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Cerebral gangliocytoma
Authors:Y. Itoh  S. Yagishita  Y. Chiba
Affiliation:(1) Department of Pathology, Kanagawa Rehabilitation Center, 516, Nanasawa, Atsugi-Shi, Kanagawa-Ken, Japan;(2) Department of Neurosurgery, Kanagawa Rehabilitation Center, 516, Nanasawa, Atsugi-Shi, Kanagawa-Ken, Japan
Abstract:
Summary We report a case of cerebral gangliocytoma (GC) with a variety of unusual structures in the tumor cells. Light microscopically, the tumor consisted of typical ganglion cells, atypical cells which has argyrophilic granules in the cytoplasm, and a few astrocytes. Electron microscopically, the tumor cells showed typical gangliocytic features, which had abundant rough endoplasmic reticula, ribosomes and cored vesicles of 90–150 nm diameter, a few 50-nm-diametered non-cored vesicles, and other common organelles in their cytoplasm. Furthermore, neoplastic ganglion cells contained a variety of abnormal structures, including membranous cytoplasmic bodies (MCB), Zebra bodies (ZB), tubular structures, branched tubular structures (BTS), concentrical laminated bodies and curvilinear bodies (CB). The MCB, ZB and CB resembled those in GM2 gangliosidosis (GMG), and the BTS that in infantile neuroaxonal dystrophy (INAD). Although the significance of these inclusions is still unknown, it is considered that some common mechanism might play a role in the metabolism of both neoplastic neuronal cells and degenerating neurons (GMG and INAD). Synapses could not be observed anywhere despite complete neuronal differentiation of many tumor cells.
Keywords:Cerebral gangliocytoma  Parieto-frontal lobe  Intracytoplasmic inclusion bodies  No synapse  Electron microscopy
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