Coca S, Moreno M, Martos J A, Rodriguez J, Barcena A, Vaquero J
Department of Pathology and Neurosurgery of Air Forces, University Hospital, Madrid, Spain.
Acta Neuropathol. 1994;87(5):537-40. doi: 10.1007/BF00294182.
We report a case of spinal cord neurocytoma in a 67-year-old man who had experienced a progressive numbness of the left foot during the previous 4 years. Magnetic resonance imaging showed a well-defined intramedullary tumor located at the T10-T11 level. The pathological examination revealed histological characteristics described in neurocytomas. The tumor cells showed a uniform small nucleus and clear or slightly eosinophilic cytoplasm with frequent perinuclear halos, resembling the picture of oligodendroglioma. Some tumor cells exhibited mature ganglion cell appearance. Electron microscopy showed cells with microtubules and dense-core vesicles in their cytoplasm and cytoplasmic process. Immunohistochemically, the majority of tumor cells expressed synaptophysin and neuron-specific enolase. We conclude that this tumor is an exceptional case of neurocytoma located in the spinal cord, and consider that the term neurocytoma can be applied to tumors with neuronal differentiation intermediate between neuroblastoma and ganglioneuroma, even if arising in CNS outside of the intracranial ventricular system.
我们报告一例67岁男性脊髓神经细胞瘤病例,该患者在过去4年中出现左足进行性麻木。磁共振成像显示在T10 - T11水平有一个边界清晰的髓内肿瘤。病理检查揭示了神经细胞瘤所描述的组织学特征。肿瘤细胞显示核小而均匀,胞质透明或略嗜酸性,核周晕常见,类似少突胶质细胞瘤的表现。一些肿瘤细胞呈现成熟神经节细胞外观。电子显微镜显示细胞胞质和胞质突起中有微管和致密核心小泡。免疫组化显示,大多数肿瘤细胞表达突触素和神经元特异性烯醇化酶。我们得出结论,该肿瘤是位于脊髓的神经细胞瘤的一个特殊病例,并认为神经细胞瘤这一术语可应用于神经母细胞瘤和神经节神经瘤之间具有神经元分化的肿瘤,即使其发生于颅内脑室系统以外的中枢神经系统。