Pneumomediastinum and subcutaneous emphysema secondary to amyopathic dermatomyositis with cryptogenic organizing pneumonia in invasive breast cancer: a case report and review of literature
Identifieur interne : 001E94 ( Istex/Corpus ); précédent : 001E93; suivant : 001E95Pneumomediastinum and subcutaneous emphysema secondary to amyopathic dermatomyositis with cryptogenic organizing pneumonia in invasive breast cancer: a case report and review of literature
Auteurs : Sung Hwan Park ; Yoon-Seup Kum ; Kyung-Chan Kim ; Jung-Yoon Choe ; Sung-Hoon Park ; Seong-Kyu KimSource :
- Rheumatology International [ 0172-8172 ] ; 2009-08-01.
English descriptors
- KwdEn :
Abstract
Abstract: Amyopathic dermatomyositis (ADM) is recognized as a variant phenotype of dermatomyositis and characterized by typical skin manifestations without evidence of muscular inflammation. While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. We report a case presented with the spontaneous pneumomediastinum and subcutaneous emphysema in both ADM and cryptogenic organizing pneumonia during adjuvant chemotherapy based on cyclophosphamide for breast cancer.
Url:
DOI: 10.1007/s00296-008-0808-0
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ISTEX:2042FA4DC1896AF1AE6A677EA2034CEC946AA53ELe document en format XML
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705-718, Daegu, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Choe, Jung Yoon" sort="Choe, Jung Yoon" uniqKey="Choe J" first="Jung-Yoon" last="Choe">Jung-Yoon Choe</name><affiliation><mods:affiliation>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Park, Sung Hoon" sort="Park, Sung Hoon" uniqKey="Park S" first="Sung-Hoon" last="Park">Sung-Hoon Park</name><affiliation><mods:affiliation>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Kim, Seong Kyu" sort="Kim, Seong Kyu" uniqKey="Kim S" first="Seong-Kyu" last="Kim">Seong-Kyu Kim</name><affiliation><mods:affiliation>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: kimsk714@cu.ac.kr</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Rheumatology International</title><title level="j" type="sub">Clinical and Experimental Investigations</title><title level="j" type="abbrev">Rheumatol Int</title><idno type="ISSN">0172-8172</idno><idno type="eISSN">1437-160X</idno><imprint><publisher>Springer-Verlag</publisher><pubPlace>Berlin/Heidelberg</pubPlace><date type="published" when="2009-08-01">2009-08-01</date><biblScope unit="volume">29</biblScope><biblScope unit="issue">10</biblScope><biblScope unit="page" from="1231">1231</biblScope><biblScope unit="page" to="1235">1235</biblScope></imprint><idno type="ISSN">0172-8172</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0172-8172</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amyopathic dermatomyositis</term><term>Breast cancer</term><term>Cryptogenic organizing pneumonia</term><term>Pneumomediastinum</term><term>Subcutaneous emphysema</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: Amyopathic dermatomyositis (ADM) is recognized as a variant phenotype of dermatomyositis and characterized by typical skin manifestations without evidence of muscular inflammation. While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. We report a case presented with the spontaneous pneumomediastinum and subcutaneous emphysema in both ADM and cryptogenic organizing pneumonia during adjuvant chemotherapy based on cyclophosphamide for breast cancer.</div></front></TEI><istex><corpusName>springer-journals</corpusName><author><json:item><name>Sung Hwan Park</name><affiliations><json:string>Department of General Surgery, Catholic University of Daegu School of Medicine, Daegu, South Korea</json:string></affiliations></json:item><json:item><name>Yoon-Seup Kum</name><affiliations><json:string>Department of Pathology, Catholic University of Daegu School of Medicine, Daegu, South Korea</json:string></affiliations></json:item><json:item><name>Kyung-Chan Kim</name><affiliations><json:string>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</json:string></affiliations></json:item><json:item><name>Jung-Yoon Choe</name><affiliations><json:string>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</json:string></affiliations></json:item><json:item><name>Sung-Hoon Park</name><affiliations><json:string>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</json:string></affiliations></json:item><json:item><name>Seong-Kyu Kim</name><affiliations><json:string>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</json:string><json:string>E-mail: kimsk714@cu.ac.kr</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Amyopathic dermatomyositis</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Breast cancer</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Cryptogenic organizing pneumonia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Pneumomediastinum</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Subcutaneous