Nishio S, Takeshita I, Kaneko Y, Fukui M
Department of Neurosurgery, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Cancer. 1992 Jul 15;70(2):529-37. doi: 10.1002/1097-0142(19920715)70:2<529::aid-cncr2820700225>3.0.co;2-0.
Three cases of patients with unusual neuronal tumors in the cerebral hemisphere are reported. All were associated with long-standing epileptic seizures. Computed tomography disclosed low-density lesions without contrast enhancement, which were interpreted as either arachnoid cysts or a cerebral infarction at initial diagnosis. Magnetic resonance imaging scans, however, revealed the lesions to be solid tumors. At surgery, the tumors were found to be relatively well demarcated, soft, and gelatinous. Histologically, all tumors were composed of small uniform stellate cells, which proliferated in a loose myxoid fibrillary matrix and resembled either oligodendroglial or astrocytic tumors. Ultrastructurally, however, all tumors showed neuronal differentiation, including numerous clear and occasional dense-core vesicles, microtubules, and a number of synapses. A review of the literature uncovered no other such cases, and therefore it was decided to classify these tumors as a distinct group of benign neuronal tumors, designated as "cerebral" neurocytoma compared with "intraventricular" neurocytoma. Related nosologic problems of neuronal tumors of the central nervous system and their possible histogenesis are also discussed.
本文报告了3例大脑半球发生罕见神经元肿瘤的患者。所有患者均伴有长期癫痫发作。计算机断层扫描显示低密度病变,无对比增强,初诊时被解释为蛛网膜囊肿或脑梗死。然而,磁共振成像扫描显示病变为实体瘤。手术中发现肿瘤边界相对清晰,质地柔软,呈胶冻状。组织学上,所有肿瘤均由小而均匀的星状细胞组成,这些细胞在疏松的黏液样纤维基质中增殖,类似少突胶质细胞瘤或星形细胞瘤。然而,超微结构显示所有肿瘤均有神经元分化,包括大量清亮的和偶尔的致密核心小泡、微管以及一些突触。文献回顾未发现其他此类病例,因此决定将这些肿瘤归为一类独特的良性神经元肿瘤,与“脑室内”神经细胞瘤相比,命名为“大脑”神经细胞瘤。本文还讨论了中枢神经系统神经元肿瘤相关的分类学问题及其可能的组织发生。