Microvascular density and vascular endothelial growth factor have little correlation with prognosis of craniopharyngioma

Surg Neurol. 2006:66 Suppl 1:S30-4. doi: 10.1016/j.surneu.2006.05.047.

Abstract

Background: Craniopharyngioma is histologically a benign epithelial tumor located in the supersellar cistern that often presents aggressive growth and repeated recurrence. The authors hypothesized that craniopharyngioma recurrence and invasive growth are angiogenesis dependent and evaluated the significance of vascularization in the prognosis of craniopharyngioma by a prospective cohort study.

Methods: The cohorts consisted of 32 patients with AE and 31 patients with SP tumor. The primary and recurrence removal specimens of the cohort patients were gathered. Microvascular density and VEGF protein in the recurrence group and recurrence-free group were detected by the immunohistochemistry avidin-biotin-peroxidase method and analyzed quantitatively through computer-assisted microscopy to evaluate the correlation of MVD and VEGF with prognosis of craniopharyngiomas.

Results: The average follow-up phase was 63.34 months; 14 of 32 patients with AE and 6 of 31 patients with SP had recurrence and underwent operation again. Although MVD and VEGF have significant difference between AE and SP (P=.000, P=.018, respectively), MVD and VEGF have no statistical difference between the recurrence group and recurrence-free group (P>.05).

Conclusions: Microvascular density and VEGF in craniopharyngioma tissue have no correlation with prognosis of the tumor, which may be explained by the minimal blood circulation in the craniopharyngioma. Adamantine epithelioma showed more tendency to recur than SP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Craniopharyngioma / blood supply*
  • Craniopharyngioma / metabolism*
  • Craniopharyngioma / surgery
  • Follow-Up Studies
  • Humans
  • Image Processing, Computer-Assisted
  • Microcirculation
  • Neoplasm Recurrence, Local / etiology*
  • Pituitary Neoplasms / blood supply*
  • Pituitary Neoplasms / metabolism*
  • Pituitary Neoplasms / surgery
  • Risk Factors
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Vascular Endothelial Growth Factor A