emphysema</value></json:item></subject><articleId><json:string>808</json:string><json:string>s00296-008-0808-0</json:string></articleId><arkIstex>ark:/67375/VQC-BZD5SMJN-0</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>Report</json:string></originalGenre><abstract>Abstract: Amyopathic dermatomyositis (ADM) is recognized as a variant phenotype of dermatomyositis and characterized by typical skin manifestations without evidence of muscular inflammation. While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. We report a case presented with the spontaneous pneumomediastinum and subcutaneous emphysema in both ADM and cryptogenic organizing pneumonia during adjuvant chemotherapy based on cyclophosphamide for breast cancer.</abstract><qualityIndicators><score>5.852</score><pdfWordCount>2556</pdfWordCount><pdfCharCount>17493</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>5</pdfPageCount><pdfPageSize>595 x 791 pts</pdfPageSize><refBibsNative>false</refBibsNative><abstractWordCount>108</abstractWordCount><abstractCharCount>816</abstractCharCount><keywordCount>5</keywordCount></qualityIndicators><title>Pneumomediastinum and subcutaneous emphysema secondary to amyopathic dermatomyositis with cryptogenic organizing pneumonia in invasive breast cancer: a case report and review of literature</title><genre><json:string>research-article</json:string></genre><host><title>Rheumatology 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While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. 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report and review of literature</ArticleTitle><ArticleCategory>Case Report</ArticleCategory><ArticleFirstPage>1231</ArticleFirstPage><ArticleLastPage>1235</ArticleLastPage><ArticleHistory><RegistrationDate><Year>2008</Year><Month>11</Month><Day>20</Day></RegistrationDate><Received><Year>2008</Year><Month>8</Month><Day>29</Day></Received><Accepted><Year>2008</Year><Month>11</Month><Day>20</Day></Accepted><OnlineDate><Year>2008</Year><Month>12</Month><Day>18</Day></OnlineDate></ArticleHistory><ArticleCopyright><CopyrightHolderName>Springer-Verlag</CopyrightHolderName><CopyrightYear>2008</CopyrightYear></ArticleCopyright><ArticleGrants Type="Regular"><MetadataGrant Grant="OpenAccess"></MetadataGrant><AbstractGrant Grant="OpenAccess"></AbstractGrant><BodyPDFGrant Grant="Restricted"></BodyPDFGrant><BodyHTMLGrant Grant="Restricted"></BodyHTMLGrant><BibliographyGrant Grant="Restricted"></BibliographyGrant><ESMGrant Grant="Restricted"></ESMGrant></ArticleGrants></ArticleInfo><ArticleHeader><AuthorGroup><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Sung</GivenName><GivenName>Hwan</GivenName><FamilyName>Park</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff2"><AuthorName DisplayOrder="Western"><GivenName>Yoon-Seup</GivenName><FamilyName>Kum</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>Kyung-Chan</GivenName><FamilyName>Kim</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>Jung-Yoon</GivenName><FamilyName>Choe</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>Sung-Hoon</GivenName><FamilyName>Park</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3" CorrespondingAffiliationID="Aff3"><AuthorName DisplayOrder="Western"><GivenName>Seong-Kyu</GivenName><FamilyName>Kim</FamilyName></AuthorName><Contact><Phone>+82-53-6503038</Phone><Fax>+82-53-6298248</Fax><Email>kimsk714@cu.ac.kr</Email></Contact></Author><Affiliation ID="Aff1"><OrgDivision>Department of General Surgery</OrgDivision><OrgName>Catholic University of Daegu School of Medicine</OrgName><OrgAddress><City>Daegu</City><Country Code="KR">South Korea</Country></OrgAddress></Affiliation><Affiliation ID="Aff2"><OrgDivision>Department of Pathology</OrgDivision><OrgName>Catholic University of Daegu School of Medicine</OrgName><OrgAddress><City>Daegu</City><Country Code="KR">South Korea</Country></OrgAddress></Affiliation><Affiliation ID="Aff3"><OrgDivision>Department of Internal Medicine</OrgDivision><OrgName>Catholic University of Daegu School of Medicine</OrgName><OrgAddress><Street>3056-6 Daemyung 4-Dong, Namgu</Street><City>Daegu</City><Postcode>705-718</Postcode><Country Code="KR">South Korea</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En" OutputMedium="All"><Heading>Abstract</Heading><Para>Amyopathic dermatomyositis (ADM) is recognized as a variant phenotype of dermatomyositis and characterized by typical skin manifestations without evidence of muscular inflammation. While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. We report a case presented with the spontaneous pneumomediastinum and subcutaneous emphysema in both ADM and cryptogenic organizing pneumonia during adjuvant chemotherapy based on cyclophosphamide for breast cancer.