Hepatic granulomas: a 10 year single centre experience
Background: Epithelioid granulomas have been reported in 2–15% of unselected liver biopsies, with numerous underlying aetiologies described. However, all UK series were reported before identification of hepatitis C virus (HCV). Aim: To evaluate the current aetiologies of hepatic granulomas and to as...
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description | Background: Epithelioid granulomas have been reported in 2–15% of unselected liver biopsies, with numerous underlying aetiologies described. However, all UK series were reported before identification of hepatitis C virus (HCV). Aim: To evaluate the current aetiologies of hepatic granulomas and to assess the prognosis for the “idiopathic” group, in which all investigations for a recognised cause were negative or normal. Methods: A retrospective review of patient case notes between 1991 and 2001; all patients who had a liver biopsy at Glasgow Royal Infirmary revealing epithelioid granulomas had their case notes and liver biopsies reviewed and a standard proforma completed. Results: Over the study period, 1662 liver biopsies were performed. Hepatic granulomas were found in 63. Of those identified, 47 were female, with a mean age of 42 years (range, 17–81). Underlying aetiologies were as follows: primary biliary cirrhosis (PBC; 23.8%), sarcoidosis (11.1%), idiopathic (11.1%), drug induced (9.5%), HCV (9.5%), PBC/autoimmune hepatitis (AIH) overlap (6.3%), Hodgkin lymphoma (6.3%), AIH (4.8%), tuberculosis (4.8%), resolving biliary obstruction (3.2%), and other single miscellaneous causes (9.5%). Of the seven patients with idiopathic hepatic granulomas, one was lost to follow up, one died of stroke, and the remaining five were well with no liver related morbidity at a mean follow up of 6.2 years. Conclusions: The aetiology of hepatic granulomas is broad ranging, with HCV an important cause in this population. Despite extensive investigations, a 10–15% of patients still had “idiopathic” hepatic granulomas. However, the prognosis for this last group appears to be excellent. |
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However, all UK series were reported before identification of hepatitis C virus (HCV). Aim: To evaluate the current aetiologies of hepatic granulomas and to assess the prognosis for the “idiopathic” group, in which all investigations for a recognised cause were negative or normal. Methods: A retrospective review of patient case notes between 1991 and 2001; all patients who had a liver biopsy at Glasgow Royal Infirmary revealing epithelioid granulomas had their case notes and liver biopsies reviewed and a standard proforma completed. Results: Over the study period, 1662 liver biopsies were performed. Hepatic granulomas were found in 63. Of those identified, 47 were female, with a mean age of 42 years (range, 17–81). Underlying aetiologies were as follows: primary biliary cirrhosis (PBC; 23.8%), sarcoidosis (11.1%), idiopathic (11.1%), drug induced (9.5%), HCV (9.5%), PBC/autoimmune hepatitis (AIH) overlap (6.3%), Hodgkin lymphoma (6.3%), AIH (4.8%), tuberculosis (4.8%), resolving biliary obstruction (3.2%), and other single miscellaneous causes (9.5%). Of the seven patients with idiopathic hepatic granulomas, one was lost to follow up, one died of stroke, and the remaining five were well with no liver related morbidity at a mean follow up of 6.2 years. Conclusions: The aetiology of hepatic granulomas is broad ranging, with HCV an important cause in this population. Despite extensive investigations, a 10–15% of patients still had “idiopathic” hepatic granulomas. However, the prognosis for this last group appears to be excellent.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jcp.56.11.850</identifier><identifier>PMID: 14600131</identifier><identifier>CODEN: JCPAAK</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; AIH ; AMA ; antimitochondrial antibodies ; autoimmune hepatitis ; Biological and medical sciences ; Biopsy ; Crohn's disease ; Digestive system ; epithelioid granulomas ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Granuloma - etiology ; Granuloma - virology ; HCV ; Hepatitis ; Hepatitis C - complications ; hepatitis C virus ; Histology ; Humans ; Immunology ; Inflammatory bowel disease ; Investigative techniques, diagnostic techniques (general aspects) ; liver biopsy ; Liver cirrhosis ; Liver Diseases - etiology ; Liver Diseases - virology ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Lymphoma ; Male ; Medical sciences ; Middle Aged ; Original ; Other diseases. Semiology ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Patients ; PBC ; primary biliary cirrhosis ; Prognosis ; Retrospective Studies ; Sarcoidosis ; Survival Analysis ; Tropical diseases ; Tuberculosis</subject><ispartof>Journal of clinical pathology, 2003-11, Vol.56 (11), p.850-853</ispartof><rights>Copyright 2003 Journal of Clinical Pathology</rights><rights>2004 INIST-CNRS</rights><rights>COPYRIGHT 2003 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2003 Copyright 2003 Journal of Clinical Pathology</rights><rights>Copyright © Copyright 