Ushida T, Sonobe H, Mizobuchi H, Toda M, Tani T, Yamamoto H
Department of Orthopedic Surgery, Kochi Medical School, Japan.
Childs Nerv Syst. 1998 Dec;14(12):751-5. doi: 10.1007/s003810050310.
The authors present clinical, radiological, and pathological features of the "widespread" type of primary spinal oligodendroglioma arising in a 12-year-old boy. The initial symptoms were gait disturbance, hypesthesia of the lower trunk, and scoliosis. Gadolinium-enhanced magnetic resonance imaging revealed an intramedullary tumor with syringomyelia. The tumor spread rapidly in a "widespread" pattern within the spinal cord between C7 and T12. One year after surgery the patient had made a poor neurological recovery despite the two-stage tumor resection. Only five cases of widespread tumors, including our case, have been described with discussion of their clinical manifestations.
作者介绍了一名12岁男孩发生的“广泛型”原发性脊髓少突胶质细胞瘤的临床、放射学和病理学特征。初始症状为步态障碍、下躯干感觉减退和脊柱侧弯。钆增强磁共振成像显示髓内肿瘤伴脊髓空洞症。肿瘤在C7至T12之间的脊髓内以“广泛”模式迅速扩散。尽管进行了两阶段肿瘤切除,但术后一年患者神经功能恢复不佳。包括我们的病例在内,仅有5例广泛型肿瘤的病例被描述并讨论了其临床表现。