Russian Journal of Pediatric SurgeryRussian Journal of Pediatric SurgeryДетская хирургия1560-95102412-0677Eco-Vector410.18821/1560-9510-2020-24-6-363-369ORIGINAL ARTICLESОРИГИНАЛЬНЫЕ СТАТЬИLaparoscopic resections of the pancreas in children with hyperinsulinismЛапароскопические резекции поджелудочной железы у детей с врождённым гиперинсулинизмомSokolovYu. Yu.СоколовЮ. Ю.Russian Federation
Moscow, 125993
125993, г. Москва
MelikyanM. A.МеликянМ. А.Russian Federation
Moscow, 117036
117036, г. Москва
EfremenkovA. M.ЕфременковА. М.Russian Federation
Artem М. Efremenkov, MD, Cand. Sc.(med), chief of department of pediatric surgery in Central Clinical Hospital with Out-patient Unit; assistant at the chair of pediatric surgery in Russian Medical Academy of Continuous Professional Education
Moscow, 125993
Ефременков Артём Михайлович, кандидат мед. наук, заведующий отделением детской хирургии ФГБУ «Центральная клиническая больница с поликлиникой» Управления делами Президента Российской Федерации; ассистент кафедры детской хирургии
Russian Medical Academy of Continuous Professional Education, Doletsky Department of Pediatric SurgeryФГБУ ДПО «Российская медицинская академия непрерывного профессионального образования» Министерства здравоохранения Российской ФедерацииEndocrinology Research CentreФГБУ»Национальный медицинский исследовательский центр эндокринологии» Министерства здравоохранения Российской ФедерацииBashlaeva Children HospitalГБУЗ «Детская городская клиническая больница имени З.А. Башляевой Департамента здравоохранения города Москвы»1812202024636336917022021170220212020https://jps-nmp.ru/jour/article/view/4сongenitalhyperinsulinismlaparoscopypancreatectomychildrenврождённый гиперинсулинизмлапароскопияпанкреатэктомиядети1. Dunne M.J., Kane C., Shepherd R.M., et al. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor. N Engl J Med. 1997; 336(10): 703-6.2. Hussain K., Hindmarsh P., Aynsley-Green A. Neonates with symptomatic hyperinsulinemic hypoglycemia generate inappropriately low serum cortisol counterregulatory hormonal responses. J Clin Endocrinol Metab. 2003; 88 (9): 4342-7.3. Меликян М. А., Карева М. А. Врожденный гиперинсулинизм: Пособие для врачей. М.: Практика; 2015.4. Palladino A.A., Bennett M.J., Stanley C.A. Hyperinsulinism in infancy and childhood: when an insulin level is not always enough. Ann Biol Clin (Paris). 2009; 67: 3: 245-4.5. Kapoor R.R., Flanagan S.E., James C. et al. Hyperinsulinaemic hypoglycaemia. Arch Dis Child. 2009; 94: 450-7.6. Меликян М.А. Врожденный гиперинсулинизм. Проблемы эндокринологии. 2010; 56(6); 41-7.7. Adzick N.S., De Leon D.D., States L.J., Lord K., Bhatti T.R., Becker S.A., Stanley C.A. Surgical treatment of congenital hyperinsulinism: Results from 500 pancreatectomies in neonates and children. J Pediatr Surg. 2019 Jan; 54(1): 27-32.8. Fékété C. N., de Lonlay P., Jaubert F. et al. The surgical management of congenital hyperinsulinemic hypoglycemia in infancy. J Pediatr Surg. 2004; 39: 267-9.9. Sidler M., Shah P., Ashworth M., De Coppi P. Laparoscopic resection of pancreatic neck lesion with Roux-en-Y pancreatico-jejunostomy. 