Image diagnoses for "red"
912 results with 4583 images

Teleangiectasia macularis eruptiva perstans: discrete, moderately itchy, disseminated, 0.2-0.5 cm large, roundish, red or reddish-brown spots interspersed with telangiectasia; urticarial reaction when rubbed vigorously over the spot (Darier's sign).

Keratosis follicularis (pilaris): Inflammatory, follicularly bound horny papules on the lower leg

Calcinosis cutis dystrophica: ulceration with a rock-hard, irregular base and reddened periulcerous surroundings; accumulation e.g. in systemic scleroderma

Erythema multiforme: multiple red plaques with central blistering, the lesions are confluent on the left and right edge of the image.

Psoriasis guttata: de novo occurred, 0.1-2.0 cm large, reddish, rough papules and plaques with fine-lamellar scaling in a 26-year-old woman, preceded by a feverish flu-like infection.

Ear fistula and cyst, congenital findings,congenital, no symptoms so far. The external fistula opening impresses as an unattractive red nodule with central porus.

Primary cutaneous marginal zone lymphoma: localized red (surface smooth) plaque with circulatory margins, known for several months and only moderately consistent, no evidence of systemic involvement.

Dermatomyositis: Flat red plaques on the end phalanges. Hyperkeratotic nail folds

Condylomata gigantea: cauliflower-like, exophytic and locally infiltrating fibroepithelial prollferates in the anal and peerianal region; known HIV infection.

Chronic inpatient psoriasis: typical infestation pattern.

haematoma, nail haematoma. nail alteration after slight crush trauma. striped, red and blue-black spots (splinter hemorrhages). since red and black shades are present at the same time, this finding speaks against a melanotic pigmentation.

Stevens-Johnson syndrome: acute with accompanying fever, occurred extensive, painful erosions of the red of the lips, lip mucosa and tongue in a 17-year-old woman. A few days later multiromic exanthema of the runp and face. The cause was probably the intake of ibuprofen.

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)