- This is an incomplete list, which may never be able to satisfy certain standards for completion.
- See also Category:Cutaneous conditions and ICD-10 Chapter XII
There are many conditions of or affecting the human integumentary system—the organ system that covers the entire surface of the body and is composed of skin, hair, nails, and related muscle and glands.[1] The major function of this system is as a barrier against the external environment.[2] The skin weighs an average of four kilograms, covers an area of two square meters, and is made of three distinct layers: the epidermis, dermis, and subcutaneous tissue.[1] There are two main types of human skin: glabrous skin, the non-hairy skin on the palms and soles (also referred to as the "palmoplantar" surfaces), and hair-bearing skin.[3] Within the latter type, there are hairs in structures called pilosebaceous units, each with hair follicle, sebaceous gland, and associated arrector pili muscle.[4] 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.[5] The epidermis is the most superficial layer of skin, a squamous epithelium with several strata: the stratum corneum, stratum lucidum, stratum granulosum, stratum spinosum, and stratum basale.[6] Nourishment is provided to these layers via diffusion from the dermis, since the epidermis is without direct blood supply. The epidermis contains four cell types: keratinocytes, melanocytes, Langerhans cells, and the Merkels cell. Of these, keratinocytes are the major component, constituting roughly 95 percent of the epidermis.[3] 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.[3] In normal skin, the rate of production equals the rate of loss; it takes about two weeks 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.[7] The dermis is the layer of skin between the epidermis and subcutaneous tissue, and comprises two sections, the papillary and reticular dermis.[8] The superficial papillary dermis interdigitates with the overlying rete ridges of the epidermis, between which the two layers interact through the basement membrane zone.[8] Structural components of the dermis are collagen, elastic fibers, and extrafibrillar matrix (previously called ground substance).[8] Within these components are the pilosebaceous units, arrector pili muscles, and the eccrine and apocrine glands.[6] 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.[6] The function of blood vessels within the dermis is twofold: to supply nutrition and regulate temperature.[3] The subcutaneous tissue is a layer of fat between the dermis and underlying fascia.[9] 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.[3] The main cellular component of this tissue is the adipocyte, or fat cell.[9] The structure of this tissue is composed of septal (i.e. linear strands) and lobular compartments, which differ in microscopic appearance.[6] Functionally, the subcutaneous fat insulates the body, absorbs trauma, and serves as a reserve energy source.[9] Conditions of the human integumentary system constitute a broad spectrum of diseases, also known as dermatoses, as well as several nonpathologic states (like, in certain circumstances, melanonychia and racquet nails).[10] While only a small number of skin diseases account for most visits to the physician, thousands of skin conditions have been described.[9] Classification of these conditions often presents many nosological challenges, since underlying etiologies and pathogenetics are often not known.[10][11] 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), and so on.[12] Clinically, the diagnosis of any particular skin condition is made by gathering pertinent information regarding the presenting skin lesion(s), including the location (such as arms, head, legs), symptoms (pruritus, pain), duration (acute or chronic), arrangement (solitary, generalized, annular, linear), morphology (macules, papules, vesicles), and color (red, blue, brown, black, while, yellow).[13] [edit] Acneiform eruptions See also Category:Acneiform eruptions Acneiform eruptions are caused by changes in the pilosebaceous unit.[14][15] - Acne aestivalis (Mallorca acne)[nb 1]
- Acne conglobata
- Acne cosmetica
- Acne fulminans (Acute febrile ulcerative acne)
- Acne keloidalis (Acne keloidalis nuchae, Dermatitis papillaris capillitii, Folliculitis keloidalis, Folliculitis keloidis nuchae, Nuchal keloid acne)
- Acne mechanica
- Acne medicamentosa
- Acne miliaris necrotica (Acne varioliformis)
- Acne vulgaris
- Acne with facial edema (Solid facial edema)
- Acneiform eruptions
- Blepharophyma
- Erythrotelangiectatic rosacea (Erthemaotelangiectatic rosacea)
- Excoriated acne (Acne excoriée des jeunes filles, Picker's acne)
- Glandular rosacea
- Gnathophyma
- Gram-negative rosacea
- Granulomatous facial dermatitis
- Granulomatous perioral dermatitis
- Halogen acne
- Hidradenitis suppurativa (Acne inversa, Verneuil's disease)
- Idiopathic facial aseptic granuloma
- Infantile acne
- Lupoid rosacea (Granulomatous rosacea, Micropapular tuberculid, Rosacea-like tuberculid of Lewandowsky)
- Lupus miliaris disseminatus faciei
- Metophyma
- Neonatal acne (Acne infantum, Acne neonatorum)
- Occupational acne
- Ophthalmic rosacea (Ocular rosacea, Ophthalmorosacea)
- Otophyma
- Persistent edema of rosacea (Chronic upper facial erythematous edema, Morbihan's disease, Rosaceous lymphedema)
- Pomade acne
- Papulopustular rosacea
- Perifolliculitis capitis abscedens et suffodiens (Dissecting cellulitis of the scalp, Dissecting folliculitis, Perifolliculitis capitis abscedens et suffodiens of Hoffman)
- Perioral dermatitis
- Periorbital dermatitis (Periocular dermatitis)
- Pyoderma faciale (Rosacea fulminans)
- Rhinophyma
- Rosacea (Acne rosacea)
- Rosacea conglobata
- Rosacea fulminans
- SAPHO syndrome
- Steroid rosacea
- Tropical acne
[edit] Autoinflammatory See also Category:Autoinflammatory syndromes Autoinflammatory syndromes are a group of inherited disorders characterized by bouts of inflammatory skin lesions and periodic fevers.[16][17] [edit] Chronic blistering See also Category:Chronic blistering cutaneous conditions Chronic blistering cutaneous conditions have a prolonged course and present with vesicles and bullae.[18][19] [edit] Conditions of the mucous membranes See also Category:Conditions of the mucous membranes Conditions of the mucous membranes involve the moist linings of the eyes, nose, mouth, and anus.[2] - Acatalasemia (Takahara's disease)
- Acquired dyskeratotic leukoplakia
- Actinic cheilitis
- Acute necrotizing ulcerative gingivitis (Acute necrotizing ulcerative gingivostomatitis, Trench mouth, Vincent's disease)
- Allergic contact cheilitis
- Angina bullosa haemorrhagica
- Angular cheilitis (Perlèche)
- Behçet syndrome (Oculo-oral-genitial syndrome)
- Black hairy tongue
- Caviar tongue
- Cheilitis exfoliativa
- Cheilitis glandularis
- Cheilitis granulomatosa
- Cutaneous sinus of dental origin (Dental sinus)
- Cyclic neutropenia
- Drug-induced ulcer of the lip
- Eosinophilic ulcer of the oral mucosa
- Epidermization of the lip
- Epulis
- Epulis fissuratum (Granuloma fissuratum)
- Eruptive lingual papillitis
- Erythroplakia (Erythroplasia)
- Fissured tongue (Furrowed tongue, Lingua plicata, Plicated tongue, Scrotal tongue)
- Geographic tongue (Begnign migratory glossitis, Benign migratory stomatitis, Glossitis areata exfoliativa, Glossitis areata migrans, Lingua geographica, Stomatitis areata migrans, Transitory benign plaques of the tongue)
- Leukoplakia
- Leukoplakia with tylosis and esophageal carcinoma
- Major aphthous ulcer (Periadenitis mucosa necrotica recurrens)
