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蕈样肉芽肿(MF)侵犯中枢神经系统(CNS),极为少见且诊断、治疗困难.本文报导1例治疗成功.患者男性,58岁.3年前出现皮肤损害,据临床特点和显微镜下有Pautrier氏小脓肿的典型皮肤改变而诊断为MF.无皮肤外损害.局部用氮芥治疗直至6个月前入院时.体检见脸、手、下肢和阴茎部位有较多的散在性斑块,两侧腹股沟淋巴腺肿大,肝脾未触及,神经系统检查正常.血红蛋白13.4克,血小板182,000,白细胞7,100,中性
Mycosis fungoides (MF) invade the central nervous system (CNS), is extremely rare and difficult to diagnose and treat.This article reports the successful treatment of one patient, male, aged 58. Three years ago, skin lesions occurred and, according to clinical features and under the microscope The typical cutaneous changes of Pautrier’s small abscess were diagnosed as MF without external damage and topical treatment with nitrogen mustard until 6 months before admission showed more scattered plaque on the face, hands, lower extremities and penis, On both sides of the inguinal lymph nodes, liver and spleen did not touch, normal nervous system examination. Hemoglobin 13.4 grams, 182,000 platelets, white blood cells 7,100, neutral