O'Neill B P, Illig J J
Department of Neurology, Mayo Clinic, Rochester, MN 55905.
Mayo Clin Proc. 1989 Aug;64(8):1005-20. doi: 10.1016/s0025-6196(12)61228-2.
Primary central nervous system lymphomas constitute less than 2% of primary brain tumors. Although their cause is unknown, they are in some way related to immunosuppression. The typical patient is a middle-aged man who displays the syndrome of a subacute mass lesion. These tumors most commonly occur as a single, bulky mass in the hemispheric white matter or the deep gray matter, but multiple tumors occur in approximately a fourth of the patients. The findings on computed tomography are distinctive and nearly pathognomonic. The majority of these tumors are B-cell lymphomas with aggressive histologic changes. Surgical intervention should be reserved for tissue diagnosis because surgical removal does not seem to influence the outcome. Conventional therapy consists of whole-brain irradiation with or without chemotherapy. The prognosis for patients with such tumors is grim, the median duration of survival being less than 2 years with conventional therapy and the 5-year survival being less than 5%.
原发性中枢神经系统淋巴瘤占原发性脑肿瘤的比例不到2%。尽管其病因不明,但在某种程度上与免疫抑制有关。典型患者为中年男性,表现为亚急性肿块病变综合征。这些肿瘤最常表现为半球白质或深部灰质中的单个大肿块,但约四分之一的患者会出现多个肿瘤。计算机断层扫描的表现具有独特性,几乎具有诊断意义。这些肿瘤大多数是具有侵袭性组织学改变的B细胞淋巴瘤。手术干预应仅用于组织诊断,因为手术切除似乎并不影响预后。传统治疗包括全脑放疗,可联合或不联合化疗。此类肿瘤患者的预后很差,采用传统治疗时,中位生存期不到2年,5年生存率不到5%。