Encouraging option of multi-staged gross total resection for a C11orf-RelA fusion-positive supratentorial anaplastic ependymoma

Brain Tumor Pathol. 2017 Oct;34(4):160-164. doi: 10.1007/s10014-017-0297-5. Epub 2017 Aug 22.

Abstract

Ependymomas are primary neuroepithelial malignancies that mainly occur during childhood, and arise from ependymal cells along the ventricular systems of the CNS. Recently, it was elucidated that two-thirds of supratentorial (ST) ependymomas harbor oncogenic fusions of RELA, whose protein product is the principal effector of canonical NF-κB signaling. RELA fusion proteins activate signaling for tumor proliferation and malignant progression, resulting in poorer prognoses in these patients compared to those in patients with other ST ependymomas. In this study, we encountered a case of C11orf-RelA fusion-positive ST anaplastic ependymoma that was diagnosed in first tumor resection surgery of multi-staged gross total resection with molecular evidence. In ependymomas, regardless of tumor location or pathological grade, subtotal resection is associated with higher rates of mortality compared with GTR. Molecular analysis based on the application of recent molecular knowledge for ST ependymomas performs a role in appropriate and individualized treatment strategies.

Keywords: Ependymoma; RelA; Supratentrial.

Publication types

  • Case Reports

MeSH terms

  • Cerebral Ventricles*
  • Child, Preschool
  • Disease Progression
  • Ependymoma / diagnosis*
  • Ependymoma / genetics*
  • Ependymoma / pathology
  • Ependymoma / surgery*
  • Female
  • Gene Fusion / genetics*
  • Humans
  • Molecular Diagnostic Techniques
  • NF-kappa B
  • Neurosurgical Procedures / methods*
  • Proteins / genetics*
  • Signal Transduction / genetics
  • Supratentorial Neoplasms / diagnosis*
  • Supratentorial Neoplasms / genetics*
  • Supratentorial Neoplasms / pathology
  • Supratentorial Neoplasms / surgery*
  • Transcription Factor RelA / genetics*

Substances

  • C11orf95 protein, human
  • NF-kappa B
  • Proteins
  • RELA protein, human
  • Transcription Factor RelA