منابع مشابه
A Rare Extrahepatic Biliary Anomaly
In a case operated on for calculous jaundice the right and left hepatic ducts drained directly into the gallbladder and the cystic duct was the only route by which hepatic bile reached the duodenum. Exploration of the inside of the gallbladder was a crucial step for the discovery of the anomaly. Continuity of bile drainage was secured by the preservation of a portion of the gallbladder which co...
متن کاملExtrahepatic biliary cystadenoma: a rare cause of biliary obstruction.
Biliary cystadenoma is a rare tumor of the biliary tree and a rare cause of obstructive jaundice. Most are intrahepatic, and pure extrahepatic biliary cystadenoma is less common. Cases are more common in women. Unless suspected, diagnosis of extrahepatic biliary cystadenoma is often delayed. Here, we report the case of a young woman with extrahepatic biliary cystadenoma who presented at Raja Is...
متن کاملResection of hepaticocystic duct which is a rare anomaly of the extrahepatic biliary system: a case report
INTRODUCTION There are several variations in the morphologic characteristics of the extrahepatic biliary system. A hepaticocystic duct is one of the rare variations. CASE PRESENTATION A 69-year-old Asian man underwent a cholecystectomy for cholelithiasis. His cystic duct was not detected during surgery. An intraoperative cholangiography revealed that his common hepatic ducts drained directly ...
متن کاملCongenital Extrahepatic Biliary Atresia
Case 1. The elder of two sibs, this boy was born on May 21, 1965 to unrelated healthy parents aged 29 (mother) and 30 years (father). Birthweight was 2820 g.; delivery was by forceps. His mother had 'influenza' between the fifth and sixth months of the pregnancy which had been otherwise normal. There was no previous foetal loss. Four generations of the family, comprising, in addition to the par...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: HPB Surgery
سال: 1989
ISSN: 0894-8569
DOI: 10.1155/1989/49560