Multiple rib infarcts: a rare form of osteonecrosis in antiphospholipid syndrome
ON has obvious association with various systemic conditions, including sickle cell disease, prolonged glucocorticoid treatment, alcohol abuse, and Gaucher's disease, and several factors, such as vascular thrombosis, mechanical defects, cellular damage, embolisation, changes in intraosseous pres...
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Veröffentlicht in: | Annals of the rheumatic diseases 2004-04, Vol.63 (4), p.457-458 |
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description | ON has obvious association with various systemic conditions, including sickle cell disease, prolonged glucocorticoid treatment, alcohol abuse, and Gaucher's disease, and several factors, such as vascular thrombosis, mechanical defects, cellular damage, embolisation, changes in intraosseous pressure, or trauma, have been proposed in its pathogenesis. 1 For rheumatological diseases, a pathogenic relationship between aPL and ON has been proposed on the basis of clinical observations of patients with APS who developed ON in the absence of glucocorticoid treatment. 2, 3 Several studies showed a correlation between aPL and ON in patients with systemic lupus erythematosus, 4- 6 and Belmonte et al 7 suggested a possible association of aPL with ON in patients with HIV infection. [...]owing to the hypercoagulable potential of aPL, vascular occlusion or thrombotic vasculopathy related to the aPL was also thought to be the underlying pathogenetic mechanism. [...]the prothrombotic potential of aPL and the above described clinical features of this patient suggest that aPL are directly implicated in the aetiopathogenesis of ON. |
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[...]owing to the hypercoagulable potential of aPL, vascular occlusion or thrombotic vasculopathy related to the aPL was also thought to be the underlying pathogenetic mechanism. [...]the prothrombotic potential of aPL and the above described clinical features of this patient suggest that aPL are directly implicated in the aetiopathogenesis of ON.</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/ard.2003.006197</identifier><identifier>PMID: 15020344</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and European League Against Rheumatism</publisher><subject>Adult ; antiphospholipid syndrome ; Antiphospholipid Syndrome - diagnostic imaging ; Antiphospholipid Syndrome - etiology ; Antiphospholipid Syndrome - pathology ; Female ; HIV ; Human immunodeficiency virus ; Humans ; Immunology ; Laboratories ; Letter ; Mixed Connective Tissue Disease - complications ; Mixed Connective Tissue Disease - diagnostic imaging ; Mixed Connective Tissue Disease - pathology ; osteonecrosis ; Osteonecrosis - complications ; Osteonecrosis - diagnostic imaging ; Osteonecrosis - pathology ; Pathogenesis ; Patients ; Radionuclide Imaging ; Rheumatic diseases ; rib infarction ; Ribs - diagnostic imaging ; Ribs - pathology ; Sickle cell anemia ; Sickle cell disease</subject><ispartof>Annals of the rheumatic diseases, 2004-04, Vol.63 (4), p.457-458</ispartof><rights>Copyright 2004 by Annals of the Rheumatic Diseases</rights><rights>COPYRIGHT 2004 BMJ Publishing Group Ltd.</rights><rights>Copyright: 2004 Copyright 2004 by Annals of the Rheumatic Diseases</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b536t-3a85ade45f6ac8b697eefd536e280df9a462dcc8d6603f4a5c47a7be9ac0bdbb3</citedby><cites>FETCH-LOGICAL-b536t-3a85ade45f6ac8b697eefd536e280df9a462dcc8d6603f4a5c47a7be9ac0bdbb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1754939/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1754939/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15020344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoo, W-H</creatorcontrib><title>Multiple rib infarcts: a rare form of osteonecrosis in antiphospholipid syndrome</title><title>Annals of the rheumatic diseases</title><addtitle>Ann Rheum Dis</addtitle><description>ON has obvious association with various systemic conditions, including sickle cell disease, prolonged glucocorticoid treatment, alcohol abuse, and Gaucher's disease, and several factors, such as vascular thrombosis, mechanical defects, cellular damage, embolisation, changes in intraosseous pressure, or trauma, have been proposed in its pathogenesis. 1 For rheumatological diseases, a pathogenic relationship between aPL and ON has been proposed on the basis of clinical observations of patients with APS who developed ON in the absence of glucocorticoid treatment. 2, 3 Several studies showed a correlation between aPL and ON in patients with systemic lupus erythematosus, 4- 6 and Belmonte et al 7 suggested a possible association of aPL with ON in patients with HIV infection. [...]owing to the hypercoagulable potential of aPL, vascular occlusion or thrombotic vasculopathy related to the aPL was also thought to be the underlying pathogenetic mechanism. [...]the prothrombotic potential of aPL and the above described clinical features of this patient suggest that aPL are directly implicated in the aetiopathogenesis of ON.