Schild S E, Wharen R E, Menke D M, Folger W N, Colón-Otero G
Department of Radiation Oncology, Mayo Clinic Scottsdale, AZ 85259.
Mayo Clin Proc. 1995 Mar;70(3):256-60. doi: 10.4065/70.3.256.
Non-Hodgkin's lymphomas arising in the spinal cord are extremely rare. Only eight single case reports have been well confirmed in the literature. Herein we describe a 59-year-old woman with symptoms attributable to a spinal cord lesion. Physical examination revealed neurologic deficits but no evidence of tumor elsewhere. Although several imaging studies were performed, only magnetic resonance imaging with use of gadolinium revealed the exact site and extent of the lesion. Laminectomy and direct examination of the spinal cord disclosed a discolored region at the level of the 11th thoracic vertebra. A biopsy specimen was obtained, and pathologic examination revealed an intermediate grade, mixed cell lymphoma of T-cell origin. Radiotherapy was administered to the lesion and adjacent region of the spinal cord with use of 6-MV photons and an anteroposterior-posteroanterior technique; the total dose was 45 Gy in 23 fractions. No chemotherapy was given. After 3 years of follow-up, the neurologic signs and symptoms were stable, and repeated magnetic resonance imaging with use of gadolinium showed no residual tumor. In addition to the case report, we review the literature on primary lymphomas of the central nervous system and discuss treatment recommendations.
脊髓原发性非霍奇金淋巴瘤极为罕见。文献中仅有8例单病例报告得到充分证实。在此,我们描述一名59岁女性,其出现了归因于脊髓病变的症状。体格检查发现神经功能缺损,但未发现其他部位有肿瘤迹象。尽管进行了多项影像学检查,但只有使用钆剂的磁共振成像显示了病变的确切部位和范围。椎板切除术及对脊髓的直接检查发现第11胸椎水平有一变色区域。获取了活检标本,病理检查显示为T细胞来源的中级混合细胞淋巴瘤。使用6兆伏光子及前后-后前技术对病变及脊髓相邻区域进行了放射治疗;总剂量为45 Gy,分23次给予。未进行化疗。经过3年随访,神经体征和症状稳定,再次使用钆剂的磁共振成像显示无残留肿瘤。除了该病例报告外,我们还回顾了中枢神经系统原发性淋巴瘤的文献并讨论了治疗建议。