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Updated: Aug 14, 2026

Laparoscopic Common Bile Duct Exploration Followed by Primary Suture Using a Modified Bile Duct Incision
Published on: May 2, 2025
Management of an epidermoid cyst of the intrahepatic ducts
Bill Chiu1, Hector Melin-Aldana, Riccardo A Superina
1Department of Surgery, Children's Memorial Hospital, Chicago, IL 60614, USA.
Insights
This study describes the first case of an epidermoid cyst in the biliary tree of an infant. Surgical intervention and a Roux-en-Y cyst jejunostomy were performed to manage the rare biliary cyst.
Area of Science:
- Hepatobiliary surgery
- Pediatric surgery
- Gastroenterology
Background:
- Epidermoid cysts are rare, typically occurring in the skin or central nervous system.
- Congenital biliary tract abnormalities can present with diverse cystic lesions.
- The occurrence of epidermoid cysts within the biliary tree has not been previously documented.
Observation:
- A neonate presented with a prenatally detected intrahepatic cyst.
- Radioisotope imaging confirmed communication between the cyst and the biliary tree.
- Ultrasound at six months revealed echogenic material within the cyst, suggesting blood or biliary debris.
Findings:
- The cyst was surgically located at the confluence of the hepatic ducts, involving the common hepatic duct.
- Complete cyst resection was performed, preserving the orifices of the left and right hepatic ducts and the common bile duct.
- A Roux-en-Y cyst jejunostomy was established for biliary drainage and future monitoring.
Implications:
- This case establishes the existence of epidermoid cysts in the biliary tree.
- The surgical approach highlights a viable method for managing such rare congenital anomalies.
- The created cyst jejunostomy allows for surveillance of the remnant for potential malignant transformation.
Abstract:
Epidermoid cysts of the biliary tree have not previously been described. A baby boy presented with a prenatally diagnosed echolucent intrahepatic cyst. Postnatal radioisotope study of the liver demonstrated that the cyst communicated with the biliary tree. Follow-up ultrasound at 6 months demonstrated that the cyst was filled with echogenic material consistent with either blood or biliary debris. Due to the potential for obstruction and cholangitis, surgery was planned. The cyst was located at the confluence of the right and left hepatic ducts and involved all of the common hepatic duct. The entire cyst was resected except for the patch containing 3 duct orifices: the opening of both hepatic ducts as well as the orifice leading to the common bile duct. A Roux-en-Y cyst jejunostomy was created to allow drainage of both left and right hepatic ducts. The connection also provided access to the cyst remnant through the common duct for future endoscopic monitoring of potential malignant transformation.
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