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Vol. 9 No. Supplement 1 (2016)

December 2016

Biliary mucinous cystic neoplasm: a case report and review of the literature

  • Mohammad Taghi Safari
  • Shabnam Shahrokh
  • Mohammad Bagher Miri
  • Forough Foroughi
  • Amir Sadeghi

Gastroenterology and Hepatology from Bed to Bench, Vol. 9 No. Supplement 1 (2016), 8 December 2016
https://doi.org/10.22037/ghfbb.v0i0.938 Published: 2016-12-08

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Abstract

Hepatobiliary cystadenomas (HBC) is a rare neoplasm which comprising less than one percent of liver cystic neoplasms. Although it’s known as a benign tumor, but they have a potential for neoplastic transformation. Making a proper diagnosis and ruling out of other differential diagnosis is important because of different treatment. In the present study, we described a case of HBC manifested as idiopathic dominant biliary stricture in common hepatic duct (CHD), on the basis of spiral CT scan and MRI, and elevated CA19-9. With a probable diagnosis of malignant biliary stricture, she underwent ERCP and cholangioscopy that were non-diagnostic and final diagnosis was made surgically. HBCs usually found incicentally as a cystic lesion and biliary stricture without visible cyst in imaging like that seen in cholangiocarcinoma is very unlikely. In truth, this patient is an unusual manifestation of one rare disease.

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How to Cite

Safari, M. T., Shahrokh, S., Miri, M. B., Foroughi, F., & Sadeghi, A. (2016). Biliary mucinous cystic neoplasm: a case report and review of the literature. Gastroenterology and Hepatology from Bed to Bench, 9(Supplement 1). https://doi.org/10.22037/ghfbb.v0i0.938
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Print ISSN: 2008-2258
Online ISSN: 2008-4234

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