- Median rhomboid glossitis
- Melanocytic oral lesion
- Melkersson–Rosenthal syndrome
- Mucocele
- Mucosal lichen planus
- Mucosal squamous cell carcinoma
- Oral Crohn's disease
- Oral florid papillomatosis
- Oral hairy leukoplakia
- Oral melanosis
- Osseous choristoma of the tongue
- Peripheral ameloblastoma
- Plasma cell cheilitis (Plasma cell gingivitis, Plasma cell orificial mucositi)
- Plasmoacanthoma
- Proliferative verrucous leukoplakia
- Pyogenic granuloma (Granuloma gravidarum, Pregnancy tumor)
- Pyostomatitis vegetans
- Recurrent aphthous stomatitis (Aphthosis, Canker sores)
- Recurrent intraoral herpes simplex infection
- Smooth tongue (Atrophic glossitis, Bald tongue, Hunter glossitis, Moeller)
- Stomatitis nicotina (Smoker's keratosis, Smoker's patches)
- Torus palatinus
- Trumpeter's wart
- Vestibular papillomatosis
- White sponge nevus (White sponge nevus of Cannon)
[edit] Conditions of the skin appendages See also Category:Conditions of the skin appendages Conditions of the skin appendages are those affecting the glands of the skin, hair, nails, and arrector pili muscles.[1] - Accessory nail of the fifth toe
- Acne necrotica
- Acquired generalized hypertrichosis (Acquired hypertrichosis lanuginosa)
- Acquired perforating dermatosis (Acquired perforating collagenosis)
- Acrokeratosis paraneoplastica of Bazex (Bazex' syndrome)
- Acute paronychia
- Alopecia areata
- Alopecia neoplastica
- Anagen effluvium
- Androgenetic alopecia
- Anhidrosis (Hypohidrosis)
- Anonychia
- Acroosteolysis
- Beau's lines
- Blue nails
- Bromidrosis (Apocrine bromhidrosis, Fetid sweat, Malodorous sweating, Osmidrosis)
- Bubble hair deformity
- Central centrifugal cicatricial alopecia
- Chevron nail (Herringbone nail)
- Chromhidrosis (Colored sweat)
- Chronic paronychia
- Cicatricial alopecia
- Clubbing (Drumstick fingers, Hippocratic fingers, Watch-glass nails)
- Congential onychodysplasia of the index fingers
- Disseminate and recurrent infundibulofolliculitis
- Erosive pustular dermatitis of the scalp (Erosive pustular dermatosis of the scalp)
- Erythromelanosis follicularis faciei et colli
- Folliculitis decalvans
- Folliculitis nares perforans
- Fox–Fordyce disease
- Frontal fibrosing alopecia
- Generalized congenital hypertrichosis (Congenital hypertrichosis lanuginosa)
- Generalized hyperhidrosis
- Graham-Little syndrome
- Granulosis rubra nasi
- Green nails
- Gustatory hyperhidrosis
- Hair casts (Pseudonits)
- Hair follicle nevus (Vellus hamartoma)
- Half and half nails
- Hangnail
- Hapalonychia
- Hirsutism
- Hook nail
- Hot comb alopecia
- Intermittent hair–follicle dystrophy
- Keratosis pilaris atropicans
- Kinking hair (Acquired progressive kinking)
- Koenen's tumor (Koenen's periungual fibroma)
- Koilonychia (Spoon nails)
- Kyrle disease
- Leukonychia (White nails)
- Lichen planopilaris (Acuminatus, Follicular lichen planus, Lichen planus follicularis, Peripilaris)
- Lichen planus of the nails
- Lichen spinulosus (Keratosis spinulosa)
- Localized acquired hypertrichosis
- Localized congenital hypertrichosis
- Longitudinal erythronychia
- Loose anagen syndrome
- Lupus erythematosus
- Malalignment of the nail plate
- Male-pattern baldness
- Marie Unna hereditary hypotrichosis
- Median nail dystrophy (Dystrophia unguis mediana canaliformis, Median canaliform dystrophy of Heller, Solenonychia)
- Mees' lines
- Melanonychia
- Menkes kinky hair syndrome
- Monilethrix (Beaded hairs)
- Muehrcke's lines
- Nail–patella syndrome (Fong syndrome, Hereditary osteoonychodysplasia)
- Neoplasms of the nailbed
- Noncicatricial alopecia
- Onychauxis
- Onychoatrophy
- Onychocryptosis (Ingrown nail, Unguis incarnatus)
- Onychogryphosis
- Onycholysis
- Onychomadesis
- Onychomatricoma
- Onychophagia (Nail biting)
- Onychophosis
- Onychoptosis defluvium (Alopecia unguium)
- Onychorrhexis (Brittle nails)
- Onychoschizia
- Onychotillomania
- Palmoplantar hyperhidrosis (Emotional hyperhidrosis)
- Parakeratosis pustulosa
- Patterned acquired hypertrichosis
- Perforating folliculitis
- Pili annulati (Ringed hair)
- Pili bifurcati
- Pili multigemini
- Pili pseudoannulati (Pseudo pili annulati)
- Pili torti (Twisted hairs)
- Pincer nails (Omega nails, Trumpet nails)
- Pityriasis amiantacea (Tinea amiantacea)
- Platonychia
- Plica neuropathica (Felted hair)
- Pressure alopecia
- Pseudofolliculitis barbae
- Pseudopelade of Brocq (Alopecia cicatrisata)
- Psoriatic nails
- Pterygium inversum unguis (Ventral pterygium)
- Pterygium unguis (Dorsal pterygium)
- Purpura of the nail beds
- Racquet nails (Nail en raquette)
- Recurrent palmoplantar hidradenitis (Idiopathic plantar hidradenitis)
- Red lunulae
- Ross’ syndrome
- Shell nail syndrome
- Splinter hemorrhage
- Spotted lunulae
- Staining of the nail plate
- Stippled nails
- Subungual hematoma
- Telogen effluvium
- Terry's nails
- Traction alopecia
- Traumatic anserine folliculosis
- Triangular alopecia (Temporal alopecia)
- Trichomycosis axillaris
- Trichorrhexis invaginata (Bamboo hair)
- Trichorrhexis nodosa
- Trichostasis spinulosa
- Tufted folliculitis
- Tumor alopecia
- Twenty-nail dystrophy (Trachyonychia)
- Uncombable hair syndrome (Cheveux incoiffable, Pili trianguli et canaliculi, Spun-glass hair)
- Wooly hair (Woolly hair)
- Wooly hair nevus (Woolly hair nevus)
- X-linked hypertrichosis
[edit] Conditions of the subcutaneous fat See also Category: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.[20][21][22] [edit] Connective tissue diseases See also Category:Connective tissue diseases Connective tissue diseases are caused by a complex array of autoimmune responses that target or affect collagen or ground substance.[23] [edit] Abnormalities of dermal fibrous and elastic tissue See also Category:Abnormalities of dermal fibrous and elastic tissue Abnormalities of dermal fibrous and elastic tissue are caused by problems in the regulation of collagen synthesis and/or degradation.[24] [edit] Dermal and subcutaneous growths See also Category: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.[1] - Accessory tragus (Ear tag, Preauricular appendages, Preauricular tags)
- Acquired progressive lymphangioma (Benign lymphangioendothelioma)
- Acral arteriolar ectasia
- 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 sebaceum
- African cutaneous Kaposi sarcoma
- African lymphadenopathic Kaposi sarcoma
- Aggressive infantile fibromatosis
- AIDS-associated Kaposi sarcoma
- Ainhum (Bankokerend, Dactylolysis spontanea, Sukhapakla)
- Angiofibroma
- Angiokeratoma of Mibelli (Telangiectatic warts)
- Angiokeratoma of the scrotum (Fordyce's disease, Fordyce's spot)
- Angiokeratomas
- Angioleiomyoma (Vascular leiomyoma)
- Angiolipoleiomyoma
- Angiolipoma
- Angiolymphoid hyperplasia with eosinophilia
- Angioma serpiginosum
- Angiosarcoma
- Aponeurotic fibroma (Calcifying aponeurotic fibroma, Juvenile aponeurotic fibroma)
- Arteriovenous fistula
- Atypical fibroxanthoma
- Benign lipoblastomatosis
- Capillary aneurysms
- Carcinoid
- Cavernous venous malformations
- Cherry angiomas (De Morgan spots, Senile angiomas)
- Chondrodermatitis nodularis chronica helicis (Chondrodermatitis nodularis helicis)
- Chondroid lipoma
- Chordoma
- Classic Kaposi sarcoma
- Collagenous fibroma (Desmoplastic fibroblastoma)
- Composite hemangioendothelioma
- Congenital cartilaginous rest of the neck (Cervical accessory tragus, Wattle)
- Congenital smooth muscle hamartoma
- Connective tissue nevus
- Cutaneous endometriosis
- Cutaneous meningioma (Rudimentary meningocele)
- Cutaneous myxoma
