Image diagnoses for "brown"
361 results with 1409 images

Nevus Spitz. reflected light microscopy of the previously clinically imaged nevus. irregular pigmentation; radial-strictive basic architecture, which is particularly visible at the edges, no vascular polymorphies.

nevus melanocytic acral: completely sympotmless, congenital melanocytic, nevus that covers the sole and back of the foot. bizarre lateral borders, different shades of brown and black. six-monthly controls are indicated.

Scleroderma circumscripts (type band-shaped circumscripts scleroderma). 32-year-old woman, for years progressive symptoms. no significant symptoms. no restrictions in mobility.

Argyrie: diffuse, completely symptom-free brown coloration of the facial areas in the area of exposed areas, which does not recede even in the winter months.

Incontinentia pigmenti, type Bloch-Sulzberger (back part): a few weeks old girl with grouped blisters and extensive erosions.

Papillomatosis cutis carcinoides. cauliflower-like, dirty greyish brown vegetation, slightly bleeding.

Dermatofibroma, hemosiderin storing tumor on the lower leg of a 64-year-old female patient.

Dyskeratosis follicularis (Darier's disease).

Adenoma sebaceum: diffuse distribution of skin-coloured, shiny papules and plaques. conspicuously bizarre telangiectasias, partly present in the papules and in the surrounding area. no folliculitis, no comedones.

Granuloma anulare, classic type . borderline, in the centre skin-coloured, smooth, painless, firm plaque with the formation of an indicated ring shape without scaling over the middle joint of the left middle finger (fingers are predilection sites). no itching.

Melanoma malignes, nodular: A solitary node that has existed for years, has been growing for more than a year, is firm, sharply defined, smooth on the surface, not hairy, and has bled repeatedly in recent weeks.

Hyperpigmentation caloric: Net-like hyperpigmentation caused by regular application of heat. No complaints.

Adenoma sebaceum: disseminated, densely packed, chronically stationary (no dynamic development), completely asymptomatic, reddish-brownish, 0.1-0.4 cm in size, red, reddish-brown and skin-coloured, individually standing and aggregated papules with symmetrical, centrofacial emphasis; slight seborrhoea; no comedones.

Unusually large keloid that appeared after a flesh wound, otherwise banal wounds healed keloid-free.

Papillomatosis cutis lymphostatica: Initial findings with flat keratotic deposits.

Keratoacanthoma: Typicalclinical aspect with peripheral wall and central horn plug.

Cornu cutaneum: existing for several months; painless, bleeding from time to time when shaving Histological: actinic keratosis

type i neurofibromatosis, peripheral type or classic cutaneous form. since puberty slowly increasing formation of these soft, skin-coloured or slightly brownish, painless papules and nodules. characteristic for neurofibromas are consistency and the bell-button phenomenon (the papules can be pressed into the skin under pressure). on the flanks on both sides large café-au-lait spots up to 8 cm in diameter. the simultaneous detection of several café-au-lait spots secured the clinical diagnosis here.