Morgello S, Petito C K, Mouradian J A
Department of Pathology, New York Hospital-Cornell University Medical Center, NY 10021.
Clin Neuropathol. 1990 Jul-Aug;9(4):205-15.
Primary central nervous system (CNS) lymphomas were studied in fifteen autopsied patients with the acquired immunodeficiency syndrome (AIDS). Using the working formulation for non-Hodgkin's lymphomas, the tumors were classified as large cell (7 patients), mixed large and small cell (6 patients), small cleaved cell (1 patient), and unclassifiable (1 patient). The mixed lymphomas displayed unusual features characterized by a high mitotic rate and the presence of numerous medium-sized cells (5 to 10 mus), not classifiable using the working formulation. Focal T cell and lymphoplasmacytoid B cell infiltrates accompanied lymphoma cells at the periphery of and remote from solid tumor masses in 9 cases. Immunohistochemical analysis of the lymphomas suggested B cell neoplasms. All of these patients had concurrent CNS and systemic cytomegalovirus (CMV) infections. The CNS infections were of both viral (CMV, human immunodeficiency virus (HIV), varicella zoster virus (VZV), progressive multifocal leukoencephalopathy (PML) and non-viral (toxoplasmosis, candidiasis) etiology. In the general AIDS population at our institution, the autopsy incidence of CNS infections and systemic CMV was 63% and 60%, respectively. In contrast, the incidence for both these entities was 0% in otherwise healthy, non-AIDS patients with CNS lymphoma supports the hypothesis that viral infection plays a role in the pathogenesis of CNS lymphoma in the immunocompromised. Polyclonal lymphoplasmacytoid B and T cell infiltrates accompanying lymphoma may produce diagnostic difficulties on surgical biopsy. As these infiltrates were a frequent feature in this study, we caution that their recognition does not argue against the presence of CNS lymphoma.
对15例获得性免疫缺陷综合征(AIDS)患者进行尸检,研究原发性中枢神经系统(CNS)淋巴瘤。根据非霍奇金淋巴瘤的工作分类法,这些肿瘤被分类为大细胞型(7例)、大细胞与小细胞混合型(6例)、小裂细胞型(1例)和无法分类型(1例)。混合型淋巴瘤表现出不寻常的特征,其特点是有丝分裂率高,且存在许多中等大小的细胞(5至10微米),根据工作分类法无法分类。9例患者在实体瘤块周边及远离实体瘤块处,局灶性T细胞和淋巴浆细胞样B细胞浸润伴随淋巴瘤细胞。淋巴瘤的免疫组化分析提示为B细胞肿瘤。所有这些患者均同时患有中枢神经系统和全身性巨细胞病毒(CMV)感染。中枢神经系统感染的病因既有病毒性的(CMV、人类免疫缺陷病毒(HIV)、水痘带状疱疹病毒(VZV)、进行性多灶性白质脑病(PML)),也有非病毒性的(弓形虫病、念珠菌病)。在我们机构的普通AIDS人群中,中枢神经系统感染和全身性CMV的尸检发生率分别为63%和6[X]%。相比之下,在其他方面健康的非AIDS中枢神经系统淋巴瘤患者中,这两种情况的发生率均为0%。这支持了病毒感染在免疫受损患者中枢神经系统淋巴瘤发病机制中起作用的假说。伴随淋巴瘤的多克隆淋巴浆细胞样B细胞和T细胞浸润可能会给手术活检带来诊断困难。由于这些浸润在本研究中是常见特征,我们提醒,识别出这些浸润并不排除中枢神经系统淋巴瘤的存在。