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Generation and Quantitative Characterization of Functional and Polarized Biliary Epithelial Cysts
Published on: May 16, 2020
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Biliary Cystadenoma in a Child: A Rare Entity
Sohail Ahmad1,2, Subrat Kumar Sahoo2, Aditya Arvind Manekar2
1Department of General Surgery, Darbhanga Medical College, Darbhanga, Bihar.
Journal of Indian Association of Pediatric Surgeons
|January 4, 2024
Summary
Biliary cystadenoma is a rare liver tumor. This case highlights a hepatic biliary cystadenoma in a 3-year-old girl, emphasizing the need for surgical removal.
Area of Science:
- Hepatobiliary surgery
- Pediatric oncology
- Gastroenterology
Background:
- Biliary cystadenoma is a rare, potentially malignant hepatic cystic lesion.
- It typically affects middle-aged females and is uncommon in children.
Observation:
- A 3-year-old girl presented with a gradually enlarging right upper abdominal mass.
- Imaging revealed a multiloculated and septated cystic lesion in the liver.
Findings:
- The lesion was diagnosed as a hepatic biliary cystadenoma.
- Complete surgical excision with clear margins was achieved.
Implications:
- This case expands the understanding of biliary cystadenoma presentation in pediatric patients.
- Early diagnosis and complete surgical resection are crucial for favorable outcomes in pediatric biliary cystadenoma.
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