</description><subject>Adult</subject><subject>antiphospholipid syndrome</subject><subject>Antiphospholipid Syndrome - diagnostic imaging</subject><subject>Antiphospholipid Syndrome - etiology</subject><subject>Antiphospholipid Syndrome - pathology</subject><subject>Female</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunology</subject><subject>Laboratories</subject><subject>Letter</subject><subject>Mixed Connective Tissue Disease - complications</subject><subject>Mixed Connective Tissue Disease - diagnostic imaging</subject><subject>Mixed Connective Tissue Disease - pathology</subject><subject>osteonecrosis</subject><subject>Osteonecrosis - complications</subject><subject>Osteonecrosis - diagnostic imaging</subject><subject>Osteonecrosis - pathology</subject><subject>Pathogenesis</subject><subject>Patients</subject><subject>Radionuclide Imaging</subject><subject>Rheumatic diseases</subject><subject>rib infarction</subject><subject>Ribs - diagnostic imaging</subject><subject>Ribs - pathology</subject><subject>Sickle cell anemia</subject><subject>Sickle cell disease</subject><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</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>eNqFkd9rFDEQx4Mo9qw--yYLvgl7TS7ZZNcHoR7WX2ftg_oassnkmnN3c032SvvfO8cerUJBQgjJfOabmfkS8pLROWNcnpjk5gtK-ZxSyRr1iMyYkHW5oJI-JjOKkVI0Uh2RZzlv8EprVj8lR6yiC8qFmJGLb7tuDNsOihTaIgzeJDvmt4UpkklQ-Jj6Ivoi5hHiADbFHDJihRkw6zJm3F3YBlfk28Gl2MNz8sSbLsOLw3lMfp59-LH8VK6-f_y8PF2VbcXlWHJTV8aBqLw0tm5lowC8wxAsaup8Y4RcOGtrJyXlXpjKCmVUC42xtHVty4_Ju0l3u2t7cBaGMZlOb1PoTbrV0QT9b2QIl3odrzVTlWh4gwKvDwIpXu0gj3oTd2nAmhFRqhZVUyukyolamw40zieimF3DAKiJE_EBn08ZqzjylCM_f4DH5aAP9sGEkylhP9ucwN-1wKjee6zRY733WE8eY8arvzu_5w-m3tcc0LWbu7hJv7VUXFX6_NdSr75efDkX78_0Evk3E9_2m__-_gdHDsB9</recordid><startdate>200404</startdate><enddate>200404</enddate><creator>Yoo, W-H</creator><general>BMJ Publishing Group Ltd and European League Against Rheumatism</general><general>BMJ Publishing Group Ltd</general><general>Elsevier Limited</general><scope>BSCLL</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>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>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>200404</creationdate><title>Multiple rib infarcts: a rare form of osteonecrosis in antiphospholipid syndrome</title><author>Yoo, W-H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b536t-3a85ade45f6ac8b697eefd536e280df9a462dcc8d6603f4a5c47a7be9ac0bdbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>antiphospholipid syndrome</topic><topic>Antiphospholipid Syndrome - diagnostic imaging</topic><topic>Antiphospholipid Syndrome - etiology</topic><topic>Antiphospholipid Syndrome - pathology</topic><topic>Female</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunology</topic><topic>Laboratories</topic><topic>Letter</topic><topic>Mixed Connective Tissue Disease - complications</topic><topic>Mixed Connective Tissue Disease - diagnostic imaging</topic><topic>Mixed Connective Tissue Disease - pathology</topic><topic>osteonecrosis</topic><topic>Osteonecrosis - complications</topic><topic>Osteonecrosis - diagnostic imaging</topic><topic>Osteonecrosis - pathology</topic><topic>Pathogenesis</topic><topic>Patients</topic><topic>Radionuclide Imaging</topic><topic>Rheumatic diseases</topic><topic>rib infarction</topic><topic>Ribs - diagnostic imaging</topic><topic>Ribs - pathology</topic><topic>Sickle cell anemia</topic><topic>Sickle cell disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yoo, W-H</creatorcontrib><collection>Istex</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>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>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>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological 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>PubMed Central (Full Participant titles)</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoo, W-H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple rib infarcts: a rare form of osteonecrosis in antiphospholipid syndrome</atitle><jtitle>Annals of the rheumatic diseases</jtitle><addtitle>Ann Rheum Dis</addtitle><date>2004-04</date><risdate>2004</risdate><volume>63</volume><issue>4</issue><spage>457</spage><epage>458</epage><pages>457-458</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>ON has obvious association with various systemic conditions, including sickle cell disease, prolonged glucocorticoid treatment, alcohol abuse, and Gaucher's disease, and several factors, such as vascular thrombosis, mechanical defects, cellular damage, embolisation, changes in intraosseous pressure, or trauma, have been proposed in its pathogenesis. 1 For rheumatological diseases, a pathogenic relationship between aPL and ON has been proposed on the basis of clinical observations of patients with APS who developed ON in the absence of glucocorticoid treatment. 2, 3 Several studies showed a correlation between aPL and ON in patients with systemic lupus erythematosus, 4- 6 and Belmonte et al 7 suggested a possible association of aPL with ON in patients with HIV infection. [...]owing to the hypercoagulable potential of aPL, vascular occlusion or thrombotic vasculopathy related to the aPL was also thought to be the underlying pathogenetic mechanism. [...]the prothrombotic potential of aPL and the above described clinical features of this patient suggest that aPL are directly implicated in the aetiopathogenesis of ON.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and European League Against Rheumatism</pub><pmid>15020344</pmid><doi>10.1136/ard.2003.006197</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult antiphospholipid syndrome Antiphospholipid Syndrome - diagnostic imaging Antiphospholipid Syndrome - etiology Antiphospholipid Syndrome - pathology Female HIV Human immunodeficiency virus Humans Immunology Laboratories Letter Mixed Connective Tissue Disease - complications Mixed Connective Tissue Disease - diagnostic imaging Mixed Connective Tissue Disease - pathology osteonecrosis Osteonecrosis - complications Osteonecrosis - diagnostic imaging Osteonecrosis - pathology Pathogenesis Patients Radionuclide Imaging Rheumatic diseases rib infarction Ribs - diagnostic imaging Ribs - pathology Sickle cell anemia Sickle cell disease |
title | Multiple rib infarcts: a rare form of osteonecrosis in antiphospholipid syndrome |
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