic eczema) == Disturbances of pigmentation ==
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 syndromeArgyriaArsenic poisoning |alt=Depigmented patches on the posterior hand and fingers • Berlin syndrome • Pigmentation changes caused by the bioaccumulation of pigments, e.g. CanthaxanthinChédiak–Higashi syndromeChrysiasisCross–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 hereditariaElejalde syndrome (Griscelli syndrome type 1) • Eruptive hypomelanosisFamilial progressive hyperpigmentationGalli–Galli diseaseGriscelli syndrome type 2 (partial albinism with immunodeficiency) • Griscelli syndrome type 3Hemochromatosis (bronze diabetes) • Hemosiderin hyperpigmentationHermansky–Pudlak syndromeIdiopathic guttate hypomelanosis (leukopathia symmetrica progressiva) • Iron metallic discolorationKlein–Waardenburg syndromeLead poisoningLeukodermaMelanoma-associated leukodermaMelasma (chloasma faciei, mask of pregnancy) • Mukamel syndromeNecklace of VenusNevus anemicus |alt=Multiple, hypopigmented macules and patches on the leg of an adult • Nevus depigmentosus (nevus achromicus) • Ocular albinismOculocutaneous albinismPallister–Killian syndromePeriorbital hyperpigmentationPhotoleukomelanodermatitis of KoboriPhylloid hypomelanosisPiebaldismPigmentatio reticularis faciei et colliPityriasis albaPoikiloderma of CivattePoikiloderma vasculare atrophicansPostinflammatory hyperpigmentation (postinflammatory hypermelanosis) • Postinflammatory hypopigmentationProgressive macular hypomelanosisQuadrichrome vitiligoReticular pigmented anomaly of the flexures (dark dot disease, Dowling–Degos' disease) • Reticulate acropigmentation of KitamuraRevesz syndromeRiehl melanosisScratch dermatitis (flagellate pigmentation from bleomycin) • Segmental vitiligoShah–Waardenburg syndromeShiitake mushroom dermatitis (flagellate mushroom dermatitis, mushroom worker's disease, shiitake-induced toxicoderma) • Tar melanosis (melanodermatitis toxica lichenoides) • Tietz syndromeTitanium metallic discolorationTransient neonatal pustular melanosis (transient neonatal pustulosis, lentigines neonatorum) • Trichrome vitiligoVagabond's leukomelanodermaVasospastic maculeVitiligoVitiligo ponctuéVogt–Koyanagi–Harada syndromeWaardenburg syndromeWende–Bauckus syndrome (Pegum syndrome) • Woronoff's ringX-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
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) |alt=Multiple small subcorneal pustules on erythematous patches • Adverse reaction to biologic agentsAdverse reaction to cytokinesAllopurinol hypersensitivity syndromeAnticoagulant-induced skin necrosisAnticonvulsant hypersensitivity syndromeBromodermaBullous drug reaction (bullous drug eruption, generalized bullous fixed drug eruption, multilocular bullous fixed drug eruption) • Chemotherapy-induced acral erythema (palmoplantar erythrodysesthesia syndrome) • Chemotherapy-induced hyperpigmentationDrug-induced acneDrug-induced angioedemaDrug-related gingival hyperplasiaDrug-induced lichenoid reaction (drug-induced lichen planus, lichenoid drug eruption) • Drug-induced lupus erythematosusDrug-induced nail changesDrug-induced pigmentationDrug-induced urticariaDrug reaction with eosinophilia and systemic symptomsErythema multiforme major (erythema multiforme minor–erythema multiforme von Hebra) • Exudative hyponychial dermatitisFixed drug reactionHalogenodermaHeparin necrosisHIV disease-related drug reactionHydroxyurea dermopathyInjection site reactionIododermaLeukotriene receptor antagonist-associated Churg–Strauss syndromeLinear IgA bullous dermatosis (linear IgA dermatosis) • Photosensitive drug reactionRed man syndromeSevere cutaneous adverse reactions (includes DRESS syndrome, Steven Johnson syndrome, Toxic epidermal necrolysis, Stevens-Johnson/toxic epidermal necrolysis overlap syndrome, and Acute generalized exanthematous pustulosis) • Scleroderma-like reaction to taxanesSerum sickness-like reactionSteroid acneSteroid folliculitisStevens–Johnson syndromeSulfonamide hypersensitivity syndromeTexier's diseaseToxic epidermal necrolysis (Lyell's syndrome) • Urticarial erythema multiformeVitamin K reactionWarfarin necrosis == Endocrine-related ==
