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Case report: Obstructive jaundice caused by biliary cystadenoma.
Yun-Cheng Li1, An-da Shi1, Kang-Shuai Li1
1Department of General Surgery, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
Frontiers in Oncology
|April 17, 2023
Summary
This case report details a rare intrahepatic biliary cystadenoma presenting as jaundice in a 56-year-old woman. Surgical resection confirmed the diagnosis, highlighting the diagnostic challenges of this uncommon biliary tumor.
Area of Science:
- Hepatobiliary surgery
- Gastroenterology
- Oncology
Background:
- Biliary cystadenoma, also known as mucinous cystic neoplasm with low-grade intraepithelial neoplasia, is a rare cystic tumor originating from the biliary epithelium.
- The etiology of biliary cystadenoma remains unclear, posing diagnostic challenges.
Observation:
- A 56-year-old woman presented with jaundice, poor appetite, and epigastric pain, with elevated total bilirubin and carbohydrate antigen 19-9 (CA19-9).
- Imaging revealed a large intrahepatic cystic lesion with common bile duct dilation and thickening, suggestive of either biliary cystadenoma or malignancy.
Findings:
- Histopathology confirmed a mucinous cystadenoma of the liver and hilar bile duct.
- The tumor presented macroscopically as a polypoid mass extending along the bile duct and a cystic-solid mass in the liver.
Implications:
- This case underscores the importance of considering biliary cystadenoma in the differential diagnosis of intrahepatic cystic lesions presenting with jaundice.
- Accurate diagnosis and surgical resection are crucial for managing biliary cystadenoma, despite its rarity and potential for diagnostic ambiguity.
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