- Cutis marmorata telangiectatica congenita (Congenital generalized phlebectasia, Van Lohuizen syndrome)
- Cystic lymphatic malformation
- Dermal dendrocyte hamartoma
- Dermatofibroma (Fibrous dermatofibroma, Fibrous histiocytoma)
- Dermatofibrosarcoma protuberans
- Desmoid tumor
- Diffuse cutaneous mastocytosis
- Diffuse infantile fibromatosis
- Dupuytren's contracture (Palmar fibromatosis)
- Eccrine angiomatous hamartoma
- Elastofibroma dorsi
- Encephalocele
- Endovascular papillary angioendothelioma (Dabska tumor)
- Epithelioid hemangioendothelioma
- Epithelioid sarcoma
- Erythrodermic mastocytosis
- Familial myxovascular fibromas
- Fascial hernia
- Fibromatosis colli (Sternomastoid tumor of infancy)
- Fibrous hamatoma of infancy
- Fibrous papule of the nose (Benign solitary fibrous papule, Fibrous papule of the face)
- Folded skin with scarring (Michelin tire baby syndrome)
- Ganglioneuroma
- Generalized eruption of cutaneous mastocytosis (adult type)
- Generalized eruption of cutaneous mastocytosis (childhood type) (Urticaria pigmentosa)
- Genital leiomyoma (Dartoic leiomyoma)
- Giant cell tumor of the tendon sheath
- Glomeruloid hemangioma
- Glomus tumor (Glomangioma)
- Granular cell tumor (Abrikossoff's tumor)
- Hemangiopericytoma
- Hibernoma
- Immunosuppression-associated Kaposi sarcoma
- Infantile digital fibromatosis (Inclusion body fibromatosis, Infantile digital myofibroblastoma, Reye tumor)
- Infantile hemangioma (Capillary hemangioma, Strawberry hemangioma)
- Infantile myofibromatosis
- Infantile neuroblastoma
- Infantile systemic hyalinosis
- Intradermal spindle cell lipoma
- Intravascular papillary endothelial hyperplasia
- Juvenile hyaline fibromatosis
- Kaposiform hemangioendothelioma
- Kasabach–Merritt syndrome (Hemangioma with thrombocytopenia)
- Keloid (Keloidal scar)
- Kimura's disease
- Klippel–Trenaunay syndrome (Angioosteohypertrophy syndrome, Hemangiectatic hypertrophy)
- Knuckle pads (Heloderma)
- Leiomyosarcoma
- Lipoma
- Liposarcoma
- Lymphangiectasis (Lymphangioma)
- Lymphangiomatosis
- Malignant fibrous histiocytoma
- Mast cell sarcoma
- Meningocele
- Metastatic carcinoma
- Microvenular hemangioma
- Midline nevus flammeus (Angel's kiss, Salmon patch)
- Multifocal lymphangioendotheliomatosis
- Multiple cutaneous leiomyoma (Pilar leiomyoma)
- Nasal glioma (Cephalic brainlike heterotopias)
- Neural fibrolipoma
- Neuroma cutis
- Neurothekeoma (Nerve sheath myxoma)
- Nevus anemicus
- Nevus flammeus (Capillary malformation, Port-wine stain)
- Nevus flammeus nuchae (Stork bite)
- Nevus lipomatosus superficialis
- Nevus oligemicus
- Nodular fasciitis (Nodular pseudosarcomatous fasciits, Subcutaneous pseudosarcomatous fibromatosis)
- Oral submucous fibrosis
- Pachydermodactyly
- Paraneoplastic syndrome
- Pearly penile papules
- Peyronie's disease (Induratio penis plastica)
- Phakomatosis pigmentovascularis
- Plantar fibromatosis
- Pleomorphic lipoma
- Plexiform fibrohistiocytic tumor
- Proliferating angioendotheliomatosis
- Prominent inferior labial artery
- Pseudo-ainhum
- Retiform hemangioendothelioma
- Schwannoma (Neurilemmoma)
- Solitary angiokeratoma
- Solitary cutaneous leiomyoma
- Solitary mastocytoma
- Solitary neurofibroma
- Spider angioma (Nevus araneus, Spider nevus, Vascular spider)
- Spindle-cell hemangioendothelioma
- Spindle-cell lipoma
- Subungual exostosis
- Superficial acral fibromyxoma
- Superficial lymphatic malformation (Lymphangioma circumscriptum)
- Systemic mastocytosis
- Targetoid hemosiderotic hemangioma
- Telangiectasia
- Telangiectasia macularis eruptiva perstans
- Teratoma
- Tufted angioma (Angioblastoma)
- Umbilical granuloma
- Universal angiomatosis (Generalized telangiectasia)
- Venous lake (Phlebectases)
- Verrucous vascular malformation (Angiokeratoma circumscriptum naeviforme)
- Wildervanck syndrome
- Xanthelasmoidal mastocytosis
- Zosteriform metastasis
[edit] Dermatitis See also Category:Dermatitis Dermatitis is a general term for "inflammation of the skin."[25] [edit] Atopic See also Category:Atopic dermatitis Atopic dermatitis is a chronic dermatitis associated with a hereditary tendency to develop allergies to food and inhalant substances.[26][27] - Atopic dermatitis (Atopic eczema, Disseminated neurodermatitis, Flexural eczema, Infantile eczema, Prurigo diathsique)
[edit] Contact See also Category:Contact dermatitis Contact dermatitis is caused by certain substances coming in contact with the skin.[28][29] [edit] Eczema See also Category:Eczema Eczema refers to a broad range of conditions that begin as spongiotic dermatitis and may progress to a lichenified stage.[30] [edit] Pustular See also Category:Pustular dermatitis Pustular dermatitis is an inflammation of the skin that presents with pustular lesions.[31] [edit] Seborrheic See also Category:Seborrheic dermatitis Seborrheic dermatitis is a chronic, superficial, inflammatory disease characterized by scaling on an erythematous base.[32] [edit] Disturbances of pigmentation See also Category:Disturbances of human 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.[33][34] [edit] Drug eruptions See also Category:Drug eruptions Drug eruptions are adverse drug reactions that present with cutaneous manifestations.[35][36] [edit] Endocrine-related See also Category:Endocrine-related cutaneous conditions Endocrine conditions often present with cutaneous findings as the skin interacts with the endocrine system in many ways.[37] [edit] Epidermal nevi, neoplasms, cysts See also Category:Epidermal nevi, neoplasms, cysts Epidermal nevi, neoplasms, cysts are skin lesions that develop from the epidermal layer of the skin.[6] - 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 (Solar keratosis)
- Adenoid squamous cell carcinoma (Pseudoglandular squamous cell carcinoma)
- Aggressive digital papillary adenocarcinoma (Digital papillary adenocarcinoma)
- Apocrine gland carcinoma
- Apocrine nevus
- Arsenical keratosis
- Balanitis plasmacellularis (Balanoposthitis chronica circumscripta plasmacellularis, Zoon's balanitis)
- Basal cell carcinoma
- Basaloid follicular hamartoma
- Basaloid squamous cell carcinoma
- Benign lichenoid keratosis (Lichen planus-like keratosis)
- Birt–Hogg–Dubé syndrome
- Bowen's disease (Squamous cell carcinoma in situ)
- Branchial cyst (Branchial cleft cyst)
- Bronchogenic cyst
- Ceruminoma
- Cicatricial basal cell carcinoma (Morpheaform basal cell carcinoma, Morphoeic basal cell carcinoma)
- 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 radiation keratosis
- Chronic scar keratosis (Chronic cicatrix keratosis)
- Clonal seborrheic keratosis
- Common seborrheic keratosis (Basal cell papilloma, Solid seborrheic keratosis)
- Congenital preauricular fistula (Ear pit, Congenital auricular fistula, Preauricular sinus and cyst)
- Cowden syndrome (Cowden's disease, Multiple hamartoma syndrome)
- Cutaneous ciliated cyst
- Cutaneous columnar cyst
- Cutaneous horn (Cornu cutaneum)
- Cylindroma (Dermal eccrine cylindroma)
- Cystic basal cell carcinoma
- Dermatosis papulosa nigra
- Dermoid cyst
- 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)
- Eruptive vellus hair cyst
- Erythroplasia of Queyrat
- Extramammary Paget's disease
- Fibroepithelioma
- Fibroepithelioma of Pinkus
- Fibrofolliculoma
- Folliculosebaceous cystic hamartoma
- Generalized eruptive keratoacanthoma (Generalized eruptive keratoacanthoma of Grzybowski)
- Giant solitary trichoepithelioma
- Hidradenoma papilliferum
- Hidrocystoma
- Hydrocarbon keratosis (Pitch keratosis, Tar keratosis, Tar wart)
- Hyperkeratosis lenticularis perstans (Flegel's disease)
- Hyperkeratosis of the nipple and areola
