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A case of idiopathic granulomatous hypophysitis

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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.
All Author(s)
C. H. Chung ; M. S. Song ; H. D. Cho ; S. Jeong du ; Y. J. Kim ; H. G. Bae ; S. J. Kim
Issued Date
2012
Type
Article
Keyword
Granulomatous hypophysitisHeadacheHypopituitarism
Publisher
대한내과학회
Korean Association of Internal Medicine
ISSN
1226-3303 ; 2005-6648
Citation Title
The Korean journal of internal medicine
Citation Volume
27
Citation Number
3
Citation Start Page
346
Citation End Page
349
Language(ISO)
eng
DOI
10.3904/kjim.2012.27.3.346
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/3220
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