Image diagnoses for "Leg/Foot"
410 results with 1189 images

Purpura thrombocytopenic: Hemorrhagic spots with a tendency to confluence, existing on both lower legs with emphasis on the extensor sides. It is a drug-induced form of a thrombotic- thrombocytopenic purpura with hemolytic microangiopathic anemia and central nervous failure symptoms. The trigger was the ingestion of non-steroidal anti-inflammatory drugs. Sudden onset with fever, disorientation, stupor.

Churg-Strauss Syndrome. circumscribed, borderline red, in the centre brown-yellow (here beginning of infiltrate formation and regression), in the area of the red areas rough, moderately pressure tolerated plaques and nodules in a 40-year-old man. known allergic bronchial asthma and seasonal rhinitis allergica. rennet: eosinophilia 45%; IgE >1000U/ml

Churg-Strauss syndrome: encircled central granulomatous regression zone (see histological preparation 1); on the right side the progression zone is outlined (see histological preparation 2).

Acute urticaria: acutely occurring, itchy exanthema with circulatory, also anular wheals.

Acute urticaria: Acute exanthema with multiple red wheals localized on the trunk and extremities, disseminated, flatly elevated, severely itching.

Acute urticaria. detailed view

Kaposi sarcoma classic: large, red moderately sharply defined, painless plaques.

Hyalinosis cutis et mucosae: psoriasiform, scaly plaques on both knees. No itching.

Linear IgA dermatosis: urticarial plaques with staggered vesicle and bladder formations.

Necrobiosis lipoidica: a condition that has existed for years and is constantly worsening; no diabetes mellitus known.

Necrobiosis lipoidica: detailed picture with pronounced atrophy of the surface epithelium.

Lymphomatoid papulosis: chronic, relapsing, completely asymptomatic clinical picture with multiple, 0.3 - 1.2 cm large, flat, scaly papules and nodules as well as ulcers. 35-year-old otherwise healthy man.

Dermatoliposclerosis. 64-year-old female patient with known CVI. For years increasing hardening of the distal and middle US third (so-called bottle bone). Extensive hyperpigmentation of the skin with coarse increase in consistency.

Dermatoliposclerosis. 64-year-old female patient with known CVI. For years increasing hardening of the distal and middle third of the US (so-called bottle bone). Extensive hyper - and depigmentation of the skin with wood-like, coarse increase in consistency.

Scar sarcoidosis: Since about 9 months development of completely symptom-free plaque in an old irritation-free scar on the knee.

Erythema multiforme: suddenly occurring, itchy, disseminated exanthema with cocard-like plaques which has been present for 4 days. here the finding on the lower leg. striated arrangement after external stimulus. s. isomorphism (Koebner phenomenon).

Ecchymosis syndrome, painful seti 6 months of recurrent, painful, extensive skin bleeding on the abodes and extremities in an otherwise healthy 69-year-old female patient

Granulomatosis disciformis chronica et progressiva: solitary, non-infiltrated, polycyclically limited, brown, symptomless, slow-growing spot.

Granulomatosis disciformis chronica et progressiva: solitary, non-infiltrated, brown, symptomless, slow-growing focal point (palpable only as a spot).

Leishmaniasis cutane: after a holiday in Tunisia appeared, little symptomatic, roundish, red-brown ulcerated nodules.

Malformation, vascular: mixed venous/arterial malformation with circumscribed soft tissue swelling; evidence of arterio-venous shunts; no cutaneous involvement.

Merkel cell carcinoma: rapidly growing non-symptomatic nodule, in a 73-year-old female patient

Merkel cell carcinoma: detailed view.

Myxoedema pretiabiales: circumscribed, blurred, yellowish-reddish, firm, hardly compressible, otherwise symptomless swellings; here a partial symptom of Graves' disease; typical is the orange peel-like surface of the swelling.

Pretibial myxoedema: close-up.