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Published on: February 28, 2025
Gallstone pancreatitis in children: atypical presentation and review
Samir Akel1, Mohammad Khalifeh, Madeleine Makhlouf Akel
1Department of Surgery, American University of Beirut Medical Centre, 113-6044/A10, Beirut, Lebanon. sa37@aub.edu.lb
Insights
Gallstone pancreatitis is rare in children but can cause jaundice. Early diagnosis and surgical intervention are crucial for successful treatment and recovery in pediatric patients.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Surgical Gastroenterology
Background:
- Pancreatitis in children is uncommon, with causes including trauma, infection, and anatomical abnormalities.
- Gallstone pancreatitis is a particularly rare condition in infants and young children.
Observation:
- A 17-month-old girl presented with a month of jaundice, conjugated hyperbilirubinemia, acute pancreatitis, and pseudo-hyponatremia due to hyperlipidemia.
- Imaging revealed an obstruction at the Ampulla of Vater without choledochal cysts or pancreatic masses.
Findings:
- The patient underwent urgent decompressive cholecystostomy and intraoperative cholecystography.
- Subsequent cholecystectomy with common bile duct exploration, stone extraction, and sphincterotomy led to an uneventful recovery.
Implications:
- Acute gallstone pancreatitis in pediatric patients can manifest as jaundice or abdominal pain.
- Prompt recognition, accurate diagnosis, and timely surgical management are essential for favorable outcomes in children with gallstone pancreatitis.
Unlabelled:
Pancreatitis in children is less common than in adults and is mostly related to trauma, infection and anatomical anomalies. Gallstone pancreatitis is an even rarer entity in infants and children. We present an unusual case of gallstone pancreatitis in a 17- month-old girl who presented with jaundice of 1 month duration. The laboratory studies showed conjugated hyperbilirubinaemia with associated acute pancreatitis and pseudo-hyponatraemia secondary to the markedly elevated lipid profile. Further evaluations revealed obstruction at the Ampulla of Vater with no evidence of a choledochal cyst and no mass lesion seen in the pancreas. The patient initially underwent urgent decompressive cholecystostomy with intraoperative cholecystography. When the biochemical parameters improved, the patient underwent formal cholecystectomy with common bile duct exploration, extraction of multiple impacted stones in the ampullary region and Fogarty balloon sphincterotomy. The post-operative course was uneventful.
Conclusion:
Acute gallstone pancreatitis in children may present as jaundice or abdominal pain. Recognition, early diagnosis and surgical intervention are the mainstay for a good outcome.
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