ArticleCureus2025
Neonatal Choledocholithiasis: A Rare but Challenging Surgical Scenario.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
8 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Choledocholithiasis is a rare diagnosis in neonates, and there are no standard management guidelines for this population. Additionally, endoscopic retrograde cholangiopancreatography (ERCP) is often not an option due to the small size of the common bile duct and non-availability of appropriately sized neonatal endoscopes. We present the cases of two neonates with choledocholithiasis. Both patients underwent open cholecystectomy with common bile duct exploration. The biliary stones were not removable, and therefore both underwent a Roux-en-Y hepaticojejunostomy. Both neonates have done well postoperatively. While hyperbilirubinemia is common in neonates, choledocholithiasis is challenging to diagnose. Diagnosis requires a broad differential and the use of abdominal ultrasound. While ERCP is the gold standard in adults, it is difficult to perform in neonates. Therefore, other treatment modalities involving laparoscopic and open surgery may be necessary. There is a need for improved management guidelines and endoscopic treatment options for neonates with choledocholithiasis.
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