Granulomatous Hypophysitis

Common Name(s)

Granulomatous Hypophysitis

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Granulomatous Hypophysitis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Granulomatous Hypophysitis" returned 16 free, full-text research articles on human participants. First 3 results:

A case of idiopathic granulomatous hypophysitis.
 

Author(s): Nilufer Ozdemir Kutbay, Mustafa Berker, Figen Soylemezoglu, Hatice Ozisik, Banu Sarer Yurekli

Journal: Hormones (Athens). 2017 Jul;16(3):331-332.

 

Last Updated: 31 Dec 1969

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Granulomatous hypophysitis: a case of severe headache.
 

Author(s): Sharifah Faradila Wan Muhamad Hatta, M Farhan Hamdan, Siti Aishah Md Ali, Rohana Abdul Ghani

Journal:

 

Idiopathic granulomatous hypophysitis (GH) is an uncommon inflammatory disease of the pituitary with impairment of pituitary gland function due to infiltration by lymphocytes, plasma cells and macrophages. We report the case of a 39-year-old woman who presented with worsening of headaches ...

Last Updated: 31 Dec 1969

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Granulomatous hypophysitis - A rare pathology: Review of three cases.
 

Author(s): Biswaranjan Nayak, Ram Kumar Goyal, Rajiv Maharshi, Debabrata Biswal, Prafulla Kumar Sahoo

Journal: Neurol India. ;64(2):343-5.

 

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Granulomatous Hypophysitis" returned 3 free, full-text review articles on human participants. First 3 results:

Idiopathic granulomatous hypophysitis: a systematic review of 82 cases in the literature.
 

Author(s): Benjamin H M Hunn, William G Martin, Steven Simpson, Catriona A Mclean

Journal: Pituitary. 2014 Aug;17(4):357-65.

 

Idiopathic granulomatous hypophysitis (IGH) is a rare inflammatory disease of the pituitary. There is debate in the scientific literature as to whether IGH represents a continuum of disease with lymphocytic hypophysitis or has a distinct pathogenesis. Due to the rare nature of the ...

Last Updated: 31 Dec 1969

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Primary granulomatous hypophysitis: a case report and literature review.
 

Author(s): Shao-bo Su, Da-jian Zhang, Shu-yuan Yue, Jian-ning Zhang

Journal: Endocr. J.. 2011 ;58(6):467-73.

 

Primary granulomatous hypophysitis (PGH) is a rarely occurred inflammatory disease of unknown etiology. We retrospective review a case of PGH treated by microsurgical transsphenoidal approach and review the appropriately documented cases of PGH collected from the literatures. The ...

Last Updated: 31 Dec 1969

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Granulomatous hypophysitis: two case reports and literature review.
 

Author(s): Jian Shi, Jian-Min Zhang, Qun Wu, Gao Chen, Hong Zhang, Wen-Liang Bo

Journal: J Zhejiang Univ Sci B. 2009 Jul;10(7):552-8.

 

Granulomatous hypophysitis (GRH) is extremely rare and commonly presents with chronic inflammatory of the enlarged pituitary gland. In our study, 66-year-old and 57-year-old women, both Chinese, were diagnosed with GRH presenting preoperatively definite imageology characters as pituitary ...

Last Updated: 31 Dec 1969

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Clinical Trial Information This information is provided by ClinicalTrials.gov

There are currently no open clinical trials for this condition.