- Ichthyosis hystrix
- Infiltrative basal cell carcinoma
- Inflammatory linear verrucous epidermal nevus
- Irritated seborrheic keratosis (Basosquamous cell acanthoma, Inflamed seborrheic keratosis)
- Keratin implantation cyst
- Keratoacanthoma
- Keratoacanthoma centrifugum marginatum
- Linear verrucous epidermal nevus (Linear epidermal nevus, Verrucous epidermal nevus)
- Malignant acrospiroma (Malignant poroma, Porocarcinoma)
- Malignant mixed tumor (Malignant chondroid syringoma)
- Malignant pilomatricoma (Pilomatrical carcinoma, Pilomatrix carcinoma)
- Malignant trichilemmal cyst
- Mantleoma
- Marjolin's ulcer
- Median raphe cyst
- Melanoacanthoma (Pigmented seborrheic keratosis)
- Merkel cell carcinoma (Trabecular carcinoma)
- Microcystic adnexal carcinoma (Sclerosing sweat duct carcinoma)
- Micronodular basal cell carcinoma
- Milia
- Mixed tumor (Chondroid syringoma)
- Mucinous carcinoma
- Muir–Torre syndrome
- Multiple familial trichoepithelioma (Brooke–Spiegler syndrome, Epithelioma adenoides cysticum)
- Multiple keratoacanthomas (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)
- 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)
- Omphalomesenteric duct cyst (Omphalomesenteric duct remnant, Vitelline cyst)
- Paget's disease of the breast
- Papillary eccrine adenoma (Tubular apocrine adenoma)
- Perifollicular fibroma
- Phakomatosis pigmentokeratotica
- Pigmented basal cell carcinoma
- Pigmented hairy epidermal nevus syndrome
- Pilar cyst (Trichilemmal cyst, Isthmus-catagen cyst)
- Pilar sheath acanthoma
- Pilomatricoma (Calcifying epithelioma of Malherbe, Malherbe calcifying epithelioma, Pilomatrixoma)
- Pilonidal sinus (Pilonidal cyst)
- Polypoid basal cell carcinoma
- Pore-like basal cell carcinoma
- Primary cutaneous adenoid cystic carcinoma
- Proliferating epidermoid cyst
- Proliferating trichilemmal cyst
- Pseudocyst of the auricle (Auricular endochondrial pseudocyst)
- Pseudoepitheliomatous keratotic and micaceous balanitis
- PUVA keratosis
- Reactional keratosis
- Reticulated seborrheic keratosis (Adenoid seborrheic keratosis)
- Rodent ulcer (Jacobi ulcer)
- Schimmelpenning syndrome
- Sebaceoma (Sebaceous epithelioma)
- Sebaceous adenoma
- Sebaceous carcinoma
- Sebaceous hyperplasia
- Seborrheic keratosis (Seborrheic verruca, Senile keratosis, Senile wart)
- Seborrheic keratosis with squamous atypia
- Signet-ring cell squamous cell carcinoma
- Solitary keratoacanthoma (Subungual keratoacanthoma)
- Solitary trichoepithelioma
- Spindle cell squamous 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, 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
- Thyroglossal duct cyst
- Trichilemmal carcinoma
- Trichilemmoma
- Trichoadenoma
- Trichoblastoma
- Trichodiscoma
- Trichofolliculoma
- Tumor of the follicular infundibulum
- Unilateral palmoplantar verrucous nevus
- Urethral caruncle
- Verrucous carcinoma (Ackerman tumor, Carcinoma cuniculatum)
- Verrucous cyst (Cystic papilloma)
- Viral keratosis
- Warty dyskeratoma (Isolated dyskeratosis follicularis)
- Waxy keratosis of childhood (Kerinokeratosis papulosa)
- Zoon's vulvitis
- Zosteriform speckled lentiginous nevus
[edit] Erythemas See also Category:Erythemas Erythemas are reactive skin conditions in which there is blanchable redness.[1][7] [edit] Genodermatoses See also Category:Genodermatoses Genodermatoses are inherited genetic skin conditions often grouped into three categories: chromosomal, single gene, and polygenetic.[38][39] - 18q deletion syndrome
- Acrodermatitis enteropathica
- Acrokeratosis verruciformis (Acrokeratosis verruciformis of Hopf)
- Acrokeratotic poikiloderma (Hyperkeratosis–hyperpigmentation syndrome, Kindler syndrome, Weary–Kindler syndrome)
- Adams–Oliver syndrome
- Adducted thumbs syndrome
- AEC syndrome (Ankyloblepharon filiforme adenatum – ectodermal dysplasia – cleft palate syndrome, Hay–Wells syndrome)
- Albright's hereditary osteodystrophy
- Apert syndrome (Acrocephalosyndactyly)
- Aplasia cutis congenita (Cutis aplasia, Congenital absence of skin, Congenital scars)
- Ataxia telangiectasia (Louis–Bar syndrome)
- Atrichia with papular lesions
- 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 (APECED syndrome)
- Bart syndrome
- BIDS syndrome
- Bloom syndrome (Bloom–Torre–Machacek syndrome)
- Cardio-facio-cutaneous syndrome (Cardiofaciocutaneous syndrome)
- Cartilage–hair hypoplasia (McKusick type metaphyseal chondrodysplasia)
- Carvajal syndrome
- CHILD syndrome (Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome)
- CHIME syndrome (Zunich–Kaye syndrome, Zunich neuroectodermal syndrome)
- Chondrodysplasia punctata
- Cicatricial junctional epidermolysis bullosa
- Cockayne syndrome
- Conradi–Hünermann syndrome (Conradi–Hünermann–Happle syndrome, X-linked dominant chondrodysplasia punctata)
- Costello syndrome
- Cronkhite–Canada syndrome
- Crouzon syndrome
- Crow–Fukase syndrome (POEMS syndrome)
- Cutis verticis gyrata
- Darier's disease (Darier–White disease, Keratosis follicularis)
- Disseminated superficial actinic porokeratosis
- Disseminated superficial porokeratosis
- Dominant dystrophic epidermolysis bullosa
- Dyskeratosis congenita (Zinsser–Cole–Engman syndrome)
- Dystrophic epidermolysis bullosa
- Ectodermal dysplasia
- Ectodermal dysplasia with corkscrew hairs
- EEC syndrome (Ectrodactyly – ectodermal dysplasia – cleft 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 variabilis (Erythrokeratodermia figurata variabilis, Keratosis extremitatum progrediens, Keratosis palmoplantaris transgrediens et progrediens, Mendes da Costa type erythrokeratodermia, Progressive symmetric erythrokeratoderma)
- Familial benign chronic pemphigus (Familial benign pemphigus, Hailey–Hailey disease)
- Fanconi syndrome (Familial pancytopenia, Familial panmyelophthisis)
- Focal dermal hypoplasia (Goltz syndrome)
- Follicular atrophoderma
- Franceschetti–Klein syndrome (Mandibulofacial dysostosis)
- Generalized atrophic benign epidermolysis bullosa
- Generalized epidermolysis bullosa simplex (Koebner variant of generalized epidermolysis bullosa simplex)
- Generalized trichoepithelioma
- Hallerman–Streiff syndrome
- Harlequin-type ichthyosis (Harlequin fetus)
- Hereditary sclerosing poikiloderma
- Hidrotic ectodermal dysplasia (Alopecia congenita with keratosis palmoplantaris, Clouston syndrome, Fischer–Jacobsen–Clouston syndrome, Keratosis palmaris with drumstick fingers, Palmoplantar keratoderma and clubbing)
- Hypohidrotic ectodermal dysplasia (Anhidrotic ectodermal dysplasia, Christ–Siemens–Touraine syndrome)
- IBIDS syndrome (Tay's syndrome, Trichothiodystrophy)
- Ichthyosis bullosa of Siemens
- Ichthyosis follicularis (Ichthyosis follicularis with alopecia and photophobia syndrome)
- Ichthyosis linearis circumflexa
- Ichthyosis prematurity syndrome
- Ichthyosis vulgaris
- Incontinentia pigmenti (Bloch–Sulzberger disease)
- Incontinentia pigmenti achromians (Hypomelanosis of Ito)
- IPEX syndrome
- Junctional epidermolysis bullosa
- Junctional epidermolysis bullosa gravis (Epidermolysis bullosa letalis, Herlitz disease, Herlitz epidermolysis bullosa, Lethal junctional epidermolysis bullosa)
- Junctional epidermolysis bullosa with pyloric atresia
- Keratitis–ichthyosis–deafness syndrome (Desmons' syndrome, Ichthyosiform erythroderma with corneal involvement and deafness, KID syndrome, Senter syndrome)
- Keratolytic winter erythema (Erythrokeratolysis hiemalis, Oudtshoorn skin)
- Keratosis follicularis spinulosa decalvans (Siemens-1 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
- Klinefelter syndrome
- Klippel–Feil syndrome
