De novo malignant craniopharyngioma: case report and literature review

J Neurooncol. 2011 Jun;103(2):381-6. doi: 10.1007/s11060-010-0382-7. Epub 2010 Sep 3.

Abstract

Malignant or anaplastic craniopharyngioma, first described in 1987 by Akachi and coworkers, is a rare occurring craniopharyngioma characterized by cytologic atypia and poor prognosis. Fifteen cases have been previously reported, two of which have been defined de novo, i.e. not developing from a previously treated benign craniopharyngioma; both these patients died in the early post-operative period. Herein we describe the case of a 66-year-old female who presented with visual disturbance and radiological evidence of a sellar and suprasellar tumor. The patient underwent trans-sphenoidal biopsy followed by pterional craniotomy with partial tumor removal. Histological diagnosis documented a malignant adamantinomatous type craniopharyngioma. The patient received adjuvant radiotherapy with a significant tumor reduction. She remained in good clinical conditions for 10 months; she deteriorated and died, due to tumor progression, 15 months after diagnosis. Malignant craniopharyngioma is a rare primary malignant tumor of the sellar region. This is the first case of de novo malignant craniopharyngioma with significant follow-up.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aged
  • Combined Modality Therapy
  • Craniopharyngioma / pathology*
  • Craniopharyngioma / therapy
  • Fatal Outcome
  • Female
  • Humans
  • Immunohistochemistry
  • Neurosurgical Procedures
  • Pituitary Neoplasms / pathology*
  • Pituitary Neoplasms / therapy
  • Radiotherapy