Endocrine-related
Endocrine conditions often present with cutaneous findings as the skin 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) |alt=Blackened necrosis of multiple toes on an adult foot • Acral dry gangreneAcromegalyAddison's diseaseAdrenal adenomaAdrenal carcinomaAdrenal hyperplasiaAlopecia–nail dystrophy–ophthalmic complications–thyroid dysfunction–hypohidrosis–ephelides and enteropathy–respiratory tract infections syndrome (ANOTHER syndrome) • ArrhenoblastomaCretinismCushing's syndrome |alt=Hyperpigmented plaque with velvety textural change within the axillary fold of an adult • Excess ovarian androgen release syndrome (ovarian SAHA syndrome) • Familial acanthosis nigricans (acanthosis nigricans type II) • Growth hormone deficiencyHyperandrogenism–insulin resistance–acanthosis nigricans syndrome (HAIR-AN syndrome) • HyperparathyroidismHyperprolactinemic SAHA syndromeHyperthyroidismHypoparathyroidismHypothyroidismLeydig cell tumorMultiple 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) • MyxedemaPanhypopituitarismPersistent adrenarche syndrome (adrenal SAHA syndrome) • Polycystic ovarian syndromeSeborrhoea–acne–hirsutism–alopecia (SAHA syndrome) • Thyroid acropachy == Eosinophilic ==
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 infancyArthropod assaultEosinophilic cellulitis (Wells' syndrome) • Eosinophilic fasciitis (Shulman's syndrome) • Eosinophilic granulomaEosinophilic granulomatosis with polyangiitisEosinophilic 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) |alt=Solitary, large, white to yellow erosion on the inner lower lip of a child • Eosinophilic vasculitisErythema toxicum neonatorum (erythema toxicum, toxic erythema of the newborn) • Granuloma facialeHypereosinophiliaHypereosinophilic syndromeIncontinentia pigmenti (Bloch–Siemens syndrome, Bloch–Sulzberger disease, Bloch–Sulzberger syndrome) • Itchy red bump disease (papular dermatitis) • Juvenile xanthogranulomaKimura's diseaseNodules–eosinophilia–rheumatism–dermatitis–swelling syndromePachydermatous eosinophilic dermatitisPapular eruption of blacksPapuloerythroderma of OfujiPruritic papular eruption of HIV disease == Epidermal nevi, neoplasms, and cysts ==
Epidermal nevi, neoplasms, and cysts
Epidermal nevi, neoplasms, and cysts are skin lesions that develop from the epidermal layer of the skin. • Polypoid basal cell carcinomaPore-like basal cell carcinomaPrimary cutaneous adenoid cystic carcinomaProliferating 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 balanitisPUVA keratosisRasmussen syndromeReactional keratosisReticulated seborrheic keratosis (adenoid seborrheic keratosis) • Rodent ulcer (Jacobi ulcer) • Schimmelpenning syndrome (Schimmelpenning–Feuerstein–Mims syndrome) • Sebaceoma (sebaceous epithelioma) • Sebaceous adenomaSebaceous carcinomaSebaceous hyperplasiaSebaceous nevus syndromeSeboacanthomaSeborrheic keratosis (seborrheic verruca, senile wart) • Seborrheic keratosis with squamous atypiaSignet-ring cell squamous cell carcinomaSolitary keratoacanthoma (subungual keratoacanthoma) • Solitary trichoepitheliomaSpindle cell squamous cell carcinoma (spindle cell carcinoma) • SpiradenomaSquamous cell carcinoma |alt=Ulceration and crusting over a skin lesion on the front of an adult nose • 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) • SyringomaSystematized epidermal nevusThermal keratosisTrichilemmal carcinomaTrichilemmal cyst (isthmus-catagen cyst, pilar cyst) • TrichilemmomaTrichoadenoma (trichoadenoma of Nikolowski) • TrichoblastomaTrichoblastic fibromaTrichodiscomaTrichofolliculomaUnilateral palmoplantar verrucous nevusUrethral caruncleVerrucous carcinomaVerrucous cyst (cystic papilloma) • Viral keratosisWarty dyskeratoma (isolated dyskeratosis follicularis) • Waxy keratosis of childhood (kerinokeratosis papulosa) • Zoon's vulvitisZosteriform speckled lentiginous nevus == Erythemas ==
