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Papillary Glioneuronal Tumor with Highly Degenerative Pseudopapillary Structure Accompanied by Specific Abortive Glial Cells : A Case Report Michimasa EBATO 1,3 , Akira TSUNODA 1 , Chikashi MARUKI 1 , Furitsu IKEYA 1 , Motoi OKADA 2 1Department of Neurosurgery, Koshigaya Municipal Hospital 2Department of Pathology, Koshigaya Municipal Hospital Keyword: papillary glioneuronal tumor , mixed neuronal and glioneuronal tumor , GFAP , synaptophysin , S−100 protein pp.1185-1190
Published Date 2003/11/10
DOI https://doi.org/10.11477/mf.1436902461
  • Abstract
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Recently, unusual examples of tumors of the mixed glioneuronal type have been reported, including the papillary glioneuronal tumor (PGNT). A 23-year-old woman with a 2-3 months history of headache and insomnia presented with a tumor. Neuroimaging showed a right temporal lobe cystic tumor with a mural nodule enhanced by contrast medium. She underwent gross total resection of the tumor. The tumor was histologically marked by a mixture of glial and neural components.


Copyright © 2003, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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