2003 Journal of Clinical Pathology 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b589t-5fade5ac71265ce8f87c017277175ec93d149779963733479c41abde6a0181853</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770104/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1770104/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15248817$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14600131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gaya, D R</creatorcontrib><creatorcontrib>Thorburn, D</creatorcontrib><creatorcontrib>Oien, K A</creatorcontrib><creatorcontrib>Morris, A J</creatorcontrib><creatorcontrib>Stanley, A J</creatorcontrib><title>Hepatic granulomas: a 10 year single centre experience</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><description>Background: Epithelioid granulomas have been reported in 2–15% of unselected liver biopsies, with numerous underlying aetiologies described. However, all UK series were reported before identification of hepatitis C virus (HCV). Aim: To evaluate the current aetiologies of hepatic granulomas and to assess the prognosis for the “idiopathic” group, in which all investigations for a recognised cause were negative or normal. Methods: A retrospective review of patient case notes between 1991 and 2001; all patients who had a liver biopsy at Glasgow Royal Infirmary revealing epithelioid granulomas had their case notes and liver biopsies reviewed and a standard proforma completed. Results: Over the study period, 1662 liver biopsies were performed. Hepatic granulomas were found in 63. Of those identified, 47 were female, with a mean age of 42 years (range, 17–81). Underlying aetiologies were as follows: primary biliary cirrhosis (PBC; 23.8%), sarcoidosis (11.1%), idiopathic (11.1%), drug induced (9.5%), HCV (9.5%), PBC/autoimmune hepatitis (AIH) overlap (6.3%), Hodgkin lymphoma (6.3%), AIH (4.8%), tuberculosis (4.8%), resolving biliary obstruction (3.2%), and other single miscellaneous causes (9.5%). Of the seven patients with idiopathic hepatic granulomas, one was lost to follow up, one died of stroke, and the remaining five were well with no liver related morbidity at a mean follow up of 6.2 years. Conclusions: The aetiology of hepatic granulomas is broad ranging, with HCV an important cause in this population. Despite extensive investigations, a 10–15% of patients still had “idiopathic” hepatic granulomas. However, the prognosis for this last group appears to be excellent.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>AIH</subject><subject>AMA</subject><subject>antimitochondrial antibodies</subject><subject>autoimmune hepatitis</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Crohn's disease</subject><subject>Digestive system</subject><subject>epithelioid granulomas</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Granuloma - etiology</subject><subject>Granuloma - virology</subject><subject>HCV</subject><subject>Hepatitis</subject><subject>Hepatitis C - complications</subject><subject>hepatitis C virus</subject><subject>Histology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Inflammatory bowel disease</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>liver biopsy</subject><subject>Liver cirrhosis</subject><subject>Liver Diseases - etiology</subject><subject>Liver Diseases - virology</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Lymphoma</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Other diseases. Semiology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Patients</subject><subject>PBC</subject><subject>primary biliary cirrhosis</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><subject>Sarcoidosis</subject><subject>Survival Analysis</subject><subject>Tropical diseases</subject><subject>Tuberculosis</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</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>eNqFkctrFEEQxgdRzCZ69CoDoniZtWumX5ODEBbjqkEhRK9Nb2_N2uu87J4JyX9vrTtkVQLSh37Ur796fEnyDNgcoJBvtq6fC0nnuRbsQTIDrvKMA5cPkxljOWSl4vIoOY5xyxgUCorHyRGFdxeYJXKJvR28SzfBtmPdNTaepjYFlt6iDWn07abG1GE7BEzxpsfgsXX4JHlU2Tri02k_Sb6ev7taLLOLL-8_LM4uspXQ5ZCJyq5RWKcgl8KhrrRyDFSuFCiBrizWwEulylIWqii4Kh0Hu1qjtAw0aFGcJG_3uv24anD9uw5bmz74xoZb01lv_o60_rvZdNcGlGLAOAm8mgRC93PEOJjGR4d1bVvsxmhoHlzTIAl88Q-47cbQUnOkpYHlRSkZUdme2tgajW-rjrK6DbZIybsWK0_PZ0CCWvN8V__8Hp7WGhvv7v0wJXChizFgddcrMLMz3JDhRkg6GzKc-Od_DuhATw4T8HICbHS2rshm5-OBEznXGtQhsY8D3tzFbfhhpCqUMJ-_LYz8eFl-Or9cmiviX-_5VbP9T42_AN_VzFw</recordid><startdate>20031101</startdate><enddate>20031101</enddate><creator>Gaya, D R</creator><creator>Thorburn, D</creator><creator>Oien, K A</creator><creator>Morris, A J</creator><creator>Stanley, A J</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ</general><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>Copyright 2003 Journal of Clinical Pathology</general><scope>BSCLL</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20031101</creationdate><title>Hepatic granulomas: a 10 year single centre experience</title><author>Gaya, D R ; Thorburn, D ; Oien, K A ; Morris, A J ; Stanley, A