Erythemas
|alt=Large erythematous patch in the pattern of a "bull's-eye" on a woman's posterior upper arm Erythemas are reactive skin conditions in which there is 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 multiformeErythema multiforme minor (herpes simplex-associated erythema multiforme) • Erythema palmareGeneralized erythemaNecrolytic acral erythemaNecrolytic migratory erythema (glucagonoma syndrome) == Genodermatoses ==
Genodermatoses
Genodermatoses are inherited genetic skin conditions often grouped into three categories: chromosomal, single gene, and polygenetic. • 18q deletion syndromeAcrodermatitis enteropathicaAcrogeria (Gottron syndrome) • Acrokeratosis verruciformis (acrokeratosis verruciformis of Hopf) • Adams–Oliver syndromeAdducted thumbs syndromeAlbright's hereditary osteodystrophyAngelman syndromeApert syndrome (acrocephalosyndactyly) • Arthrogryposis–renal dysfunction–cholestasis syndromeAtaxia 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 syndromeBart syndromeBazex–Dupré–Christol syndrome (Bazex syndrome, follicular atrophoderma and basal cell carcinomas) • Beare–Stevenson cutis gyrata syndromeBloom syndrome (Bloom–Torre–Machacek syndrome) • Blue rubber bleb nevus syndromeBrittle hair–intellectual impairment–decreased fertility–short stature syndromeCantú syndromeCardio-facio-cutaneous syndrome (cardiofaciocutaneous syndrome) • Cartilage–hair hypoplasia (McKusick type metaphyseal chondrodysplasia) • Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndromeChildhood tumor syndromeChondrodysplasia punctataCicatricial junctional epidermolysis bullosaCraniosynostosis–anal anomalies–porokeratosis syndromeCockayne syndromeColobomas 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 syndromeCronkhite–Canada syndromeCrouzon syndromeCutis verticis gyrataDarier's disease (Darier–White disease, dyskeratosis follicularis, keratosis follicularis) |alt=Many hyperkeratotic, vegetative, and hyperpigmented papules in a zosteriform pattern on the right lateral lower extremity of an adult • DeSanctis–Cacchione syndromeDisseminated superficial actinic porokeratosisDisseminated superficial porokeratosisDolichol kinase deficiencyDominant dystrophic epidermolysis bullosaDyskeratosis congenita (Zinsser–Cole–Engman syndrome) • Dystrophic epidermolysis bullosaEctodermal dysplasiaEctodermal dysplasia with corkscrew hairsEctrodactyly–ectodermal dysplasia–cleft syndrome (EEC syndrome, split hand–split foot–ectodermal dysplasia–cleft syndrome) • Epidermolysis bullosa herpetiformis (Dowling–Meara epidermolysis bullosa simplex) • Epidermolysis bullosa simplexEpidermolysis bullosa simplex of OgnaEpidermolysis bullosa simplex with mottled pigmentationEpidermolysis bullosa simplex with muscular dystrophyEpidermolytic 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 progressivaFocal dermal hypoplasia (Goltz syndrome) • Follicular atrophodermaFranceschetti–Klein syndrome (mandibulofacial dysostosis) • Gardner's syndrome (familial colorectal polyposis) • Gastrocutaneous syndromeGeneralized atrophic benign epidermolysis bullosaGeneralized epidermolysis bullosa simplex (Koebner variant of generalized epidermolysis bullosa simplex) • Generalized trichoepitheliomaGiant axonal neuropathy with curly hairGingival fibromatosis with hypertrichosisHaber syndromeHallerman–Streiff syndromeHarlequin-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 |alt=Small, red, monomorphic skin lesions on