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Y-Shaped Vesica Fellea Duplex Gallbladder Causing Acute Biliary Pancreatitis
Eyad Gadour1, Zeinab Hassan2, Abdalla Hassan1
1Gastroenterology and Hepatology, University Hospitals of Morecambe Bay National Health Service Foundation Trust, Lancaster, GBR.
Gallbladder duplication is a rare congenital anomaly. This case highlights diagnostic challenges and the importance of careful imaging for managing associated biliary pancreatitis.
Area of Science:
- Gastroenterology and Hepatology
- Embryology and Developmental Biology
- Diagnostic Imaging
Background:
- Gallbladder duplication is a rare congenital anomaly arising from the splitting of the gallbladder primordium in early embryonic development.
- While often asymptomatic, symptomatic cases can manifest with abdominal complaints, potentially leading to cholecystitis, cholangitis, biliary colic, or pancreatitis.
Observation:
- A case report details a 35-year-old female presenting with acute gallstone pancreatitis.
- Initial radiological diagnosis was challenging, necessitating advanced imaging techniques.
Findings:
- Magnetic resonance cholangiopancreatography (MRCP) and blood tests aided in diagnosis.
- Endoscopic retrograde cholangiopancreatography (ERCP) confirmed the diagnosis of duplex gallbladder and cleared the bile duct.
Implications:
- Duplex gallbladder may be associated with other biliary anomalies, increasing the risk of complications like biliary pancreatitis.
- Accurate diagnosis is critical, as gallbladder duplication can be missed on standard imaging, requiring meticulous surgical planning for cholecystectomy to avoid bile duct and vascular injury.
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