Mineura K, Sawataishi J, Sasajima T, Kowada M, Sugawara A, Ebina K
Neurosurgical Service, Akita University Hospital, Japan.
J Neurooncol. 1993 Jun;16(3):235-42. doi: 10.1007/BF01057040.
Primary central nervous system (CNS) involvement of non-Hodgkin's lymphoma is uncommon and a vast majority of reported cases are of B-cell origin. We present a 52-year-old woman with primary peripheral T-cell lymphoma of the brain. Immunostaining of paraffin-embedded sections proved tumor cells to be positive for T-cell markers MT1 and UCHL1, and negative for B-cell markers MB1, and 4KB5. Radiotherapy combined with steroid therapy rendered neurologic recovery and complete tumor remission confirmed by computed tomography and magnetic resonance imaging. From a review of documented 19 cases of primary CNS T-cell lymphoma including the present case, this disease is characterized by poor prognosis among CNS lymphomas.
原发性中枢神经系统(CNS)非霍奇金淋巴瘤受累情况并不常见,且绝大多数报告病例起源于B细胞。我们报告一例52岁女性原发性脑外周T细胞淋巴瘤。石蜡包埋切片的免疫染色显示肿瘤细胞T细胞标志物MT1和UCHL1呈阳性,B细胞标志物MB1和4KB5呈阴性。放疗联合类固醇治疗使患者神经功能恢复,计算机断层扫描和磁共振成像证实肿瘤完全缓解。回顾包括本病例在内的19例原发性中枢神经系统T细胞淋巴瘤文献,该病在中枢神经系统淋巴瘤中预后较差。