Case-based review: Ependymomas in adults

David Cachia, Derek R. Johnson, Timothy J. Kaufmann, Stephen Lowe, Samuel Andersen, Adriana Olar, Samuel Lewis Cooper, Bruce M. Frankel, Mark R. Gilbert

Research output: Contribution to journalArticle

Abstract

Ependymomas are rare primary central nervous system (CNS) tumors in adults. They occur most commonly in the spinal cord, and have classically been graded histologically into World Health Organization (WHO) grades I, II, or III based on the level of anaplasia. Recent data are showing that genetic heterogeneity occurs within the same histological subgroup and that ependymomas arising from different CNS locations have different molecular signatures. This has renewed interest in developing targeting therapies based on molecular profiles especially given the variable outcomes with radiation and the poor results with cytotoxic agents. In this paper, we present the case of a 46-year-old woman with a classic presentation of spinal cord ependymoma and discuss the current histopathological and molecular classification for ependymomas as well as current guidelines for patient management.

Original languageEnglish (US)
Pages (from-to)142-153
Number of pages12
JournalNeuro-Oncology Practice
Volume5
Issue number3
DOIs
StatePublished - Aug 3 2018

Keywords

  • Adults
  • Chemotherapy
  • Ependymoma
  • Radiation
  • Surgery

ASJC Scopus subject areas

  • Medicine (miscellaneous)

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  • Cite this

    Cachia, D., Johnson, D. R., Kaufmann, T. J., Lowe, S., Andersen, S., Olar, A., Cooper, S. L., Frankel, B. M., & Gilbert, M. R. (2018). Case-based review: Ependymomas in adults. Neuro-Oncology Practice, 5(3), 142-153. https://doi.org/10.1093/nop/npy026