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Pineal germ cell tumors: Two cases with review of histopathologies and biomarkers. | LitMetric

Pineal germ cell tumors: Two cases with review of histopathologies and biomarkers.

J Clin Neurosci

Department of Neurosurgery, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States; Department of Radiation Oncology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States; Department of Head and Neck Surgery, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States; Jonsson Comprehensive Cancer Center, University of California, Los Angeles, Los Angeles, CA, United States. Electronic address:

Published: April 2017

AI Article Synopsis

  • * These tumors likely arise from the misplacement of totipotent stem cells during early development, primarily growing along the pineal-suprasellar axis in the brain, leading to varied symptoms based on their location.
  • * The study reviews two specific cases of pineal GCTs and discusses the significance of histopathologies and biomarkers in their management and outcomes.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8908809PMC
http://dx.doi.org/10.1016/j.jocn.2016.12.024DOI Listing

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