Abstract:
:Hypophysitis, which is often accompanied by pituitary dysfunction, is classified into several subtypes based on the cause, histology, and the location of inflammation in the pituitary gland. A definitive diagnosis requires pituitary biopsy, which is invasive, and the process is limited to specialized clinical settings. In this opinion paper, we review the literature associated with hypophysitis, and provide the guidelines of the Japan Endocrine Society for the diagnosis and treatment of autoimmune and IgG4-related hypophysitis.
journal_name
Endocr Jjournal_title
Endocrine journalauthors
Takagi H,Iwama S,Sugimura Y,Takahashi Y,Oki Y,Akamizu T,Arima Hdoi
10.1507/endocrj.EJ19-0569subject
Has Abstractpub_date
2020-04-28 00:00:00pages
373-378issue
4eissn
0918-8959issn
1348-4540journal_volume
67pub_type
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