V:ari cells:generalized, but only moderately pronounced exanthema with erythema, vesicles, papules, papulopustules on the stem of a 24-year-old female patient.
Mycosis fungoides tumor stage: long term known Mycosis fungoides. recurrent plaques and nodules, which wet and crust on their surface from a certain size and thickness. now first infestation of the conjunctiva.
Primary cutaneous follicular center lymphoma: Condition after treatment of an alopecia areata with DNCB about 20 years ago; for several months now, formation of smooth, painless plaques and nodules, which, according to a biopsy, affected the entire anterior half of the capillitium.
Mycosis fungoides tumor stage: mycosis fungoides has been known for several years. for several months continuous appearance of plaques and nodules on face, trunk and extremities. findings in 2013
Condylomata gigantea. 39-year-old patient has had rapidly growing, perianal, localised, extensive papillomatous, sometimes nodular, superficially fissured vegetation for about 12 months. HPV typing revealed HPV types 6 and 18.
Carcinoma, carcinoma of the lip (spinocellular carcinoma of the lower lip, existing for years) Small basal cell carcinoma of the corresponding upper lip.
Primary cutaneous anaplastic large cell (CD 30+) lymphoma. Painless, slowly progressive skin ulcer (62-year-old, otherwise healthy woman) which has been present for several months and treated as "pyoderma". Conspicuously raised wall of the ulcer and distinct induration of the reddened edges.
Melanoma, malignant, acrolentiginous.Here: amelanotic malignant melanoma: Chronic inpatient tumor in an 80-year-old patient, existing since 2 years, localized at a pressure-exposed site, flat, sharply defined, slightly painful, similar to an ulcer, slightly raised, flat, ulcerated. The diagnosis as primary tumor was made by finding a metastasis. Note: The diagnosis of malignant melanoma in the presented case can only be made histologically. Clinically, at best, a suspected malignant tumor can be made, which must be clarified histologically.
Hemangioma of the infant. 6-month-old girl (premature birth): Swelling of the left lower lid of a 6-month-old girl (premature birth) existing since the 2nd month of life, progressive in size, flat, blue, soft, not painful, encompassing the whole lower lid.
lymphoma, cutaneous T-cell lymphoma, large-cell, CD30-positive. detailed view: multiple, chronically dynamic, increasing, non-displaceable, confluent, hemispherical nodules covering a total area of 6 x 6 cm with hard, central, red part and deep, crater-shaped ulceration in a 64-year-old patient. the ulceration is covered with thick, yellowish coatings. the surrounding area of the ulceration is raised, livid-red and partly erosive weeping.
Dermatofibrosarcoma protuberans. solitary, chronically dynamic, continuously growing for 4-5 years, poorly delimitable to the side and depth, woody solid, smooth, bumpy, red node. the lateral depth extension clearly exceeds the protuberant part (iceberg phenomenon).
Angiodysplasia. 44-year-old female patient. Monoorganic, solitary, vascular malformation with very low tendency of growth for about 3-4 years. Blurred, reddish-livid, soft swelling as a consequence of a vascular proliferation limited to the dysplasia area. Bizarrely configured vascular dilatations in the vicinity of the soft tissue swelling.
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