Image diagnoses for "Torso", "Plaque (raised surface > 1cm)"
275 results with 969 images

Toxic epidermal necrolysis: Large, superficial, towel-like detachment of the skin after ingestion of allopurinol.

Dyskeratosis follicularis (Darier's disease).

Lichen planus exanthematicus: small papular lichen planus with aggregation of the efflorescences to larger plaques, danger of erythroderma.

Mycosis fungoides. patch stage (early form of mycosis fungoides) Sharply limited, scaly erythema existing for several years. atrophic wrinkling of the skin on the shoulder. no significant clinical symptoms, especially no itching. low functional livedo (upper arm left). treatment in this stage blanching and with PUVA therapy.

Scabies. line and hook-shaped, reddened, infiltrated ducts on the field skin, considerable itching.

Circumscribed scleroderma: white moderately indurated plaques, the broad red border is striking.

Lichen sclerosus et atrophicus: General view of a bullous form: In the region of the lower right buttocks a sharply defined plaque of about 7 x 3.5 cm in size with a parchment-like folded skin surface in a 66-year-old female patient.

Leiomyoma (segmental cutaneous leiomyomatosis): Multiple, reddish-brownish papules in the upper abdomen, lateral thorax and back of a 49-year-old man.

Lupus erythematosus subacutely cutaneous (Rowell's sydrome): symmetrical, up to 3.0 cm large, partly confluent plaques that have existed for several weeks, ANA and SSA+.

Dyskeratosis follicularis (Darier's disease): non-itching, chronically persistent, disseminated papules.

Still Syndrome adultes: maculo-papular (sometimes urticarial aspect) exanthema in 53-year-old patient with recurrent fever attacks, distinct feeling of illness, arthralgias, relevantly increased inflammatory parameters, negative ANA and rheumatoid factor; no monoclonal gammopathy (DD: Schnitzler Syndrome)

DRESS: Detailed picture. 4 weeks after taking carbemazepine, occurrence of this generalized maculo-papular exanthema.

Angry back: Multiple "false positive" and clinically irrelevant test reactions in epicutaneous testing. 48h reading.

Connective tissue nevus, lumbosacral. 30-year-old woman, in whom these changes had been present since earliest childhood. Clinically, in the sacral region, sharply defined, very firm, partly rubbery, slightly raised above the skin level, cobblestone-like arranged, whitish papules and plaques with smooth surface are found. Localization and clinic are characteristic for the diagnosis. Secondary findings are angiofibromas in the face.

Nevus, melanocytic, dysplastic. 1.5 x 0.8 cm in size, differently structured, multicoloured melanocytic nevus, with a blurred brown soft brown papule in the centre, surrounded by a ring-shaped, reddish-brownish plaque.

Lupus erythermatodes tumidus:recurrent disease patternforseveral years. no itching, no other subjective complaints. significant improvement of symptoms after treatment with antimalarials.