Primary Intracranial Germ-Cell Tumors: A Retrospective Analysis with Special Reference to Long-Term Results of Treatment and the Behavior of Rare Types of Tumors

Authors

  • N. Sakai Department of Neurosurgery, Gifu University, School of Medicine, Gifu, Japan
  • H. Yamada Department of Neurosurgery, Gifu University, School of Medicine, Gifu, Japan
  • T. Andoh Department of Neurosurgery, Gifu University, School of Medicine, Gifu, Japan
  • T. Hirata Department of Neurosurgery, Gifu University, School of Medicine, Gifu, Japan
  • K. Shimizu Department of Neurosurgery, Gifu University, School of Medicine, Gifu, Japan
  • J. Shinoda Department of Neurosurgery, Gifu University, School of Medicine, Gifu, Japan

DOI:

https://doi.org/10.3109/02841868809090317

Keywords:

Brain neoplasms, germ-cell tumor, germinom, teratoma, radiotherapy, extracranial metastasis

Abstract

Thirty cases of primary intracranial germ-cell tumors were reviewed with reference to the effect of treatment. Histologically, there were 23 pure germinomas, while the remaining tumors had more unusual histology; 3 of these were teratomas, and 4 germ-cell tumors with the admixture of yolk sac tumor (YST) or embryonal carcinoma (EMC). Three of these rare cases are presented. The performed surgery and radiotherapy, seemed adequate for pure germinomas, and all these cases lived tumor-free after an observation time of 13 to 139 months although 4 patients developed intellectual retardation or cerebral dullness after radiotherapy. Four cases with YST and EMC elements, indicated by the elevation of AFP and HCG values in serum, were resistant to radio-and chemotherapy and developed, despite surgically total removal of the tumor, intra-or extracranial metastases. A review of the literature is included.

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Published

1988-01-01

How to Cite

Sakai, N. ., Yamada, H. ., Andoh, T. ., Hirata, T., Shimizu, K. ., & Shinoda, J. . (1988). Primary Intracranial Germ-Cell Tumors: A Retrospective Analysis with Special Reference to Long-Term Results of Treatment and the Behavior of Rare Types of Tumors. Acta Oncologica, 27(1), 43–50. https://doi.org/10.3109/02841868809090317