
Atopic dermatitis (overview) L20.-
Eczema atopic (overview): severe atopic eczema existing for years, mainly flexural in adolescence, generalized for 2 years now. massive constant itching, intensified after sweating. numerous scratch marks.

Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk and both legs. No evidence of soft tissue hypertrophy so far. No AV fistulas. Here is a detailed picture of the sole of the foot.

Psoriasis vulgaris L40.00
psoriasis vulgaris. treated psoriasis vulgaris. the previously existing typical psoriatic plaques are replaced by red spots with marginal hyperpigmentation. the treatment was carried out locally with dithranol [cignolin]. scaling no longer present. the brewing discoloration of the lesional surroundings are reversible discolorations of the nromal skin by diathranol. the diagnosis "psoriasis" is doubtless due to the known anamnesis.

Purpura thrombocytopenic M31.1; M69.61(Thrombozytopenie)
Purpura thrombocytopenic: acutely occurring, partly large-area, partly punctiform, non-anemic spots with a tendency to confluence; sudden onset with fever, multiple thromboses, disorientation, stupor; it is a drug-induced form of thrombotic thrombocytopenic purpura with hemolytic microangiopathic anemia at the base of an infectious disease and a previously unknown drug allergy.

Acrocyanosis I73.81; R23.0;
Acrocyanosis in age-atrophied, shiny skin, alternating temperature-dependent colouring from medium red to deep red.

Asymmetrical nevus flammeus Q82.5
Nevus flammeus (port wine stain): congenital erythema in the facial region (capillary vascular malformation), localized in V2 distribution, completely without symptoms; control image after 4 years

Purpura pigmentosa progressive L81.7
Purpura pigmentosa progressiva: aetiologically unexplained (medication?) pronounced clinical picture that has been changing for several months with symmetrically distributed, disseminated, non-itching, yellow-brown, spots (detailed picture).

Dermatomyositis (overview) M33.-
Dermatomyositis. Gottron papules in a 72-year-old woman. Smaller, striated, reddish-livid papules appear, which confluent in the region of the end phalanges to form flat plaques. Strongly pronounced nail fold capillaries on dig. III and V. The Keining sign was strongly positive in the clinical examination.

Maculopapular cutaneous mastocytosis Q82.2
Urticaria pigmentosa: general view: about 0.5-1.0cm large, disseminated, oval or round, brownish-red spots. only when rubbed, increased redness of the spots with accompanying itching. also in warm showers or baths increased redness and clearly palpable elevation of the lesions.

Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome: extensive vascular malformation with extensive nevus flammeus affecting the trunk and both arms. So far no evidence of soft tissue hypertrophy. No AV fistulas.

Erysipelas A46
erysipelas. extensive redness and swelling of the left foot in a 71-year-old man. on the left back of the foot there is a sharply limited overheated erythema with flame-like runners of 15 x 15 cm in size. the back of the foot is circumferentially enlarged and painful. secondary findings are the palpation of single, enlarged, pressure-dolent lymph nodes in the corresponding lymph drainage area of the groin region.

Erythronychia longitudinalis; L60.9 L60.8

Asteatotic dermatitis L30.8
Desiccation dermatitis: slight, pityriasiform scaling with a characteristic craquelée pattern with linear cracking

Erysipelas bullous
Erysipelas bullöses: acuteextensive, sharply defined, painful reddening and plaque with circumscribed large blisters; entry portal: tinea pedum.

Unilateral naevoid telangiectasia syndrome I78.8
Teleangiectasia syndrome, naevoides; for about 20 years existing, blurred redness of finest telangiectasia on the forearm of a 66-year-old woman.