- Lamellar ichthyosis (Collodion baby)
- Lelis syndrome
- Lenz–Majewski syndrome
- Linear and whorled nevoid hypermelanosis (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
- McCusick syndrome
- Mitis junctional epidermolysis bullosa (Nonlethal junctional epidermolysis bullosa)
- Multiple lentigines syndrome (Cardiocutaneous syndrome, Gorlin syndrome II, Lentiginosis profusa syndrome, LEOPARD syndrome, Progressive cardiomyopathic lentiginosis)
- Multiple sulfatase deficiency
- Naegeli–Franceschetti–Jadassohn syndrome (Chromatophore nevus of Naegeli)
- Netherton's 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
- Odonto–Tricho–Ungual–Digital–Palmar syndrome
- Pachydermoperiostosis (Idiopathic hypertrophic osteoathorpathy, Touraine–Solente–Gole syndrome)
- Pachyonychia congenita type I (Jadassohn–Lewandown–Sky syndrome)
- Pachyonychia congenita type II (Jackson–Lawler pachyonychia congenita, Jackson–Sertoli syndrome)
- Papillon–Lefèvre syndrome
- Peeling skin syndrome (Continual peeling skin syndrome, Familial continual skin peeling, Idiopathic deciduous skin, Keratolysis exfoliativa congenita)
- Pfeiffer syndrome
- PIBI(D)S syndrome
- Pityriasis rotunda (Pityriasis circinata)
- Plaque-type porokeratosis (Classic porokeratosis, Porokeratosis Mibelli)
- Polyostotic fibrous dysplasia (Albright's disease)
- Popliteal pterygium syndrome
- Porokeratosis
- Porokeratosis palmaris et plantaris disseminata
- Progeria (Hutchinson–Gilford progeria syndrome, Hutchinson–Gilford syndrome)
- Progressive symmetric erythrokeratodermia (Erythrokeratodermia progressiva symmetrica)
- Proteus syndrome
- Punctate porokeratosis
- Rapp–Hodgkin syndrome (Rapp–Hodgkin ectodermal dysplasia syndrome)
- Recessive dystrophic epidermolysis bullosa (Hallopeau–Siemens variant of epidermolysis bullosa)
- Refsum's disease (Heredopathia atactica polyneuritiformis)
- Relapsing linear acantholytic dermatosis
- Restrictive dermopathy
- Rhizomelic chondrodysplasia punctata (Peroxisomal biogenesis disorder complementation group 11)
- Rombo syndrome
- Rothmund–Thomson syndrome (Poikiloderma congenitale)
- Rud syndrome
- Scleroatrophic syndrome of Huriez (Huriez syndrome, Palmoplantar keratoderma with sclerodactyly, Scleroatrophic and keratotic dermatosis of the limbs, Sclerotylosis)
- Sjögren–Larsson syndrome
- Tooth and nail syndrome (Hypodontia with nail dysgenesis, Witkop syndrome)
- Transient bullous dermolysis of the newborn
- Treacher Collins 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 (Cranio-carpo-tarsal 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
[edit] Infection-related See also Category:Infection-related cutaneous conditions Infection-related cutaneous conditions may be caused by bacteria, fungi, yeast, viruses, and/or parasites.[40] [edit] Bacterium-related See also Category:Bacterium-related cutaneous conditions 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.[40][41] - Aeromonas infection
- African tick bite fever
- Arcanobacterium haemolyticum infection
- Bacillary angiomatosis
- Bejel (Endemic syphilis)
- Blastomycosis-like pyoderma
- Blistering distal dactylitis
- Borderline lepromatous leprosy
- Borderline leprosy
- Borderline tuberculoid leprosy
- Botryomycosis
- Brucellosis (Undulant fever)
- Bullous impetigo
- Cat-scratch disease
- Cellulitis
- Chancre
- Chancroid (Soft chancre, Ulcus molle)
- Chlamydial infection
- Chronic lymphangitis
- Chronic recurrent erysipelas
- Chronic undermining burrowing ulcers (Meleney gangrene)
- Chromobacteriosis infection
- Cutaneous actinomycosis
- Cutaneous anthrax infection
- Cutaneous diphtheria infection
- Cutaneous group B streptococcal infection
- Cutaneous Pasteurella hemolytica infection
- Cutaneous Streptococcus iniae infection
- Dermatitis gangrenosa (Gangrene of the skin)
- Desert sore (Barcoo rot, Diphtheric desert sore, Septic sore, Veldt sore)
- Ecthyma
- Ecthyma gangrenosum
- Ehrlichiosis
- Elephantiasis nostras
- Endemic typhus
- Epidemic typhus
- Erysipelas (Ignis sacer, Saint Anthony's fire)
- Erysipeloid of Rosenbach
- Erythema marginatum
- Erythrasma
- External otitis
- Folliculitis
- Fournier gangrene of the penis or scrotum
- Furunculosis (Boil)
- Gas gangrene (Clostridial myonecrosis)
- Glanders (Equinia, Farcy, Malleus)
- Gonococcemia
- Gram-negative folliculitis
- Gram-negative toe web infection
- Granuloma inguinale (Donovanosis, Granuloma venereum, Ulcerating sclerosing granuloma)
- Green nail syndrome
- Group JK corynebacterium sepsis
- Haemophilus influenzae cellulitis
- Helicobacter cellulitis
- Histoid leprosy
- Hospital furunculosis
- Hot tub folliculitis (Pseudomonas aeruginosa folliculitis)
- Impetigo contagiosa
- Lepromatous leprosy
- Leptospirosis (Fort Bragg fever, Pretibial fever, Weil's disease)
- Listeriosis
- Lyme disease
- Lymphogranuloma venereum
- Malakoplakia (Malacoplakia)
- Mediterranean spotted fever (Boutonneuse fever)
- Melioidosis (Whitmore's disease)
- Meningococcemia
- Mycoplasma infection
- Necrotizing fascitis
- Nocardiosis
- Oroya fever (Carrion's disease)
- Pasteurella multocida infection
- Pasteurellosis
- Perineal dermatitis
- Pinta
- Pitted keratolysis (Keratoma plantare sulcatum)
- Plague
- Primary gonococcal dermatitis
- Pyogenic paronychia
- Pyomyositis
- Q fever
- Queensland tick typhus
- Rat-bite fever
- Rhinoscleroderma
- Rickettsialpox
- Rocky Mountain spotted fever
- Salmonellosis
- Scarlet fever
- Scrub typhus (Tsutsugamushi fever)
- Shigellosis
- Staphylococcal scalded skin syndrome
- Streptococcal intertrigo
- Superficial pustular folliculitis (Impetigo of Bockhart, Superficial folliculitis)
- Sycosis vulgaris (Barber's itch, Sycosis barbae)
- Syphilis
- Toxic shock syndrome
- Trench fever (Five day fever, Quintan fever, Urban trench fever)
- Tropical ulcer (Aden ulcer, Jungle rot, Malabar ulcer, Tropical phagedena)
- Tuberculoid leprosy
- Tularemia (Deer fly fever, Ohara's disease)
- Verruga peruana
- Vibrio vulnificus infection
- Yaws (Bouba, Frambesia, Pian)
[edit] Mycobacterium-related See also Category:Mycobacterium-related cutaneous conditions Mycobacterium-related cutaneous conditions are caused by mycobacterium infections.[40] [edit] Mycosis-related See also Category:Mycosis-related cutaneous conditions Mycosis-related cutaneous conditions are caused by fungi or yeasts, and may present as either a superficial or deep infection of the skin.[40] [edit] Parasitic infestations, stings, and bites See also Category:Parasitic infestations, stings, and bites of the skin Parasitic infestations, stings, and bites in humans are caused by several groups of animals belonging to the following phyla: Arthropoda, Chordata, Cnidaria, Nemathelminthes, Platyhelminthes, Annelida, and Protozoa.[40] - Acanthamoeba infection
- Amebiasis cutis
- Ant sting
- Arachnidism
- Balamuthia infection
- Bee and wasp stings
- Blister beetle dermatitis (Paederus dermatitis)
- Bristleworm sting
- Caripito itch
- Caterpillar dermatitis
- Centipede bite
- Cheyletiella dermatitis
- Chigger bite
- Cimicosis (Bedbug bites)
- 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
- Demodex mite bite
- Dogger Bank itch
- Dracunculiasis (Dracontiasis, Guinea worm disease, Medina worm)
- Echinococcosis (Hydatid disease)
- Elephant skin
- Elephantiasis tropica (Elephantiasis arabum)
- Enterobiasis (Oxyuriasis, Pinworm infection, Seatworm infection)
- Erisipela de la costa
- Funnel web spider bite
- Gamasoidosis
- Gnathostomiasis (Larva migrans profundus)
- Grain itch (Barley itch, Mattress itch, Prairie itch, Straw itch)
- Grocer's itch
