Apollo Medicine (Jan 2019)

Supratentorial ependymoma: A rare presentation in an adolescent

  • Dilip Rajasekharan,
  • Kanjithanda Subbaiah Bopaiah,
  • Aumir Moin,
  • Jayanth Bannur Nagaraja

DOI
https://doi.org/10.4103/am.am_19_19
Journal volume & issue
Vol. 16, no. 3
pp. 161 – 163

Abstract

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Ependymomas are rare primary glial tumors that arise from ependymal cells found in the central nervous system. While usually intracranial, they rarely arise from the supratentorial parenchyma. They have a variable clinical course and are aggressive in nature. Among the important prognostic factors include tumor location, histology, and extent of resection. Total surgical excision is the rule. Diagnosis is confirmed by histopathology. Suspicion of an ependymoma must, however, be borne in mind while dealing with a supratentorial space-occupying lesion.

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