Image diagnoses for "brown"
361 results with 1409 images

Fibroma molle. numerous, stalked, pendulous, soft, skin-coloured or slightly brownish, symptomless outgrowths in the area of the axilla

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.

Basal cell carcinoma, sclerodermiformes. solitary, chronically stationary (growth imperceptible since 5 years); firm, symptomless, red, centrally rough (crustal deposit), otherwise smooth, shiny plaques. transition into nodules.

Basal cell carcinoma nodular: Slowly growing, symptomless, surface smooth lump, existing for several years; conspicuous bizarre vascular structure.

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.

Prurigo nodularis: Multiple, chronically stationary, disseminated, isolated, sharply defined, raised, round, calotte-like, coarse, grayish grey to dirty grey, very itchy, rough nodules with a verruciform surface.

Mycobacteriosis, atpyic.

Verrucae vulgares. up to 0.6 cm in size, skin-coloured to yellowish, aggregated to a wart bed, rough papules and nodules with a verrucous surface. Vitiligo known for a long time.

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

Self-tanner: uneven browning of the cheek area after application of a self-tanning external layer.

Granuloma anulare disseminatum: non-painful, non-itching, disseminated, large-area plaques that appeared on the trunk and extremities of a 52-year-old patient. No diabetes mellitus. No other systemic diseases known.

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

Lentigo maligna with transition to a lentigo maligna melanoma: 68-year-old man, presenting in practice because of eczema. On questioning the completely symptomless "spot" on the earlobe has slowly grown over the years. Excision with histology: Both parts of a lentigo maligna and (central) parts of a lentigo maligna melanoma, TD 0.4mm, pT1a.

Onychogrypose: 10-nail onychogrypose in cases of perennial erythrodermia of unknown etiology.

Lymphangioma progressive: large brownish-red plaques, which fray into small flat plaques at the edges. No complaints. We aregratefulto Dr. U. Ammanfor submitting this image.

Nevus, melanocytic. Type: Acral, acquired melanocytic nevus.