Giant cell angiofibroma or localized periorbital lymphedema?
Identifieur interne : 006386 ( Istex/Corpus ); précédent : 006385; suivant : 006387Giant cell angiofibroma or localized periorbital lymphedema?
Auteurs : Michael C. Lynch ; Catherine G. Chung ; Charles S. Specht ; Michael Wilkinson ; Loren E. ClarkeSource :
- Journal of Cutaneous Pathology [ 0303-6987 ] ; 2013-12.
Abstract
Giant cell angiofibroma represents a rare soft tissue neoplasm with a predilection for the orbit. We recently encountered a mass removed from the lower eyelid of a 56‐year‐old female that histopathologically resembled giant cell angiofibroma. The process consisted of haphazardly arranged CD34‐positive spindled and multinucleated cells within an edematous, densely vascular stroma. However, the patient had recently undergone laryngectomy and radiotherapy for a laryngeal squamous cell carcinoma. A similar mass had arisen on the contralateral eyelid, and both had developed several months post‐therapy. Lymphedema of the orbit can present as tumor‐like nodules and in some cases may share histopathologic features purported to be characteristic of giant cell angiofibroma. A relationship between giant cell angiofibroma and lymphedema has not been established, but our case suggests there may be one. The potential overlap of these two conditions should be recognized, as should other entities that may enter the differential diagnosis.
Url:
DOI: 10.1111/cup.12225
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ISTEX:D4EA5C723196CCF27BF3340577107CE2599821FFLe document en format XML
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Specht</name><affiliation><mods:affiliation>Department of Pathology, The Penn State Hershey Medical Center, Hershey, PA, USA</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</mods:affiliation></affiliation></author><author><name sortKey="Wilkinson, Michael" sort="Wilkinson, Michael" uniqKey="Wilkinson M" first="Michael" last="Wilkinson">Michael Wilkinson</name><affiliation><mods:affiliation>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</mods:affiliation></affiliation></author><author><name sortKey="Clarke, Loren E" sort="Clarke, Loren E" uniqKey="Clarke L" first="Loren E." last="Clarke">Loren E. 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Lynch</name><affiliation><mods:affiliation>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</mods:affiliation></affiliation><affiliation><mods:affiliation>Michael C. Lynch, MDDepartment of Pathology, Penn State Hershey Medical Center, H179, 500 University Drive, PO Box 850, Hershey, PA 17033, USATel: +1 717 531 8993Fax: +1 717 531 7741e‐mail:</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: mlynch1@hmc.psu.edu</mods:affiliation></affiliation></author><author><name sortKey="Chung, Catherine G" sort="Chung, Catherine G" uniqKey="Chung C" first="Catherine G." last="Chung">Catherine G. Chung</name><affiliation><mods:affiliation>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</mods:affiliation></affiliation></author><author><name sortKey="Specht, Charles S" sort="Specht, Charles S" uniqKey="Specht C" first="Charles S." last="Specht">Charles S. Specht</name><affiliation><mods:affiliation>Department of Pathology, The Penn State Hershey Medical Center, Hershey, PA, USA</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</mods:affiliation></affiliation></author><author><name sortKey="Wilkinson, Michael" sort="Wilkinson, Michael" uniqKey="Wilkinson M" first="Michael" last="Wilkinson">Michael Wilkinson</name><affiliation><mods:affiliation>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</mods:affiliation></affiliation></author><author><name sortKey="Clarke, Loren E" sort="Clarke, Loren E" uniqKey="Clarke L" first="Loren E." last="Clarke">Loren E. Clarke</name><affiliation><mods:affiliation>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Journal of Cutaneous Pathology</title><title level="j" type="alt">JOURNAL OF CUTANEOUS PATHOLOGY</title><idno type="ISSN">0303-6987</idno><idno type="eISSN">1600-0560</idno><imprint><biblScope unit="vol">40</biblScope><biblScope unit="issue">12</biblScope><biblScope unit="page" from="1059">1059</biblScope><biblScope unit="page" to="1062">1062</biblScope><biblScope unit="page-count">4</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2013-12">2013-12</date></imprint><idno type="ISSN">0303-6987</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0303-6987</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract">Giant cell angiofibroma represents a rare soft tissue neoplasm with a