Tatter S B, Borges L F, Louis D N
Neurosurgical Service, Massachusetts General Hospital, Boston.
J Neurosurg. 1994 Aug;81(2):288-93. doi: 10.3171/jns.1994.81.2.0288.
Central neurocytoma is a neuronal neoplasm that occurs supratentorially in the lateral or third ventricles. The authors report the clinical, neuroradiological, and neuropathological features of two neurocytomas arising in the spinal cord of two men, aged 65 and 49 years. The patients presented with progressive neurological deficits referable to the cervical spinal cord. Magnetic resonance imaging revealed isodense intramedullary spinal cord tumors at the C3-4 level. Both tumors were initially misdiagnosed as gliomas. In Case 1 the correct diagnosis was made after electron microscopy revealed neuronal features. Immunostaining in Case 2 revealed that tumor cells were positive for synaptophysin and negative for glial fibrillary acidic protein, strongly indicating a neuronal tumor. It is suggested that this spinal cord neoplasm be included under the designation "central neurocytoma."
中枢神经细胞瘤是一种发生于幕上侧脑室或第三脑室的神经元肿瘤。作者报告了两名分别为65岁和49岁男性脊髓中发生的神经细胞瘤的临床、神经放射学和神经病理学特征。患者表现为与颈髓相关的进行性神经功能缺损。磁共振成像显示C3 - 4水平髓内等密度脊髓肿瘤。这两个肿瘤最初均被误诊为胶质瘤。病例1在电子显微镜显示神经元特征后做出了正确诊断。病例2的免疫染色显示肿瘤细胞突触素阳性,胶质纤维酸性蛋白阴性,强烈提示为神经元肿瘤。建议将这种脊髓肿瘤纳入“中枢神经细胞瘤”这一命名范畴。