Magnetic resonance imaging in the diagnosis of idiopathic giant-cell granulomatous hypophysitis: a rare cause of hyperprolactinaemia.

M N Pamir, T A Zirh, M M Ozek, A Sav, C Erzen, T Erbengi
{"title":"Magnetic resonance imaging in the diagnosis of idiopathic giant-cell granulomatous hypophysitis: a rare cause of hyperprolactinaemia.","authors":"M N Pamir,&nbsp;T A Zirh,&nbsp;M M Ozek,&nbsp;A Sav,&nbsp;C Erzen,&nbsp;T Erbengi","doi":"10.1055/s-2008-1052286","DOIUrl":null,"url":null,"abstract":"<p><p>Idiopathic giant cell granulomatous hypophysitis is a rare disorder of pituitary gland characterised by a chronic inflammatory process. It can also be an extremely rare cause of hyperprolactinaemia. In this paper, we present our experience with two cases of idiopathic giant cell granulomatous hypophysitis manifested by hyperprolactinaemia, and their neuroradiological evaluation including preoperative MRI studies in one of them, and discuss our findings in the light of the literature.</p>","PeriodicalId":76208,"journal":{"name":"Neurochirurgia","volume":"36 1","pages":"20-5"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1055/s-2008-1052286","citationCount":"15","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurochirurgia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/s-2008-1052286","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15

Abstract

Idiopathic giant cell granulomatous hypophysitis is a rare disorder of pituitary gland characterised by a chronic inflammatory process. It can also be an extremely rare cause of hyperprolactinaemia. In this paper, we present our experience with two cases of idiopathic giant cell granulomatous hypophysitis manifested by hyperprolactinaemia, and their neuroradiological evaluation including preoperative MRI studies in one of them, and discuss our findings in the light of the literature.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
磁共振成像诊断特发性巨细胞肉芽肿性垂体炎:一种罕见的高泌乳素血症病因。
特发性巨细胞肉芽肿性垂体炎是一种罕见的垂体疾病,其特征是慢性炎症过程。它也可能是高泌乳素血症的一个极其罕见的原因。在本文中,我们介绍了两例以高泌乳素血症为表现的特发性巨细胞肉芽肿性垂体炎的经验,以及他们的神经放射学评估,包括其中一例的术前MRI检查,并结合文献讨论了我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Relative postnatal growth of the basal regions of the cranial fossa]. A trans-orofacial approach for the removal of an extracranial meningioma in the skull base. [Supratentorial glioma: analysis of clinical and temporal parameters in 163 cases]. [Clinical aspects and pathology of intracranial subependymoma--18 personal cases and review of the literature]. Tumors of the nasal cavity occurring after hypophysectomy.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1