predilection for the orbit. We recently encountered a mass removed from the lower eyelid of a 56‐year‐old female that histopathologically resembled giant cell angiofibroma. The process consisted of haphazardly arranged CD34‐positive spindled and multinucleated cells within an edematous, densely vascular stroma. However, the patient had recently undergone laryngectomy and radiotherapy for a laryngeal squamous cell carcinoma. A similar mass had arisen on the contralateral eyelid, and both had developed several months post‐therapy. Lymphedema of the orbit can present as tumor‐like nodules and in some cases may share histopathologic features purported to be characteristic of giant cell angiofibroma. A relationship between giant cell angiofibroma and lymphedema has not been established, but our case suggests there may be one. The potential overlap of these two conditions should be recognized, as should other entities that may enter the differential diagnosis.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>lymphedema</json:string><json:string>giant cell</json:string><json:string>multinucleated</json:string><json:string>brous</json:string><json:string>brous tumor</json:string><json:string>pathol</json:string><json:string>john wiley sons</json:string><json:string>multinucleated cells</json:string><json:string>radiotherapy</json:string><json:string>histopathologic</json:string><json:string>multinucleated giant cells</json:string><json:string>differential diagnosis</json:string><json:string>cutan pathol</json:string><json:string>penn state hershey</json:string><json:string>eyelid</json:string><json:string>localized</json:string><json:string>hershey</json:string><json:string>histopathologic features</json:string><json:string>pleomorphic lipoma</json:string><json:string>surg pathol</json:string><json:string>localized periorbital lymphedema</json:string><json:string>adjuvant radiotherapy</json:string><json:string>right eyelid</json:string><json:string>resection specimen</json:string><json:string>spindle cells</json:string><json:string>surgical debulking</json:string><json:string>cell carcinoma</json:string><json:string>case series</json:string><json:string>brous septa</json:string><json:string>orbital masses</json:string><json:string>localized lymphedema</json:string><json:string>orbital</json:string></teeft></keywords><author><json:item><name>Michael C. Lynch</name><affiliations><json:string>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</json:string><json:string>Michael C. Lynch, MDDepartment of Pathology, Penn State Hershey Medical Center, H179, 500 University Drive, PO Box 850, Hershey, PA 17033, USATel: +1 717 531 8993Fax: +1 717 531 7741e‐mail:</json:string><json:string>E-mail: mlynch1@hmc.psu.edu</json:string></affiliations></json:item><json:item><name>Catherine G. Chung</name><affiliations><json:string>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</json:string></affiliations></json:item><json:item><name>Charles S. Specht</name><affiliations><json:string>Department of Pathology, The Penn State Hershey Medical Center, Hershey, PA, USA</json:string><json:string>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</json:string></affiliations></json:item><json:item><name>Michael Wilkinson</name><affiliations><json:string>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</json:string></affiliations></json:item><json:item><name>Loren E. 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We recently encountered a mass removed from the lower eyelid of a 56‐year‐old female that histopathologically resembled giant cell angiofibroma. The process consisted of haphazardly arranged CD34‐positive spindled and multinucleated cells within an edematous, densely vascular stroma. However, the patient had recently undergone laryngectomy and radiotherapy for a laryngeal squamous cell carcinoma. A similar mass had arisen on the contralateral eyelid, and both had developed several months post‐therapy. Lymphedema of the orbit can present as tumor‐like nodules and in some cases may share histopathologic features purported to be characteristic of giant cell angiofibroma. A relationship between giant cell angiofibroma and lymphedema has not been established, but our case suggests there may be one. 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Lynch, MD Department of Pathology, Penn State Hershey Medical Center, H179, 500 University Drive, PO Box 850, Hershey, PA 17033, USA Tel: +1 717 531 8993 Fax: +1 717 531 7741 e‐mail: mlynch1@hmc.psu.edu</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Catherine G.