Pituitary carcinoma: a clinicopathological review

Neurosurgery. 2005 May;56(5):1066-74; discussion 1066-74.

Abstract

Pituitary carcinomas are rare tumors; less than 100 well-documented cases have been reported to date. Such tumors are aggressive and associated with a high mortality rate. The molecular events leading to the development of pituitary carcinomas are largely unknown. Recent studies have only begun to shed light on the probable mechanisms of tumor initiation and progression. A review of the clinicopathological and molecular genetic characteristics of pituitary carcinomas is presented.

Publication types

  • Review

MeSH terms

  • Adenoma / diagnosis
  • Adenoma / surgery
  • Carcinoma / diagnosis
  • Carcinoma / surgery
  • Diagnosis, Differential
  • Humans
  • Pituitary Neoplasms / diagnosis
  • Pituitary Neoplasms / pathology
  • Pituitary Neoplasms / surgery*