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特发性肉芽肿性垂体炎 1 例报告。

A case of idiopathic granulomatous hypophysitis.

机构信息

Department of Internal Medicine, Soonchunhyang University College of Medicine, Cheonan, Korea.

出版信息

Korean J Intern Med. 2012 Sep;27(3):346-9. doi: 10.3904/kjim.2012.27.3.346. Epub 2012 Sep 1.

DOI:10.3904/kjim.2012.27.3.346
PMID:23019401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3443729/
Abstract

Granulomatous hypophysitis is a rare pituitary condition that commonly presents with enlargement of the pituitary gland. A 31-year-old woman was admitted to the hospital with a severe headache and bitemporal hemianopsia. Magnetic resonance imaging (MRI) showed an 18 × 10-mm sellar mass with suprasellar extension and compression of the optic chiasm. Interestingly, brain MRI had shown no abnormal finding 4 months previously. On hormonal examination, hypopituitarism with mild hyperprolactinemia was noted. The biopsy revealed granulomatous changes with multinucleated giant cells. We herein report this rare case and discuss the relevant literature.

摘要

肉芽肿性垂体炎是一种罕见的垂体疾病,常表现为垂体增大。一名 31 岁女性因剧烈头痛和双颞侧偏盲入院。磁共振成像(MRI)显示 18×10mm 的鞍内肿块伴鞍上扩展,压迫视交叉。有趣的是,4 个月前的脑部 MRI 未见异常。在激素检查中,发现垂体功能减退伴轻度高泌乳素血症。活检显示有多核巨细胞的肉芽肿性改变。我们在此报告这一罕见病例,并讨论相关文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5de/3443729/96950fe9ac49/kjim-27-346-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5de/3443729/8abb9df76232/kjim-27-346-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5de/3443729/806dd669f9c6/kjim-27-346-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5de/3443729/96950fe9ac49/kjim-27-346-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5de/3443729/8abb9df76232/kjim-27-346-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5de/3443729/806dd669f9c6/kjim-27-346-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5de/3443729/96950fe9ac49/kjim-27-346-g003.jpg

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本文引用的文献

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Granulomatous hypophysitis--an interesting and rare cause mimicking pituitary mass.肉芽肿性垂体炎——一种酷似垂体肿块的有趣且罕见的病因。
J Assoc Physicians India. 2007 Sep;55:653-4.
2
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N Z Med J. 2005 Mar 11;118(1211):U1355.
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Autoimmune hypophysitis.自身免疫性垂体炎
Neuroradiol J. 2022 Oct;35(5):545-562. doi: 10.1177/19714009221100983. Epub 2022 May 22.
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Imaging findings in hypophysitis: a review.垂体炎的影像学表现:综述。
Radiol Med. 2020 Mar;125(3):319-328. doi: 10.1007/s11547-019-01120-x. Epub 2019 Dec 20.
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14th EUNOS Congress: PORTO, PORTUGAL, 16-19 JUNE 2019.第14届欧洲神经肿瘤学会大会:葡萄牙波尔图,2019年6月16日至19日。
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Clin Case Rep. 2017 Jun 1;5(7):1147-1151. doi: 10.1002/ccr3.1007. eCollection 2017 Jul.
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Idiopathic Granulomatous Hypophysitis Mimicking Pituitary Abscess.酷似垂体脓肿的特发性肉芽肿性垂体炎
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Idiopathic granulomatous hypophysitis.特发性肉芽肿性垂体炎
Neurosurg Focus. 1996 Jul 15;1(1):e7. doi: 10.3171/foc.1996.1.6.8.
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The spectrum and significance of primary hypophysitis.原发性垂体炎的谱系及意义
J Clin Endocrinol Metab. 2001 Mar;86(3):1048-53. doi: 10.1210/jcem.86.3.7265.
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Idiopathic granulomatous hypophysitis: clinical and imaging features.特发性肉芽肿性垂体炎:临床及影像学特征
Neuroradiology. 1997 Jan;39(1):7-11. doi: 10.1007/s002340050357.
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Lymphocytic and granulomatous hypophysitis: experience with nine cases.淋巴细胞性和肉芽肿性垂体炎:9例经验
Neurosurgery. 1997 Apr;40(4):713-22; discussion 722-3. doi: 10.1097/00006123-199704000-00010.