</forename><surname>Chung</surname></persName><affiliation><orgName>Department of Pathology</orgName><orgName>The Penn State Hershey Medical Center</orgName><address><settlement type="city">Hershey</settlement><region>PA</region><country key="US">USA</country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Charles S.</forename><surname>Specht</surname></persName><affiliation><orgName>Department of Pathology</orgName><orgName>The Penn State Hershey Medical Center</orgName><address><settlement type="city">Hershey</settlement><region>PA</region><country key="US">USA</country></address></affiliation><affiliation><orgName>Department of Ophthalmology</orgName><orgName>The Penn State Hershey Medical Center</orgName><address><settlement type="city">Hershey</settlement><region>PA</region><country key="US">USA</country></address></affiliation></author><author xml:id="author-0003"><persName><forename type="first">Michael</forename><surname>Wilkinson</surname></persName><affiliation><orgName>Department of Ophthalmology</orgName><orgName>The Penn State Hershey Medical Center</orgName><address><settlement type="city">Hershey</settlement><region>PA</region><country key="US">USA</country></address></affiliation></author><author xml:id="author-0004"><persName><forename type="first">Loren E.</forename><surname>Clarke</surname></persName><affiliation><orgName>Department of Pathology</orgName><orgName>The Penn State Hershey Medical Center</orgName><address><settlement type="city">Hershey</settlement><region>PA</region><country key="US">USA</country></address></affiliation></author><idno type="istex">D4EA5C723196CCF27BF3340577107CE2599821FF</idno><idno type="DOI">10.1111/cup.12225</idno><idno type="unit">CUP12225</idno><idno type="toTypesetVersion">file:CUP.CUP12225.pdf</idno></analytic><monogr><title level="j" type="main">Journal of Cutaneous Pathology</title><title level="j" type="alt">JOURNAL OF CUTANEOUS PATHOLOGY</title><idno type="pISSN">0303-6987</idno><idno type="eISSN">1600-0560</idno><idno type="book-DOI">10.1111/(ISSN)1600-0560</idno><idno type="book-part-DOI">10.1111/cup.2013.40.issue-12</idno><idno type="product">CUP</idno><imprint><biblScope unit="vol">40</biblScope><biblScope unit="issue">12</biblScope><biblScope unit="page" from="1059">1059</biblScope><biblScope unit="page" to="1062">1062</biblScope><biblScope unit="page-count">4</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2013-12"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract style="main" xml:id="cup12225-abs-0001"><head>Abstract</head><p xml:id="cup12225-para-0001">Giant cell angiofibroma represents a rare soft tissue neoplasm with a predilection for the orbit. We recently encountered a mass removed from the lower eyelid of a 56‐year‐old female that histopathologically resembled giant cell angiofibroma. The process consisted of haphazardly arranged <hi rend="fc">CD34</hi>‐positive spindled and multinucleated cells within an edematous, densely vascular stroma. However, the patient had recently undergone laryngectomy and radiotherapy for a laryngeal squamous cell carcinoma. A similar mass had arisen on the contralateral eyelid, and both had developed several months post‐therapy. Lymphedema of the orbit can present as tumor‐like nodules and in some cases may share histopathologic features purported to be characteristic of giant cell angiofibroma. A relationship between giant cell angiofibroma and lymphedema has not been established, but our case suggests there may be one. The potential overlap of these two conditions should be recognized, as should other entities that may enter the differential diagnosis.</p></abstract><textClass><keywords><term xml:id="cup12225-kwd-0001">giant cell angiofibroma</term><term xml:id="cup12225-kwd-0002">herniated orbital fat</term><term xml:id="cup12225-kwd-0003">lymphedema</term><term xml:id="cup12225-kwd-0004">massive localized lymphedema</term></keywords><classCode scheme="articleCategory">Case Report</classCode><classCode scheme="tocHeading1">Case Reports</classCode></textClass><langUsage><language ident="EN"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/D4EA5C723196CCF27BF3340577107CE2599821FF/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component type="serialArticle" version="2.0" xml:lang="en" xml:id="cup12225"><header xml:id="cup12225-hdr-0001"><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi>10.1111/(ISSN)1600-0560</doi><issn type="print">0303-6987</issn><issn type="electronic">1600-0560</issn><idGroup><id type="product" value="CUP"></id></idGroup><titleGroup><title type="main" sort="JOURNAL OF CUTANEOUS PATHOLOGY">Journal of Cutaneous Pathology</title><title type="short">J Cutan Pathol</title></titleGroup></publicationMeta><publicationMeta level="part" position="120"><doi origin="wiley">10.1111/cup.2013.40.issue-12</doi><copyright ownership="publisher">© 2013 John Wiley & Sons A/S. 