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Updated: Jun 26, 2026

Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
Polycystic hepatic disease
I Copaci1, Mihaela Enache, C Jurcut
13rd Internal Medicine Department, Carol Davila Central Clinical Emergency Military Hospital, Bucharest, Romania. iulian_copaci@yahoo.com
Abstract:
Polycystic hepatic disease is a very rare hereditary disease. Most of the patients have no symptoms but sometimes they present abdominal discomfort, fever, jaundice. Almost half of the patients associate renal cysts. Rarely, the cysts may appear in other organs such as the pancreas, the spleen or the lung. We present a case of polycystic hepatic disease. In our patient the cysts replace almost the entire hepatic structure. However, the hepatic functional tests were normal.
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