- Hookworm disease (Ancylostomiasis, Ground itch, Necatoriasis, Uncinariasis)
- Human trypanosomiasis
- Hydroid dermatitis
- Jellyfish dermatitis
- Ked itch
- Larva currens
- Latrodectism
- Leech bite
- Leopard skin
- Lizard bite
- Lizard skin
- Loaiasis (Calabar swelling, Fugitive swelling, Loa loa, Tropical swelling)
- Loxoscelism
- Mal morando
- Millipede burn
- Mosquito bite
- Moth dermatitis
- Mucocutaneous leishmaniasis (Espundia, Leishmaniasis americana)
- Myiasis
- Necrotic cutaneous loxoscelism
- Nematode dermatitis
- Norwegian scabies
- Onchocerciasis
- Pediculosis capitis
- Pediculosis corporis (Pediculosis vestimenti, Vagabond's disease)
- Pediculosis pubis (Crabs)
- Pneumocystosis
- Portuguese man-of-war dermatitis
- Post-kala-azar dermal leishmaniasis
- Pulicosis (Flea bites)
- Reduviid bite
- Scabies
- Scorpion sting
- Sea anemone dermatitis
- Sea urchin injury
- Seabather's eruption
- Seaweed dermatitis
- Snake bite
- Sowda
- Sparganosis
- Stingray injury
- Swimmer's itch (Schistosome cercarial dermatitis)
- Tarantula bite
- Tick bite
- Toxoplasmosis
- Trichinosis
- Trichomoniasis
- Tungiasis
- Visceral leishmaniasis (Dumdum fever, Kala-azar)
- Visceral schistosomiasis (Bilharziasis)
- Viscerotropic leishmaniasis
- Wheat warehouse itch
[edit] Virus-related See also Category:Virus-related cutaneous conditions Virus-related cutaneous conditions are caused by two main groups of viruses–DNA and RNA types–both of which are obligatory intracellular parasites.[40] [edit] Lichenoid eruptions See also Category:Lichenoid eruptions Lichenoid eruptions are dermatoses related to the unique, common inflammatory disorder lichen planus, which affects the skin, mucous membranes, nails, and hair.[42][43] [edit] Lymphoid-related See also Category:Lymphoid-related cutaneous conditions Lymphoid-related cutaneous conditions are a group of disorders characterized by collections of lymphocyte cells within the skin.[44] - Acquired ichthyosis (Ichthyosis acquisita)
- Adult T-cell leukemia/lymphoma
- Angiocentric lymphoma (Nasal/nasal type NK/T-cell lymphoma)
- 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 (Lymphadenosis benigna cutis, Lymphocytoma cutis, Pseudolymphoma, Spiegler–Fendt sarcoid)
- Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns
- Cutaneous lymphoid hyperplasia with nodular pattern (Nodular pattern of cutaneous lymphoid hyperplasia)
- Cutaneous myelofibrosis
- 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
- Hypereosinophilic syndrome
- Intravascular large B-cell lymphoma (Angiotropic large cell lymphoma, Malignant angioendotheliomatosis)
- Jessner lymphocytic infiltrate of the skin (Jessner lymphocytic infiltration of the skin, Jessner–Kanof lymphocytic infiltration of the skin, Lymphocytic infiltrate of Jessner)
- Lennert lymphoma (Lymphoepitheliod lymphoma)
- Leukemia cutis
- 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 (Leukemids)
- Pagetoid reticulosis (Acral mycoses fungoides, Localized epidermotropic reticulosis, Mycosis fungoides palmaris et plantaris, 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
- 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
- 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)
[edit] Melanocytic nevi and neoplasms See also Category: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, but which lack dendritic processes.[45] - Acral lentiginous melanoma
- Acral nevus (Melanocytic nevus of acral skin, Melanocytic nevus with intraepidermal ascent of cells)
- Amelanotic blue nevus (Hypomelanotic blue nevus)
- Amelanotic melanoma
- Balloon cell nevus
- Becker nevus
- Benign melanocytic nevus (Banal nevus, Nevocytic nevus)
- Blue nevus
- Blue nevus of Jadassohn–Tiche (Common blue nevus, Nevus ceruleus)
- Carney complex (LAMB syndrome, NAME syndrome)
- Cellular blue nevus
- Centrofacial lentiginosis
- Deep penetrating nevus
- Desmoplastic melanoma
- Dysplastic nevus
- Dysplastic nevus syndrome (B-K mole syndrome, Familial atypical multiple mole-melanoma syndrome, Familial melanoma syndrome)
- Ephelis (Freckle)
- Epithelioid and spindle-cell nevus (Benign juvenile melanoma, Spitz nevus)
- Epithelioid blue nevus
- Generalized lentiginosis
- Giant pigmented nevus (Bathing trunk nevus, Giant hairy nevus)
- Halo nevus (Leukoderma acquisitum centrifugum, Perinevoid vitiligo, Sutton nevus)
- Inherited patterned lentiginosis in black persons
- Ink spot lentigo (Sunburn lentigo)
- Lentigo maligna (Lentiginous melanoma on sun-damaged skin)
- Lentigo maligna melanoma
- Lentigo simplex
- Malignant blue nevus
- Medium-sized congenital nevocytic nevus
- Melanoacanthoma
- Melanocytic tumors of uncertain malignant potential
- Mongolian spot
- Moynahan syndrome
- Mucosal lentigines (Labial and penile and vulvar melanosis, Melanotic macules)
- Mucosal melanoma
- Nevus of Ito (Nevus fuscoceruleus acromiodeltoideus)
- Nevus of Ota (Nevus fuscoceruleus ophthalmomaxillaris, Oculodermal melanocytosis)
- Nevus spilus (Speckled lentiginous nevus, Zosteriform lentiginous nevus)
- Nodular melanoma
- Partial unilateral lentiginosis
- Peutz–Jeghers syndrome
- Polypoid melanoma
- Pseudomelanoma (Recurrent nevus)
- PUVA lentigines
- Small-sized congenital nevocytic nevus
- Soft-tissue melanoma (Clear-cell sarcoma, Melanoma of the soft parts)
- Solar lentigo (Lentigo senilis, Liver spots)
- Superficial spreading melanoma (Superficially spreading melanoma)
[edit] Monocyte- and macrophage-related See also Category:Monocyte- and macrophage-related cutaneous conditions Monocyte- and macrophage-related cutaneous conditions are characterized histologically by infiltration of the skin by monocyte and/or macrophage cells.[8] [edit] Mucinoses See also Category:Mucinoses Mucinoses are a group of conditions caused by dermal fibroblasts producing abnormally large amounts of mucopolysaccharides.[2] [edit] Neurocutaneous See also Category:Neurocutaneous conditions Neurocutaneous conditions are due organic nervous system disease or are psychiatric in etiology.[46][47] [edit] Noninfectious immunodeficiency-related See also Category:Noninfectious immunodeficiency-related cutaneous conditions Noninfectious immunodeficiency-related cutaneous conditions are caused by T-cell and/or B-cell dysfunction.[48][49] [edit] Nutrition-related See also Category:Malnutrition Nutrition-related cutaneous conditions are caused by malnutrition due to an improper or inadequate diet.[50][51] [edit] Papulosquamous hyperkeratotic See also Category:Papulosquamous hyperkeratotic skin diseases Papulosquamous hyperkeratotic skin conditions are those that present with papules and scales caused by a thickening of the stratum corneum.[7] - Acrokeratoelastoidosis of Costa
- Aquagenic wrinkling of the palms (Acquired aquagenic syringeal acrokeratoderma)
- Camisa disease
- Complex keratoderma
- Confluent and reticulated papillomatosis (Confluent and reticulated papillomatosis of Gougerot and Carteaud, Familial cutaneous papillomatosis, Familial occurrence of confluent and reticulated papillomatosis)
- Corneodermatosseous syndrome (CDO syndrome)
- Diffuse epidermolytic palmoplantar keratoderma (Palmoplantar keratoderma cum degeneratione granulosa Vörner, Vörner's epidermolytic palmoplantar 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)
- Diffuse palmoplantar keratoderma
- Digitate dermatosis (Xanthoerythrodermia perstans)
- Exfoliative dermatitis (Dermatitis exfoliativa, Erythroderma, Red man syndrome)
- Florid cutaneous papillomatosis
- Focal acral hyperkeratosis (Acrokeratoelastoidosis lichenoides, Degenerative collagenous plaques of the hand)