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Published by John Wiley & Sons Ltd</copyright><eventGroup><event type="manuscriptReceived" date="2013-08-25"></event><event type="manuscriptRevised" date="2013-08-24"></event><event type="manuscriptAccepted" date="2013-08-24"></event><event type="xmlCreated" agent="Laserwords Private Ltd." date="2013-09-17"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.2.6 mode:FullText" date="2013-11-26"></event><event type="publishedOnlineAccepted" date="2013-09-04"></event><event type="publishedOnlineEarlyUnpaginated" date="2013-10-03"></event><event type="firstOnline" date="2013-10-03"></event><event type="publishedOnlineFinalForm" date="2013-11-26"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.6.4 mode:FullText" date="2015-10-03"></event></eventGroup><numberingGroup><numbering type="pageFirst">1059</numbering><numbering type="pageLast">1062</numbering></numberingGroup><correspondenceTo><lineatedText xml:id="cup12225-lntxt-0001"><line xml:id="cup12225-line-0001">Michael C. Lynch, MD</line><line xml:id="cup12225-line-0002">Department of Pathology, Penn State Hershey Medical Center, H179, 500 University Drive, PO Box 850, Hershey, PA 17033, USA</line><line xml:id="cup12225-line-0003">Tel: +1 717 531 8993</line><line xml:id="cup12225-line-0004">Fax: +1 717 531 7741</line><line xml:id="cup12225-line-0005">e‐mail: <email>mlynch1@hmc.psu.edu</email></line></lineatedText></correspondenceTo><selfCitationGroup><citation type="self" xml:id="cup12225-cit-0000"><author><familyName>Lynch</familyName> <givenNames>MC</givenNames></author>, <author><familyName>Chung</familyName> <givenNames>CG</givenNames></author>, <author><familyName>Specht</familyName> <givenNames>CS</givenNames></author>, <author><familyName>Wilkinson</familyName> <givenNames>M</givenNames></author>, <author><familyName>Clarke</familyName> <givenNames>LE</givenNames></author>. <articleTitle>Giant cell angiofibroma or localized periorbital lymphedema?</articleTitle></citation></selfCitationGroup><linkGroup><link type="toTypesetVersion" href="file:CUP.CUP12225.pdf"></link></linkGroup></publicationMeta><contentMeta><titleGroup><title type="main">Giant cell angiofibroma or localized periorbital lymphedema?</title><title type="short">Giant cell angiofibroma</title><title type="shortAuthors">Lynch <b>et al.</b></title></titleGroup><creators><creator creatorRole="author" xml:id="cup12225-cr-0001" affiliationRef="#cup12225-aff-0001" corresponding="yes"><personName><givenNames>Michael C.</givenNames>
<familyName>Lynch</familyName></personName></creator><creator creatorRole="author" xml:id="cup12225-cr-0002" affiliationRef="#cup12225-aff-0001"><personName><givenNames>Catherine G.</givenNames>
<familyName>Chung</familyName></personName></creator><creator creatorRole="author" xml:id="cup12225-cr-0003" affiliationRef="#cup12225-aff-0001 #cup12225-aff-0002"><personName><givenNames>Charles S.</givenNames>
<familyName>Specht</familyName></personName></creator><creator creatorRole="author" xml:id="cup12225-cr-0004" affiliationRef="#cup12225-aff-0002"><personName><givenNames>Michael</givenNames>
<familyName>Wilkinson</familyName></personName></creator><creator creatorRole="author" xml:id="cup12225-cr-0005" affiliationRef="#cup12225-aff-0001"><personName><givenNames>Loren E.</givenNames>
<familyName>Clarke</familyName></personName></creator></creators><affiliationGroup xml:id="cup12225-affgp-0001"><affiliation countryCode="US" type="organization" xml:id="cup12225-aff-0001"><orgDiv>Department of Pathology</orgDiv><orgName>The Penn State Hershey Medical Center</orgName><address><city>Hershey</city><countryPart>PA</countryPart><country>USA</country></address></affiliation><affiliation countryCode="US" type="organization" xml:id="cup12225-aff-0002"><orgDiv>Department of Ophthalmology</orgDiv><orgName>The Penn State Hershey Medical Center</orgName><address><city>Hershey</city><countryPart>PA</countryPart><country>USA</country></address></affiliation></affiliationGroup><keywordGroup type="author"><keyword xml:id="cup12225-kwd-0001">giant cell angiofibroma</keyword><keyword xml:id="cup12225-kwd-0002">herniated orbital fat</keyword><keyword xml:id="cup12225-kwd-0003">lymphedema</keyword><keyword