Image diagnoses for "brown"
357 results with 1404 images

Pustulosis palmaris et plantaris: square: grouped pustules, low collateral erythema. encircled: confluent pustule. pustules: sterile

Granuloma faciale: Multiple, reddish-brown, blurred and irregularly configured, symptomless plaque in a 52-year-old man. No known secondary diseases, no drug anemia. The finding has been present for several months and is slowly progressive. Detailed view of multiple facial plalues.

Granuloma anulare, subcutaneous type. 8-9 years old, developed on the stretching side, deeply situated, coarse, flat, confluent papules with indicated anular arrangement in a 38-year-old patient. Small nodules on the sides of the fingers and on the back of the hand, particularly pronounced on digitus III. Painfulness on touch or pressure as well as restriction of movement on digitus I.

Necrobiosis lipoidica: chronic, sharply defined, flat, centrally atrophic, smooth plaque with clearly brown-red tinged edges; shining through of the underlying veins is characteristic.

Becker nevus: planar and spatter-like hyperpigmentation, focal hypertrichosis in the region of the lateral thoracic wall in young men; hardly visible at birth, postpubertal expression.

Melanoma, malignant, lentigo-maligna melanoma, bizarrely configured brown-black spot on UV-damaged skin on the nose, centrally low infiltration, development since about 8 years.

Erythema dyschromicum perstans. 49-year-old male. Several months old with extensive gray-brown patches on the trunk. No itching. No drug history?

Seborrhoeic keratosis in different stages of development: Papules marked with arrows, plaques encircled, nodes marked rectangularly.

Keratosis areolae mammae acquisita in age-related atrophic, slightly exsiccated, scaly skin.

Melanonychia striata longitudinalis. 4 months" (realistic is a duration of years) of persistent brown longitudinal stripes on the fingers of the right hand in a 64-year-old Turkish man. Mainly Laugier-Hunziker-Baran syndrome. Malignancy was excluded.

Comedo: multiple, chronically stationary, 0.5-1 mm large, firm, asymptomatic, grey, rough follicular papules with enlarged follicles, localized in the nasolabial fold; sebaceous content can be expressed on pressure.

Scleroderma ligamentous: for years slowly progressive, only moderately indurated ligamentous morphea in a 42-year-old woman; no movement restrictions of the joints.

Venous insufficiency chronic: pronounced congestive dermatitis with extensive induration of both lower legs.

Erythema gyratum repens: close-up.

Keratosis areolae mammae naeviformis: Chronically inpatient, for years unchanged, limited to nipple and areola, moderately consistent, symptomless, brown, rough (warty) plaque in a 45-year-old man.

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

Dyskeratosis follicularis. chronic dynamic, partly loosely disseminated, partly grouped standing, partly aggregated to plaques, brown papules first manifested in childhood. distinct itching with excoriations on the skin lesions.

Kaposi's sarcoma HIV-associated: red-brown, symptomless plaques

melanosis neurocutanea. multiple, sharply defined, pigmented, black spots, plaques and nodules on head, upper extremities and upper trunk. in the area of the middle and lower trunk there is a large melanocytic nevus. evidence of leptomeningeal melanosis.

Linea fusca. sharply defined, linear, brown, smooth, non-pruritic hyperpigmentation in a 28-year-old pregnant woman in 24th week of pregnancy. the line runs from the symphysis pubica upwards to the epigastrium. the clinical picture is diagnostically conclusive.