- Focal palmoplantar keratoderma
- Focal palmoplantar keratoderma with oral mucosal hyperkeratosis (Hereditary painful callosity syndrome, Keratosis follicularis, Keratosis palmoplantaris nummularis)
- Howel–Evans syndrome (Familial keratoderma with carcinoma of the esophagus, Palmoplantar ectodermal dysplasia type III, Palmoplantar keratoderma associated with esophageal cancer, Tylosis)
- Keratoderma
- Keratoderma climactericum (Climacteric keratoderma)
- Keratolysis exfoliativa (Lamellar dyshidrosis, 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)
- 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)
- Mal de Meleda (Acral keratoderma, Mutilating palmoplantar keratoderma of the Gamborg–Nielsen type, Palmoplantar ectodermal dysplasia type VIII)
- 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, Polykeratosis of Touraine)
- Pachyonychia congenita
- Palmoplantar keratoderma
- Palmoplantar keratoderma and spastic paraplegia (Charcot–Marie–Tooth disease with palmoplantar keratoderma and nail dystrophy)
- Palmoplantar keratoderma of Sybert (Greither palmoplantar keratoderma, Keratosis extremitatum hereditaria progrediens, Keratosis palmoplantaris transgrediens et progrediens)
- Pityriasis rosea
- Pityriasis rubra pilaris
- Porokeratosis plantaris discreta
- Punctate palmoplantar keratoderma
- Schöpf–Schulz–Passarge syndrome (Eyelid cysts with palmoplantar keratoderma and hypodontia and hypotrichosis)
- Simple keratoderma
- Small-plaque parapsoriasis (Chronic superficial dermatitis)
- Spiny keratoderma (Porokeratosis punctata palmaris et plantaris, Punctate keratoderma, Punctate porokeratosis of the palms and soles)
- Striate keratoderma
- Striate palmoplantar keratoderma (Acral keratoderma, Brünauer–Fuhs–Siemens type, Keratosis palmoplantaris varians, Wachter keratoderma, Wachters palmoplantar keratoderma)
- Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy
- Syndromic keratoderma
- Tyrosinemia type II (Oculocutaneous tyrosinemia, Richner–Hanhart syndrome)
- Vohwinkel syndrome (Keratoma hereditaria mutilans, Mutilating keratoderma of Vohwinkel)
[edit] Pruritic See also Category:Pruritic skin conditions Pruritus, commonly known as itchiness, is a sensation exclusive to the skin, and characteristic of many skin conditions.[52][53] [edit] Psoriasis See also Category:Psoriasis Psoriasis is a common, chronic, and recurrent inflammatory disease of the skin characterized by circumscribed, erythematous, dry, scaling plaques.[54][55][56] [edit] Reactive neutrophilic See also Category:Reactive neutrophilic cutaneous conditions Reactive neutrophilic cutaneous conditions constitute a spectrum of disease mediated by neutrophils, and typically associated with underlying diseases, such as inflammatory bowel disease and hematologic malignancy.[57][58] [edit] Recalcitrant palmoplantar eruptions See also Category:Recalcitrant palmoplantar eruptions Recalcitrant palmoplantar eruptions are skin conditions of the palms and soles which are resistant to treatment.[2] - 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 palmaris et plantaris)
- Pustular bacterid
[edit] Resulting from errors in metabolism See also Category:Skin conditions resulting from errors in metabolism Skin conditions resulting from errors in metabolism are caused by enzymatic defects that lead to an accumulation or deficiency of various cellular components, including, but not limited to, amino acids, carbohydrates, and lipids.[10] - Acute intermittent porphyria
- Adrenoleukodystrophy (Schilder's disease)
- Alkaptonuria
- Angiokeratoma corporis diffusum (Anderson–Fabry disease, Fabry disease)
- B-mannosidase deficiency
- CADASIL syndrome
- Carotenosis
- 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
- Familial alpha-lipoprotein deficiency (Tangier disease)
- Familial apoprotein CII deficiency
- Familial combined hyperlipidemia (Multiple-type hyperlipoproteinemia)
- Familial defective apolipoprotein B-100
- Familial dysbetalipoproteinemia (Broad beta disease)
- Familial hypertriglyceridemia
- Farber disease (Fibrocytic dysmucopolysaccharidosis, Lipogranulomatosis)
- Fucosidosis
- Gaucher's disease
- Gout (Podagra, Urate crystal arthropathy, Urate deposition disease)
- Hartnup disease
- Hepatoerythropoietic porphyria
- Hereditary coproporphyria
- Heredofamilial amyloidosis
- Hunter syndrome
- Hurler syndrome (Gargoylism, Mucopolysaccharidosis I)
- Hyaluronidase deficiency (Mucopolysaccharidosis IX)
- Iatrogenic calcinosis cutis
- Idiopathic scrotal calcinosis (Idiopathic calcified nodules of the scrotum)
- Lafora's disease
- Lesch–Nyhan syndrome (Juvenile gout)
- Lichen amyloidosis
- Limited joint mobility
- Lipoid proteinosis (Hyalinosis cutis et mucosae, Urbach–Wiethe disease)
- Lipoprotein lipase deficiency (Chylomicronemia)
- Macular amyloidosis
- Medication-induced hyperlipoproteinemia
- Metastatic calcinosis cutis
- Morquio's disease (Mucopolysaccharidosis 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
- Secondary cutaneous amyloidosis
- Secondary systemic amyloidosis
- Sialidosis
- Subepidermal calcified nodule (Solitary congenital nodular calcification, Winer's nodular calcinosis)
- Transient erythroporphyria of infancy (Purpuric phototherapy-induced eruption)
- Traumatic calcinosis cutis
- Tuberoeruptive xanthoma
- Tumoral calcinosis
- Variegate porphyria (Mixed hepatic porphyria, Mixed porphyria, South African genetic porphyria)
- Verruciform xanthoma
- Waxy skin
- Wilson's disease (Hepatolenticular degeneration)
- Xanthelasma palpebrarum (Xanthelasma)
- Xanthoma diabeticorum
- Xanthoma planum (Plane xanthoma)
- Xanthoma striatum palmare
- Xanthoma tendinosum
- Xanthoma tuberosum
[edit] Resulting from physical factors See also Category:Skin conditions resulting from physical factors Skin conditions resulting from physical factors occur due to a number of causes, including, but not limited to, hot and cold temperatures, friction, moisture, and ionizing radiation.[2] - Abrasion
- Acrocyanosis
- Actinic prurigo (Familial polymorphous light eruption of American Indians, Hereditary polymorphous light eruption of American Indians, Hutchinson's summer prurigo, Hydroa aestivale)
- Acute radiodermatitis
- Beryllium granuloma
- Black heel (Calcaneal petechiae, Chromidrose plantaire, Talon noir)
- Brachioradial pruritis
- Callus
- Carbon stain
- Chilblains (Pernio, Perniosis)
- Chronic actinic dermatitis (Actinic reticuloid, Chronic photosensitivity dermatitis, Persistent light reactivity, Photosensitive eczema)
- Chronic radiodermatitis
- Clavus (Corn)
- Colloid milium
- Coral cut
- Dermatosis neglecta
- Electrical burn
- Eosinophilic, polymorphic, and pruritic eruption associated with radiotherapy
- Equestrian perniosis
- Erythema ab igne
- Erythrocyanosis crurum
- Fracture blister
- Friction blister
- Frostbite
- Hot tar burn
- Hydroa vacciniforme
- Kairo cancer
- Kang cancer
- Kangri ulcer
- Mercury granuloma
- Miliaria crystalline (Sudamina)
- Miliaria profunda
- Miliaria pustulosa
- Miliaria rubra (Prickly heat)
- Narcotic dermopathy
- Occlusion miliaria
- Painful fat herniation (Painful piezogenic pedal papules)
- Peat fire cancer
- Photoaging (Dermatoheliosis)
- Photosensitivity with HIV infection
- Phototoxic tar dermatitis
- Phytophotodermatitis (Berloque dermatitis)
- Polymorphous light eruption
- Postmiliarial hypohidrosis
- Pressure ulcer (Decubitus ulcer)
- Pseudoverrucous papules and nodules
- Radiation cancer
- Sclerosing lymphangiitis
- Silica granuloma
- Silicone granuloma
- Solar erythema
- Subcutaneous emphysema
- Sunburn
- Tattoo
- Thermal burn
