Case ReportOpen Access

Hepatorenal Polycystosis Complicated By Hepatic Cirrhosis: A Case Report

ยทยทยทยทยทยทยท
DOI: 10.23958/ijirms/vol06-i12/1288ยท Pages: 888 - 890ยท Vol. 6, No. 12, (2021)ยท Published: December 2, 2021
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Abstract

Polycystic liver disease is most commonly associated with autosomal dominant polycystic kidney disease. Hepatic cysts are the most common extrarenal manifestation of autosomal dominant polycystic kidney disease. The progression to cirrhosis remains rare, and the data is sparse, the only curative treatment is liver transplantation. We report the case of a young patient with hepato-renal polycystosis at the stage of cirrhosis.

Keywords

Cirrhosishepato-renal polycysticsportal hypertensionhematemisisliver transplantationcase report
Author details
Meryem Aouroud
Department of Gastroenterology CHU Mohammed VI Marrakesh
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Mariama Jarti
Department of Gastroenterology CHU Mohammed VI Marrakesh
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Marj Zohour Haida
Department of Gastroenterology CHU Mohammed VI Marrakesh
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Abderahmane Jallouli
Department of Gastroenterology CHU Mohammed VI Marrakesh
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Adil Ait Errami
Department of Gastroenterology CHU Mohammed VI Marrakesh
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Sofia Oubaha
Department of Physiology, Cadi Ayad University CHU Mohammed VI Marrakesh
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Zouhour Samlani
Department of Gastroenterology CHU Mohammed VI Marrakesh
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Khadija Krati
Department of Gastroenterology CHU Mohammed VI Marrakesh
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