
Juvenile dermatomyositis M33.0

Acrodermatitis chronica atrophicans L90.4
Acrodermatitis chronica atrophicans. livid, blurred, variable coloured erythema of the left hand in comparison to the healthy right hand. skin atrophically shiny, hyperesthetic.

Erysipelas bullous
Erysipelas bullöses: acuteareal, sharply defined, painful reddening and plaque and areal blistering in the area of the lower leg. entry portal: macerated tinea pedum. fever, chills, lymphangitis and lymphadenitis also exist.

Keratosis actinica erythematous type L57.00
Keratosis actinica erythematous type: multiple red, rough, slightly painful plaques when spread over the skin, existing for years.

Chronic actinic dermatitis (overview) L57.1
Dermatitis chronic actinic: Chronic laminar eczema reaction which is essentially limited to the exposed skin areas Typical of chronic actinic dermatitis and thus distinguishable from a toxic light reaction (type acute solar dermatitis) is the blurred transition (eczematous scattering reactions) from lesional to healthy skin.

Asymmetrical nevus flammeus Q82.5
Vascular (capillary) malformation (so-called naevus flammeus): Congenital, generalized, irregularly configured, spotty erythema from the scalp to the sole of the foot in a 5-year-old boy, developed according to age. Here changes of the sole of the foot.

Adult dermatomyositis M33.1
dermatomyositis: reflected light microscopy. hyperkeratotic nail folds. pathologically increased and enlarged torqued capillaries. older bleeding into the nail fold.

Purpura thrombocytopenic M31.1; M69.61(Thrombozytopenie)
Thrombocytopenic purpura: colorful picture of a symmetrical, orthostatic purpura with fresh, punctiform, red bleeding.

Erythema infectiosum B08.30
Erythema infectiosum: less symptomatic exanthema with reticular erythema of the upper extremity.

Diffuse cutaneous mastocytosis Q82.2
Mastocytosis diffuse of the skin: Disseminated large-area mastocytosis of the skin (type Ia); no systemic involvement detectable (detailed picture)

Drug effect adverse drug reactions (overview) L27.0

Amyloidosis systemic (overview) E85.9
Amyloidosis systemic: Flat light brown, symptomless plaques on both backs of the hands and fingers; recurrent fresh haemorrhages after banal traumas.

Erythema infectiosum B08.30
Erythema infectiosum: partly anular partly reticular erythema on the lower extremity.

Dermatomyositis (overview) M33.-
Dermatomyositis (overview): Extensive, indicated striated erythema with reddish-livid papules which confluent in the region of the end phalanges to form extensive plaques; strongly pronounced nail fold capillaries.

Erythrosis interfollicularis colli L57.3

Asymmetrical nevus flammeus Q82.5
Naevus flammeus (Port-wine stain): congenitalerythema in the facial region (capillary vascular malformation), localized in V2 distribution, completely without symptoms. 4-month-old boy, developed according to age.

Atopic dermatitis in children and adolescents L20.8
Childhood eczema atopic: skin lesions in a 12-year-old boy. Back of the hand gray, dry, lichenified. No dermatitis. No itching.