[Pediatric supratentorial oligodendrogliomas: Marseilles and Lyons experiences]

Neurochirurgie. 2005 Sep;51(3-4 Pt 2):400-9. doi: 10.1016/s0028-3770(05)83499-x.
[Article in French]

Abstract

Background and purpose: The goal of this study was to analyze the main aspects of oligodendrogliomas observed in children.

Method: The records of 35 children aged 15 years or younger (23 from Marseilles and 12 from Lyons) were reviewed. Clinical signs and symptoms, imaging findings (CT scan and pre- and post-operative MRI), extent of surgical resection, histology according to the WHO and Ste-Anne grading and survival were analysed. Considering all these factors, a statistical analyzis was undertaken in order to identify prognostic factors.

Discussion and conclusion: Oligodendrogliomas are rare tumors in children. The most important differential diagnosis to discuss is dysembryoplastic neuroepithelial tumor. Our study allowed us to distinguish several subgroups of patients with a different prognosis: thalamic tumors with a dismal prognosis versus hemispheric tumors. A group of cortical tumors we called "DNT-like" (hemispheric cortical tumor, isolated epilepsy, without neurological deficit and reased ICP, without edema and mass effect on MRI) with an excellent prognosis like the group with epilepsy. Histological grading (grade A/grade B and grade II/grade III) is also a prognostic factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Catchment Area, Health
  • Child
  • Diagnosis, Differential
  • Female
  • France / epidemiology
  • Functional Laterality
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Neoplasms, Neuroepithelial / pathology
  • Oligodendroglioma / diagnosis
  • Oligodendroglioma / mortality
  • Oligodendroglioma / surgery*
  • Postoperative Care
  • Supratentorial Neoplasms / diagnosis
  • Supratentorial Neoplasms / mortality
  • Supratentorial Neoplasms / surgery*
  • Survival Rate
  • Teratoma / pathology
  • Thalamus / pathology
  • Thalamus / surgery