Image diagnoses for "Torso"
551 results with 2173 images

Graft-versus-Host Disease, chronic: 1.5 years after stem cell transplantation, large-area scleroderma with significant movement restriction, significant reduction of the AZ

Bilateral naevus verrucosus in an infant. No symptoms. Psoriasiform aspect of the plaques running in the Blaschko lines, scattered, reddish, slightly infiltrated, scaly.

Eczema, photoallergic. 78-year-old female patient. Taking diuretics because of lymphedema. After first exposure to sunlight in spring, blurred erythema, reddened papules as well as flat, scaly plaques (sternal area) appeared in light-exposed areas.

Type I neurofibromatosis, peripheral type: detailed picture of generalized clinical picture; circumscribed soft protuberant neurofibroma of the sole of the foot.

Primary cutaneous marginal zone lymphoma: livid to erythematous plaques in a 64-year-old female patient, which appeared for the first time 12 monthsago . Clearly indurated efflorescences on otherwise apparently free skin. No scratch excoriations, no scaling, no pruritus.

artefacts. numerous, partly excoriated papules in the sense of scratch artefacts on the breasts of a 34-year-old woman. the patient denies the artefact component. rapid healing under bandages (diagnostically almost proving an artificial mechanism)

Pemphigus chronicus benignus familiaris: multiple, chronically dynamic (changing course), little itchy, sharply defined, red, rough, scaly, also erosive plaques

Syphilide, papular. multiple, acute, still increasing, generalized (trunk, extremities, palms, soles of feet affected), predominantly isolated, 0.1-0.3 cm in size, confluent in places (chest region), red or reddish-brownish, rough, slightly scaly papules or plaques. There is also fatigue, generalized, non-painful lymphadenopathy and positive syphilis serology. Typically, infestation of palms and soles of feet occurs.

Type I Neurofibromatosis (peripheral type): Numerous soft papules and nodules; multiple smaller and larger café-au-lait spots.

Café-au-lait stains: in neurofibromatosis type I. 2 medium brown homogeneously coloured light brown rounded spots.

Lupus erythematosus chronicus discoides: chronic cutaneous lupus erythematosus that has been present for several years, progressive, disseminated, scarring, chronic cutaneous lupus erythematosus, no evidence of systemic involvement (no ANA, no DNA antibodies).

Molluscum contagiosum: multiple Mollusca contagiosa, here grouped, indicated linearly arranged, detailed view.

Naevus Spitz: a slightly raised, sharply defined, irregularly pigmented tumour that has existed for several months.

Circumscripts of scleroderma (plaque-type). 24 months ago, a progressive, 26 x 21 cm large, flat, partially white-porcelain-like indurated area appeared for the first time in a 21-year-old patient. Additional findings were extensive brownish hyperpigmentation as well as multiple, partly very dark pigmented nevi in a trunk accentuated distribution.

Lyme borreliosis: erythema chronicum migrans, which has been present for several weeks and continues to grow

Tyrosine kinase inhibitors: UAW: acne-like, follicular, pustular exanthema

Pityriasis lichenoides chronica