A case of diffuse congenital hyperinsulinism in which continuous glucose monitoring contributed to the choice of a treatment strategy following a subtotal pancreatectomy-Reference-Cited by-同舟云学术

A case of diffuse congenital hyperinsulinism in which continuous glucose monitoring contributed to the choice of a treatment strategy following a subtotal pancreatectomy

Published:2024 Issue:3 Volume:33 Page:174-180
ISSN:0918-5739
Container-title:Clinical Pediatric Endocrinology
language:en
Short-container-title:Clin Pediatr Endocrinol

Author:

Zukeran Hiroaki¹,Akiba Kazuhisa¹²,Higuchi Shinji³,Mori Jun³,Yorifuji Tohru⁴,Hasegawa Yukihiro¹⁵

Affiliation:

1. Division of Endocrinology and Metabolism, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan

2. Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan

3. Division of Pediatric Endocrinology and Metabolism, Children’s Medical Center, Osaka City General Hospital, Osaka, Japan

4. 2nd Department of Internal Medicine, Date Red Cross Hospital, Hokkaido, Japan

5. Department of Pediatrics, Tama-Hokubu Medical Center, Tokyo, Japan

Publisher

Japanese Society for Pediatric Endocrinology

Link

https://www.jstage.jst.go.jp/article/cpe/33/3/33_2023-0086/_pdf

Reference16 articles.

1. 1. Banerjee, I, Salomon-Estebanez, M, Shah, P, Nicholson, J, Cosgrove, KE, Dunne, MJ. Therapies and outcomes of congenital hyperinsulinism-induced hypoglycaemia. Diabet Med 2019;36: 9–21.

2. 2. Yorifuji, T, Horikawa, R, Hasegawa, T, Adachi, M, Soneda, S, Minagawa, M, et al. (on behalf of The Japanese Society for Pediatric Endocrinology and The Japanese Society of Pediatric Surgeons). Clinical practice guidelines for congenital hyperinsulinism. Clin Pediatr Endocrinol 2017;26: 127–52.

3. 3. Snider, KE, Becker, S, Boyajian, L, Shyng, SL, MacMullen, C, Hughes, N, et al. Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. J Clin Endocrinol Metab 2013;98: E355–63.

4. 4. Kapoor, RR, Flanagan, SE, Arya, VB, Shield, JP, Ellard, S, Hussain, K. Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism. Eur J Endocrinol 2013;168: 557–64.

5. 5. de Lonlay, P, Fournet, JC, Rahier, J, Gross-Morand, MS, Poggi-Travert, F, Foussier, V, et al. Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy. J Clin Invest 1997;100: 802–7.