the back of an adult arm • Heterochromia iridumHolocarboxylase synthetase deficiencyHypohidrotic ectodermal dysplasia (anhidrotic ectodermal dysplasia, Christ–Siemens–Touraine syndrome) • Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndromeHypotrichosis–lymphedema–telangiectasia syndromeIchthyosis–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 circumflexaIchthyosis prematurity syndromeIchthyosis vulgaris (autosomal dominant ichthyosis, ichthyosis simplex) • Ichthyosis with confettiNeonatal ichthyosis–sclerosing cholangitis syndrome (ichthyosis–sclerosing cholangitis syndrome, NISCH syndrome) • Incontinentia pigmenti achromians (hypomelanosis of Ito) • Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndromeJaffe–Campanacci syndromeJohanson–Blizzard syndromeJohnson–McMillin syndromeJoubert syndromeJunctional epidermolysis bullosaJunctional epidermolysis bullosa gravis (epidermolysis bullosa letalis, Herlitz disease, Herlitz epidermolysis bullosa, Herlitz syndrome, lethal junctional epidermolysis bullosa) • Junctional epidermolysis bullosa with pyloric atresiaKabuki 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 syndromeKeratosis 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 pilarisKindler 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 syndromeKlippel–Feil syndromeLamellar ichthyosis (collodion baby) • Legius syndrome (neurofibromatosis type 1-like syndrome) • Lelis syndromeLenz–Majewski syndromeLeschke syndromeLethal acantholytic epidermolysis bullosaLhermitte–Duclos diseaseLinear 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 porokeratosisLocalized epidermolysis bullosa simplex (Weber–Cockayne syndrome, Weber–Cockayne variant of generalized epidermolysis bullosa simplex) • Mandibuloacral dysplasiaMarinesco–Sjögren syndromeMcCune–Albright syndromeMcCusick syndromeMetageriaMicrophthalmia–dermal aplasia–sclerocornea syndromeMitis junctional epidermolysis bullosa (nonlethal junctional epidermolysis bullosa) • Mitochondrial myopathy–encephalopathy–lactic acidosis–stroke syndromeMultiple lentigines syndrome (cardiocutaneous syndrome, Gorlin syndrome II, lentiginosis profusa syndrome, LEOPARD syndrome, progressive cardiomyopathic lentiginosis) • Multiple pterygium syndromeMultiple sulfatase deficiency (Austin disease, mucosulfatidosis) • Naegeli–Franceschetti–Jadassohn syndrome (chromatophore nevus of Naegeli) • Netherton syndromeNeurofibromatosis type 1 (von Recklinghausen's disease) |alt=Many small to large, skin colored nodules on the trunk of an adult • 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 syndromeOculocerebrocutaneous syndrome (Delleman–Oorthuys syndrome) • Oculodentodigital dysplasiaOdonto-tricho-ungual-digital-palmar syndromeOliver–McFarlane syndromeOrofaciodigital syndromePachydermoperiostosis (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 syndromePhotosensitivity–ichthyosis–brittle sulfur-deficient hair–impaired intelligence–decreased fertility–short stature syndromePityriasis rotunda (pityriasis circinata, tinea circinata) • Plate-like osteoma cutisPlaque-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 syndromePorokeratosisPorokeratosis palmaris et plantaris disseminataPrader–Willi syndromeProgeria (Hutchinson–Gilford progeria syndrome, Hutchinson–Gilford syndrome, progeria syndrome) • Progressive osseous heteroplasiaProgressive symmetric erythrokeratodermia (erythrokeratodermia progressiva symmetrica) • Proteus syndromeProteus-like syndromePunctate porokeratosisRapp–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 dermatosisRestrictive dermopathy |alt=Thick, fish-like scales on an adult lower leg • Rhizomelic chondrodysplasia punctata (autosomal recessive chondrodysplasia punctata type 1, chondrodystrophia calcificans punctata, peroxisomal biogenesis disorder complementation group 11) • Rombo