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垂体自身免疫:30年后

Pituitary autoimmunity: 30 years later.

作者信息

Caturegli Patrizio, Lupi Isabella, Landek-Salgado Melissa, Kimura Hiroaki, Rose Noel R

机构信息

Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States.

出版信息

Autoimmun Rev. 2008 Sep;7(8):631-7. doi: 10.1016/j.autrev.2008.04.016. Epub 2008 May 8.

Abstract

Pituitary autoimmunity encompasses a spectrum of conditions ranging from histologically proven forms of lymphocytic hypophysitis to the presence of pituitary antibodies in apparently healthy subjects. Hypophysitis is a rare but increasingly recognized disorder that typically presents as a mass in the sella turcica. It mimics clinically and radiologically other non-functioning sellar masses, such as the more common pituitary adenoma. Hypophysitis shows a striking temporal association with pregnancy, and it has been recently described during immunotherapies that block CTLA-4. Several candidate pituitary autoantigens have been described in the last decade, although none has proven useful as a diagnostic tool. This review summarizes the advances made in the field since the publication of the first review on pituitary autoimmunity, and the challenges that await clarification.

摘要

垂体自身免疫涵盖一系列病症,从组织学证实的淋巴细胞性垂体炎形式到表面健康的受试者体内存在垂体抗体。垂体炎是一种罕见但越来越被认识到的疾病,通常表现为蝶鞍区的肿块。它在临床和放射学上类似于其他无功能的鞍区肿块,如更常见的垂体腺瘤。垂体炎与妊娠有显著的时间关联,并且最近在阻断CTLA-4的免疫治疗期间也有描述。在过去十年中已经描述了几种候选垂体自身抗原,尽管没有一种被证明可作为诊断工具。本综述总结了自首次发表关于垂体自身免疫的综述以来该领域取得的进展以及有待阐明的挑战。

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本文引用的文献

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