Image diagnoses for "brown"
372 results with 1434 images

Incontinentia pigmenti, Bloch-Sulzberger type: a few weeks old girl with flat and streaky, inflammatory, in places hardly noticeable blistery skin changes.

Naevus melanocytic: Large congenital completely unattractive melanocyticnaevus.

Nevus, melanocytic. type: Congenital melanocytic nevus. solitary, chronically stationary, constant size for 12 months, indolent, sharply defined, axisymmetric, 0.6 cm diameter, dark brown, smooth nodule.

Tinea corporis:unusually elongated, non-pretreated, large-area tinea in known HIV infection.

Addison's disease: the palms of the previously described patient. pigmentation of the palm lines as well as the finger wrinkles. hyperpigmentation at traumatized areas typical for Addison's disease (here: calluses)

Condylomata acuminata: in the 20-year-old patient, these brownish, partly isolated, partly aggregated to large beds of verrucous papules and plaques have existed for about 1/2 year (?).

Melanoma malignant superficially spreading: Exceptionally large, 6.0x4.0 cm in diameter, malignant melanoma of the SSM type with nodular part. No bleeding, no oozing. The patient carefully clothed the melanoma-bearing area when exposed to the sun.

melanodermatitis toxica. chronic stationary (no growth dynamics), large, blurred, symptomless (only cosmetically disturbing), brown, spots. probably chronic, photoxic dermatitis due to frequent use of "refreshing tissues". DD. Chloasma.

Circumscriptal scleroderma (plaque-type/variant: Atrophodermia idiopathica et progressiva) Survey picture of the trunk: 2 years ago for the first time appeared, since then size progressive, large-area, erythematous-livid to brown, confluent, discreetly indurated spots and plaques in the region of the trunk in a 68-year-old female patient. In the region of the lower abdomen on the right side clearly sclerosed plaques of whitish color with partly distinctly atrophic surface and partly livid margins are found.

Granulomatosis disciformis chronica et progressiva: Large, hyperpigmented, borderline infiltrated foci with atrophic surface.

Chloasma gravidarum perstans: Chronic stationary, no longer increasing, periorally localized, smooth, brown spots in a 29-year-old woman 14 months after delivery.

Hyperpigmentation, postinflammatory. overview image: Chronic stationary, multiple, disseminated or confluent, brown-red or brownish smooth spots on the lower legs of a 26-year-old patient. The spots developed over a longer period of time from brown-red, verrucous plaques that had developed in the context of a lichen planus verrucosus.

Acanthosis nigricans benigna: blurred brown-black spots and plaques. the plaques are characterized by a slightly sooted, leathery surface. no subjective symptoms.

Auricular appendix: chronically stationary, existing since birth, not growing for many years, without symptoms, sharply defined, firm, smooth, skin-coloured to brownish nodules.

Neurofibromatosis peripheral: Café au lait spots in neurofibromatosis type I.