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中枢神经细胞瘤:5例临床病理研究及文献复习

Central neurocytoma: clinico-pathological study of 5 cases and review of the literature.

作者信息

Maiuri F, Spaziante R, De Caro M L, Cappabianca P, Giamundo A, Iaconetta G

机构信息

Department of Neurosurgery and Pathology, School of Medicine, University Federico II, Naples, Italy.

出版信息

Clin Neurol Neurosurg. 1995 Aug;97(3):219-28. doi: 10.1016/0303-8467(95)00031-e.

Abstract

Five cases of central neurocytoma, confirmed by immunohistochemical and electron microscopy studies, are reported and 127 cases from the literature are reviewed. Central neurocytomas are more frequent than previously thought, and will be diagnosed with increasing frequency in the future, if intraventricular tumors with histological aspect of oligodendroglioma or ependymoma will be routinely studied by immunohistochemistry and electron microscopy. The occurrence of an intraventricular tumor with a typical MR aspect in a young patient should suggest preoperatively the diagnosis of neurocytoma. The positivity for synaptophysin and neuron specific enolase, the negativity for neurofilament protein and glial fibrillary acid protein, and the finding of elements of neuronal differentiation on electron microscopy, are the main pathological features of these tumors. Complete removal of the tumor mass without radiotherapy is the treatment of choice. The prognosis is usually favorable without recurrence.

摘要

报告了5例经免疫组织化学和电子显微镜研究确诊的中枢神经细胞瘤,并对文献中的127例病例进行了回顾。中枢神经细胞瘤比以前认为的更为常见,如果对具有少突胶质细胞瘤或室管膜瘤组织学特征的脑室内肿瘤常规进行免疫组织化学和电子显微镜检查,未来其诊断频率将会增加。年轻患者出现具有典型磁共振成像表现的脑室内肿瘤,术前应提示神经细胞瘤的诊断。突触素和神经元特异性烯醇化酶阳性、神经丝蛋白和胶质纤维酸性蛋白阴性,以及电子显微镜下发现神经元分化的成分,是这些肿瘤的主要病理特征。不进行放疗而完全切除肿瘤肿块是首选治疗方法。预后通常良好,无复发。

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