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Title: Non-functioning well-differentiated neuroendocrine tumor of the extrahepatic bile duct: an unusual suspect? Author: Sethi H, Madanur M, Srinivasan P, Portmann B, Heaton N, Rela M. Journal: Hepatobiliary Pancreat Dis Int; 2007 Oct; 6(5):549-52. PubMed ID: 17897922. Abstract: BACKGROUND: Neuroendocrine tumors (NETs) arising in the biliary tree are extremely rare, and 37 cases were identified in the English literature. METHODS: A well-differentiated NET was found arising from the junction of the cystic and common hepatic ducts, in a 51-year-old male presenting with pedal edema and weight loss with abnormal liver enzymes and a normal serum bilirubin level. No mass was seen on radiological imaging and biopsy of the liver was suggestive of an early cholangiopathy. A bile leak complicating the liver biopsy led to an ERCP that demonstrated a filling defect suggestive of a mass in the common bile duct (CBD). RESULTS: He underwent a successful excision of the tumor with a Roux-en-Y hepaticojejunostomy. The diagnosis of NET was made on histological and immunohistochemical analysis of the resected specimen. He remains well and disease free 22 months after surgery. CONCLUSIONS: Recognition of biliary NET continues to be a challenge and an increased awareness of these tumors in rare sites will result in optimal management of these tumors.[Abstract] [Full Text] [Related] [New Search]