A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy-Reference-Cited by-同舟云学术

A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy

Published:2017 Issue:4 Volume:26 Page:251-257
ISSN:0918-5739
Container-title:Clinical Pediatric Endocrinology
language:en
Short-container-title:Clin Pediatr Endocrinol

Author:

Wada Keisuke¹,Kobayashi Hironori¹,Moriyama Aisa¹,Haneda Yasuhiro¹,Mushimoto Yuichi¹,Hasegawa Yuki¹,Onigata Kazumichi¹,Kumori Koji²,Ishikawa Noriyoshi³,Maruyama Riruke³,Sogo Tsuyoshi⁴,Murphy Lynne⁵,Taketani Takeshi¹

Affiliation:

1. Department of Pediatrics, School of Medicine, Shimane University, Shimane, Japan

2. Department of Digestive and General Surgery, School of Medicine, Shimane University, Shimane, Japan

3. Department of Pathology, Shimane University Hospital, Shimane, Japan

4. Department of Pediatric Hepatology and Gastroenterology, Saiseikai Yokohama City Tobu Hospital, Kanagawa, Japan

5. Department of Medical English Education, School of Medicine, Shimane University, Shimane, Japan

Publisher

Japanese Society for Pediatric Endocrinology

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

https://www.jstage.jst.go.jp/article/cpe/26/4/26_2017-0014/_pdf

Reference13 articles.

1. 1. Dateki, S. combined pituitary hormone deficiency. In : Yokoya S, Ogata T, Ozono K editors. Pediatric endocrinology 2nd edition revised, Tokyo: SHINDAN TO CHIRYO SHA; 2016. p.225–8 (in Japanese).

2. 2. Ashikari, Y, Ito, K, Sugiura, T, Endo, T, Kato, S, Ishida, A, et al. Distinguishing congenital combined pituitary hormone deficiency from biliary atresia as a cause of cholestasis in infants. J Jpn Pediatr Soc 2014;118: 653–60(in Japanese).

3. 3. Al-Hussaini, A, Almutairi, A, Mursi, A, Alghofely, M, Asery, A. Isolated cortisol deficiency: a rare cause of neonatal cholestasis. Saudi J Gastroenterol 2012;18: 339–41.

4. 4. Mauvais, FX, Gonzales, E, Davit-Spraul, A, Jacquemin, E, Brauner, R. Cholestasis reveals severe cortisol deficiency in neonatal pituitary stalk interruption syndrome. PLoS ONE 2016;11: e0147750.

5. 5. Sheehan, AG, Martin, SR, Stephure, D, Scott, RB. Neonatal cholestasis, hypoglycemia, and congenital hypopituitarism. J Pediatr Gastroenterol Nutr 1992;14: 426–30.

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