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pubmed-article:16181390pubmed:abstractTextWe report a 26-year-old woman with congenital hepatic fibrosis (CHFib), adult polycystic kidney disease, type II diabetes mellitus, and von Willebrand disease, who despite persistent advice to the contrary because of severe portal hypertension, had 5 pregnancies delivering 6 healthy infants over 8 yr. During this time, she experienced several episodes of esophageal variceal bleeding and severe ascites with persistently normal liver and renal function. CHFib is one of the prototypes of portal hypertension with preserved hepatocellular function. Although pregnancy is ill-advised in most women with portal hypertension and particularly with severe manifestations, this report illustrates the importance of preserved hepatocellular function for the outcome of pregnancy in these patients.lld:pubmed
pubmed-article:16181390pubmed:languageenglld:pubmed
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pubmed-article:16181390pubmed:pagination2359-61lld:pubmed
pubmed-article:16181390pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:16181390pubmed:year2005lld:pubmed
pubmed-article:16181390pubmed:articleTitleMultiple normal deliveries in a woman with severe portal hypertension due to congenital hepatic fibrosis: the importance of preserved hepatocellular function.lld:pubmed
pubmed-article:16181390pubmed:affiliationCenter for Liver Diseases, Division of Hepatology, University of Miami Leonard M. Miller School of Medicine, Miami, Florida 33136, USA.lld:pubmed
pubmed-article:16181390pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16181390pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:16181390pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed