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Journal article

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

Abstract:

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 disease, previous descriptions have been limited to single case reports or small series. In the present study, a systematic review of the literature was performed for cases of IGH. 82 cases met inclusion criteria. D...

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Publication status:
Published
Peer review status:
Peer reviewed
Version:
Publisher's version

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Publisher copy:
10.1007/s11102-013-0510-4

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Institution:
University of Oxford
Department:
Oxford, MSD, Physiology Anatomy and Genetics
Role:
Author
Publisher:
Springer US Publisher's website
Journal:
Pituitary Journal website
Volume:
17
Issue:
4
Pages:
357-365
Publication date:
2014-08-05
DOI:
EISSN:
1573-7403
ISSN:
1386-341X
URN:
uuid:65741e97-075e-4c74-aad8-c80b5b0ee3a4
Source identifiers:
438774
Local pid:
pubs:438774

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