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A Case of Idiopathic Granulomatous Hypophysitis

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 suprasel...

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Autores principales: Chung, Chul Ho, Song, Min Soo, Cho, Hyun Deuk, Jeong, Du Shin, Kim, Yeo Joo, Bae, Hack Gun, Kim, Sang Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443729/
https://www.ncbi.nlm.nih.gov/pubmed/23019401
http://dx.doi.org/10.3904/kjim.2012.27.3.346
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author Chung, Chul Ho
Song, Min Soo
Cho, Hyun Deuk
Jeong, Du Shin
Kim, Yeo Joo
Bae, Hack Gun
Kim, Sang Jin
author_facet Chung, Chul Ho
Song, Min Soo
Cho, Hyun Deuk
Jeong, Du Shin
Kim, Yeo Joo
Bae, Hack Gun
Kim, Sang Jin
author_sort Chung, Chul Ho
collection PubMed
description 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.
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spelling pubmed-34437292012-09-27 A Case of Idiopathic Granulomatous Hypophysitis Chung, Chul Ho Song, Min Soo Cho, Hyun Deuk Jeong, Du Shin Kim, Yeo Joo Bae, Hack Gun Kim, Sang Jin Korean J Intern Med Case Report 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. The Korean Association of Internal Medicine 2012-09 2012-09-01 /pmc/articles/PMC3443729/ /pubmed/23019401 http://dx.doi.org/10.3904/kjim.2012.27.3.346 Text en Copyright © 2012 The Korean Association of Internal Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Chung, Chul Ho
Song, Min Soo
Cho, Hyun Deuk
Jeong, Du Shin
Kim, Yeo Joo
Bae, Hack Gun
Kim, Sang Jin
A Case of Idiopathic Granulomatous Hypophysitis
title A Case of Idiopathic Granulomatous Hypophysitis
title_full A Case of Idiopathic Granulomatous Hypophysitis
title_fullStr A Case of Idiopathic Granulomatous Hypophysitis
title_full_unstemmed A Case of Idiopathic Granulomatous Hypophysitis
title_short A Case of Idiopathic Granulomatous Hypophysitis
title_sort case of idiopathic granulomatous hypophysitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443729/
https://www.ncbi.nlm.nih.gov/pubmed/23019401
http://dx.doi.org/10.3904/kjim.2012.27.3.346
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