Giangaspero F, Cenacchi G, Losi L, Cerasoli S, Bisceglia M, Burger P C
Institute of Anatomic Pathology, Ospedale Bufalini, Cesena, Italy.
Am J Surg Pathol. 1997 Feb;21(2):206-12. doi: 10.1097/00000478-199702000-00011.
The clinicopathological features of a series of neuronal and mixed neuronal and astrocytic neoplasms of the CNS are described. Patients were aged 5 to 63 years. Six cases were composed predominantly of small round cells with clear cytoplasm resembling central neurocytoma but lacked the characteristic intraventricular location of that tumor. The remaining five cases had similar neurocytomatous features associated with a benign astrocytic component. Ganglion cells and hyalinization vessels were observed in both groups. The growth fraction evaluated with monoclonal antibody Ki67Mib1 was low, ranging from 1 to 1.5%. Immunohistochemical detection of synaptophysin played a crucial role in identifying the neuronal nature of these neoplasms and was instrumental in distinguishing them from oligodendrogliomas, with which they are readily confused. The neuronal nature of the oligodendroglial-like cells was confirmed ultrastructurally in one case. The present cases, together with others reported previously, suggest that neoplasms of the CNS with "neurocytic" components are more frequent than generally assumed and expand the morphologic spectrum of neuronal and mixed neuronal-glial tumors. Except for one patient who died postoperatively, all patients were alive at follow-up ranging from 6 to 80 months.
本文描述了一系列中枢神经系统神经元性肿瘤以及神经元和星形细胞混合性肿瘤的临床病理特征。患者年龄在5岁至63岁之间。6例主要由胞质清亮的小圆形细胞构成,类似于中枢神经细胞瘤,但缺乏该肿瘤特征性的脑室内位置。其余5例具有类似神经细胞瘤的特征,并伴有良性星形细胞成分。两组均可见神经节细胞和玻璃样变血管。用单克隆抗体Ki67Mib1评估的增殖分数较低,范围为1%至1.5%。突触素的免疫组化检测在确定这些肿瘤的神经元性质方面起关键作用,有助于将它们与易与之混淆的少突胶质细胞瘤区分开来。在1例中通过超微结构证实了少突胶质细胞样细胞的神经元性质。目前的这些病例以及先前报道的其他病例表明,具有“神经细胞瘤”成分的中枢神经系统肿瘤比一般认为的更为常见,并扩展了神经元和神经元 - 胶质混合性肿瘤的形态学谱。除1例患者术后死亡外,所有患者在6至80个月的随访期内均存活。