Role of aetiology in the progression, regression, and parenchymal remodelling of liver disease: implications for liver biopsy interpretation.
Identifieur interne : 001D47 ( PubMed/Corpus ); précédent : 001D46; suivant : 001D48Role of aetiology in the progression, regression, and parenchymal remodelling of liver disease: implications for liver biopsy interpretation.
Auteurs : Alberto Quaglia ; Venancio A. Alves ; Charles Balabaud ; Prithi S. Bhathal ; Paulette Bioulac-Sage ; James M. Crawford ; Amar P. Dhillon ; Linda Ferrell ; Maria Guido ; Prodromos Hytiroglou ; Yasuni Nakanuma ; Valerie Paradis ; Dale C. Snover ; Neil D. Theise ; Swan N. Thung ; Wilson M S. Tsui ; Dirk J. Van LeeuwenSource :
- Histopathology [ 1365-2559 ] ; 2016.
English descriptors
- KwdEn :
- Acute Disease, Biopsy, Carcinoma, Hepatocellular (etiology), Carcinoma, Hepatocellular (pathology), Chronic Disease, Disease Progression, Humans, Liver (pathology), Liver Cirrhosis (complications), Liver Cirrhosis (pathology), Liver Diseases (complications), Liver Diseases (pathology), Liver Neoplasms (etiology), Liver Neoplasms (pathology), Liver Regeneration, Male, Middle Aged, Parenchymal Tissue (pathology).
- MESH :
- complications : Liver Cirrhosis, Liver Diseases.
- etiology : Carcinoma, Hepatocellular, Liver Neoplasms.
- pathology : Carcinoma, Hepatocellular, Liver, Liver Cirrhosis, Liver Diseases, Liver Neoplasms, Parenchymal Tissue.
- Acute Disease, Biopsy, Chronic Disease, Disease Progression, Humans, Liver Regeneration, Male, Middle Aged.
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
Links to Exploration step
pubmed:26918878Le document en format XML
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<author><name sortKey="Balabaud, Charles" sort="Balabaud, Charles" uniqKey="Balabaud C" first="Charles" last="Balabaud">Charles Balabaud</name>
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</affiliation>
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<author><name sortKey="Ferrell, Linda" sort="Ferrell, Linda" uniqKey="Ferrell L" first="Linda" last="Ferrell">Linda Ferrell</name>
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<author><name sortKey="Guido, Maria" sort="Guido, Maria" uniqKey="Guido M" first="Maria" last="Guido">Maria Guido</name>
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</author>
<author><name sortKey="Hytiroglou, Prodromos" sort="Hytiroglou, Prodromos" uniqKey="Hytiroglou P" first="Prodromos" last="Hytiroglou">Prodromos Hytiroglou</name>
<affiliation><nlm:affiliation>Department of Pathology, Aristotle University Medical School, Thessaloniki, Greece.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Nakanuma, Yasuni" sort="Nakanuma, Yasuni" uniqKey="Nakanuma Y" first="Yasuni" last="Nakanuma">Yasuni Nakanuma</name>
<affiliation><nlm:affiliation>Department of Diagnostic Pathology, Shizuoka Cancer Center, Shizuoka, Japan.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Paradis, Valerie" sort="Paradis, Valerie" uniqKey="Paradis V" first="Valerie" last="Paradis">Valerie Paradis</name>
<affiliation><nlm:affiliation>Pathology Department, Beaujon Hospital, Clichy, France.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Snover, Dale C" sort="Snover, Dale C" uniqKey="Snover D" first="Dale C" last="Snover">Dale C. Snover</name>
<affiliation><nlm:affiliation>Department of Pathology, Fairview Southdale Hospital, Edina, MN, USA.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Theise, Neil D" sort="Theise, Neil D" uniqKey="Theise N" first="Neil D" last="Theise">Neil D. Theise</name>
<affiliation><nlm:affiliation>Departments of Pathology and Medicine (Division of Digestive Diseases), Beth Israel Medical Center of Albert Einstein College of Medicine, New York, NY, USA.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Thung, Swan N" sort="Thung, Swan N" uniqKey="Thung S" first="Swan N" last="Thung">Swan N. Thung</name>
<affiliation><nlm:affiliation>Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.</nlm:affiliation>
</affiliation>
</author>
<author><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>
<affiliation><nlm:affiliation>Department of Pathology, Caritas Medical Centre, Hong Kong, China.</nlm:affiliation>
</affiliation>
</author>
<author><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>
<affiliation><nlm:affiliation>Section of Gastroenterology and Hepatology, Dartmouth Medical School, Hanover, NH, USA.</nlm:affiliation>
</affiliation>
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<term>Biopsy</term>
<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="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" 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>
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<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>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26918878</PMID>
<DateCreated><Year>2016</Year>
<Month>05</Month>
<Day>06</Day>
</DateCreated>
<DateCompleted><Year>2017</Year>
<Month>11</Month>
<Day>01</Day>
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<DateRevised><Year>2017</Year>
<Month>11</Month>
<Day>01</Day>
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<JournalIssue CitedMedium="Internet"><Volume>68</Volume>
<Issue>7</Issue>
<PubDate><Year>2016</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Histopathology</Title>
<ISOAbbreviation>Histopathology</ISOAbbreviation>
</Journal>
<ArticleTitle>Role of aetiology in the progression, regression, and parenchymal remodelling of liver disease: implications for liver biopsy interpretation.</ArticleTitle>
<Pagination><MedlinePgn>953-67</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1111/his.12957</ELocationID>
<Abstract><AbstractText>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.</AbstractText>
