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垂体癌:临床病理综述

Pituitary carcinoma: a clinicopathological review.

作者信息

Scheithauer Bernd W, Kurtkaya-Yapicier Ozlem, Kovacs Kalman T, Young William F, Lloyd Ricardo V

机构信息

Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, Minnesota 55901, USA.

出版信息

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.

摘要

垂体癌是罕见肿瘤;迄今为止,仅有不到100例记录完备的病例被报道。这类肿瘤具有侵袭性,且死亡率很高。导致垂体癌发生的分子事件在很大程度上尚不清楚。最近的研究才刚刚开始揭示肿瘤起始和进展的可能机制。本文对垂体癌的临床病理和分子遗传学特征进行了综述。

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