原位型乳头状汗管囊腺癌
[Abstract]:A case of primary papillary sweating cystadenocarcinoma is reported. Patient male, 64 years old. The lumber plaque increased for 10 years and increased by 1 year. Dermatological examination: waist about 10 cm in diameter, reddish color, moist surface, not smooth, hard touch. Pathological examination of skin lesions: excessive keratinization associated with incomplete keratinization, callus formation, some epidermis sunken to form capsule-like structure, papillae protuberance visible, cystic wall composed of lamellar squamous epithelium, cell arrangement disorder. Some nuclei were deeply stained, pathological mitotic images and plasmacytes were found in the stroma. Immunohistochemical examination showed that carcinoembryonic antigen (CEA), epithelial membrane antigen (EMA), keratin (CK) 7 was localized positive, nuclear proliferation antigen (Ki-67) was about 60% positive, P63 was positive, and liquid protein (GCDFP)-15 of giant cyst disease was negative. Diagnosis: primary papillary sweating cystadenocarcinoma.
【作者单位】: 重庆市中医院皮肤科;
【分类号】:R739.5
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