
Atopic dermatitis (overview) L20.-
Eczema atopic (overview): severe, universal (erythrodermic) atopic eczema. exacerbation phase since about 3 months. patient with rhinitis and conjunctivitis with pollinosis. total IgE >1.000IU.

Urticaria (overview) L50.8
Angioedema: idiopathic, acute and for the first time opened angioedema with massive swelling of the upper and lower eyelids.

Ilven Q82.5
ILVEN: 5-year-old girl in whom flat and linear plaques in a characteristic arrangement along the Blaschko lines were noticed since the first year of life (not detectable at birth). This bizarre pattern marks the changes as a cutaneous mosaic and thus as a harmlessoma of the skin. For half a year the inflammatory character has been increasing.

Atopic dermatitis (overview) L20.-
Extrinsic atopiceczema: eminently chronic, somewhat asymmetrical eczema with blurred, itchy, red, rough, flat plaques. known (only slightly pronounced) rhinoconjunctivitis allergica. I.A. variable course with activity spurts ("overnight"). IgE normal. no atopic FA.

Acne conglobata L70.1
Acne conglobata. Numerous open comedones, inflammatory papules, flat atrophic scars.

Seborrheic dermatitis of adults L21.9
dermatitis, seborrhoeic: 58-year-old patient with negative self- and family history of psoriasis. recurrent HV in the seboohoeic zones of the trunk for years. no itching. improvement in summer. multiple, chronically inpatient, figured, borderline, temporarily itching, moderately scaly, clearly borderline hardly elevated plaques.

Urticaria vasculitis M31.8
Urticarial vasculitis. 33-year-old female patient with distinct reduction of the az. 3 weeks of recurrent febrile attacks (CRP and SPA massively increased) and a distinct feeling of illness accompanied by a maculo-papular, moderately itchy exanthema. Histological: Evidence of a leukocytoclastic "small vessel vasculitis". The clinical differentiation from urticaria is possible by marking a persistent efflorescence for several days (marking test). Recurrent and changing arthritis.

Anticonvulsant hypersensitivity syndrome T88.7

Circumscribed scleroderma L94.0
scleroderma circumscripts (plaque-type). large,circumcircumscribed, red-violet, smooth plaque with centrally embedded yellow-white indurations. the surface here is shiny like parchment. there is a feeling of tension. no pain. DD: scleroderma-like borreliosis!

Pityriasis lichenoides chronica L41.1
Pityriasis lichenoides chronica, colorful picture with inflammatory papules of different size, central excoriations.

Bullous Pemphigoid L12.0
Pemphigoid, bullous. general view: maximum exacerbated clinical picture on trunk and extremities of a 66-year-old female patient. Multiple, acute, generalized, symmetrical, flexurally accentuated, 0.3-1.0 cm large, isolated and grouped, partly hemorrhagic, bulging blisters on flat erythema and plaques. Older, healing blisters are partly burst open, eroded or encrusted.

Solar dermatitis L55.-
Dermatitis solaris. almost universal, succulent erythema in a 30-year-old patient (skin type II) after intensive, several hours of sunbathing in the midday sun. accompanying strong sensation of heat, chills and circulatory weakness about 7 hours after exposure to the sun.

Erythema multiforme, minus-type L51.0
Erythema multiforme: multiple red plaques with central blister formation, on the left edge of the picture the lesions are confluent.

Granuloma anulare plaque type
Granuloma anulare, plaque type: Multiple, completely symptom-free, smooth, homogeneously stained (no prominent marginal structures) plaques.

Acne (overview) L70.0
Acne vulgaris: numerous, sometimes painful keloids, after Acne vulgaris has largely healed

Radiodermatitis chronic L58.1
Chronic radiodermatitis: Condition following radiation of a bronchial carcinoma.

Mycosis fungoides C84.0
Mycosis fungoides: Plaque stage. 32-year-old male with multiple, disseminated, 1.0-5.0 cm large, moderately itchy, hardly consistency increased, red, rough plaques; clinically and histologically no detectable LK infection.