syndromeRothmund–Thomson syndrome (poikiloderma congenitale) • Rud syndromeSay syndromeScalp–ear–nipple syndrome (Finlay–Marks syndrome) • Schindler disease (Kanzaki disease, alpha-N-acetylgalactosaminidase deficiency) • Schinzel–Giedion syndromeScleroatrophic syndrome of Huriez (Huriez syndrome, palmoplantar keratoderma with scleroatrophy, palmoplantar keratoderma with sclerodactyly, scleroatrophic and keratotic dermatosis of the limbs, sclerotylosis) • Segmental neurofibromatosisSenter syndrome (Desmons' syndrome) • Shabbir syndrome (laryngo–onycho–cutaneous syndrome) • Silver–Russell syndromeSjögren–Larsson syndromeSkin fragility syndrome (plakophilin 1 deficiency) • Smith–Lemli–Opitz syndromeSturge–Weber syndromeSupernumerary nipples–uropathies–Becker's nevus syndromeTerminal osseous dysplasia with pigmentary defectsTooth and nail syndrome (hypodontia with nail dysgenesis, Witkop syndrome) • Townes–Brocks syndromeTransient bullous dermolysis of the newborn |alt=Frontal image of a child's face showing large hyperkeratotic papules and plaques with some induration suspicious for actinic keratoses and early squamous cell carcinomas • Treacher Collins syndrome (Treacher Collins–Franceschetti syndrome) • Tricho–dento–osseous syndromeTricho–rhino–phalangeal syndromeTuberous sclerosis (Bourneville disease, epiloia) • Turner syndromeUlnar–mammary syndromeVan Der Woude syndromeVon Hippel–Lindau syndromeWatson syndromeWerner syndrome (adult progeria) • Westerhof syndromeWhistling syndrome (craniocarpotarsal syndrome, distal arthrogryposis type 2, Freeman–Sheldon syndrome, Windmill–Vane–Hand syndrome) • Wilson–Turner syndromeWolf–Hirschhorn syndrome (4p- syndrome) • X-linked ichthyosis (steroid sulfatase deficiency, X-linked recessive ichthyosis) • X-linked recessive chondrodysplasia punctataXeroderma pigmentosum (Cockayne syndrome complex) • XXYY genotypeZimmermann–Laband syndrome == Infection-related ==
Infection-related
Infection-related cutaneous conditions may be caused by bacteria, fungi, yeast, viruses, or parasites. Bacterium-related Bacterium-related cutaneous conditions often have distinct morphologic characteristics that may be an indication of a generalized systemic process or simply an isolated superficial infection. • Aeromonas infectionAfrican tick bite feverAmerican tick bite fever (Rickettsia parkeri infection) • Arcanobacterium haemolyticum infectionBacillary angiomatosisBejel (endemic syphilis) • Blastomycosis-like pyoderma (pyoderma vegetans) • Blistering distal dactylitisBotryomycosisBrill–Zinsser diseaseBrucellosis (Bang's disease, Malta fever, undulant fever) • Bubonic plagueBullous impetigoCat scratch disease (cat scratch fever, English–Wear infection, inoculation lymphoreticulosis, subacute regional lymphadenitis) • Cellulitis |alt=Redness and mild swelling of an adult leg • ChancreChancroid (soft chancre, ulcus molle) • Chlamydial infectionChronic lymphangitisChronic recurrent erysipelasChronic undermining burrowing ulcers (Meleney gangrene) • Chromobacteriosis infectionCondylomata lataCutaneous actinomycosisCutaneous anthrax infectionCutaneous C. diphtheriae infection (Barcoo rot, diphtheric desert sore, septic sore, Veldt sore) • Cutaneous group B streptococcal infectionCutaneous Pasteurella hemolytica infectionCutaneous Streptococcus iniae infectionDermatitis gangrenosa (gangrene of the skin) • EcthymaEcthyma gangrenosumEhrlichiosis ewingii infectionElephantiasis nostrasEndemic typhus (murine typhus) • Epidemic typhus (epidemic louse-borne typhus) • Erysipelas (ignis sacer, Saint Anthony's fire) • Erysipeloid of RosenbachErythema marginatumErythrasmaExternal otitis (otitis externa, swimmer's ear) |alt=Exudate over a background of redness on the external ear canal of an adult • FelonFlea-borne spotted feverFlinders Island spotted feverFlying squirrel