Oligodendroglioma showing pleomorphic xanthoastrocytoma-like perivascular microlesion: With IDH1, TERT promoter mutation and 1p/19q codeletion detected in both components

Pathol Int. 2020 Jan;70(1):40-46. doi: 10.1111/pin.12880. Epub 2019 Dec 19.

Abstract

We report a histological and genetic study of concurrent oligodendroglioma and a microscopic pleomorphic xanthoastrocytoma (PXA)-like lesion in a 48-year-old male. He presented with generalized seizure, and magnetic resonance imaging revealed a nonenhanced left frontal lobe mass suggesting low-grade glioma. The patient underwent craniotomy and tumor resection. Histopathological examination of the surgical specimen showed an oligodendroglioma with a PXA-like element; the latter measured 0.9 mm and occupied a Virchow-Robin space of the superficial cortex. The whole tumor had no elevated mitotic activity, microvascular proliferation or necrosis. Each component was immunohistochemically isocitrate dehydrogenase (IDH1)-R132H positive, p53 negative and ATRX positive. Genetic analyses clarified identical IDH1 G395A mutation, promoter C228T mutation and 1p/19q codeletion in both elements. Careful integration of histology and telomerase reverse transcriptase (TERT) molecular parameters revealed that this case was an oligodendroglioma showing PXA-like features, rather than a collision tumor. This case provides further insights into the gliomagenesis.

Keywords: 1p/19q-codeletion; IDH; oligodendroglioma; pleomorphic xanthoastrocytoma.

Publication types

  • Case Reports

MeSH terms

  • Astrocytoma / pathology
  • Brain Neoplasms / diagnosis
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / pathology*
  • Gene Deletion
  • Humans
  • Isocitrate Dehydrogenase / genetics
  • Male
  • Middle Aged
  • Mutation
  • Oligodendroglioma / diagnosis
  • Oligodendroglioma / genetics*
  • Oligodendroglioma / pathology*
  • Promoter Regions, Genetic / genetics
  • Telomerase / genetics

Substances

  • Isocitrate Dehydrogenase
  • IDH1 protein, human
  • TERT protein, human
  • Telomerase