Image diagnoses for "Torso"
542 results with 2145 images

Mycosis fungoides: tumor stage. 53-year-old man with multiple, disseminated, 1.0-5.0 cm large, in places also large, moderately itchy, clearly consistency increased, red, rough, confluent plaques (nodules)

Pustulose, subcorneal. 6-year-old boy with infantile form of the disease. Craniocaudal erupted pustules after fever attack, disseminated over the whole integument. Whole integument almost completely reddened, flat flat infiltrations of the skin with fine lamellar scaling.

Café-au-lait spots: in discrete neurofibromatosis type I. Several medium brown spots in the area of the lower and middle abdomen.

Angioimmunoblastic T-cell lymphoma: Dress syndrome in AIP.  Figure taken from: Mangana Jet al. (2017)

Erythema anulare centrifugum: characteristic (fresh) lesions with peripherally progressive plaques, which are peripherally palpable as well limited (like a wet wolfaden) Histological clarification necessary.

Xanthoma disseminatum: Overview with disseminated, symmetrically distributed asymptomatic papules.

Erythrokeratodermia progressiva symmetrica. close-up: Dirty-brown hyperkeratosis in the area of the trunk.

Boils: painful, highly inflammatory, putrid, centrally fluctuating lump.

Kaposi sarcoma HIV-associated: flat, symptomless plaques; HIV infection known for several years.

Haematoma: not quite fresh haematoma of the shoulder region after a fall; blurred boundaries of the discoloration.

Parapsorisis en petites plaques: completely symptom-free red (hardly palpable), slightly scaly plaques; recurrent course for years; improvement in the summer months or under UV therapy.

lupus erythematosus acute-cutaneous: clinical picture known for several years, occurring within 14 days, at the time of admission still with intermittent course. anular pattern. in the current intermittent phase fatigue and exhaustion. ANA 1:160; anti-Ro/SSA antibodies positive. DIF: LE - typical.

psoriasis guttata. small, exanthematic form of psoriasis after streptococcal infection. only slight scaling (due to pre-treatment). note the indicated linear patterns (koebner phenomenon). the auspitz phenomenon (finest punctiform bleeding after removal of the uppermost scaly layer with a wooden spatula) can still be triggered even in these pre-treated lesions and is therefore an excellent diagnostic sign (best triggered in the small papules).

Folliculitis superficial: slightly painful follicular (staphylogenic) pyoderma with yellowish central necrosis and severe perifollicular erythema.

Teleangiectasia macularis eruptiva perstans. 54-year-old patient with a generalized macular clinical picture which has existed for years and shows a constant progression. Itching in case of heat exposure and mechanical exposure of the affected areas.

Malformations vascular: Blue-rubber-bleb syndrome with deeply cutaneous/subcutaneously situated, surprisingly firm nodules.

Dermatitis, seborrhoeic: 62-year-old patient with a negative family history of psoriasis. recurrent HV on the trunk for years. no itching. multiple, chronically inpatient, figured, borderline, sometimes itchy, moderately scaly, clearly borderline hardly elevated plaques.

Morphea type or plaque type of circumscribed scleroderma: slightly idurated irregularly bordered white plaque with a parchment-like, scale-free surface; discreet, light red rimythema.