typhusFolliculitisFournier 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 folliculitisGram-negative toe web infectionGranuloma 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 syndromeGroup JK Corynebacterium sepsisHaemophilus influenzae cellulitisHelicobacter cellulitisHospital furunculosisHot tub folliculitis (Pseudomonas aeruginosa folliculitis) • Human granulocytotropic anaplasmosisHuman monocytotropic ehrlichiosisImpetigo contagiosaJapanese spotted feverLeptospirosis (Fort Bragg fever, pretibial fever, Weil's disease) • ListeriosisLudwig's anginaLupoid sycosisLyme 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) • MeningococcemiaMissouri Lyme diseaseMycoplasma infectionNecrotizing fasciitis (flesh-eating bacteria syndrome) • Neonatal toxic shock-like exanthematous diseaseNocardiosisNoma neonatorumNorth Asian tick typhusOphthalmia neonatorum |alt=Redness and swelling of an ear • Oroya fever (Carrion's disease) • PasteurellosisPerianal cellulitis (perineal dermatitis, streptococcal perianal disease) • Periapical abscessPintaPitted keratolysis (keratolysis plantare sulcatum, keratoma plantare sulcatum, ringed keratolysis) • PlaguePrimary gonococcal dermatitisPseudomonal pyodermaPseudomonas hot-foot syndromePyogenic paronychiaPyomyositisQ feverQueensland tick typhusRat-bite feverRecurrent toxin-mediated perineal erythemaRhinoscleromaRickettsia aeschlimannii infectionRickettsialpoxRocky Mountain spotted feverSaber shin (anterior tibial bowing) • Saddle noseSalmonellosisScarlet feverScrub typhus (Tsutsugamushi fever) • ShigellosisStaphylococcal scalded skin syndrome (pemphigus neonatorum, Ritter's disease) • Streptococcal intertrigoSuperficial pustular folliculitis (impetigo of Bockhart, superficial folliculitis) • Sycosis vulgaris (barber's itch, sycosis barbae) • SyphilidSyphilis (lues) • Tick-borne lymphadenopathyToxic 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 peruanaVibrio vulnificus infectionYaws (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 leprosyBorderline leprosyBorderline tuberculoid leprosyBuruli ulcer (Bairnsdale ulcer, Searl ulcer, Searle's ulcer) |alt=Ulceration of the skin over the back of a teenager's hand • Erythema induratum (Bazin disease) • Histoid leprosyLepromatous leprosyLeprosy (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 infectionMycobacterium haemophilum infectionMycobacterium kansasii infectionPapulonecrotic tuberculidPrimary inoculation tuberculosis (cutaneous primary complex, primary tuberculous complex, tuberculous chancre) • Rapid-growing Mycobacterium infectionScrofuloderma (tuberculosis cutis colliquativa) • Tuberculosis cutis orificialis (acute tuberculous ulcer, orificial tuberculosis) • Tuberculosis verrucosa cutis (lupus verrucosus, prosector's wart, warty tuberculosis) • Tuberculous cellulitisTuberculous 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. • Acanthamoeba infectionAmebiasis cutisAnt stingArachnidismBaker's itchBalamuthia infectionBedbug infestation (bedbug bite, cimicosis) • Bee and wasp stingsBlister beetle dermatitisBombardier beetle burnBristleworm sting |alt=Multiple, red, linear plaques on the extremity • Centipede biteCheyletiella dermatitisChigger biteCoolie itchCopra itchCoral dermatitisCreeping 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 cutisDemodex folliculitis, usually caused by the Demodex folliculorum mite • Dogger Bank itchDracunculiasis (dracontiasis, guinea worm disease, Medina worm) • Echinococcosis (hydatid disease) • Elephantiasis tropica (elephantiasis arabum) • Elephant skinEnterobiasis (oxyuriasis, pinworm infection, seatworm infection) • Erisipela de la costaFeather pillow dermatitisFunnel web spider biteGamasoidosisGnathostomiasis (larva migrans profundus) • Grain itch (barley itch, mattress itch, prairie itch, straw itch) • Grocer's