Identification of factors contributing to hepatomegaly in severely burned children
Hepatomegaly is a common postmortem observation in severely burned children, with the liver often tripling in size when compared with normal livers for age, weight, and sex. Lesions identified at autopsy include deposition of large and small fat droplets in the hepatocyte, congestion, centrilobular...
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Veröffentlicht in: | Shock (Augusta, Ga.) Ga.), 2005-12, Vol.24 (6), p.523-528 |
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description | Hepatomegaly is a common postmortem observation in severely burned children, with the liver often tripling in size when compared with normal livers for age, weight, and sex. Lesions identified at autopsy include deposition of large and small fat droplets in the hepatocyte, congestion, centrilobular necrosis, and cholestasis. The present study was designed to identify the primary causes of hepatomegaly in severely burned children postmortem. For this purpose, 41 autopsies were reviewed and, when available, blood and tissue samples were studied. Histopathologic findings showed that large intrahepatocytic fat droplets within hepatocytes and cholestasis were important contributors to hepatomegaly. Liver density and wet/dry weight ratios significantly decreased with increasing liver size. Hepatocyte volume increased with increasing liver size (P < 0.001) as did total fat content (P < 0.001). The liver enzymes, alanine aminotransferase and aspartate aminotransferase, remained normal except within 5 to 10 days of injury and 5 to 10 days of death. Triglycerides made up 4% to 70% of the total fat, with the percentage of triglycerides increasing with the severity of hepatomegaly. Saturated fatty acids represented about 85% of the total fatty acids in normal-sized livers, whereas in the largest livers (400% of predicted), only 25% of the fatty acids were saturated. This study provides evidence that 85% to 90% of the hepatomegaly observed in severely burned children postmortem is associated with hepatocyte enlargement, which includes up to 19% intracellular fat. Increases in extracellular protein, intracellular glycogen, and fluid accumulation may make a minor contribution to postburn hepatomegaly. |
doi_str_mv | 10.1097/01.shk.0000187981.78901.ee |
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Lesions identified at autopsy include deposition of large and small fat droplets in the hepatocyte, congestion, centrilobular necrosis, and cholestasis. The present study was designed to identify the primary causes of hepatomegaly in severely burned children postmortem. For this purpose, 41 autopsies were reviewed and, when available, blood and tissue samples were studied. Histopathologic findings showed that large intrahepatocytic fat droplets within hepatocytes and cholestasis were important contributors to hepatomegaly. Liver density and wet/dry weight ratios significantly decreased with increasing liver size. Hepatocyte volume increased with increasing liver size (P < 0.001) as did total fat content (P < 0.001). The liver enzymes, alanine aminotransferase and aspartate aminotransferase, remained normal except within 5 to 10 days of injury and 5 to 10 days of death. Triglycerides made up 4% to 70% of the total fat, with the percentage of triglycerides increasing with the severity of hepatomegaly. Saturated fatty acids represented about 85% of the total fatty acids in normal-sized livers, whereas in the largest livers (400% of predicted), only 25% of the fatty acids were saturated. This study provides evidence that 85% to 90% of the hepatomegaly observed in severely burned children postmortem is associated with hepatocyte enlargement, which includes up to 19% intracellular fat. Increases in extracellular protein, intracellular glycogen, and fluid accumulation may make a minor contribution to postburn hepatomegaly.</description><identifier>ISSN: 1073-2322</identifier><identifier>EISSN: 1540-0514</identifier><identifier>DOI: 10.1097/01.shk.0000187981.78901.ee</identifier><identifier>PMID: 16317382</identifier><language>eng</language><publisher>Augusta, GA: BioMedical Press</publisher><subject>Age Factors ; Alanine Transaminase - metabolism ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Aspartate Aminotransferases - metabolism ; Biological and medical sciences ; Blood and lymphatic vessels ; Burns - complications ; Burns - enzymology ; Burns - pathology ; Cardiology. Vascular system ; Child ; Child, Preschool ; Cytoplasm - enzymology ; Cytoplasm - pathology ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Emergency and intensive care: burns ; Female ; Hepatocytes - enzymology ; Hepatocytes - pathology ; Hepatomegaly - enzymology ; Hepatomegaly - etiology ; Hepatomegaly - pathology ; Humans ; Intensive care medicine ; Liver - enzymology ; Liver - pathology ; Male ; Medical sciences ; Necrosis - enzymology ; Necrosis - pathology ; Organ Size ; Sex Factors ; Trauma Severity Indices ; Triglycerides - metabolism</subject><ispartof>Shock (Augusta, Ga.), 2005-12, Vol.24 (6), p.523-528</ispartof><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-54c01e8501ab298f3ff7cd797c30d52202d699d504a5e5d08626292e620c04a33</citedby><cites>FETCH-LOGICAL-c417t-54c01e8501ab298f3ff7cd797c30d52202d699d504a5e5d08626292e620c04a33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17332116$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16317382$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BARROW, Robert E</creatorcontrib><creatorcontrib>HAWKINS, Hal K</creatorcontrib><creatorcontrib>AARSLAND, Asle</creatorcontrib><creatorcontrib>COX, Robert</creatorcontrib><creatorcontrib>ROSENBLATT, Judah</creatorcontrib><creatorcontrib>BARROW, Laura N</creatorcontrib><creatorcontrib>JESCHKE, Marc G</creatorcontrib><creatorcontrib>HERNDON, David N</creatorcontrib><title>Identification of factors contributing to hepatomegaly in severely burned children</title><title>Shock (Augusta, Ga.)</title><addtitle>Shock</addtitle><description>Hepatomegaly is a common postmortem observation in severely burned children, with the liver often tripling in size when compared with normal livers for age, weight, and sex. Lesions identified at autopsy include deposition of large and small fat droplets in the hepatocyte, congestion, centrilobular necrosis, and cholestasis. The present study was designed to identify the primary causes of hepatomegaly in severely burned children postmortem. For this purpose, 41 autopsies were reviewed and, when available, blood and tissue samples were studied. Histopathologic findings showed that large intrahepatocytic fat droplets within hepatocytes and cholestasis were important contributors to hepatomegaly. Liver density and wet/dry weight ratios significantly decreased with increasing liver size. Hepatocyte volume increased with increasing liver size (P < 0.001) as did total fat content (P < 0.001). The liver enzymes, alanine aminotransferase and aspartate aminotransferase, remained normal except within 5 to 10 days of injury and 5 to 10 days of death. Triglycerides made up 4% to 70% of the total fat, with the percentage of triglycerides increasing with the severity of hepatomegaly. Saturated fatty acids represented about 85% of the total fatty acids in normal-sized livers, whereas in the largest livers (400% of predicted), only 25% of the fatty acids were saturated. This study provides evidence that 85% to 90% of the hepatomegaly observed in severely burned children postmortem is associated with hepatocyte enlargement, which includes up to 19% intracellular fat. Increases in extracellular protein, intracellular glycogen, and fluid accumulation may make a minor contribution to postburn hepatomegaly.</description><subject>Age Factors</subject><subject>Alanine Transaminase - metabolism</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Aspartate Aminotransferases - metabolism</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Burns - complications</subject><subject>Burns - enzymology</subject><subject>Burns - pathology</subject><subject>Cardiology. Vascular system</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cytoplasm - enzymology</subject><subject>Cytoplasm - pathology</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>Emergency and intensive care: burns</subject><subject>Female</subject><subject>Hepatocytes - enzymology</subject><subject>Hepatocytes - pathology</subject><subject>Hepatomegaly - enzymology</subject><subject>Hepatomegaly - etiology</subject><subject>Hepatomegaly - pathology</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Liver - enzymology</subject><subject>Liver - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Necrosis - enzymology</subject><subject>Necrosis - pathology</subject><subject>Organ Size</subject><subject>Sex Factors</subject><subject>Trauma Severity Indices</subject><subject>Triglycerides - metabolism</subject><issn>1073-2322</issn><issn>1540-0514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF1rVDEQhkNR2lr9C3IQ9O6sk-TkJPFOih-FglDqdcgmk270bLImOYX-e6Nd2LmZ4eWZGXgIeUdhQ0HLj0A3dfd7A72oklrRjVS6h4hn5JKKCUYQdHrRZ5B8ZJyxC_Kq1l8AbOJanpMLOnMquWKX5O7GY2oxRGdbzGnIYQjWtVzq4HJqJW7XFtPD0PKww4NteY8PdnkaYhoqPmLBPm_XktAPbhcXXzC9Ji-DXSq-OfYr8vPrl_vr7-Ptj283159vRzdR2UYxOaCoBFC7ZVoFHoJ0XmrpOHjBGDA_a-0FTFag8KBmNjPNcGbgesb5FfnwfPdQ8p8VazP7WB0ui02Y12pmpaYJxNzBT8-gK7nWgsEcStzb8mQomH9GDVDTjZqTUfPfqEHsy2-PX9btHv1p9aiwA--PgK3OLqHY5GI9cZJzRjv9F_wPgJ8</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>BARROW, Robert E</creator><creator>HAWKINS, Hal K</creator><creator>AARSLAND, Asle</creator><creator>COX, Robert</creator><creator>ROSENBLATT, Judah</creator><creator>BARROW, Laura N</creator><creator>JESCHKE, Marc G</creator><creator>HERNDON, David N</creator><general>BioMedical Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20051201</creationdate><title>Identification of factors contributing to hepatomegaly in severely burned children</title><author>BARROW, Robert E ; HAWKINS, Hal K ; AARSLAND, Asle ; COX, Robert ; ROSENBLATT, Judah ; BARROW, Laura N ; JESCHKE, Marc G ; HERNDON, David N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-54c01e8501ab298f3ff7cd797c30d52202d699d504a5e5d08626292e620c04a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Age