Image diagnoses for "brown"
373 results with 1439 images
Results forbrown

Syringome disseminated D23.L
Syringome disseminated: 78-year-old male patient. the brownish-red subjectively completely asymptomatic papules; they would have existed "forever". spreading flat only on the right forearm on the inside. the diagnosis was confirmed bioptically.

Papillomatosis cutis lymphostatica I89.0
Papillomatosis cutis lymphostatica: massive findings with papillomatous growths on the back of the foot and toes; chronic lymphedema after recurrent erysipelas.

Acuminate condyloma A63.0
Condylomata acuminata, perianal and extraanal soft cauliflower-like tumors.

Acromegaly E22.0
Acromegaly: 43-year-old patient with known acromegaly. Noticeable increase in size of the lower extremities. Simultaneous development of excessive varicosis with consecutive chronic venous insufficiency (CVI).

Diffuse cutaneous mastocytosis Q82.2
Diffuse cutaneous mastocytosis, with uniform waxy skin texture and artificial blistering, peau-dórange-like skin aspect.

Nevus melanocytic dysplastic D48.5

Chronic prurigo L28.1
Differential diagnosis of Prurigo nodularis: Lichen planus verrucosus: Isolated and aggregated, massively itchy, scratched papules and nodules in the area of the lower leg (resistance to therapy; progression over years).

Nevus melanocytic (overview) D22.-
Usual melanocytic nevus. Chronic stationary, 0.2-2.0 cm in size, sharply defined, soft, light to dark brown, indolent, smooth papules and plaques in the breast area of a 22-year-old woman. No increase in pigmentation or size is noticeable.

Argyria L81.8
Argyrie: diffuse, grey to greyish-blackish, metallically shiny, diffuse discolouration of the facial skin due to deposition of silver complexes The patient worked for decades in a silver-processing company

Granuloma anulare disseminatum L92.0
Granuloma anulare disseminatum: partial manifestation. non-painful, non-itching, disseminated, large-area plaques that appeared on the trunk and extremities of a 65-year-old patient. no diabetes mellitus. no other systemic diseases known.

Becker's nevus D22.5
Becker-Naevus: Since birth existing, extensive hyperpigmentation in the area of the right hip in a 7-year-old boy; typical for the Becker-Naevus is the bizarre bordering as well as the follicular accentuation in the pigment zones.

Keratosis seborrhoic (papillomatous type) L82
Multiple seborrhoeic keratoses in different stages of development. 2.0 cm in diameter in the centre, dark brown seborrhoeic keratosis. Characteristic is the punched surface.

Darian sign
Urticaria pigmentosa of childhood: extensive redness and urticarial reaction in the lesions after mechanical irritation.

Circumscribed scleroderma L94.0
Scleroderma circumscripts (plaque-type; pattern of chessboard-like cutaneous mosaic - see below mosaic dermatosis acquired)

Maculopapular cutaneous mastocytosis Q82.2
Urticaria pigmentosa:multiple, chronically stationary, known for 1 year, no longer increasing for 3 months, mainly localised on the trunk, 0.2-0.4 cm in size, blurred, red to reddish-brownish, smooth spots. no spontaneous itching. after warm bathing, the spots are bright red, eleated and itchy (wheals). lively redness and wheals appear even after mechanical irritation.









