Image diagnoses for "brown"
357 results with 1404 images

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

Lichen sclerosus of the vulva: Infestation of vulva and anus in a figure of eight form.

Melanocytic nevus. Type: Congenital melanocytic nevus. Repigmented scar after partial resection.

type i neurofibromatosis, peripheral type or classic cutaneous form. numerous smaller and larger soft, predominantly pigmented, practical nodules and nodules. in the larger nodules the so-called "bell-button phenomenon" can be detected. the palpating finger penetrates the deep dermis as if through a fascial gap. few café-au-lait spots. papules and nodules. only isolated rather discreet café-au-lait spots.

Circumscripts of scleroderma (small-heart plaque or confetti type): disseminated, symptomless, 0.1-0.2 cm large, confetti-like, white spots/papules with (incident light microscopic) detectable, atropically shiny surface. The skin lesions have now been discovered (by chance) after sunbathing. Histology: No evidence of Lichen sclerosus.

Necrobiosis lipoidica: Overview of the left thigh: Approx. 3 cm large, slightly elevated, erythematous plaque without ulcerations.

Acne, keloid acne. Acne vulgaris cured with scar keloids.

Becker-Naevus: chronically stationary, planar, splatter-like light brown pigmented, rough, sharply defined stain; no change in pigmentation in the last 20 months compared to the previous findings

Keloids in dark skin: Training on pre-existing folliculitis.

Late syphilis: asymmetrical, scarred, bizarrely configured, brown, surface smooth plaques.

 

Generalized GVHD: chronic, generalized, poikilodermatic skin changes, with circumscribed calluses, atrophy and reticular hyperpigmentation.

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

Scabies: Months old, disseminated, fresh and older, erythematous, scaly, papules, plaques (ganglion structures); multiple scratch artifacts and erosions; 45-year-old neglected patient.

Amyloidosis systemic: Flat light brown, symptomless plaques on both backs of the hands and fingers; recurrent fresh haemorrhages after banal traumas.

Melanonychia: Longitudinally over the nail plate running brown-black discoloration (pigmentation).

Onychodystrophy. Traumatic onychodystrophy with splinter hemorrhage.

Amyloidosis macular cutaneous: Large, long-standing, continuously spreading, blurred, symmetrical, light to medium brown spots and plaques; histological evidence of the amyloid.

Lentigo maligna: a slow-growing, completely symptom-free spot that has been known for years; histologically, no invasiveness (transition to lentigo maligna melanoma) could be detected even in cut series.

Purpura pigmentosa progressiva: aetiologically unexplained (medication?) pronounced clinical picture that has been changing for several months with symmetrically distributed, disseminated, non-itching, yellow-brown, spots (detailed picture).