Itami J, Mori S, Arimizu N, Inoue S, Lee M, Uno K
Jpn J Clin Oncol. 1986 Dec;16(4):407-12.
A case of primary intramedullary spinal cord malignant lymphoma is described. The patient was a 24-year-old female with a preceding history of a lupus-erythematosus-like disorder. The presenting symptom of the spinal cord tumor was spastic paresis of the lower extremities. Radiological examinations including magnetic resonance imaging (MRI) of the spinal cord revealed an intramedullary tumor from levels C2 to T6. A decompressive laminectomy was performed with the pathological diagnosis of poorly differentiated lymphocytic lymphoma with T-cell surface marker. Postoperative cerebrospinal radiation up to 40.5 Gy was performed. The patient is alive without disease 18 months after completion of the therapy. MRI proved to be a very useful method for evaluation of the response to therapy and for follow-up. Primary involvement of the spinal cord with non-Hodgkin's lymphoma is unusual and this is the ninth case of primary intramedullary spinal cord lymphoma reported.
本文描述了一例原发性脊髓恶性淋巴瘤病例。患者为一名24岁女性,既往有类似红斑狼疮样疾病史。脊髓肿瘤的主要症状是下肢痉挛性轻瘫。包括脊髓磁共振成像(MRI)在内的影像学检查显示,C2至T6水平存在髓内肿瘤。进行了减压性椎板切除术,病理诊断为具有T细胞表面标志物的低分化淋巴细胞淋巴瘤。术后进行了高达40.5 Gy的脑脊液放疗。治疗完成18个月后,患者存活且无疾病。MRI被证明是评估治疗反应和随访的非常有用的方法。脊髓原发性非霍奇金淋巴瘤并不常见,这是报道的第九例原发性脊髓髓内淋巴瘤病例。