Image diagnoses for "Torso"
551 results with 2173 images

Rowell's syndrome: acute "multiform" exanthema in subacute cutaneous lupus erythematosus.

Keratosis seborhoeic: A slow-growing, broad-based, brown-black nodule that has been present for years; a lateral view shows the knot's sloppy growth pattern particularly well.

Side effects of vemurafenib: Erythroderma with pronounced keratosis areolae mammae (acquisita) under vemurafenib therapy.

Leprosy (overview): Borderlinelepromatous leprosy (BB), plaques and dome-shaped punch-out lesions.

Pemphigoid gestationis. itchy, since 4 weeks existing exanthema with multiple, generalized, symmetric, truncated, large red plaques with isolated, bulging blisters. picture reminds of an erythema exsudativum multiforme.

Hyperpigmentation, caloric by regular warming at a heating stove. detailed view.

Neurofibroma in Type I Neurofibromatosis: Multiple Neurofibromas

Lymphangioma circumscriptum: Densely aggregated vesicles, usually with haemorrhagic content (so-called haematolymphangioma).

Leiomyoma. Close up of the multiple leiomyomas described above.

Primary cutaneous follicular center lymphoma: chronically active, increasing for 12 months, localized on the trunk and upper extremities, disseminated, 0.3-0.7 cm in size, asymptomatic, hemispherical, firm, smooth, red papules and nodes.

Herpes simplex recidivans: recurrent, in this case very extensive, multilocular herpes simplex infection in an HIV-infected person at intervals of 6-8 months

Comedo (giant comedo): approx. 2.0 cm large, firm knot with a black, keratotic centre about 0.3 cm in size.

Erythrokeratodermia progressiva symmetrica. extensive, sharply defined, brown-yellow discoloured, scaly and hardened plaques existing since the 2nd LJ, which had already appeared on other parts of the trunk, but healed there in the meantime. occasional slight itching.

Lichen planus. overview with pathognomic fine-tissue architecture of the LP. ligamentous (not reaching into the deeper parts of the dermis) lymphocytic infiltrate which is "crowded" closely to the epithelium. moderate, continuous acanthosis and hypergranulosis as well as severe orthohyperkeratosis. in the right section of the picture distinct cleft formation in the area of the dermo-epidermal junction zone.

ecchymosis syndrome, painful, intermittent manifestation of painful skin bleeding in a 48-year-old man. initial development of oedematous, overheated, pressure-sensitive erythema. subsequent development of skin bleeding and slow expansion of the skin changes. scarless healing after 1-2 weeks. in the present case, there was a severely pronounced clinical picture with multiple accompanying symptoms, especially fever, weight loss, fatigue, muscle and headaches, arthralgia, epistaxis, haemoptysis and haematuria.

Dermatitis herpetiformis: chronically recurrent course of the disease. persists for about 3 years. disseminated, burning, partly also stinging urticarial papules, papulo vesicles and erosions.

Mammilla, accessory. 0.6 cm high, solitary, brown plaque, clearly grown during puberty, localized in the so-called embryonic lactiferous ridge, without symptoms, with a central pointed conical papule and a coarse-fielded surface.

Dermatosis, acute febrile neutrophils (Sweet Syndrome): suddenly appearing inflammatory, succulent, livid red papules that have conflued into larger and plaques, combined with fever and feeling of illness.

Nevus, melanocytic, halo-nevus. solitary, depigmented, oval, sharply defined, smooth, white patch with central, sharply defined, brown, slightly raised papule. 27-year-old patient with multiple halo-nevi is shown here.

Syphilis acquisita: maculo-papular exanthema.