Recent developments in liver pathology
Hepatocellular carcinoma is the sixth most common malignancy and the third leading cause of cancer deaths worldwide, making pathologic identification of precursor lesions essential. Recent molecular genetic, pathologic, and clinical data have led to the stratification of hepatic adenomas into subgro...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2009-07, Vol.133 (7), p.1078-1086 |
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description | Hepatocellular carcinoma is the sixth most common malignancy and the third leading cause of cancer deaths worldwide, making pathologic identification of precursor lesions essential. Recent molecular genetic, pathologic, and clinical data have led to the stratification of hepatic adenomas into subgroups with unique molecular profiles and varying potential for malignant transformation, as well as to the reclassification of telangiectatic focal nodular hyperplasia as telangiectatic adenoma. Clinical, morphologic, and molecular genetic studies have also established juvenile hemochromatosis and pediatric nonalcoholic steatohepatitis as entities distinct from their adult counterparts.
To review the recent molecular genetic characterization of telangiectatic hepatic adenomas and juvenile hemochromatosis, as well as the recent clinicopathologic characterization of pediatric nonalcoholic steatohepatitis.
Literature review, personal experience, and material from the University of Chicago.
Basic science and translational research have led to the classification of many pathologic entities of the liver according to molecular genetic and protein expression profiles that correspond to traditional morphologic categories. Insights into signal transduction pathways that are activated in, and protein expression patterns unique to, an individual disease may lead to the development of new therapeutic agents and novel diagnostic biomarkers. |
doi_str_mv | 10.1043/1543-2165-133.7.1078 |
format | Article |
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To review the recent molecular genetic characterization of telangiectatic hepatic adenomas and juvenile hemochromatosis, as well as the recent clinicopathologic characterization of pediatric nonalcoholic steatohepatitis.
Literature review, personal experience, and material from the University of Chicago.
Basic science and translational research have led to the classification of many pathologic entities of the liver according to molecular genetic and protein expression profiles that correspond to traditional morphologic categories. Insights into signal transduction pathways that are activated in, and protein expression patterns unique to, an individual disease may lead to the development of new therapeutic agents and novel diagnostic biomarkers.</description><identifier>ISSN: 1543-2165</identifier><identifier>ISSN: 0003-9985</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.1043/1543-2165-133.7.1078</identifier><identifier>PMID: 19642734</identifier><identifier>CODEN: APLMAS</identifier><language>eng</language><publisher>United States: College of American Pathologists</publisher><subject>Adenoma - diagnosis ; Adenoma - genetics ; Adenoma - pathology ; Adolescent ; Adult ; Biomarkers, Tumor - genetics ; Carcinoma, Hepatocellular - epidemiology ; Cellular signal transduction ; Child ; Child, Preschool ; Development and progression ; Diagnosis ; DNA methylation ; Fatty Liver - diagnosis ; Fatty Liver - genetics ; Fatty Liver - pathology ; Gene mutations ; Genetic aspects ; Hemochromatosis - diagnosis ; Hemochromatosis - genetics ; Hemochromatosis - pathology ; Humans ; Hyperplasia ; Liver cancer ; Liver Neoplasms - diagnosis ; Liver Neoplasms - genetics ; Liver Neoplasms - pathology ; Mass spectrometry ; Mutation ; Pediatrics ; Physiological aspects ; Protein expression ; Proteins ; Risk Factors ; Scientific imaging ; Signal transduction ; Tumors ; X chromosomes</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2009-07, Vol.133 (7), p.1078-1086</ispartof><rights>COPYRIGHT 2009 College of American Pathologists</rights><rights>Copyright College of American Pathologists Jul 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-c025c49186f7be9e5bfb19786a5c833fb0ad10956be79b10ffd274f53ae8a27f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19642734$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yan, Benjamin C</creatorcontrib><creatorcontrib>Hart, John A</creatorcontrib><title>Recent developments in liver pathology</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>Hepatocellular carcinoma is the sixth most common malignancy and the third leading cause of cancer deaths worldwide, making pathologic identification of precursor lesions essential. Recent molecular genetic, pathologic, and clinical data have led to the stratification of hepatic adenomas into subgroups with unique molecular profiles and varying potential for malignant transformation, as well as to the reclassification of telangiectatic focal nodular hyperplasia as telangiectatic adenoma. Clinical, morphologic, and molecular genetic studies have also established juvenile hemochromatosis and pediatric nonalcoholic steatohepatitis as entities distinct from their adult counterparts.
To review the recent molecular genetic characterization of telangiectatic hepatic adenomas and juvenile hemochromatosis, as well as the recent clinicopathologic characterization of pediatric nonalcoholic steatohepatitis.
Literature review, personal experience, and material from the University of Chicago.