<CopyrightInformation>© 2016 John Wiley & Sons Ltd.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Quaglia</LastName>
<ForeName>Alberto</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Institute of Liver Studies, King's College Hospital and King's College, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Alves</LastName>
<ForeName>Venancio A</ForeName>
<Initials>VA</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, University of São Paulo School of Medicine, São Paulo, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Balabaud</LastName>
<ForeName>Charles</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Inserm, U1053, Bordeaux University 2, Bordeaux, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bhathal</LastName>
<ForeName>Prithi S</ForeName>
<Initials>PS</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, University of Melbourne, Melbourne, VIC, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bioulac-Sage</LastName>
<ForeName>Paulette</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, CHU Bordeaux, Bordeaux, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Crawford</LastName>
<ForeName>James M</ForeName>
<Initials>JM</Initials>
<AffiliationInfo><Affiliation>Department of Pathology and Laboratory Medicine, Hofstra Northwell School of Medicine, Hempstead, NY, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Dhillon</LastName>
<ForeName>Amar P</ForeName>
<Initials>AP</Initials>
<AffiliationInfo><Affiliation>Department of Cellular Pathology, UCL Medical School, London, UK.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Ferrell</LastName>
<ForeName>Linda</ForeName>
<Initials>L</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, University of California, San Francisco, CA, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Guido</LastName>
<ForeName>Maria</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Medicine-DIMED, Pathology Unit, University of Padova, Padova, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Hytiroglou</LastName>
<ForeName>Prodromos</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, Aristotle University Medical School, Thessaloniki, Greece.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Nakanuma</LastName>
<ForeName>Yasuni</ForeName>
<Initials>Y</Initials>
<AffiliationInfo><Affiliation>Department of Diagnostic Pathology, Shizuoka Cancer Center, Shizuoka, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Paradis</LastName>
<ForeName>Valerie</ForeName>
<Initials>V</Initials>
<AffiliationInfo><Affiliation>Pathology Department, Beaujon Hospital, Clichy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Snover</LastName>
<ForeName>Dale C</ForeName>
<Initials>DC</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, Fairview Southdale Hospital, Edina, MN, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Theise</LastName>
<ForeName>Neil D</ForeName>
<Initials>ND</Initials>
<AffiliationInfo><Affiliation>Departments of Pathology and Medicine (Division of Digestive Diseases), Beth Israel Medical Center of Albert Einstein College of Medicine, New York, NY, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Thung</LastName>
<ForeName>Swan N</ForeName>
<Initials>SN</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Tsui</LastName>
<ForeName>Wilson M S</ForeName>
<Initials>WM</Initials>
<AffiliationInfo><Affiliation>Department of Pathology, Caritas Medical Centre, Hong Kong, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>van Leeuwen</LastName>
<ForeName>Dirk J</ForeName>
<Initials>DJ</Initials>
<AffiliationInfo><Affiliation>Section of Gastroenterology and Hepatology, Dartmouth Medical School, Hanover, NH, USA.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Onze Lieve Vrouwe Gasthuis, Amsterdam, the Netherlands.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><CollectiveName>International Liver Pathology Study Group</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016454">Review</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2016</Year>
<Month>04</Month>
<Day>28</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Histopathology</MedlineTA>
<NlmUniqueID>7704136</NlmUniqueID>
<ISSNLinking>0309-0167</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000208" MajorTopicYN="N">Acute Disease</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001706" MajorTopicYN="N">Biopsy</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006528" MajorTopicYN="N">Carcinoma, Hepatocellular</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002908" MajorTopicYN="N">Chronic Disease</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018450" MajorTopicYN="N">Disease Progression</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008099" MajorTopicYN="N">Liver</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008103" MajorTopicYN="N">Liver Cirrhosis</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008107" MajorTopicYN="N">Liver Diseases</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008113" MajorTopicYN="N">Liver Neoplasms</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008115" MajorTopicYN="N">Liver Regeneration</DescriptorName>
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<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">biopsy</Keyword>
<Keyword MajorTopicYN="N">end stage liver disease</Keyword>
<Keyword MajorTopicYN="N">fibrosis</Keyword>
<Keyword MajorTopicYN="N">liver cirrhosis</Keyword>
<Keyword MajorTopicYN="N">liver regeneration</Keyword>
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<PubMedPubDate PubStatus="medline"><Year>2017</Year>
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<ArticleId IdType="doi">10.1111/his.12957</ArticleId>
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