Familial occurrence of polymorphous oligodendroglioma

Neurosurgery. 1994 Apr;34(4):732-6; discussion 736. doi: 10.1227/00006123-199404000-00025.

Abstract

A case of familial polymorphous oligodendroglioma, occurring in a brother and sister, is presented. Polymorphous oligodendrogliomas have a characteristic histopathology consisting of scattered multinucleated giant cells against a typical oligodendroglial background. The oligodendroglial character of the tumors was underlined by positive immunostaining for antigalactocerebroside, anticarbonic anhydrase, and anti-leu-7, without expression of glial fibrillary acidic protein. Both tumors were immunopositive for p53, suggesting a mutation in the p53 gene. No incidence of cancer was recorded in the family. This is the first report of familial occurrence of this particular subtype of oligodendroglioma.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / pathology
  • Brain Neoplasms / surgery
  • Child
  • Fatal Outcome
  • Female
  • Frontal Lobe / pathology
  • Frontal Lobe / surgery
  • Humans
  • Male
  • Microscopy, Electron
  • Neoplastic Syndromes, Hereditary / genetics*
  • Neoplastic Syndromes, Hereditary / pathology
  • Neoplastic Syndromes, Hereditary / surgery
  • Oligodendroglioma / genetics*
  • Oligodendroglioma / pathology
  • Oligodendroglioma / surgery
  • Parietal Lobe / pathology
  • Parietal Lobe / surgery
  • Temporal Lobe / pathology
  • Temporal Lobe / surgery