Idiopathic Inflammatory Myopathy with Diffuse Alveolar Damage
Identifieur interne : 001F34 ( Istex/Corpus ); précédent : 001F33; suivant : 001F35Idiopathic Inflammatory Myopathy with Diffuse Alveolar Damage
Auteurs : C.-S. Lee ; T.-L. Chen ; C.-Y. Tzen ; F.-J. Lin ; M.-J. Peng ; C.-L. Wu ; P.-J. ChenSource :
- Clinical Rheumatology [ 0770-3198 ] ; 2002-09-01.
English descriptors
Abstract
Abstract:: Interstitial lung disease (ILD) in patients with myositis is defined by the presence of interstitial changes on radiographic examination. The reported prevalence of ILD varies from 0% to nearly 50%. However, only rarely has the pathological pattern of diffuse alveolar damage (DAD) associated with idiopathic inflammatory myopathy (IIM) been reported. We report five patients with IIM (one with dermatomyositis, one with polymyositis, and three with amyopathic dermatomyositis) and respiratory failure. Four underwent open lung biopsy with pathological proof of diffuse alveolar damage (DAD). Despite intensive immunosuppressive therapy, all of them died. In addition to the case reports, we discuss DAD in patients with IIM.
Url:
DOI: 10.1007/s100670200104
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Chen</name><affiliation><mods:affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Clinical Rheumatology</title><title level="j" type="abbrev">Clin Rheumatol</title><idno type="ISSN">0770-3198</idno><idno type="eISSN">1434-9949</idno><imprint><publisher>Springer-Verlag</publisher><pubPlace>London</pubPlace><date type="published" when="2002-09-01">2002-09-01</date><biblScope unit="volume">21</biblScope><biblScope unit="issue">5</biblScope><biblScope unit="page" from="391">391</biblScope><biblScope unit="page" to="396">396</biblScope></imprint><idno type="ISSN">0770-3198</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0770-3198</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Key words:Diffuse alveolar damage – Idiopathic inflammatory myopathy – Respiratory failure</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract:: Interstitial lung disease (ILD) in patients with myositis is defined by the presence of interstitial changes on radiographic examination. The reported prevalence of ILD varies from 0% to nearly 50%. However, only rarely has the pathological pattern of diffuse alveolar damage (DAD) associated with idiopathic inflammatory myopathy (IIM) been reported. We report five patients with IIM (one with dermatomyositis, one with polymyositis, and three with amyopathic dermatomyositis) and respiratory failure. Four underwent open lung biopsy with pathological proof of diffuse alveolar damage (DAD). Despite intensive immunosuppressive therapy, all of them died. In addition to the case reports, we discuss DAD in patients with IIM.</div></front></TEI><istex><corpusName>springer-journals</corpusName><author><json:item><name>C.-S. Lee</name><affiliations><json:string>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</json:string></affiliations></json:item><json:item><name>T.-L. Chen</name><affiliations><json:string>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</json:string></affiliations></json:item><json:item><name>C.-Y. Tzen</name><affiliations><json:string>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</json:string></affiliations></json:item><json:item><name>F.-J. Lin</name><affiliations><json:string>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</json:string></affiliations></json:item><json:item><name>M.-J. Peng</name><affiliations><json:string>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</json:string></affiliations></json:item><json:item><name>C.-L. Wu</name><affiliations><json:string>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</json:string></affiliations></json:item><json:item><name>P.-J. Chen</name><affiliations><json:string>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Key words:Diffuse alveolar damage – Idiopathic inflammatory myopathy – Respiratory failure</value></json:item></subject><articleId><json:string>210500391</json:string><json:string>Art1</json:string></articleId><arkIstex>ark:/67375/VQC-BB968HJM-M</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>OriginalPaper</json:string></originalGenre><abstract>Abstract:: Interstitial lung disease (ILD) in patients with myositis is defined by the presence of interstitial changes on radiographic examination. The reported prevalence of ILD varies from 0% to nearly 50%. However, only rarely has the pathological pattern of diffuse alveolar damage (DAD) associated with idiopathic inflammatory myopathy (IIM) been reported. We report five patients with IIM (one with dermatomyositis, one with polymyositis, and three with amyopathic dermatomyositis) and respiratory failure. Four underwent open lung biopsy with pathological proof of diffuse alveolar damage (DAD). Despite intensive immunosuppressive therapy, all of them died. 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The reported prevalence of ILD varies from 0% to nearly 50%. However, only rarely has the pathological pattern of diffuse alveolar damage (DAD) associated with idiopathic inflammatory myopathy (IIM) been reported. We report five patients with IIM (one with dermatomyositis, one with polymyositis, and three with amyopathic dermatomyositis) and respiratory failure. Four underwent open lung biopsy with pathological proof of diffuse alveolar damage (DAD). Despite intensive immunosuppressive therapy, all of them died. 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The reported prevalence of ILD varies from 0% to nearly 50%. However, only rarely has the pathological pattern of diffuse alveolar damage (DAD) associated with idiopathic inflammatory myopathy (IIM) been reported. We report five patients with IIM (one with dermatomyositis, one with polymyositis, and three with amyopathic dermatomyositis) and respiratory failure. Four underwent open lung biopsy with pathological proof of diffuse alveolar damage (DAD). Despite intensive immunosuppressive therapy, all of them died. In addition to the case reports, we discuss DAD in patients with IIM.</Para></Abstract><KeywordGroup Language="En"><Keyword>Key words:Diffuse alveolar damage – Idiopathic inflammatory myopathy – Respiratory failure</Keyword></KeywordGroup><ArticleNote Type="Misc"><SimplePara>Received: 18 June 2001 / Accepted: 6 March 2002</SimplePara></ArticleNote></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Idiopathic Inflammatory Myopathy with Diffuse Alveolar Damage</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Idiopathic Inflammatory Myopathy with Diffuse Alveolar Damage</title></titleInfo><name type="personal" displayLabel="corresp"><namePart type="given">C.-S.</namePart><namePart type="family">Lee</namePart><affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T.-L.</namePart><namePart type="family">Chen</namePart><affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C.-Y.</namePart><namePart type="family">Tzen</namePart><affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F.-J.</namePart><namePart type="family">Lin</namePart><affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M.-J.</namePart><namePart type="family">Peng</namePart><affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C.-L.</namePart><namePart type="family">Wu</namePart><affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">P.-J.</namePart><namePart type="family">Chen</namePart><affiliation>Mackay Memorial Hospital, Taipei, Taiwan, Taiwan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>Springer-Verlag</publisher><place><placeTerm type="text">London</placeTerm></place><dateIssued encoding="w3cdtf">2002-09-01</dateIssued><copyrightDate encoding="w3cdtf">2002</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><abstract lang="en">Abstract:: Interstitial lung disease (ILD) in patients with myositis is defined by the presence of interstitial changes on radiographic examination. The reported prevalence of ILD varies from 0% to nearly 50%. However, only rarely has the pathological pattern of diffuse alveolar damage (DAD) associated with idiopathic inflammatory myopathy (IIM) been reported. We report five patients with IIM (one with dermatomyositis, one with polymyositis, and three with amyopathic dermatomyositis) and respiratory failure. Four underwent open lung biopsy with pathological proof of diffuse alveolar damage (DAD). Despite intensive immunosuppressive therapy, all of them died. 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