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.