Image diagnoses for "Torso"
566 results with 2210 images

Acne cystica: In acne-typical distribution besides numerous (black) comedones and bridge comedones, numerous skin-coloured sebum retention cysts.

Lichen planus exanthematicus. 4 months old, distinctly itchy exanthema with pinhead-sized, slightly raised, partly isolated, but also aggregated to larger plaques, smooth, shiny, red papules. Streaky arrangement of the efflorescences in scratch or rub marks (Koebner phenomenon; seeleft half of the buttocks).

Syphilis (early syphilis): macular, chronic exanthema. in places fading erythema is also found. detailed view.

Urticaria pigmentosa: approx. 0.5-1.0 cm in size, disseminated, roundish, brownish-red spots. Only when rubbed, the spots become more red with accompanying itching. Increased redness and itching even in warm showers or baths.

Dermatitis medusica: In this general view, 3 weeks after the contact event, a solitary, linearly shaped, rough, strongly increased in consistency, flatly elevated, finely lamellar scaling plaque with scabbing in a 50-year-old man is shown. During a Mediterranean holiday, painful punctures on the back caused by contact with a jellyfish were first shown. The tentacles of the cnidarian could only be removed from the back with difficulty, then formation of bleeding at the adhesion sites. Immediately after contact, formation of streaky, pale erythema.

Exanthema subitum. exanthema with centrifugal spread from the trunk to the neck and back of the head. recess of the face.

Paget, M. of the nipple. unilateral, symptom-free, therapy-resistant, red, painless, slowly growing plaque of the nipple existing for several months. In the meantime, extensive infiltration of the skin beyond the areola. Previously, there was an erythema of the nipple which did not heal under an anti-eczematous therapy.

generalized cGVHD: generalized, scleroderma-like, hardly itchy generalized skin disease. graft-versus-host disease occurred about 2 years after stem cell transplantation. poikiloderma with bunchy, hyper- and depigmented indurated plaques.

Café-au-lait spots: in neurofibromatosis type I. Several medium brown spots in the lumbar region.

Sézary syndrome: universal redness with generalized lymphadenopathy; massive itching combined with pain when the integument dries out.

Xanthogranuloma adultes: 15 x 12 cm, solid, painless, skin-coloured tumour that has been growing slowly for several years; no systemic involvement detectable.

Chronic actinic skin damage: pronounced chronic light damage to the skin with poikilodermatic skin; years of excessive, chronic sun exposure.

Kindler Syndrome: since birth, recurrent blistering after banal trauma; now poikilodermatous appearance.

Melanoma, malignant, nodular. solitary, chronically active, growing rapidly in the last 4 weeks, occasionally bleeding slightly, 0.7 cm high, smooth, black lump on brown plaque.

Psoriasis vulgaris: chronic inpatient, therapy-resistant, intertriginous psoriasis.

Mycosis fungoides tumor stage: for years, previously known mycosis fungoides; for about several months, formation of less symptomatic red plaques and nodules,

Mycosis fungoides follikulotrope: 10-year-old girl with generalized folliculotropic Mycosis fungoides. foudroyant course of the disease which made a stem cell transplantation necessary

Parapsoriasis en grandes plaques.

Mycosis fungoides, folliculotropic. 3-year-old clinical picture with strongly itchy, moderately sharply defined, follicular red plaques.

Graft-versus-host disease. 3-15 months after transplantation, a reaction due to the transmission of allogenic immunocompetent T-lymphocytes. extensive dermatosclerosis with numerous, bizarre, skin-coloured papules and plaques.

Lichen simplex chronicus in dark skin. 0.1-0.2 cm large, marginally disseminated, firm brown-black (red shade is missing) papules, which have confluated into a flat plaque in the centre of the lesion. Permanent itching, which increases under stress.