- Traumatic asphyxia
- Trench foot
- Tropical anhidrotic asthenia
- Tropical immersion foot (Paddy foot)
- 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
[edit] Urticaria and angioedema See also Category:Urticaria and angioedema Urticaria is a vascular reaction of the skin characterized by the appearance of wheals, which are firm, elevated swelling of the skin.[59] Angioedema, which can occur alone or with urticaria, is characterized by a well-defined, edematous swelling that involves subcutaneous tissues, abdominal organs, and/or upper airway.[60] [edit] Vascular-related See also Category:Vascular-related cutaneous conditions Vascular-related cutaneous conditions result from dysfunction of the blood and/or blood vessels in the dermis, or lymphatics in the subcutaneous tissues.[7] - Aagenaes syndrome
- Acroangiodermatitis of Mali (Mali acroangiodermatitis)
- Acute hemorrhagic edema of infancy (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
- Calciphylaxis
- Cholesterol embolus (Warfarin blue toe syndrome)
- Churg–Strauss syndrome
- Cryofibrinogenemic purpura
- Cryoglobulinemic purpura
- Cryoglobulinemic vasculitis
- Cutaneous polyarteritis nodosa
- Cutaneous small-vessel vasculitis (Cutaneous leukocytoclastic angiitis, Cutaneous leukocytoclastic vasculitis, Cutaneous necrotizing venulitis, Hypersensitivity angiitis)
- Deep venous thrombosis
- Disseminated intravascular coagulation
- Drug-induced purpura
- Drug-induced thrombocytopenic purpura
- Ducas and Kapetanakis pigmented purpura
- Epidemic dropsy
- Erythema elevatum diutinum
- Erythromelalgia (Acromelalgia, Erythermalgia)
- Factitial lymphedema (Hysterical edema)
- Fibrinolysis syndrome (Defibrinating syndrome, Hypofibrinogenemia)
- Food-induced purpura
- Generalized essential telangiectasia
- Giant-cell arteritis
- Gougerot–Blum syndrome (Pigmented purpuric lichenoid dermatitis)
- Granuloma faciale
- Hematopoietic ulcer
- Henoch–Schönlein purpura
- Hereditary hemorrhagic telangiectasia (Osler's disease, Osler–Weber–Rendu disease)
- Idiopathic thrombocytopenic purpura (Autoimmune thrombocytopenic purpura, Werlhof's disease)
- Lichen aureus
- 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
- Majocchi's disease (Purpura annularis telangiectodes)
- Malignant atrophic papulosis (Degos' disease)
- Marshall–White syndrome
- Microscopic polyangiitis
- Mondor's disease
- Mucocutaneous lymph node syndrome (Kawasaki's disease)
- Neuropathic ulcer (Mal perforans)
- Nonne–Milroy–Meige syndrome (Hereditary lymphedema)
- Obstructive purpura
- Orthostatic purpura (Stasis purpura)
- Painful bruising syndrome (Autoerythrocyte sensitization, Gardner–Diamond syndrome, Psychogenic purpura)
- Paroxysmal hand hematoma (Achenbach syndrome)
- Paroxysmal nocturnal hemoglobinuria
- 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
- Schamberg's disease
- Secondary lymphedema
- 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
- Unilateral nevoid telangiectasia
- Urticarial vasculitis
- Venous insufficiency ulceration
- Waldenström hyperglobulinemic purpura (Purpura hyperglobulinemica)
- Waldenström macroglobulinemia
- Wegener granulomatosis
- Yellow nail syndrome (Primary lymphedema associated with yellow nails and pleural effusion)
- ^ 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.
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- ^ Krueger JG, Bowcock A (2005). "Psoriasis pathophysiology: current concepts of pathogenesis". Ann Rheum Dis 64 (Suppl 2): ii30–6. doi:10.1136/ard.2004.031120. PMID 15708932.
- ^ Callen JP (2002). "Neutrophilic dermatoses". Dermatol Clin 20 (3): 409–19. doi:10.1016/S0733-8635(02)00006-2. PMID 12170875.
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- ^ Clarke P (2004). "Urticaria". Aust Fam Physician 33 (7): 501–3. PMID 15301166. http://www.racgp.org.au/afp/200407/14489.
- ^ Muller BA (2004). "Urticaria and angioedema: a practical approach". Am Fam Physician 69 (5): 1123–8. PMID 15023012.
[edit] Further reading - Bickers DR, Athar M (2006). "Oxidative stress in the pathogenesis of skin disease". J Invest Dermatol 126 (12): 2565–75. doi:10.1038/sj.jid.5700340. PMID 17108903.
- Fawcett RS, Linford S, Stulberg DL (2004). "Nail abnormalities: clues to systemic disease". Am Fam Physician 69 (6): 1417–24. PMID 15053406.
- Gawkrodger DJ (2004). "Occupational skin cancers". Occup Med (Lond) 54 (7): 458–63. doi:10.1093/occmed/kqh098. PMID 15486177.
- Harries MJ, Lear JT (2004). "Occupational skin infections". Occup Med (Lond) 54 (7): 441–9. doi:10.1093/occmed/kqh096. PMID 15486175.
- Luba MC, Bangs SA, Mohler AM, Stulberg DL (2003). "Common benign skin tumors". Am Fam Physician 67 (4): 729–38. PMID 12613727. http://www.aafp.org/afp/20030215/729.html.
- Mancini AJ (2004). "Skin". Pediatrics 113 (4 Suppl): 1114–9. PMID 15060207. http://pediatrics.aappublications.org/cgi/content/full/113/4/S1/1114.
- Maurer TA (2005). "Dermatologic manifestations of HIV infection" (PDF). Top HIV Med 13 (5): 149–54. PMID 16377853. http://www.iasusa.org/pub/topics/2005/issue5/149.pdf.
- McLaughlin MR, O'Connor NR, Ham P (2008). "Newborn skin: Part II. Birthmarks". Am Fam Physician 77 (1): 56–60. PMID 18236823. http://www.aafp.org/afp/20080101/56.html.
- Mulinari-Brenner F, Bergfeld WF (2003). "Hair loss: diagnosis and management" (PDF). Cleve Clin J Med 70 (8): 705–6, 709–10, 712. doi:10.3949/ccjm.70.8.705. PMID 12959397. http://www.ccjm.org/content/70/8/705.full.pdf.
- O'Connor NR, McLaughlin MR, Ham P (2008). "Newborn skin: Part I. Common rashes". Am Fam Physician 77 (1): 47–52. PMID 18236822. http://www.aafp.org/afp/20080101/47.html.
- Pãunescu MM, Feier V, Pãunescu M, Dorneanu F, Sisak A, Ambros-Rudolph CM (2008). "Dermatoses of pregnancy" (PDF). Acta Dermatovenerol Alp Panonica Adriat 17 (1): 4–11. PMID 18454263. http://ibmi.mf.uni-lj.si/acta-apa/acta-apa-08-1/1.pdf.
- Pont MS, Elster AD (1992). "Lesions of skin and brain: modern imaging of the neurocutaneous syndromes" (PDF). AJR Am J Roentgenol 158 (6): 1193–203. PMID 1590106. http://www.ajronline.org/cgi/reprint/158/6/1193.pdf.
- Richens J (2004). "Genital manifestations of tropical diseases". Sex Transm Infect 80 (1): 12–7. doi:10.1136/sti.2003.004093. PMID 14755029.
- Scott LA, Stone MS (2003). "Viral exanthems". Dermatol Online J 9 (3): 4. PMID 12952751. http://dermatology.cdlib.org/93/reviews/viral/scott.html.
- Springer K, Brown M, Stulberg DL (2003). "Common hair loss disorders". Am Fam Physician 68 (1): 93–102. PMID 12887115. http://www.aafp.org/afp/20030701/93.html.
- Stulberg DL, Clark N, Tovey D (2003). "Common hyperpigmentation disorders in adults: Part I. Diagnostic approach, café au lait macules, diffuse hyperpigmentation, sun exposure, and phototoxic reactions". Am Fam Physician 68 (10): 1955–60. PMID 14655804. http://www.aafp.org/afp/20031115/1955.html.
- Stulberg DL, Clark N, Tovey D (2003). "Common hyperpigmentation disorders in adults: Part II. Melanoma, seborrheic keratoses, acanthosis nigricans, melasma, diabetic dermopathy, tinea versicolor, and postinflammatory hyperpigmentation". Am Fam Physician 68 (10): 1963–8. PMID 14655805. http://www.aafp.org/afp/20031115/1963.html.
- Thiers BH (1986). "Dermatologic manifestations of internal cancer" (PDF). CA Cancer J Clin 36 (3): 130–48. doi:10.3322/canjclin.36.3.130. PMID 3011224. http://caonline.amcancersoc.org/cgi/reprint/36/3/130.pdf.
- Tunzi M, Gray GR (2007). "Common skin conditions during pregnancy". Am Fam Physician 75 (2): 211–8. PMID 17263216. http://www.aafp.org/afp/20070115/211.html.
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