一个病人患有皮肤T细胞淋巴组织瘤[或称淋巴肉芽肿病(Lymphogranulomatosis)也称何杰金氏病(Hodgkin’s Disease)],在采用放疗与化疗联合疗法,获得成功之后两年里、临床上出现了塞沙利氏综合征(Sezary syndrome)。经临床组织学、电子显微镜观察之后、发现此病人为一个典型的塞沙利氏综合征的病例,其恶性细胞(塞沙利氏细胞)已侵犯到周围血液并有渗出,这种细胞很像T细胞。对该病人测定的免疫功能 One patient has cutaneous T-cell lymphoma (also known as Lymphogranulomatosis, also known as Hodgkin’s Disease). Two years after successful radiotherapy and chemotherapy therapies, clinically Sezary syndrome occurred. After clinical histology and electron microscopic observation, the patient was found to be a typical case of Seychelles syndrome. Malignant cells (Sertoli cells) have been infiltrated into peripheral blood and exudate, and the cells are very Like T cells. The patient’s immune function was measured