A rare case of congenital hypoplasia of the right hepatic lobe associated with choledocholithiasis and ectopic gallbladder was reported.
A 68-year-old man, who had bee n diagnosed as having a congenital malformation of the right hepatic lobe with choledocholithiasis and ectopic gallbladder, consulted our department to undergo surgical treatment.
Recent ERC d emonstrated a filling defect at the remnant right hepaic duct, but no stones in the common bile duct.
Percutaneous tran s hepatic cholangioscopic lithotripsy(PTCS-L) was performed preoperatively.
The extracted stone fragments proved to be bilirubin-calcium in nature. Abdominal angiography disclosed the abscence of right portal vein and right hepatic artery, and the lack of parenchymograrn of the right hepatic lobe.
These preoperative diagno s tic imagings supported our diagnosis of a congenital hypoplasia of the right hepatic lobe. Cholecystectomy, choledochotomy, operative cholangioscopy and the resection of a parapapillary duodenal diverticulum were successfully performed. Surgery, also, confirmed the our preopeative diagnosis.
His postoperative course was uneventful, and he discharged on the 22 th postoperative day.
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