itchHead lice infestation (cooties, pediculosis capitis) • Hookworm disease (ancylostomiasis, ground itch, necatoriasis, uncinariasis) • Human trypanosomiasisHydroid dermatitisIrukandji syndromeJellyfish dermatitisKed itchLarva currensLatrodectism (widow spider bite) • Leech biteLeopard skinLepidopterism (Caripito itch, caterpillar dermatitis, moth dermatitis) • Lizard skinLoaiasis (Calabar swelling, fugitive swelling, loa loa, tropical swelling) • Loxoscelism (brown recluse spider bite, necrotic cutaneous loxoscelism) • Mal morandoMillipede burnMosquito biteMucocutaneous leishmaniasis (espundia, leishmaniasis Americana) • MyiasisNairobi fly dermatitis (Kenya fly dermatitis, Nairobi eye) • Nematode dermatitisNorwegian scabies (crusted scabies) |alt=Diffuse thickening of the skin over an adult's bilateral arms and fingers • OnchocerciasisOphthalmia nodosaPaederus dermatitisPediculosis corporis (pediculosis vestimenti, Vagabond's disease) • Pediculosis pubis (crabs, phthirus pubis, phthirus pubis, pubic lice) • Pneumocystosis (often classified as fungal) • Portuguese man-of-war dermatitisPost-kala-azar dermal leishmaniasis (post-kala-azar dermatosis) • ProtothecosisPulicosis (flea bites) • Reduviid biteScabies (itch mite infestation, seven-year itch) • Scorpion stingSea anemone dermatitisSeabather's eruption (sea lice) • Sea urchin injurySeaweed dermatitisSnake biteSowdaSparganosisSpider biteStingray injurySwimmer's itch (cercarial dermatitis, schistosome cercarial dermatitis) |alt=Multiple red bumps on the lower legs and feet • Tarantula biteTick biteToxoplasmosisTrichinosisTrichomoniasisTungiasis (bicho de pie, chigoe flea bite, jigger bite, nigua, pique) • Visceral leishmaniasis (dumdum fever, kala-azar) • Visceral schistosomiasis (bilharziasis) • Viscerotropic leishmaniasisWheat warehouse itch Virus-related Virus-related cutaneous conditions are caused by two main groups of viruses–DNA and RNA types–both of which are obligatory intracellular parasites. • Alphavirus infectionAsymmetric periflexural exanthem of childhood (unilateral laterothoracic exanthem) • B virus infectionBoston exanthem diseaseBovine papular stomatitisBowenoid papulosisBuffalopoxButcher's wartChikungunya feverCondylomata acuminataCongenital rubella syndromeCowpoxCytomegalic inclusion diseaseDengue (Break-bone fever) • Disseminated herpes zosterEczema herpeticum (Kaposi's varicelliform eruption) |alt=A diffuse, generalized red rash over a newborn's entire body • Eczema vaccinatumEpidermodysplasia verruciformisEruptive pseudoangiomatosisErythema infectiosum (fifth disease, slapped cheek disease) • Exanthem of primary HIV infection (acute retroviral syndrome) • Farmyard poxGeneralized vacciniaGenital 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 diseaseHeck's disease (focal epithelial hyperplasia) • Hemorrhagic fever with renal syndromeHepatitis BHepatitis CHerpanginaHerpes gladiatorum (scrum pox) • Herpes simplexHerpes zoster oticus (Ramsay–Hunt syndrome) • Herpetic keratoconjunctivitisHerpetic sycosisHerpetic whitlowHIV-associated pruritusHuman monkeypoxHuman T-lymphotropic virus 1 infectionHuman tanapoxImmune reconstitution inflammatory syndrome (immune recovery syndrome) • Infectious mononucleosis (glandular fever) • Inflammatory skin lesions following zoster infection (isotopic response) • Intrauterine herpes simplex |alt=Multiple dark red skin lesions • Kaposi sarcomaLassa feverLipschütz ulcer (ulcus vulvae acutum) • Measles (rubeola, morbilli) • Milker's noduleModified varicella-like syndromeMolluscum contagiosumMyrmeciaNeonatal herpes simplexOphthalmic zosterOrf (contagious pustular dermatosis, ecthyma contagiosum, infectious labial dermatitis, sheep pox) • Orf-induced immunobullous diseaseOrolabial herpes (herpes labialis) • Papular purpuric gloves and socks syndromePigmented wartPostherpetic