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: Cirrhosis, hepato-renal polycystics, portal hypertension, hematemisis, liver transplantation, case report, morocco

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How to Cite
Aouroud, M., Jarti, M., Haida, M. Z., Jallouli, A., Ait Errami, A., Oubaha, S., … Krati, K. (2021). Hepatorenal Polycystosis Complicated By Hepatic Cirrhosis: A Case Report. International Journal of Innovative Research in Medical Science, 6(12), 888–890. https://doi.org/10.23958/ijirms/vol06-i12/1288

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Copyright © 2021 Meryem Aouroud Mariama Jarti Marj Zohour Haida Abderahmane Jallouli Adil Ait Errami Sofia Oubaha Zouhour Samlani Khadija Krati this is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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This work is licensed under a Creative Commons Attribution 4.0 International License.