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Ectopic gallbladder with congenital biliary dilatation: a pediatric case report
Kanako Omata1, Mariko Yoshida1, Kan Suzuki1
1Department of Pediatric Surgery, Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-8654, Japan.
Surgical Case Reports
|March 29, 2022
Summary
This case report details a rare pediatric ectopic gallbladder found alongside congenital biliary dilatation (CBD). Early recognition of ectopic gallbladder is crucial for accurate diagnosis and management in children.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Medical Imaging
Background:
- Ectopic gallbladder is a rare congenital anomaly that can lead to diagnostic challenges.
- Congenital biliary dilatation (CBD) is a serious condition requiring prompt management.
- This report focuses on a pediatric case involving both ectopic gallbladder and CBD.
Purpose of the Study:
- To report a unique pediatric case of ectopic gallbladder co-occurring with congenital biliary dilatation (CBD).
- To highlight the importance of considering ectopic gallbladder in preoperative imaging assessments.
- To describe the successful surgical management of this rare condition.
Main Methods:
- A 9-year-old girl with elevated liver enzymes was diagnosed with Todani type IV-A CBD.
- Preoperative imaging (ultrasonography, CT, MRI) failed to visualize the gallbladder, suggesting agenesis.
- Laparoscopic excision of the extrahepatic bile duct and hepaticojejunostomy were performed, revealing an ectopic gallbladder during surgery.
Main Results:
- An ectopic gallbladder, initially missed on imaging, was identified during surgery for CBD.
- The patient underwent successful laparoscopic treatment for both conditions.
- Histopathological examination confirmed the ectopic gallbladder diagnosis.
Conclusions:
- This is the first reported pediatric case of ectopic gallbladder concomitant with CBD.
- The case underscores the necessity of suspecting ectopic gallbladder when the gallbladder is not visualized preoperatively.
- Accurate diagnosis and surgical intervention are vital for favorable outcomes in such rare anomalies.

