Pineal germ cell tumors: Two cases with review of histopathologies and biomarkers
- PMID: 28189312
- PMCID: PMC8908809
- DOI: 10.1016/j.jocn.2016.12.024
Pineal germ cell tumors: Two cases with review of histopathologies and biomarkers
Abstract
Pineal germ cell tumors (GCTs) are primarily seen in pediatric and Asian populations. These tumors are divided into germinomatous and non-germinomatous GCTs (NGGCTs). GCTs are thought to arise by misplacement of totipotent stem cells en route to gonads during embryogenesis. Intracranial GCTs display an affinity to develop along the pineal-suprasellar axis and have variable manifestations dependent upon the location of the tumor. Management and outcomes are driven by histopathologies. In this study, we highlight two cases of pineal GCTs and present a review of the literature with an emphasis on histopathologies and biomarkers.
Keywords: Germ cell tumor; Germinoma; Intracranial neoplasms; Pathology; Yolk sac tumor.
Copyright © 2016. Published by Elsevier Ltd.
Conflict of interest statement
Conflicts of interest/disclosures
None.
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