Central Diabetes Insipidus Due to IgG4-related Hypophysitis That Required over One Year to Reach the Final Diagnosis Due to Symptoms Being Masked by Sialadenitis-Reference-Cited by-同舟云学术

Central Diabetes Insipidus Due to IgG4-related Hypophysitis That Required over One Year to Reach the Final Diagnosis Due to Symptoms Being Masked by Sialadenitis

Published:2022-12-01 Issue:23 Volume:61 Page:3541-3545
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Iwamoto Yuichiro¹,Mori Shigehito¹,Tatsumi Fuminori¹,Sugisaki Toshitomo¹,Dan Kazunori¹,Katakura Yukino¹,Kimura Tomohiko¹,Shimoda Masashi¹,Nakanishi Shuhei¹,Mune Tomoatsu¹,Kaneto Hideaki¹

Affiliation:

1. Division of Diabetes, Endocrinology and Metabolism, Kawasaki Medical School, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/61/23/61_9365-22/_pdf

Reference22 articles.

1. 1. Shikuma J, Kan K, Ito R, et al. Critical review of IgG4-related hypophysitis. Pituitary 20: 282-291, 2017.

2. 2. Takagi H, Iwama S, Sugimura Y, et al. Diagnosis and treatment of autoimmune and IgG4-related hypophysitis: clinical guidelines of the Japan Endocrine Society. Endocr J 67: 373-378, 2020.

3. 3. Garrahy A, Moran C, Thompson CL. Diagnosis and management of central diabetes insipidus in adults. Clin Endocrinol (Oxf) 90: 23-30, 2019.

4. 4. Fragoulis GE, Zampeli E, Moutsopoulos HM. IgG4-related sialadenitis and Sjögren's syndrome. Oral Dis 23: 152-156, 2017.

5. 5. Leporati P, Landek-Salgado MA, Lupi I, Chiovato L, Caturegli P. IgG4-related hypophysitis: a new addition to the hypophysitis spectrum. J Clin Endocrinol Metab 96: 1971-1980, 2011.

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