Severe inflammation may be caused by hyperferritinemia of pseudo-pseudo Meigs' syndrome in lupus patients: two cases reports and a literature review
Identifieur interne : 001F08 ( Istex/Corpus ); précédent : 001F07; suivant : 001F09Severe inflammation may be caused by hyperferritinemia of pseudo-pseudo Meigs' syndrome in lupus patients: two cases reports and a literature review
Auteurs : Sang Yeob Lee ; Sung Won Lee ; Won Tae ChungSource :
- Clinical Rheumatology [ 0770-3198 ] ; 2013-12-01.
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Abstract
Abstract: Pseudo-pseudo Meigs' syndrome or Tjalma syndrome is a rare manifestation of patients with systemic lupus erythematosus defined by the presence of ascites, pleural effusions, and an elevated cancer antigen 125 level. In this case, we described a patient with lupus who presented with sudden impaired renal function and subsequent development of massive ascites with marked high serum ferritin. Hyperferritinemia is one of the abnormal laboratory findings in severe inflammation with ferritin functioning as an inflammatory marker. However, its correlation with lupus activity remains unclear. Therefore, a review of the literature regarding pseudo-pseudo Meigs' syndrome associated with lupus and high ferritin level in this disease was carried out.
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DOI: 10.1007/s10067-013-2362-8
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ISTEX:F8C79F41AFC222F8F4629701CED1D077A05898F0Le document en format XML
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In this case, we described a patient with lupus who presented with sudden impaired renal function and subsequent development of massive ascites with marked high serum ferritin. Hyperferritinemia is one of the abnormal laboratory findings in severe inflammation with ferritin functioning as an inflammatory marker. However, its correlation with lupus activity remains unclear. Therefore, a review of the literature regarding pseudo-pseudo Meigs' syndrome associated with lupus and high ferritin level in this disease was carried out.</div></front></TEI><istex><corpusName>springer-journals</corpusName><author><json:item><name>Sang Yeob Lee</name><affiliations><json:string>Department of Internal Medicine and Rheumatology, Dong-A University Hospital, 3 Ga 1, Dong-daeshin dong, Seo-Gu, Busan, South Korea</json:string></affiliations></json:item><json:item><name>Sung Won Lee</name><affiliations><json:string>Department of Internal Medicine and Rheumatology, Dong-A University Hospital, 3 Ga 1, Dong-daeshin dong, Seo-Gu, Busan, South Korea</json:string></affiliations></json:item><json:item><name>Won Tae Chung</name><affiliations><json:string>Department of Internal Medicine and Rheumatology, Dong-A University Hospital, 3 Ga 1, Dong-daeshin dong, Seo-Gu, Busan, South Korea</json:string><json:string>E-mail: wtchung@dau.ac.kr</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>CA-125</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Lupus</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Meigs' syndrome</value></json:item></subject><articleId><json:string>2362</json:string><json:string>s10067-013-2362-8</json:string></articleId><arkIstex>ark:/67375/VQC-H6T9VDKT-Z</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>ReviewPaper</json:string></originalGenre><abstract>Abstract: Pseudo-pseudo Meigs' syndrome or Tjalma syndrome is a rare manifestation of patients with systemic lupus erythematosus defined by the presence of ascites, pleural effusions, and an elevated cancer antigen 125 level. 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AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Sang</GivenName><GivenName>Yeob</GivenName><FamilyName>Lee</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Sung</GivenName><GivenName>Won</GivenName><FamilyName>Lee</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1" CorrespondingAffiliationID="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Won</GivenName><GivenName>Tae</GivenName><FamilyName>Chung</FamilyName></AuthorName><Contact><Email>wtchung@dau.ac.kr</Email></Contact></Author><Affiliation ID="Aff1"><OrgDivision>Department of Internal Medicine and Rheumatology</OrgDivision><OrgName>Dong-A University Hospital</OrgName><OrgAddress><Street>3 Ga 1, Dong-daeshin dong, Seo-Gu</Street><City>Busan</City><Country Code="KR">South Korea</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En" OutputMedium="All"><Heading>Abstract</Heading><Para>Pseudo-pseudo Meigs' syndrome or Tjalma syndrome is a rare manifestation of patients with systemic lupus erythematosus defined by the presence of ascites, pleural effusions, and an elevated cancer antigen 125 level. In this case, we described a patient with lupus who presented with sudden impaired renal function and subsequent development of massive ascites with marked high serum ferritin. Hyperferritinemia is one of the abnormal laboratory findings in severe inflammation with ferritin functioning as an inflammatory marker. However, its correlation with lupus activity remains unclear. Therefore, a review of the literature regarding pseudo-pseudo Meigs' syndrome associated with lupus and high ferritin level in this disease was carried out.