Diagnosis and treatment of autoimmune and IgG4-related hypophysitis: clinical guidelines of the Japan Endocrine Society.

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 J

journal_title

Endocrine journal

authors

Takagi H,Iwama S,Sugimura Y,Takahashi Y,Oki Y,Akamizu T,Arima H

doi

10.1507/endocrj.EJ19-0569

subject

Has Abstract

pub_date

2020-04-28 00:00:00

pages

373-378

issue

4

eissn

0918-8959

issn

1348-4540

journal_volume

67

pub_type

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