Image diagnoses for "brown"
372 results with 1434 images
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Addison's disease E27.1
Addison's disease: grayish-brownish mucous membrane pigmentation of the gingiva in a 22-year-old man.

Neurofibromatosis (overview) Q85.0
Neurofibromatosis peripheral: Multiple dermal and large subcutaneous neurofibromas. Large café au lait spot (lower part of the picture). Multiple spatter-like pigment spots.

Nodular vasculitis A18.4
Erythema induratum. 52-year-old secretary has been suffering for 3 years from this moderately painful lesion running in relapses. Findings: Clinical examination o.B. Local findings: 10 cm in longitudinal diameter large, firm plaque, interspersed with cutaneous and subcutaneous nodules. In the centre scarring, on the edge deep, poorly healing ulcerations (here crusty evidence).

Facial granuloma L92.2
Granuloma faciale: Red-brown, blurred and irregularly configured, symptomless plaque in a 52-year-old man. distinct follicular prominence. no known secondary diseases, no medication anmnesia. the finding has been present for several months and is slowly progressive. detailed picture of multiple plaques in the face.

Incontinentia pigmenti (Bloch-Sulzberger) Q82.3
Incontinentia pigmenti, type Bloch-Sulzberger, garland-shaped pigmentation on the forearm along the Blaschko lines in a 10-month-old girl.

Nevus melanocytic (overview) D22.-
Nevus, melanocytic. Congenital melanocytic nevus of the spilus nevus type

Neurofibromatosis peripheral Q85.0
Type I neurofibromatosis, peripheral type: detailed picture of generalized clinical picture; circumscribed soft protuberant neurofibroma of the sole of the foot.

Herpes simplex virus infections B00.1
Herpes simplex virus infection:multilocular herpes simplex infection in zosteriform arrangement.

Melanonychia striata L60.8
Melanonychia striata longitudinalis: No pimentation of the perionychium = negative Hutchinson sign.

Atrophodermia idiopathica et progressiva L90.3
Atrophodermia idiopathica et progressiva. chronic stationary, map-like spread, brownish spots. the existing skin changes have developed within 2-3 years.

Neurofibromatosis peripheral Q85.0
Type I Neurofibromatosis (peripheral type): Numerous soft papules and nodules; multiple smaller and larger café-au-lait spots.

Café-au-lait stain L81.3
Café-au-lait stains: in neurofibromatosis type I. 2 medium brown homogeneously coloured light brown rounded spots.

Myzetome B47.9
Myzetome: Sharply limited, chronic granulomatous infection of the skin and subcutis with circumscribed, pseudotumorous swellings, as well as fistula formations ("Madura foot"), here "metastatic" new formation.

Nevus spitz D22.-
Naevus Spitz: a slightly raised, sharply defined, irregularly pigmented tumour that has existed for several months.

Onychomycosis (overview) B35.1
Tinea unguium. dystrophic onychomycosis. colorful, not painful nail discoloration (yellow-blue-green) with nail thickening. part of the nail discoloration is apparently caused by bleeding. Tr. rubrum and molds (Alternaria spp.) have been detected culturally.

Circumscribed scleroderma L94.0
Circumscripts of scleroderma (plaque-type). 24 months ago, a progressive, 26 x 21 cm large, flat, partially white-porcelain-like indurated area appeared for the first time in a 21-year-old patient. Additional findings were extensive brownish hyperpigmentation as well as multiple, partly very dark pigmented nevi in a trunk accentuated distribution.