Детская хирургия. Журнал им. Ю.Ф. Исакова. 2020; 24: 363-369
Лапароскопические резекции поджелудочной железы у детей с врождённым гиперинсулинизмом
https://doi.org/10.18821/1560-9510-2020-24-6-363-369Аннотация
Список литературы
1. 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 article
21. 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.
Russian Journal of Pediatric Surgery. 2020; 24: 363-369
Laparoscopic resections of the pancreas in children with hyperinsulinism
https://doi.org/10.18821/1560-9510-2020-24-6-363-369Abstract
References
1. 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. Melikyan M. A., Kareva M. A. Vrozhdennyi giperinsulinizm: Posobie dlya vrachei. M.: Praktika; 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. Melikyan M.A. Vrozhdennyi giperinsulinizm. Problemy endokrinologii. 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. Gubaeva D.N., Melikyan M.A., Ryzhkova D.V., Poida M.D., Bairov V.G., Sukhotskaya A.A., Sokolov Yu.Yu., Efremenkov A.M., Mitrofanova L.B., Christesen H., Nikitina I.L. Klinicheskie, geneticheskie i radionuklidnye kharakteristiki patsientov s fokal'noi formoi vrozhdennogo giperinsulinizma. Problemy endokrinologii. 2019. 65 (5); S. 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 article
21. 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. Sukhotskaya A.A., Bairov V.G., Nikitina I.L., Ryzhkova D.V., Mitrofanova L.B., Amidkhonova S.A. Khirurgicheskoe lechenie vrozhdennogo giperinsulinizma: predvaritel'nyi analiz. Detskaya khirurgiya. 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.
