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DOI: 10.1055/s-0042-114428
Endoscopic treatment of a choledochocele
Publication History
Publication Date:
14 September 2016 (online)
Choledochal cysts are bile duct anomalies that range from dilatation of the main bile duct to dilatation of the intrahepatic bile ducts (Caroli disease). The choledochocele is a cystic dilatation of the intraduodenal portion of the bile duct, and is designated type III in the Todani classification [1]; it represents less than 5 % of all choledochal cysts. When the choledochocele is symptomatic, the incidence of carcinoma is estimated to be 2.5 % and this risk increases with age [2]. Treatment by a single endoscopic sphincterotomy does not remove the risk of malignancy.
A 58-year-old woman, with a history of cholecystectomy, presented with acute pancreatitis. The etiological investigation found a choledochocele on magnetic resonance cholangiopancreatography. She was referred to North Hospital for endoscopic resection of the choledochocele.
Endoscopic retrograde cholangiopancreatography (ERCP) showed a 1.0-cm cystic mass to the proximal side of the major papilla, which suggested a type IIIA choledochocele ([Video 1]). In the first step, a 25 × 55 mm snare (Cook Medical, Bloomington, Indiana, USA) was deployed around the choledochocele. The snare was adjusted to capture the cystic dilatation and the major papilla, and then a resection was performed using endocut mode.
Quality:
In the second step, the bile duct was cannulated using a CannulaTome (Cook Medical) in order to place a 10 Fr × 9 cm plastic biliary stent (Cook Medical) following biliary sphincterotomy. The pancreatic duct was then cannulated and a 5 Fr × 3 cm plastic stent (Cook Medical) was placed.
The procedure was performed using carbon dioxide insufflation. The procedure was effective at preventing post-ERCP pancreatitis. The resection was performed without complication. The choledochocele was resected completely, and was 11 mm long in the major axis. Histological analysis confirmed the presence of a cystic lesion, with part duodenal and part biliary epithelia, and no tumor or dysplasia evident
Endoscopy_UCTN_Code_TTT_1AR_2AG
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References
- 1 Todani T, Watanabe Y, Narusue M et al. Congenital bile duct cysts: classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst. Am J Surg 1977; 134: 263-269
- 2 Law R, Topazian M. Diagnosis and treatment of choledochoceles. Clin Gastroenterol Hepatol 2014; 12: 196-203