Image diagnoses for "brown"
378 results with 1454 images

type I neurofibromatosis, peripheral type or classic cutaneous form. numerous smaller and larger soft papules and nodules. no so-called café-au-lait spots. left brood region of little conspicuous nevus anämicus (see subsequent figure). several capillary angiomas.

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

Neurofibroma in Type I Neurofibromatosis: Multiple Neurofibromas

Neurofibroma in Type I Neurofibromatosis: Multiple Neurofibromas

Naevus melanocytic: Large congenital completely unattractive melanocyticnaevus.

POEMS syndrome: flat, even hyperpigmentation with "scleroderma-like" hardening and swelling of the forearm and back of the hand.

scleroderma circumscripts (linear type): band-shaped expression of the scleroderma focus on the upper and lower leg. in the thigh area, clear atrophy of skin, subcutaneous fatty tissue (and muscles). clinical picture developed over a period of about 7 years. pulling and stabbing complaints during sports activities.

Scleroderma circumscripts: Band-like form of the scleroderma focus on the upper and lower leg. clinical picture that developed slowly over a period of about 7 years. pulling and stabbing complaints during sports activities.

Keratosis areolae mammae as side effect of a therapy with vemurafenib (see also there).

Urticaria pigmentosa adultorum: Classical form of cutaneous mastocytosis (excess of mast cells in the skin) with multiple red patches and wheals (positive Darier sign, due to the friction of the trousers) clearly protruding in the buttock area, and light brown in the adjacent lumbar area, 0.1-0.3 cm in size.

diffuse cutaneous mastocytosis, with uniform waxy skin texture and artificial (subepithelial) blistering. peau-dórange-like skin aspect. detailed view.

Mastocytosis diffuse of the skin: Disseminated large-area mastocytosis of the skin (type Ia). In addition to the conspicuous yellow-brown spots and plaques, the apparently unaffected skin is slushy thickened, in places also with protruding follicular structures. The occurrence of larger blisters after banal trauma has been reported time and again. No systemic involvement detectable.

Mastocytosis diffuse of the skin: Disseminated large-area mastocytosis of the skin (type Ia); no systemic involvement detectable (detailed picture)

ear fistula and cyst, congenital (bds). findings congenital. no complaints so far. external fistula opening impresses as an irritationless brownish nodule with central porus.

ear fistula and cyst, congenital (bds). findings congenital. no complaints so far. external fistula opening impresses as an irritationless brownish nodule with central porus.

Keratosis areolae mamillae in a patient with erythrodermic psoriasis: Only after the development of erythrodermia did bilateral keratosis areolae mammae develop.

Nevus, melanocytic, halo-nevus. numerous depigmented, roundish, sharply defined, smooth, white spots with centrally located brown, slightly raised papules. 25-year-old patient with multiple halo- or sutton nevi occurring within a few months.

Mlelanom malignes acrolentiginous: Subungual malignant melanoma. Characteristic is the stripy growth through the entire length of the nail. The arrow marks the so-called Hutchinson sign.

Melanoma, malignant, acrolentiginous, subungual and paraungual, black pigmented tumor in the fingernail area, advanced stage with destruction of the nail.

Melanoma, malignant, acrolentiginous: Complete destruction of the nail organ by tumor growth.

Amelanotic acrolentiginous malignant melanoma: A "reddish spot" that has existed for years. It is said that this broad-based red node has been formed for a few months and has bled several times.

Melanoma malignes acrolentiginous: Brown "spot" on the left small toe that has existed for many years; for several months now it has been growing in thickness, weeping and bleeding.

Acrolentiginous malignant melanoma: A brown, slowly increasing spot that has existed for years. It is said that this broad-based, ulcerated, repeatedly bleeding node has been formed for a few months. Arrows mark the non-node acrolentiginous part of the tumor. A weak pigmentation zone is encircled, which histologically also turned out to be melanoma infiltration.

Atrophodermia idiopathica et progressiva: Large, red, confluent, barely palpable, smooth, sharply defined, symptom-free patches/plaques that slowly expand over months.

papillomatosis confluens et reticularis. since several years increasing discoloration and thickening of the skin of the sternoepigastric area. similar foci still exist on the trunk and neck. no other disease known.