Pituitary carcinoma: A clinicopathological review


Scheithauer B., Kurtkaya-Yapicier O., Kovacs K., Young W., Lloyd R.

NEUROSURGERY, cilt.56, sa.5, ss.1066-1074, 2005 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 56 Konu: 5
  • Basım Tarihi: 2005
  • Doi Numarası: 10.1227/01.neu.0000157926.72826.db
  • Dergi Adı: NEUROSURGERY
  • Sayfa Sayıları: ss.1066-1074

Özet

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.