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Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults
Published on: February 28, 2025
Periampullary choledochal diverticula are not choledochal cysts
Dana C Moffatt1, Kathryn M Ziegler, Nicholas J Zyromski
1Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA. dmoffatt@sbgh.mb.ca
Gastrointestinal Endoscopy
|March 29, 2011
Summary
Small periampullary choledochal diverticula (PCD) appear to be acquired biliary anomalies, distinct from congenital choledochal cysts (CC). PCD are associated with sphincter of Oddi dysfunction and biliary hypertension, unlike CC.
Area of Science:
- Gastroenterology
- Hepatobiliary Surgery
- Biliary Tract Diseases
Background:
- Choledochal cysts (CC) are rare congenital biliary anomalies linked to malignancy.
- Small periampullary choledochal diverticula (PCD) are a newly identified biliary anomaly.
- PCD are primarily observed during ERCP procedures.
Purpose of the Study:
- To determine if PCD are congenital or acquired.
- Compare clinical presentation, management, and malignancy risk between PCD and CC.
- Differentiate PCD from CC for accurate classification and treatment.
Main Methods:
- Retrospective analysis of a medical center database (1985-2009).
- Compared data of 16 patients with PCD against 118 patients with CC.
- Reviewed ERCP, surgical pathology, billing, and imaging data.
Main Results:
- PCD patients were older, less likely female, and presented without jaundice compared to CC patients.
- PCD showed lower rates of anomalous pancreatobiliary junction and neoplasia, but higher rates of sphincter of Oddi dysfunction.
- PCD managed with ERCP (87%) vs. CC managed with surgery (80%); PCD had fewer long-term complications (6% vs. 40%).
Conclusions:
- PCD are likely acquired biliary anomalies, possibly secondary to biliary hypertension.
- PCD are frequently associated with sphincter of Oddi dysfunction.
- PCD should be distinguished from congenital choledochal cysts.
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