A Case of IgG4-Related Hypophysitis Presented with Hypopituitarism and Diabetes Insipidus
Immunoglobulin (Ig) G4-related systemic syndrome is a recently described entity characterized by elevated serum IgG4 and tissue infiltration of IgG4-positive plasma cells. Pituitary gland can be involved as hypophysitis. We report a case of a 72-year-old man, who presented with general fatigue and w...
Main Authors: | Yumi Harano, Kazufumi Honda, Yurika Akiyama, Lisa Kotajima, Hiroko Arioka |
---|---|
Format: | Article |
Language: | English |
Published: |
SAGE Publishing
2015-01-01
|
Series: | Clinical Medicine Insights: Case Reports |
Online Access: | https://doi.org/10.4137/CCRep.S15352 |
Similar Items
-
A Case of IgG4-Related Hypophysitis Presented with Hypopituitarism and Diabetes Insipidus
by: Yumi Harano, et al.
Published: (2015-03-01) -
IgG4-related hypophysitis presenting as diabetes insipidus with tubulo-interstital nephritis and mediastinal lymphadenopathy
by: Rayna Patel, et al.
Published: (2016-07-01) -
Anterior hypopituitarism secondary to biopsy-proven IgG4-related hypophysitis in a young man
by: H Joshi, et al.
Published: (2019-04-01) -
Ischemic Pituitary Apoplexy, Hypopituitarism and Diabetes Insipidus:
a Triad Unique to Necrotizing Hypophysitis
by: Miroslav Ćaćić, et al.
Published: (2018-01-01) -
IgG4-related hypothalamo-hypophysitis
by: Yuki Urushida, et al.
Published: (2021-09-01)