Persistant Hyperinsulinemic Hypoglycaemia Of Infancy And Neonates : Surgical Management And Intermediate Term Outcomes

Authors

  • Nischita Nischita
  • M Bellad
  • Bhagyajyothi
  • B. Khanagavi
  • Dr Santosh
  • B. Kurbet
  • M V. Patil

Abstract

Persistent hyperinsulinemic hypoglycaemia of infancy, also called nesidioblastosis, or congenital hyperinsulinism, is a disease characterized by hyperinsulinemia even with hypoglycaemia, which may result in brain dysfunction as the brain thrives on glucose exclusively. The other causes of this hypoglycaemia are ruled out before aggressive medical treatment. Finally, surgical treatment is advised, where the use of early surgery, which is major, involving near complete removal of the pancreas, is undertaken. Here, we try to address the management with these four cases.

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References

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Thomas CG Jr, Cuenca RE, Azizkhan RG, et al : Changing concepts of islet cell dysplasia in neonatal and infantile hyperinsulinism. World J Surg 1988; 12:598.

Arnoux JB, de Lonlay P, Ribeiro MJ et.al. Congenital hyperinsulinism. Early Hum Dev. 2010 May;86(5):287-94. Epub 2010 Jun 13.

Pierro A, Nah SA. Surgical management of congenital hyperinsulinism of infancy. Semin Pediatr Surg. 2011 Feb;20(1):50-3.

Spitz L, Buick DG, Grant OB.et al : Surgical treatment of nesidioblastosis. Pediatr Surg Int 1986;1.

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Published

2025-08-13

How to Cite

1.
Nischita N, Bellad M, Bhagyajyothi B, Khanagavi B, Santosh D, Kurbet B, Patil MV. Persistant Hyperinsulinemic Hypoglycaemia Of Infancy And Neonates : Surgical Management And Intermediate Term Outcomes. J Neonatal Surg [Internet]. 2025Aug.13 [cited 2025Oct.13];14(32S):7486-8. Available from: https://www.jneonatalsurg.com/index.php/jns/article/view/8639