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Role of aetiology in the progression, regression, and parenchymal remodelling of liver disease: implications for liver biopsy interpretation.

Identifieur interne : 003195 ( Ncbi/Curation ); précédent : 003194; suivant : 003196

Role of aetiology in the progression, regression, and parenchymal remodelling of liver disease: implications for liver biopsy interpretation.

Auteurs : Alberto Quaglia [Royaume-Uni] ; Venancio A. Alves [Brésil] ; Charles Balabaud [France] ; Prithi S. Bhathal [Australie] ; Paulette Bioulac-Sage [France] ; James M. Crawford [États-Unis] ; Amar P. Dhillon [Royaume-Uni] ; Linda Ferrell [États-Unis] ; Maria Guido [Italie] ; Prodromos Hytiroglou [Grèce] ; Yasuni Nakanuma [Japon] ; Valerie Paradis [France] ; Dale C. Snover [États-Unis] ; Neil D. Theise [États-Unis] ; Swan N. Thung [États-Unis] ; Wilson M S. Tsui [République populaire de Chine] ; Dirk J. Van Leeuwen [États-Unis]

Source :

RBID : pubmed:26918878

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English descriptors

Abstract

Clinicopathological concepts on acute and chronic liver disease have evolved rapidly during the last few years, with advances in general and specific treatment options and improved patient outcomes. The old paradigm of 'irreversibility' of cirrhosis had been challenged in major ways, and the validity of the usage of the term 'cirrhosis' has come into question. This paper addresses aetiology-based clinicopathological concepts and features that may deserve attention because they may determine disease outcome and, specifically, patterns of regression and remodelling. A variety of therapeutic interventions may influence remaining disease features after elimination of damaging agents (virus, alcohol, etc.), and determine the final clinical outcome including the risk of hepatocellular carcinoma (HCC). New concepts create new responsibilities and opportunities for the pathologist to contribute to the understanding of liver pathology and communicate this with clinical colleagues and researchers.

DOI: 10.1111/his.12957
PubMed: 26918878

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pubmed:26918878

Le document en format XML

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<name sortKey="Paradis, Valerie" sort="Paradis, Valerie" uniqKey="Paradis V" first="Valerie" last="Paradis">Valerie Paradis</name>
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<region type="state">État de New York</region>
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<name sortKey="Tsui, Wilson M S" sort="Tsui, Wilson M S" uniqKey="Tsui W" first="Wilson M S" last="Tsui">Wilson M S. Tsui</name>
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<nlm:affiliation>Department of Pathology, Caritas Medical Centre, Hong Kong, China.</nlm:affiliation>
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<name sortKey="Van Leeuwen, Dirk J" sort="Van Leeuwen, Dirk J" uniqKey="Van Leeuwen D" first="Dirk J" last="Van Leeuwen">Dirk J. Van Leeuwen</name>
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<title level="j">Histopathology</title>
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<term>Acute Disease</term>
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<term>Carcinoma, Hepatocellular (etiology)</term>
<term>Carcinoma, Hepatocellular (pathology)</term>
<term>Chronic Disease</term>
<term>Disease Progression</term>
<term>Humans</term>
<term>Liver (pathology)</term>
<term>Liver Cirrhosis (complications)</term>
<term>Liver Cirrhosis (pathology)</term>
<term>Liver Diseases (complications)</term>
<term>Liver Diseases (pathology)</term>
<term>Liver Neoplasms (etiology)</term>
<term>Liver Neoplasms (pathology)</term>
<term>Liver Regeneration</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parenchymal Tissue (pathology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Biopsie</term>
<term>Carcinome hépatocellulaire (anatomopathologie)</term>
<term>Carcinome hépatocellulaire (étiologie)</term>
<term>Cirrhose du foie ()</term>
<term>Cirrhose du foie (anatomopathologie)</term>
<term>Foie (anatomopathologie)</term>
<term>Humains</term>
<term>Maladie aigüe</term>
<term>Maladie chronique</term>
<term>Maladies du foie ()</term>
<term>Maladies du foie (anatomopathologie)</term>
<term>Mâle</term>
<term>Régénération hépatique</term>
<term>Tissu parenchymateux (anatomopathologie)</term>
<term>Tumeurs du foie (anatomopathologie)</term>
<term>Tumeurs du foie (étiologie)</term>
<term>Évolution de la maladie</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Carcinome hépatocellulaire</term>
<term>Cirrhose du foie</term>
<term>Foie</term>
<term>Maladies du foie</term>
<term>Tissu parenchymateux</term>
<term>Tumeurs du foie</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en">
<term>Liver Cirrhosis</term>
<term>Liver Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en">
<term>Carcinoma, Hepatocellular</term>
<term>Liver Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Carcinoma, Hepatocellular</term>
<term>Liver</term>
<term>Liver Cirrhosis</term>
<term>Liver Diseases</term>
<term>Liver Neoplasms</term>
<term>Parenchymal Tissue</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr">
<term>Carcinome hépatocellulaire</term>
<term>Tumeurs du foie</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Acute Disease</term>
<term>Biopsy</term>
<term>Chronic Disease</term>
<term>Disease Progression</term>
<term>Humans</term>
<term>Liver Regeneration</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Biopsie</term>
<term>Cirrhose du foie</term>
<term>Humains</term>
<term>Maladie aigüe</term>
<term>Maladie chronique</term>
<term>Maladies du foie</term>
<term>Mâle</term>
<term>Régénération hépatique</term>
<term>Évolution de la maladie</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Clinicopathological concepts on acute and chronic liver disease have evolved rapidly during the last few years, with advances in general and specific treatment options and improved patient outcomes. The old paradigm of 'irreversibility' of cirrhosis had been challenged in major ways, and the validity of the usage of the term 'cirrhosis' has come into question. This paper addresses aetiology-based clinicopathological concepts and features that may deserve attention because they may determine disease outcome and, specifically, patterns of regression and remodelling. A variety of therapeutic interventions may influence remaining disease features after elimination of damaging agents (virus, alcohol, etc.), and determine the final clinical outcome including the risk of hepatocellular carcinoma (HCC). New concepts create new responsibilities and opportunities for the pathologist to contribute to the understanding of liver pathology and communicate this with clinical colleagues and researchers.</div>
</front>
</TEI>
</record>

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