Basic science and translational research have led to the classification of many pathologic entities of the liver according to molecular genetic and protein expression profiles that correspond to traditional morphologic categories. Insights into signal transduction pathways that are activated in, and protein expression patterns unique to, an individual disease may lead to the development of new therapeutic agents and novel diagnostic biomarkers.</description><subject>Adenoma - diagnosis</subject><subject>Adenoma - genetics</subject><subject>Adenoma - pathology</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Carcinoma, Hepatocellular - epidemiology</subject><subject>Cellular signal transduction</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>DNA methylation</subject><subject>Fatty Liver - diagnosis</subject><subject>Fatty Liver - genetics</subject><subject>Fatty Liver - pathology</subject><subject>Gene mutations</subject><subject>Genetic aspects</subject><subject>Hemochromatosis - diagnosis</subject><subject>Hemochromatosis - genetics</subject><subject>Hemochromatosis - pathology</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - diagnosis</subject><subject>Liver Neoplasms - genetics</subject><subject>Liver Neoplasms - pathology</subject><subject>Mass spectrometry</subject><subject>Mutation</subject><subject>Pediatrics</subject><subject>Physiological aspects</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Risk Factors</subject><subject>Scientific imaging</subject><subject>Signal transduction</subject><subject>Tumors</subject><subject>X chromosomes</subject><issn>1543-2165</issn><issn>0003-9985</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkd1LwzAUxYMobk7_A5Hiw94689E0zeMYfsFAEH0uaXqzZaRNbdrB_nsLmzJl3Id7OPzO5cBF6JbgGcEJeyA8YTElKY8JYzMxmCI7Q-Nf-_xIj9BVCBuMsaSUXKIRkWlCBUvGaPoOGuouKmELzjfVoENk68jZLbRRo7q1d361u0YXRrkAN4c9QZ9Pjx-Ll3j59vy6mC9jzSTvYo0p14kkWWpEARJ4YQoiRZYqrjPGTIFVSbDkaQFCFgQbU1KRGM4UZIoKwyZour_btP6rh9DllQ0anFM1-D7kqeAspSkfwPt_4Mb3bT10yymhOMmEwAMU76GVcpDb2viuVXoFNbTK-RqMHew5ZZhwipkc-NkJfpgSKqtPBqZHgTUo162Dd31nfR3-gneHun1RQZk3ra1Uu8t_HsG-AbnTh2k</recordid><startdate>200907</startdate><enddate>200907</enddate><creator>Yan, Benjamin C</creator><creator>Hart, John A</creator><general>College of American Pathologists</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200907</creationdate><title>Recent developments in liver pathology</title><author>Yan, Benjamin C ; Hart, John A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-c025c49186f7be9e5bfb19786a5c833fb0ad10956be79b10ffd274f53ae8a27f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adenoma - diagnosis</topic><topic>Adenoma - genetics</topic><topic>Adenoma - pathology</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Carcinoma, Hepatocellular - epidemiology</topic><topic>Cellular signal transduction</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>DNA methylation</topic><topic>Fatty Liver - diagnosis</topic><topic>Fatty Liver - genetics</topic><topic>Fatty Liver - pathology</topic><topic>Gene mutations</topic><topic>Genetic aspects</topic><topic>Hemochromatosis - diagnosis</topic><topic>Hemochromatosis - genetics</topic><topic>Hemochromatosis - pathology</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - diagnosis</topic><topic>Liver Neoplasms - genetics</topic><topic>Liver Neoplasms - pathology</topic><topic>Mass spectrometry</topic><topic>Mutation</topic><topic>Pediatrics</topic><topic>Physiological aspects</topic><topic>Protein expression</topic><topic>Proteins</topic><topic>Risk Factors</topic><topic>Scientific imaging</topic><topic>Signal transduction</topic><topic>Tumors</topic><topic>X chromosomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yan, Benjamin C</creatorcontrib><creatorcontrib>Hart, John A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yan, Benjamin C</au><au>Hart, John A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent developments in liver pathology</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><addtitle>Arch Pathol Lab Med</addtitle><date>2009-07</date><risdate>2009</risdate><volume>133</volume><issue>7</issue><spage>1078</spage><epage>1086</epage><pages>1078-1086</pages><issn>1543-2165</issn><issn>0003-9985</issn><eissn>1543-2165</eissn><coden>APLMAS</coden><abstract>Hepatocellular carcinoma is the sixth most common malignancy and the third leading cause of cancer deaths worldwide, making pathologic identification of precursor lesions essential. Recent molecular genetic, pathologic, and clinical data have led to the stratification of hepatic adenomas into subgroups with unique molecular profiles and varying potential for malignant transformation, as well as to the reclassification of telangiectatic focal nodular hyperplasia as telangiectatic adenoma. Clinical, morphologic, and molecular genetic studies have also established juvenile hemochromatosis and pediatric nonalcoholic steatohepatitis as entities distinct from their adult counterparts.
To review the recent molecular genetic characterization of telangiectatic hepatic adenomas and juvenile hemochromatosis, as well as the recent clinicopathologic characterization of pediatric nonalcoholic steatohepatitis.
Literature review, personal experience, and material from the University of Chicago.
Basic science and translational research have led to the classification of many pathologic entities of the liver according to molecular genetic and protein expression profiles that correspond to traditional morphologic categories. Insights into signal transduction pathways that are activated in, and protein expression patterns unique to, an individual disease may lead to the development of new therapeutic agents and novel diagnostic biomarkers.</abstract><cop>United States</cop><pub>College of American Pathologists</pub><pmid>19642734</pmid><doi>10.1043/1543-2165-133.7.1078</doi><tpages>9</tpages></addata></record> |
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subjects | Adenoma - diagnosis Adenoma - genetics Adenoma - pathology Adolescent Adult Biomarkers, Tumor - genetics Carcinoma, Hepatocellular - epidemiology Cellular signal transduction Child Child, Preschool Development and progression Diagnosis DNA methylation Fatty Liver - diagnosis Fatty Liver - genetics Fatty Liver - pathology Gene mutations Genetic aspects Hemochromatosis - diagnosis Hemochromatosis - genetics Hemochromatosis - pathology Humans Hyperplasia Liver cancer Liver Neoplasms - diagnosis Liver Neoplasms - genetics Liver Neoplasms - pathology Mass spectrometry Mutation Pediatrics Physiological aspects Protein expression Proteins Risk Factors Scientific imaging Signal transduction Tumors X chromosomes |
title | Recent developments in liver pathology |
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