Please use this identifier to cite or link to this item: https://doi.org/10.1097/00019509-199810000-00004
DC FieldValue
dc.titleDouble papilla of Vater: A rare anatomic anomaly observed in endoscopic retrograde cholangiopancreatography
dc.contributor.authorRajnakova, A.
dc.contributor.authorTan, W.T.L.
dc.contributor.authorGoh, P.M.Y.
dc.date.accessioned2016-11-08T08:24:40Z
dc.date.available2016-11-08T08:24:40Z
dc.date.issued1998
dc.identifier.citationRajnakova, A., Tan, W.T.L., Goh, P.M.Y. (1998). Double papilla of Vater: A rare anatomic anomaly observed in endoscopic retrograde cholangiopancreatography. Surgical Laparoscopy and Endoscopy 8 (5) : 345-348. ScholarBank@NUS Repository. https://doi.org/10.1097/00019509-199810000-00004
dc.identifier.issn10517200
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/129620
dc.description.abstractA double papilla of Vater, with separate openings for the bile duct and the pancreatic duct, is a rare anatomic anomaly observed in endoscopic retrograde chop angiopancreatography (ERCP). We report the case of a 45- year-old Chinese man with obstructive jaundice due to common bile duct stones and gallbladder stones. During ERCP, a double papilla of Vater with separate drainage for the bile duct and the pancreatic duct was observed. As the anatomy was unusual, no sphincterotomy was performed, but a biliary stent was inserted. Subsequently, the patient underwent cholecystectomy and exploration of the common bile duct. On the 15th postoperative day, he was asymptomatic and was discharged.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1097/00019509-199810000-00004
dc.sourceScopus
dc.subjectCommon bile duct
dc.subjectDouble papilla of Vater
dc.subjectPancreatic duct
dc.typeArticle
dc.contributor.departmentSURGERY
dc.description.doi10.1097/00019509-199810000-00004
dc.description.sourcetitleSurgical Laparoscopy and Endoscopy
dc.description.volume8
dc.description.issue5
dc.description.page345-348
dc.description.codenSLENE
dc.identifier.isiut000076221400004
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