2019; 40: 71–5.10. Laje P., Stanley C.A., Palladino A.A., Becker S.A., Adzick N.S. Pancreatic head resection and Roux-en-Y pancreaticojejunostomy for the treatment of the focal form of congenital hyperinsulinism. J Pediatr Surg. 2012; 47(1): 130-5.11. Redkar R., Karkera P.J., Krishnan J., Hathiramani V. Subtotal pancreatectomy for congenital hyperinsulinism: our experience and review of literature. Indian J Surg. 2013; 77(S3): 778-82.12. Wolfsdorf J.I., Weinstein D.A. Hypoglycemia in Children, Pediatric. 5th Edition. Endocrinology. 2007; 1: 291-327.13. Губаева Д.Н., Меликян М.А., Рыжкова Д.В., Пойда М.Д., Баиров В.Г., Сухоцкая А.А., Соколов Ю.Ю., Ефременков А.М., Митрофанова Л.Б., Christesen H., Никитина И.Л. Клинические, генетические и радионуклидные характеристики пациентов с фокальной формой врожденного гиперинсулинизма. Проблемы эндокринологии. 2019. 65 (5); С. 319-29.14. Galcheva S, Demirbilek H, Al-Khawaga S, Hussain K. The genetic and molecular mechanisms of congenital hyperinsulinism. Front Endocrinol. 2019; 10: 111.15. Thomas P. M., Cote G. J., Wohilk N. et al. Mutations in the sulphonylurea receptor and familial persistent hyperinsulinemic hypoglycemia of infancy. Science. 1995; 268: 426-9.16. Thomas P. M., Yuyang Y., Lightner E. Mutation of the pancreatic islet inward rectifier, Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet. 1996; 5: 1809-12.17. Nestorowicz A., Inagaki N., Gonoi T. et al. A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes. 1997; 46: 1743-8.18. Glaser B., Thornton P. S., Otonkoski T., Junien C. The genetics of neonatal hyperinsulinism. Arch Dis Child. 2000; 82: 79-86.19. Ryan F., Devaney D., Joyce C. et al. Hyperinsulinism: molecular aetiology of focal disease. Arch Dis Child. 1998; 79: 445-7.20. Kapoor R.R., James C., Hussain K. Advances in the diagnosis and management of hyperinsulinemic hypoglycemia. Nat Clin Pract Endocrinol Metab. 2009; 5(2): 101-12. DOI: https://dx.doi.org/10.18821/1560-9510-2020-24-6-363-369 Original article21. Palladino A.A., Bennett M.J., Stanley C.A. Hyperinsulinism in infancy and childhood: when an insulin level is not always enough. Ann Biol Clin (Paris). 2009; 67(3): 245-54.22. Сухоцкая А.А., Баиров В.Г., Никитина И.Л., Рыжкова Д.В., Митрофанова Л.Б., Амидхонова С.А. Хирургическое лечение врожденного гиперинсулинизма: предварительный анализ. Детская хирургия. 2019; 23 (3): 124-7.23. Banerjee I., Salomon-Estebanez M., Shah P., Nicholson J., Cosgrove K.E., Dunne M.J. Therapies and outcomes of congenital hyperinsulinism-induced hypoglycaemia. Diabet Med J Br Diabet Assoc. 2019; 36(1): 9-21.(in Russian)24. Blomberg B.A., Moghbel M.C., Saboury B., Stanley C.A., Alavi A. The value of radiologic interventions and (18)F-DOPA PET in diagnosing and localizing focal congenital hyperinsulinism: Systematic review and meta-analysis. Mol Imaging Biol MIB Off Publ Acad Mol Imaging. 2013;15(1): 97-105.25. Salomon-Estebanez M., Flanagan S.E., Ellard S., et al. Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time. Orphanet J Rare Dis. 2016; 11: 163.26. Snider K.E., Becker S., Boyajian L. et al. Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. J Clin Endocrinol Metab. 2013; 98(2): 355-63.27. Hamilton J.P., Baker L., Kaye R. et al: Subtotal pancreatectomy in the management of severe persistent idiopathic hypoglycemia in children. Pediatrics. 1967; 39: 49-58.28. Barthlen W., Varol E., Empting S. et al. Surgery in focal congenital hyperinsulinism (CHI) - the “hyperinsulinism Germany international” experience in 30 children. Pediatr Endocrinol Rev. 2016; 14(2): 129-37.