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Updated: Jul 12, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults
Published on: February 28, 2025
Type I choledochal cysts in adults: natural history and implications for management
Sonal Walia1, Mohammed Saad2, James Butler1
1Department of Surgery, Division of Surgical Oncology, Indiana University School of Medicine, 545 Barnhill Dr, EH 535, Indianapolis, IN, 46202, USA.
Insights
Adults with type I choledochal cysts have a lower risk of cancer than previously thought. However, surgical resection carries significant risks of complications, especially in those diagnosed in childhood but not treated.
Area of Science:
- Gastroenterology and Hepatobiliary Surgery
- Surgical Oncology
- Medical Imaging
Background:
- Pediatric data suggest surgical resection for type I choledochal cysts due to a high risk (up to 60%) of malignant progression.
- Increased use of cross-sectional imaging leads to more frequent observation of isolated extrahepatic biliary tree dilation in adults.
- Current adult management strategies are extrapolated from pediatric data without specific long-term adult studies.
Purpose of the Study:
- To characterize the natural history of type I choledochal cysts specifically in adult patients.
- To evaluate the risk of malignant transformation in adults with type I choledochal cysts.
- To assess the outcomes and complications associated with surgical resection in adults.
Main Methods:
- Retrospective review of an institutional series of adult patients diagnosed with Todani type I choledochal cysts between 1990 and 2023.
- Inclusion criteria based on radiographic diagnosis from endoscopic, radiologic, and surgical databases.
- Analysis of patient demographics, clinical presentation, imaging findings, pathology, and management outcomes.
Main Results:
- 100 adult patients (median age 41 years) were identified; 93 underwent surgery, often with symptoms like biliary colic, pancreatitis, or cholangitis.
- Anomalous pancreaticobiliary ductal junction (APBDJ) was present in 83% of patients.
- The cholangiocarcinoma rate was 6% over a median follow-up of 8 years, primarily in those diagnosed in childhood but not resected; overall morbidity after resection was 50%, with high rates of bile leak (16%) and anastomotic stricture (24%).
Conclusions:
- Adults with type I choledochal cysts have a lower risk of malignant transformation than previously reported, particularly when diagnosed in adulthood.
- Malignant transformation predominantly occurs in cysts diagnosed in childhood but left unresected or bypassed.
- The decision for resection in adults must balance the lower cancer risk against significant short- and long-term surgical complication risks, including biliary fistula, stricture, and pancreatitis.
Background:
Historical pediatric data recommend surgical resection for type I choledochal cysts because of the risk of malignant progression over time (up to 60%). With the widespread use of high-resolution cross-sectional imaging, isolated dilation of the extrahepatic biliary tree has become more frequently observed. The pediatric management strategy for choledochal cysts has been extrapolated to adults, without any specific long-term data. This study aimed to characterize the natural history of choledochal cysts in adults.
Methods:
We have updated our previously published institutional series. From 1990 to 2023, all adult patients with a radiographic diagnosis of Todani type I choledochal cysts were identified from the endoscopic, radiologic, and surgical databases at a single academic institution. Patient demographics, clinical data, imaging studies, pathology, and management outcomes were reviewed.
Results:
A total of 100 patients with a median age of 41 years (range 15-78 years) and male/female ratio of 0.3 were identified. Ninety-three patients underwent surgery, including 83 (89%) with clinical symptoms with or without abnormal serologic liver function test results. Symptoms included biliary colic (62%), pancreatitis (16%), and cholangitis (11%). The median radiographic duct size was 22 mm [range 9-100]. 73% of the patients underwent Endoscopic Retrograde Cholangio-Pancreatography (ERCP) as part of their work-up. An anomalous pancreaticobiliary ductal junction (APBDJ) was identified in 83%, compared to 30% in biliary dilation from other etiology from our historical institutional cohort (p < 0.001). The median time from diagnosis to resection was 7 months (range 0.1-9 years). The cholangiocarcinoma rate was 6% during a median follow-up of 8 years [range 0.5-64yrs]. Five out of 6 (83%) malignant cysts were initially diagnosed during childhood, but were not resected or only bypassed. The overall morbidity after choledochal cyst resection was 50%, with Clavien-Dindo III-IV complications occurring in 40% of the patients. The clinically relevant bile leak rate was 16%, with no predictive features on the multivariate analysis. Bilioenteric anastomotic stricture and symptomatic retained cyst in the intrapancreatic portion of the bile duct requiring reoperation occurred in 24% and 5% of the patients, respectively.
Conclusion:
The largest Western series of type I choledochal cysts in adults confirms a lower risk of malignant transformation than previously described, occurring mostly in cysts diagnosed during childhood but not resected at that time. When diagnosed at an older age, the lower risk of cholangiocarcinoma should be weighed against the high risk of short- and long-term biliary complications associated with resection, including biliary fistula, stricture, and recurrent pancreatitis due to retained cysts within the intrapancreatic bile duct.
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