Image diagnoses for "Macule", "Leg/Foot"
76 results with 201 images

Klippel-Trénaunay syndrome: Extensive vascular malformation with a large-area nevus flammeus affecting the trunk and the right lower extremity with soft tissue hypertrophy of the right lower extremity; pelvic obliquity.

Incontinentia pigmenti achromians: Mosaic-like hypopigmentations of the left trunk and leg in a 2-year-old girl which appeared for the first time in the 4th month of life and have been progressive since then.

Vasculitis leukocytoclastic (non-IgA-associated): multiple, since 1 week existing, on both legs symmetrically localized, irregularly distributed, 0.1-0.2 cm large, confluent in places, symptomless, red, smooth spots (not compressible).

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.

Purpura pigmentosa progressiva. irregularly configured, reddish-brownish spots with petechiae that cannot be pushed away (cayenne pepper spots).

Erythromelalgia. seizure-like, painful, hyperemic, reddened and swollen skin of the hands and feet with increased sensitivity to heat. there is burning pain and oedema.

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. 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.

Teleangiectasia. Dense network of vasodilatation, distal sharp recess.

Desiccation dermatitis: slight, pityriasiform scaling with a characteristic craquelée pattern with linear cracking

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

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).

Anonychia in epidermolysis bullosa dystrophica Hallopeau-Siemens

Purpura jaune d'ocre: multiple, chronically stationary, proximally disseminated and blurred, distally confluent, symptom-free, light to dark brown, rough, scaly spots of varying intensity, located on the distal lower legs; detectable chronic venous insufficiency (CVI).

Purpura pigmentosa progressiva. incident light microscopy, blurred, yellow-brownish spots (star), in addition to punctiform, fresh bleeding (horizontal arrow) also older brown-reddish spots already in decomposition (vertical arrow). line pattern: traced skin line pattern of the skin of the lower leg

Erythema migrans: about 2-3 months old with slow peripheral expansion; painless, non-itching, circular erythema which is well distinguishable from normal skin; the bite is still centrally visible.

 

Vasculitis of small vessels. leukocytoclastic vasculitis (non-IgA-associated vasculitis)

Vasculitis leukocytoclastic (non-IgA-associated): small spotted vasculitis of both lower legs; multiple red spots (redness cannot be suppressed).

Peripheral arterial occlusive disease. Necrosis in the area of the 2nd toe in peripheral arterial occlusive disease.

Spider veins. Linear and reticular vascular ectasia in a 65-year-old patient with chronic venous insufficiency. The finding has been present for several years.

Systemic amyloidosis: persistent purpura (see legend in previous figure).