</Para></Abstract><KeywordGroup Language="En" OutputMedium="All"><Heading>Keywords</Heading><Keyword>CA-125</Keyword><Keyword>Lupus</Keyword><Keyword>Meigs' syndrome</Keyword></KeywordGroup></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Severe inflammation may be caused by hyperferritinemia of pseudo-pseudo Meigs' syndrome in lupus patients: two cases reports and a literature review</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Severe inflammation may be caused by hyperferritinemia of pseudo-pseudo Meigs' syndrome in lupus patients: two cases reports and a literature review</title></titleInfo><name type="personal"><namePart type="given">Sang</namePart><namePart type="given">Yeob</namePart><namePart type="family">Lee</namePart><affiliation>Department of Internal Medicine and Rheumatology, Dong-A University Hospital, 3 Ga 1, Dong-daeshin dong, Seo-Gu, Busan, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Sung</namePart><namePart type="given">Won</namePart><namePart type="family">Lee</namePart><affiliation>Department of Internal Medicine and Rheumatology, Dong-A University Hospital, 3 Ga 1, Dong-daeshin dong, Seo-Gu, Busan, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal" displayLabel="corresp"><namePart type="given">Won</namePart><namePart type="given">Tae</namePart><namePart type="family">Chung</namePart><affiliation>Department of Internal Medicine and Rheumatology, Dong-A University Hospital, 3 Ga 1, Dong-daeshin dong, Seo-Gu, Busan, South Korea</affiliation><affiliation>E-mail: wtchung@dau.ac.kr</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article" displayLabel="ReviewPaper" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-L5L7X3NF-P">review-article</genre><originInfo><publisher>Springer London</publisher><place><placeTerm type="text">London</placeTerm></place><dateCreated encoding="w3cdtf">2013-06-27</dateCreated><dateIssued encoding="w3cdtf">2013-12-01</dateIssued><copyrightDate encoding="w3cdtf">2013</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><abstract lang="en">Abstract: Pseudo-pseudo Meigs' syndrome or Tjalma syndrome is a rare manifestation of patients with systemic lupus erythematosus defined by the presence of ascites, pleural effusions, and an elevated cancer antigen 125 level. In this case, we described a patient with lupus who presented with sudden impaired renal function and subsequent development of massive ascites with marked high serum ferritin. Hyperferritinemia is one of the abnormal laboratory findings in severe inflammation with ferritin functioning as an inflammatory marker. However, its correlation with lupus activity remains unclear. Therefore, a review of the literature regarding pseudo-pseudo Meigs' syndrome associated with lupus and high ferritin level in this disease was carried out.</abstract><note>Case Based Review</note><subject lang="en"><genre>Keywords</genre><topic>CA-125</topic><topic>Lupus</topic><topic>Meigs' syndrome</topic></subject><relatedItem type="host"><titleInfo><title>Clinical Rheumatology</title><subTitle>Journal of the International League of Associations for Rheumatology</subTitle></titleInfo><titleInfo type="abbreviated"><title>Clin Rheumatol</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>Springer</publisher><dateIssued encoding="w3cdtf">2013-11-21</dateIssued><copyrightDate encoding="w3cdtf">2013</copyrightDate></originInfo><subject><genre>Journal-Subject-Collection</genre><topic authority="SpringerSubjectCodes" authorityURI="SC11">Medicine</topic></subject><subject><genre>Journal-Subject-Group</genre><topic authority="SpringerSubjectCodes" authorityURI="SCH">Medicine & Public Health</topic><topic authority="SpringerSubjectCodes" authorityURI="SCH57009">Rheumatology</topic></subject><identifier type="ISSN">0770-3198</identifier><identifier type="eISSN">1434-9949</identifier><identifier type="JournalID">10067</identifier><identifier type="IssueArticleCount">22</identifier><identifier type="VolumeIssueCount">12</identifier><part><date>2013</date><detail type="volume"><number>32</number><caption>vol.</caption></detail><detail type="issue"><number>12</number><caption>no.</caption></detail><extent unit="pages"><start>1823</start><end>1826</end></extent></part><recordInfo><recordOrigin>Clinical Rheumatology, 2013</recordOrigin></recordInfo></relatedItem><identifier type="istex">F8C79F41AFC222F8F4629701CED1D077A05898F0</identifier><identifier type="ark">ark:/67375/VQC-H6T9VDKT-Z</identifier><identifier type="DOI">10.1007/s10067-013-2362-8</identifier><identifier type="ArticleID">2362</identifier><identifier type="ArticleID">s10067-013-2362-8</identifier><accessCondition type="use and reproduction" contentType="copyright">Clinical Rheumatology, 2013</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-3XSW68JL-F">springer</recordContentSource><recordOrigin>Clinical Rheumatology, 2013</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/VQC-H6T9VDKT-Z/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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