Literature DB >> 16599828

Hepatorenal syndrome.

Selda Demirtaş1, Murat Can, Ayşegül Yarpuzlu.   

Abstract

This article summarizes the literature on current definition, suggested pathogenetic mechanisms and the role of laboratory assessment in the differential diagnosis of hepatorenal syndrome (HRS) from other causes of renal disease that may arise during hepatic cirrhosis and some diseases affecting both liver and kidney. It should be remembered that the main theory suggested for the pathogenesis of HRS is the arterial vasodilation hypothesis of portal hypertension, ending in type 1 and type 2 HRS, but there is no consensus supporting either mechanism as a solid theory for initiation of HRS pathogenesis to date. No laboratory test can firmly establish a diagnosis of HRS, which is mainly based on the absence of any specific cause of renal failure. Laboratory and ultrasonographic tests based on non-invasive techniques are being investigated as possible diagnostic approaches.

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Year:  2006        PMID: 16599828     DOI: 10.1515/CCLM.2006.062

Source DB:  PubMed          Journal:  Clin Chem Lab Med        ISSN: 1434-6621            Impact factor:   3.694


  1 in total

1.  Type I inositol 1, 4, 5-triphosphate receptors increase in kidney of mice with fulminant hepatic failure.

Authors:  Ying Wen; Wei Cui; Pei Liu
Journal:  World J Gastroenterol       Date:  2007-04-28       Impact factor: 5.742

  1 in total

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