dyskeratosis follicularis. presentation of multiple, chronically stationary, disseminated, red nbis rfot-brown papules localized in the submammary and upper abdomen. in these areas strong increase of skin changes, especially in summer with increased sweating.
plaque type of circumscribed scleroderma: large, circumcircularly bounded, red-violet, surface smooth plaques with centrally embedded, bizarre whitish indurations. the surface is shiny like parchment. there is a feeling of tension. no pain.
Lyme borreliosis, late stage: symptomless, blurred, morphea-like, painless plaques existing for several months (?). borrelia titer with highly specific bands positive. histo: diffuse, plasma cell-rich superficial and deep dermatitis. PCR: detection of borrelia antigens.
Granuloma anulare disseminatum: non-painful, non-itching, disseminated, large-area plaques that appeared on the trunk and extremities of a 52-year-old patient. No diabetes mellitus. No other systemic diseases known.
Lupus erythematosus, subacute-cutaneous. detail magnification: smaller scarcely scaly papules and larger anular, sharply defined, Collerette-like scaly plaques on the neck and face of a 68-year-old female patient.
Microspore: multicenter, acute, since 4 weeks existing, increasing, initially 0.2-0.3 cm large, later due to size increase and confluence up to 10 cm large, blurred, strongly itchy, red, rough plaques (scaling, crusts); highly contagious special form of Tinea corporis due to microsporum species.
Type I neurofibromatosis, peripheral type or classic cutaneous form. massive tumorous transformation of the skin with numerous generalized distributed, soft, skin-colored, partly pointed conical shaped neurofibromas on the left mamma. the CT examination (skull) did not reveal any pathological findings. no neurofibromas known in the family.
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