Takahashi M, Ishihara T, Yokota T, Uchino F, Yokoyama T, Matsumoto N
Department of Clinical Laboratories, Yamaguchi University School of Medicine, Japan.
Acta Neuropathol. 1990;80(1):98-102. doi: 10.1007/BF00294230.
An unusual cerebral tumor is reported in a 14-year-old boy. On light and electron microscopy, the constituent cells were very complex; the majority of the neoplastic cells were primitive neuroectodermal cells dispersed in myxomatous or fibrous stroma. Neoplastic neuronal cells and hypertrophic astrocytes were also observed in these areas. The neuronal cells showed a continuous spectrum of differentiation from very primitive to mature ganglion cells. Furthermore, the tumor contained a highly cellular discrete area consisting of neuroblasts and their precursor cells. From these findings, a diagnosis of composite ganglioneuroblastoma was made.
报道了一名14岁男孩患有一种罕见的脑肿瘤。在光镜和电镜下,组成细胞非常复杂;大多数肿瘤细胞是散在于黏液瘤样或纤维性基质中的原始神经外胚层细胞。在这些区域还观察到肿瘤性神经元细胞和肥大的星形胶质细胞。神经元细胞呈现出从非常原始到成熟神经节细胞的连续分化谱。此外,肿瘤包含一个由成神经细胞及其前体细胞组成的细胞密集离散区域。根据这些发现,做出了复合性神经节神经母细胞瘤的诊断。