Factors</topic><topic>Alanine Transaminase - metabolism</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Aspartate Aminotransferases - metabolism</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Burns - complications</topic><topic>Burns - enzymology</topic><topic>Burns - pathology</topic><topic>Cardiology. Vascular system</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cytoplasm - enzymology</topic><topic>Cytoplasm - pathology</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Emergency and intensive care: burns</topic><topic>Female</topic><topic>Hepatocytes - enzymology</topic><topic>Hepatocytes - pathology</topic><topic>Hepatomegaly - enzymology</topic><topic>Hepatomegaly - etiology</topic><topic>Hepatomegaly - pathology</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Liver - enzymology</topic><topic>Liver - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Necrosis - enzymology</topic><topic>Necrosis - pathology</topic><topic>Organ Size</topic><topic>Sex Factors</topic><topic>Trauma Severity Indices</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BARROW, Robert E</creatorcontrib><creatorcontrib>HAWKINS, Hal K</creatorcontrib><creatorcontrib>AARSLAND, Asle</creatorcontrib><creatorcontrib>COX, Robert</creatorcontrib><creatorcontrib>ROSENBLATT, Judah</creatorcontrib><creatorcontrib>BARROW, Laura N</creatorcontrib><creatorcontrib>JESCHKE, Marc G</creatorcontrib><creatorcontrib>HERNDON, David N</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Shock (Augusta, Ga.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BARROW, Robert E</au><au>HAWKINS, Hal K</au><au>AARSLAND, Asle</au><au>COX, Robert</au><au>ROSENBLATT, Judah</au><au>BARROW, Laura N</au><au>JESCHKE, Marc G</au><au>HERNDON, David N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of factors contributing to hepatomegaly in severely burned children</atitle><jtitle>Shock (Augusta, Ga.)</jtitle><addtitle>Shock</addtitle><date>2005-12-01</date><risdate>2005</risdate><volume>24</volume><issue>6</issue><spage>523</spage><epage>528</epage><pages>523-528</pages><issn>1073-2322</issn><eissn>1540-0514</eissn><abstract>Hepatomegaly is a common postmortem observation in severely burned children, with the liver often tripling in size when compared with normal livers for age, weight, and sex. Lesions identified at autopsy include deposition of large and small fat droplets in the hepatocyte, congestion, centrilobular necrosis, and cholestasis. The present study was designed to identify the primary causes of hepatomegaly in severely burned children postmortem. For this purpose, 41 autopsies were reviewed and, when available, blood and tissue samples were studied. Histopathologic findings showed that large intrahepatocytic fat droplets within hepatocytes and cholestasis were important contributors to hepatomegaly. Liver density and wet/dry weight ratios significantly decreased with increasing liver size. Hepatocyte volume increased with increasing liver size (P < 0.001) as did total fat content (P < 0.001). The liver enzymes, alanine aminotransferase and aspartate aminotransferase, remained normal except within 5 to 10 days of injury and 5 to 10 days of death. Triglycerides made up 4% to 70% of the total fat, with the percentage of triglycerides increasing with the severity of hepatomegaly. Saturated fatty acids represented about 85% of the total fatty acids in normal-sized livers, whereas in the largest livers (400% of predicted), only 25% of the fatty acids were saturated. This study provides evidence that 85% to 90% of the hepatomegaly observed in severely burned children postmortem is associated with hepatocyte enlargement, which includes up to 19% intracellular fat. Increases in extracellular protein, intracellular glycogen, and fluid accumulation may make a minor contribution to postburn hepatomegaly.</abstract><cop>Augusta, GA</cop><pub>BioMedical Press</pub><pmid>16317382</pmid><doi>10.1097/01.shk.0000187981.78901.ee</doi><tpages>6</tpages></addata></record> |
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source | Ovid Lippincott Williams and Wilkins Journal Legacy Archive; MEDLINE; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals |
subjects | Age Factors Alanine Transaminase - metabolism Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Aspartate Aminotransferases - metabolism Biological and medical sciences Blood and lymphatic vessels Burns - complications Burns - enzymology Burns - pathology Cardiology. Vascular system Child Child, Preschool Cytoplasm - enzymology Cytoplasm - pathology Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Emergency and intensive care: burns Female Hepatocytes - enzymology Hepatocytes - pathology Hepatomegaly - enzymology Hepatomegaly - etiology Hepatomegaly - pathology Humans Intensive care medicine Liver - enzymology Liver - pathology Male Medical sciences Necrosis - enzymology Necrosis - pathology Organ Size Sex Factors Trauma Severity Indices Triglycerides - metabolism |
title | Identification of factors contributing to hepatomegaly in severely burned children |
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