J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b589t-5fade5ac71265ce8f87c017277175ec93d149779963733479c41abde6a0181853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>AIH</topic><topic>AMA</topic><topic>antimitochondrial antibodies</topic><topic>autoimmune hepatitis</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Crohn's disease</topic><topic>Digestive system</topic><topic>epithelioid granulomas</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Granuloma - etiology</topic><topic>Granuloma - virology</topic><topic>HCV</topic><topic>Hepatitis</topic><topic>Hepatitis C - complications</topic><topic>hepatitis C virus</topic><topic>Histology</topic><topic>Humans</topic><topic>Immunology</topic><topic>Inflammatory bowel disease</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>liver biopsy</topic><topic>Liver cirrhosis</topic><topic>Liver Diseases - etiology</topic><topic>Liver Diseases - virology</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Lymphoma</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Other diseases. Semiology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Patients</topic><topic>PBC</topic><topic>primary biliary cirrhosis</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><topic>Sarcoidosis</topic><topic>Survival Analysis</topic><topic>Tropical diseases</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gaya, D R</creatorcontrib><creatorcontrib>Thorburn, D</creatorcontrib><creatorcontrib>Oien, K A</creatorcontrib><creatorcontrib>Morris, A J</creatorcontrib><creatorcontrib>Stanley, A J</creatorcontrib><collection>Istex</collection><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>ProQuest Central (Corporate)</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>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>ProQuest Central</collection><collection>BMJ Journals</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>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gaya, D R</au><au>Thorburn, D</au><au>Oien, K A</au><au>Morris, A J</au><au>Stanley, A J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatic granulomas: a 10 year single centre experience</atitle><jtitle>Journal of clinical pathology</jtitle><addtitle>J Clin Pathol</addtitle><date>2003-11-01</date><risdate>2003</risdate><volume>56</volume><issue>11</issue><spage>850</spage><epage>853</epage><pages>850-853</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><coden>JCPAAK</coden><abstract>Background: Epithelioid granulomas have been reported in 2–15% of unselected liver biopsies, with numerous underlying aetiologies described. However, all UK series were reported before identification of hepatitis C virus (HCV). Aim: To evaluate the current aetiologies of hepatic granulomas and to assess the prognosis for the “idiopathic” group, in which all investigations for a recognised cause were negative or normal. Methods: A retrospective review of patient case notes between 1991 and 2001; all patients who had a liver biopsy at Glasgow Royal Infirmary revealing epithelioid granulomas had their case notes and liver biopsies reviewed and a standard proforma completed. Results: Over the study period, 1662 liver biopsies were performed. Hepatic granulomas were found in 63. Of those identified, 47 were female, with a mean age of 42 years (range, 17–81). Underlying aetiologies were as follows: primary biliary cirrhosis (PBC; 23.8%), sarcoidosis (11.1%), idiopathic (11.1%), drug induced (9.5%), HCV (9.5%), PBC/autoimmune hepatitis (AIH) overlap (6.3%), Hodgkin lymphoma (6.3%), AIH (4.8%), tuberculosis (4.8%), resolving biliary obstruction (3.2%), and other single miscellaneous causes (9.5%). Of the seven patients with idiopathic hepatic granulomas, one was lost to follow up, one died of stroke, and the remaining five were well with no liver related morbidity at a mean follow up of 6.2 years. Conclusions: The aetiology of hepatic granulomas is broad ranging, with HCV an important cause in this population. Despite extensive investigations, a 10–15% of patients still had “idiopathic” hepatic granulomas. However, the prognosis for this last group appears to be excellent.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>14600131</pmid><doi>10.1136/jcp.56.11.850</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over AIH AMA antimitochondrial antibodies autoimmune hepatitis Biological and medical sciences Biopsy Crohn's disease Digestive system epithelioid granulomas Female Gastroenterology. Liver. Pancreas. Abdomen Granuloma - etiology Granuloma - virology HCV Hepatitis Hepatitis C - complications hepatitis C virus Histology Humans Immunology Inflammatory bowel disease Investigative techniques, diagnostic techniques (general aspects) liver biopsy Liver cirrhosis Liver Diseases - etiology Liver Diseases - virology Liver. Biliary tract. Portal circulation. Exocrine pancreas Lymphoma Male Medical sciences Middle Aged Original Other diseases. Semiology Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Patients PBC primary biliary cirrhosis Prognosis Retrospective Studies Sarcoidosis Survival Analysis Tropical diseases Tuberculosis |
title | Hepatic granulomas: a 10 year single centre experience |
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