Image diagnoses for "Torso"
551 results with 2173 images

Chronicdyskeratosis follicularis, also affecting the Rima ani (see detailed picture), intertriginous, whitish and red-brownish sooty, blurred, macerated, superficially rough, clearly increased in consistency, itchy and unpleasantly smelling plaques.

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

Parapsoriasis en plaques large: asymptomatic , moderately sharply defined, disseminated patches and easily eliminated plaques on the trunk and extremities.

Tinea corporis:unusually elongated, non-pretreated, large-area tinea in known HIV infection

urticaria chronic spontaneous: multiple, chronically recurrent, reddish, partly confluent wheals, with peripheral vasoconstriction zone. severe itching. no scaling. note: the single episode lasts a maximum of 8-12 hours (detectable by marking test).

Syphilide, papular. multiple, acute, still increasing, generalized (trunk, extremities, palms of hands, soles of feet affected), predominantly isolated, 0.1-0.3 cm large, confluent in places (chest region), red or reddish-brownish, rough, slightly scaly spots. fatigue, generalized, non-painful lymphadenopathy, positive serology.

Xanthomas, eruptive:0.1-0.3 cm large, yellow-brown, flat raised, superficially smooth and shiny, firm papules in dense seeding in a 54-year-old patient with known hyperlipoproteinaemia type IV.

Acne, steroid acne. Inflammatory follicular papules, no comedones.

Angiomatosis, bacillary. 73-year-old patient with generalized maculopapular exanthema. Generalized lymphadenopathy.

Lentigo maligna: a slow-growing, completely symptom-free spot that has been known for years; histologically, no invasiveness (transition to lentigo maligna melanoma) could be detected even in cut series.

Xanthomas, eruptive: Chronically stationary or chronically active clinical picture with multiple, on trunk and extremities localized, disseminated, 0.1-0.3 cm large, flat raised, on the surface somewhat fielded, symptomless, sharply defined, firm, smooth, yellow-red-brown papules.

Sézary syndrome: severe final febrile developmental stage. universal redness of the skin with extensive skin detachment. generalized lymphadenopathy, leukemic lymphocytic (CD4+) blood count (75-year-old female patient.

Leiomyoma (marginal area): Missing follicular structure in lesional skin (right marked side); left normal skin with encircled follicles.

Lichen planus exanthematicus.

papillomatosis confluens et reticularis. since 2 years increasing discoloration and thickening of the skin of the sternoepigastric area. occasionally slight itching. spotty and extensive, velvety, yellow-brown, hyperpigmented, blurred papules and plaques, which confluent to larger, dirty-brown areas.

Psorisis, plaque type: chronic relapsing-remitting psoriasis with larger, in places confluent plaques, as well as smaller fresh papules and plaques.

Livedo racemosa:idiopathic form without further organ changes.

Piytriasis rubra pilaris: Nappes claires