</Para></Abstract><KeywordGroup Language="En" OutputMedium="All"><Heading>Keywords</Heading><Keyword>Amyopathic dermatomyositis</Keyword><Keyword>Breast cancer</Keyword><Keyword>Cryptogenic organizing pneumonia</Keyword><Keyword>Pneumomediastinum</Keyword><Keyword>Subcutaneous emphysema</Keyword></KeywordGroup></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Pneumomediastinum and subcutaneous emphysema secondary to amyopathic dermatomyositis with cryptogenic organizing pneumonia in invasive breast cancer: a case report and review of literature</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Pneumomediastinum and subcutaneous emphysema secondary to amyopathic dermatomyositis with cryptogenic organizing pneumonia in invasive breast cancer: a case report and review of literature</title></titleInfo><name type="personal"><namePart type="given">Sung</namePart><namePart type="given">Hwan</namePart><namePart type="family">Park</namePart><affiliation>Department of General Surgery, Catholic University of Daegu School of Medicine, Daegu, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Yoon-Seup</namePart><namePart type="family">Kum</namePart><affiliation>Department of Pathology, Catholic University of Daegu School of Medicine, Daegu, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Kyung-Chan</namePart><namePart type="family">Kim</namePart><affiliation>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jung-Yoon</namePart><namePart type="family">Choe</namePart><affiliation>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Sung-Hoon</namePart><namePart type="family">Park</namePart><affiliation>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal" displayLabel="corresp"><namePart type="given">Seong-Kyu</namePart><namePart type="family">Kim</namePart><affiliation>Department of Internal Medicine, Catholic University of Daegu School of Medicine, 3056-6 Daemyung 4-Dong, Namgu, 705-718, Daegu, South Korea</affiliation><affiliation>E-mail: kimsk714@cu.ac.kr</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Report" 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">Berlin/Heidelberg</placeTerm></place><dateCreated encoding="w3cdtf">2008-08-29</dateCreated><dateIssued encoding="w3cdtf">2009-08-01</dateIssued><copyrightDate encoding="w3cdtf">2008</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><abstract lang="en">Abstract: Amyopathic dermatomyositis (ADM) is recognized as a variant phenotype of dermatomyositis and characterized by typical skin manifestations without evidence of muscular inflammation. While interstitial lung disease (ILD) is occasionally found as one of the lung manifestations in ADM patients, the development of a pneumomediastinum and/or subcutaneous emphysema in this disease entity is one of the extremely rare pulmonary complications. These latter complicated pulmonary manifestations have been usually reported in idiopathic ADM with ILD without any other associated medical conditions. We report a case presented with the spontaneous pneumomediastinum and subcutaneous emphysema in both ADM and cryptogenic organizing pneumonia during adjuvant chemotherapy based on cyclophosphamide for breast cancer.</abstract><note>Case Report</note><subject lang="en"><genre>Keywords</genre><topic>Amyopathic dermatomyositis</topic><topic>Breast cancer</topic><topic>Cryptogenic organizing pneumonia</topic><topic>Pneumomediastinum</topic><topic>Subcutaneous emphysema</topic></subject><relatedItem type="host"><titleInfo><title>Rheumatology International</title><subTitle>Clinical and Experimental Investigations</subTitle></titleInfo><titleInfo type="abbreviated"><title>Rheumatol Int</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">2009-07-29</dateIssued><copyrightDate encoding="w3cdtf">2009</copyrightDate></originInfo><subject><genre>Medicine & Public Health</genre><topic>Rheumatology</topic></subject><identifier type="ISSN">0172-8172</identifier><identifier type="eISSN">1437-160X</identifier><identifier type="JournalID">296</identifier><identifier type="IssueArticleCount">24</identifier><identifier type="VolumeIssueCount">12</identifier><part><date>2009</date><detail type="volume"><number>29</number><caption>vol.</caption></detail><detail type="issue"><number>10</number><caption>no.</caption></detail><extent unit="pages"><start>1231</start><end>1235</end></extent></part><recordInfo><recordOrigin>Springer-Verlag, 2009</recordOrigin></recordInfo></relatedItem><identifier type="istex">2042FA4DC1896AF1AE6A677EA2034CEC946AA53E</identifier><identifier type="ark">ark:/67375/VQC-BZD5SMJN-0</identifier><identifier type="DOI">10.1007/s00296-008-0808-0</identifier><identifier type="ArticleID">808</identifier><identifier type="ArticleID">s00296-008-0808-0</identifier><accessCondition type="use and reproduction" contentType="copyright">Springer-Verlag, 2008</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>Springer-Verlag, 2008</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/VQC-BZD5SMJN-0/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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