
Vasculitis (overview) L95.8

Teleangiectasia macularis eruptiva perstans Q82.2
Teleangiectasia macularis eruptiva perstans. 58-year-old patient with a generalized, spot-like clinical picture which has existed for many years and shows a constant progression; itching during sweat-inducing efforts and mechanical exposure of the affected skin areas.

Dermatomyositis (overview) M33.-
Dermatomyositis. acute, diffuse, succulent erythema of the skin and décolleté. general fatigue, muscle weakness.

Dermatomyositis (overview) M33.-
Dermatomyositis: Flat red plaques on the end phalanges. Hyperkeratotic nail folds

Purpura pigmentosa progressive L81.7
Purpura pigmentosa progressiva. reflected light microscopy, blurred, yellowish-brownish spots (haemosiderin) next to punctiform, fresh bleedings.

Erythema e calore L59.0
Erythema e calore. regular applications of heat pads for chronic back problems.

Unilateral naevoid telangiectasia syndrome I78.8

Maculopapular cutaneous mastocytosis Q82.2
Urticaria pigmentosa/progression: patient as before, 10 years later. in the meantime almost extensive infestation due to confluence of the flock. lbaortechnical indications for systemic infestation.

Airborne contact dermatitis L23.8
Airborne Contact Dermatitis: Retroauricular infection: This pattern distinguishes ACD from photoallergic eczema, where the "shadow area of the auricle" remains free.

Mononucleosis infectious B27.9
Mononuleosis, infectious. generalized (almost universal) macular exanthema.

Livedoid vasculopathy L95.0
Livedovasculopathy: changes in the sole of the foot (rather rare localization)

Klippel-trénaunay syndrome Q87.2
Klippel-Trénaunay syndrome: extensive, bilateral vascular malformation of capillary (naevus flammeus) and venous vessels (varicosis with chronic venous insufficiency - CVI); distinct soft tissue hypertrophy on the left side; no pelvic obliquity!

Mononucleosis infectious B27.9
Mononuleosis, infectious. generalized (almost universal) macular exanthema.

Mixed connective tissue disease M35.10
Mixed connective tissue disease: deep red, blurred, poicilodermatic spots and plaques; central brown discoloration, reticular scarring.

Rosacea papulopustulosa
Rosacea papulopustulosa: disseminated, intermittent papules and pustules that persist for weeks on reddened skin (questionable pretreatment with a glucocorticoid externum); variable feeling of tension of the facial skin.

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.

Purpura senilis D69.2
Purpura senilis: General view: Multiple, different ages, extensive bleeding into the skin on the left forearm of a 78-year-old man.

Chronic actinic dermatitis (overview) L57.1
Dermatitis chronic actinic (type actinic reticuloid): Large-area, severe itching, eczematous clinical picture of the face, which appeared in spring after a short UV exposure and now persisted for several months. Massive lichenification of the skin (see radial lip furrows) as an expression of the chronic inflammatory remodelling of the thickened skin.