neuralgia (zoster-associated pain) • Post-vaccination follicular eruptionProgressive vaccinia (vaccinia gangrenosum, vaccinia necrosum) • PseudocowpoxRecurrent respiratory papillomatosis (laryngeal papillomatosis) |alt=Multiple red papules scattered over a child's head, neck, trunk, and upper extremities • Rift Valley feverRoseola infantum (exanthem subitum, exanthema subitum, sixth disease) • Roseola vacciniaRubella (German measles) • Sandfly fever (Pappataci fever, phlebotomus fever) • SealpoxVaricella (chickenpox) • Variola major (smallpox) • Verruca plana (flat wart) • Verruca plantaris (plantar wart) • Verruca vulgaris (wart) • Verrucae palmares et plantaresViral-associated trichodysplasia (ciclosporin-induced folliculodystrophy) • Wasting syndromeWest Nile virus infectionZoster (herpes zoster, shingles) • Zoster sine herpete == Lichenoid eruptions ==
Lichenoid eruptions
Lichenoid eruptions are dermatoses related to the unique, common inflammatory disorder lichen planus, which affects the skin, mucous membranes, nails, and hair. • Annular lichen planus |alt=Violaceous, annular, scaly plaques on the face and scalp of an adult • Atrophic lichen planusBullous lichen planus (vesiculobullous lichen planus) • Erosive lichen planusErythema dyschromicum perstans (ashy dermatosis, dermatosis cinecienta) • Giant cell lichenoid dermatitisHepatitis-associated lichen planusHypertrophic lichen planus (lichen planus verrucosus) • Idiopathic eruptive macular pigmentationInverse lichen planusKeratosis lichenoides chronica (Nékam's disease) • Kraurosis vulvaeLichen nitidusLichen planus actinicus (actinic lichen nitidus, actinic lichen planus, lichen planus atrophicus annularis, lichen planus subtropicus, lichen planus tropicus, lichenoid melanodermatitis, lichenoid melanodermatosis, summertime actinic lichenoid eruption) • Lichen planus pemphigoidesLichen planus pigmentosusLichen planus–lichen sclerosus overlap syndromeLichen ruber moniliformisLichen sclerosus (lichen sclerosus et atrophicus) • Lichen striatus (Blaschko linear acquired inflammatory skin eruption, linear lichenoid dermatosis) • Lichen verrucosus et reticularisLichenoid trikeratosisLichenoid dermatitisLichenoid reaction of graft-versus-host diseaseLinear lichen planusMucosal lichen planusPeno-gingival syndromeUlcerative lichen planusVulvovaginal gingival syndromeVulvovaginal lichen planus == Lymphoid-related ==
Lymphoid-related
Lymphoid-related cutaneous conditions are a group of disorders characterized by collections of lymphocyte cells within the skin. • Adult T-cell leukemia/lymphomaAngiocentric 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 lymphomaCD30+ 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) |alt=A solitary, large, red papule on the left cheek of an adult male • Cutaneous lymphoid hyperplasia with bandlike and perivascular patternsCutaneous 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 skinHairy-cell leukemiaHodgkin's diseaseIchthyosis acquisita (acquired ichthyosis) • IgG4-related skin diseaseIntravascular 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 cutisLymphoma cutisLymphomatoid granulomatosisLymphomatoid papulosisMalignant histiocytosis (histiocytic medullary reticulosis) • Marginal zone B-cell lymphomaMucosa-associated lymphoid tissue lymphomaMycosis fungoidesNon-mycosis fungoides CD30− cutaneous large T-cell lymphomaNonspecific 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 |alt=A large ulcerated plaque on the leg of an adult male • PlasmacytosisPleomorphic 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 immunocytomaPrimary cutaneous marginal zone lymphomaRetiform parapsoriasisSecondary cutaneous CD30+ large cell lymphomaSézary syndromeSinus 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 ==
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