Chloasma gravidarum perstans: Chronic stationary, no longer increasing, smooth, brown spots located in the temporal region in a 29-year-old woman 14 months after delivery.
Lichen simplex chronicus indark skin. several lesions with 0.1-0.2 cm large, marginally disseminated, firm brown-black papules confluent in the centre of the lesions. permanent itching.
Lymphomatoid papulosis: chronic, relapsing, completely asymptomatic clinical picture with multiple, 0.3 - 1.2 cm large, flat, scaly papules and nodules as well as ulcers. 35-year-old otherwise healthy man.
Type I Neurofibromatosis, peripheral type or classic cutaneous form Peripheral neurofibromatosis with multiple skin-coloured to light brown, soft nodes and nodules, sometimes also stalked, bulging soft, skin-coloured dewlap on the left hip.
Keratosis areolae mammae naeviformis: Chronic stationary plaque in a 45-year-old man, unchanged for years, limited to the nipple and areola, moderately increased in consistency, without symptoms, brown, rough (warty) plaque.
Neurofibromatosis peripheral: Multiple dermal and large subcutaneous neurofibromas. Large café au lait spot (lower part of the picture). Multiple spatter-like pigment spots.
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).
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.
Type I neurofibromatosis, peripheral type: detailed picture of generalized clinical picture; circumscribed soft protuberant neurofibroma of the sole of the foot.
Atrophodermia idiopathica et progressiva. chronic stationary, map-like spread, brownish spots. the existing skin changes have developed within 2-3 years.
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