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Laparoscopic Surgery for Focal-Form Congenital Hyperinsulinism Located in Pancreatic Head

Overview
Journal Front Pediatr
Specialty Pediatrics
Date 2022 Aug 5
PMID 35928676
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Abstract

Background And Aims: Congenital hyperinsulinism of infancy (CHI) is a rare condition that may cause irreversible severe neurological damage in infants. For children in whom medical management fails, partial or near-total pancreatectomy is then required according to the type of lesion. Currently, open surgery of near-total pancreatic head resection is a mature technique for the treatment of focal-form CHI located in the head of the pancreas, but a minimally invasive laparoscopic procedure has not been reported yet. The aim of this study was to verify the feasibility, safety, and efficacy of laparoscopic pancreatic head resection and Roux-en-Y pancreaticojejunostomy for focal-form CHI.

Methods: Two infants with persistent hypoglycemia and increased insulin levels were diagnosed with CHI and underwent laparoscopic near-total pancreatic head resection due to a suboptimal response to medical therapy and the likelihood of focal disease amenable to surgery. Clinical records, operative findings, and postoperative follow-up were collected and analyzed.

Results: The operative duration was 300-330 min, and the intraoperative blood loss was minimal. The duration of postoperative abdominal drainage was 4-5 days. Neither intra- nor postoperative abdominal complications occurred. Oral feeding was resumed 3-4 days after the operation, and the blood glucose level was gradually stabilized to within the normal range. Normal blood glucose was observed in both patients over a follow-up period of 3-6 months.

Conclusions: Laparoscopic pancreatic head resection and Roux-en-Y pancreaticojejunostomy can be considered a safe and effective procedure with minimal morbidity and excellent outcomes for the treatment of focal CHI in the head of the pancreas.

References
1.
Lovvorn 3rd H, Nance M, Ferry Jr R, STOLTE L, Baker L, ONEILL Jr J . Congenital hyperinsulinism and the surgeon: lessons learned over 35 years. J Pediatr Surg. 1999; 34(5):786-92; discussion 792-3. DOI: 10.1016/s0022-3468(99)90374-3. View

2.
McAndrew H, Smith V, Spitz L . Surgical complications of pancreatectomy for persistent hyperinsulinaemic hypoglycaemia of infancy. J Pediatr Surg. 2003; 38(1):13-6; discussion 13-6. DOI: 10.1053/jpsu.2003.50001. View

3.
Palladino A, Stanley C . A specialized team approach to diagnosis and medical versus surgical treatment of infants with congenital hyperinsulinism. Semin Pediatr Surg. 2010; 20(1):32-7. DOI: 10.1053/j.sempedsurg.2010.10.008. View

4.
Zani A, Nah S, Ron O, Totonelli G, Ismail D, Smith V . The predictive value of preoperative fluorine-18-L-3,4-dihydroxyphenylalanine positron emission tomography-computed tomography scans in children with congenital hyperinsulinism of infancy. J Pediatr Surg. 2011; 46(1):204-8. DOI: 10.1016/j.jpedsurg.2010.09.093. View

5.
Al-Shanafey S, Habib Z, Alnassar S . Laparoscopic pancreatectomy for persistent hyperinsulinemic hypoglycemia of infancy. J Pediatr Surg. 2009; 44(1):134-8. DOI: 10.1016/j.jpedsurg.2008.10.120. View