Two cases of immunoglobulin G4 (IgG4)-related hypophysitis diagnosed without pituitary biopsy

Background: Immunoglobulin G4-related hypophysitis (IgG4-RH) is a rare disease, diagnosis of which typically depends on histopathology following an invasive pituitary biopsy, possibly leading to permanent hypopituitarism. Herein, we report two cases of IgG4-RH with favorable responses to glucocortic...

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Bibliographic Details
Main Authors: Wanlu Ma, Xi Wang, Min Nie, Junling Fu, Jiangfeng Mao, Xueyan Wu
Format: Article
Language:English
Published: SAGE Publishing 2020-06-01
Series:Therapeutic Advances in Endocrinology and Metabolism
Online Access:https://doi.org/10.1177/2042018820924556