xml:id="cup12225-kwd-0004">massive localized lymphedema</keyword></keywordGroup><abstractGroup><abstract type="main" xml:id="cup12225-abs-0001"><title type="main">Abstract</title><p xml:id="cup12225-para-0001">Giant cell angiofibroma represents a rare soft tissue neoplasm with a predilection for the orbit. We recently encountered a mass removed from the lower eyelid of a 56‐year‐old female that histopathologically resembled giant cell angiofibroma. The process consisted of haphazardly arranged <fc>CD34</fc>‐positive spindled and multinucleated cells within an edematous, densely vascular stroma. However, the patient had recently undergone laryngectomy and radiotherapy for a laryngeal squamous cell carcinoma. A similar mass had arisen on the contralateral eyelid, and both had developed several months post‐therapy. Lymphedema of the orbit can present as tumor‐like nodules and in some cases may share histopathologic features purported to be characteristic of giant cell angiofibroma. A relationship between giant cell angiofibroma and lymphedema has not been established, but our case suggests there may be one. The potential overlap of these two conditions should be recognized, as should other entities that may enter the differential diagnosis.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Giant cell angiofibroma or localized periorbital lymphedema?</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Giant cell angiofibroma</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Giant cell angiofibroma or localized periorbital lymphedema?</title></titleInfo><name type="personal"><namePart type="given">Michael C.</namePart><namePart type="family">Lynch</namePart><affiliation>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</affiliation><affiliation>Michael C. Lynch, MDDepartment of Pathology, Penn State Hershey Medical Center, H179, 500 University Drive, PO Box 850, Hershey, PA 17033, USATel: +1 717 531 8993Fax: +1 717 531 7741e‐mail:</affiliation><affiliation>E-mail: mlynch1@hmc.psu.edu</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Catherine G.</namePart><namePart type="family">Chung</namePart><affiliation>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Charles S.</namePart><namePart type="family">Specht</namePart><affiliation>Department of Pathology, The Penn State Hershey Medical Center, Hershey, PA, USA</affiliation><affiliation>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Michael</namePart><namePart type="family">Wilkinson</namePart><affiliation>Department of Ophthalmology, The Penn State Hershey Medical Center, PA, Hershey, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Loren E.</namePart><namePart type="family">Clarke</namePart><affiliation>Department of Pathology, The Penn State Hershey Medical Center, PA, Hershey, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="case-report" displayLabel="caseStudy"></genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2013-12</dateIssued><dateCreated encoding="w3cdtf">2013-09-17</dateCreated><dateCaptured encoding="w3cdtf">2013-08-25</dateCaptured><dateValid encoding="w3cdtf">2013-08-24</dateValid><edition>Lynch MC, Chung CG, Specht CS, Wilkinson M, Clarke LE. Giant cell angiofibroma or localized periorbital lymphedema?</edition><copyrightDate encoding="w3cdtf">2013</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract>Giant cell angiofibroma represents a rare soft tissue neoplasm with a predilection for the orbit. We recently encountered a mass removed from the lower eyelid of a 56‐year‐old female that histopathologically resembled giant cell angiofibroma. The process consisted of haphazardly arranged CD34‐positive spindled and multinucleated cells within an edematous, densely vascular stroma. However, the patient had recently undergone laryngectomy and radiotherapy for a laryngeal squamous cell carcinoma. A similar mass had arisen on the contralateral eyelid, and both had developed several months post‐therapy. Lymphedema of the orbit can present as tumor‐like nodules and in some cases may share histopathologic features purported to be characteristic of giant cell angiofibroma. A relationship between giant cell angiofibroma and lymphedema has not been established, but our case suggests there may be one. The potential overlap of these two conditions should be recognized, as should other entities that may enter the differential diagnosis.</abstract><subject><genre>keywords</genre><topic>giant cell angiofibroma</topic><topic>herniated orbital fat</topic><topic>lymphedema</topic><topic>massive localized lymphedema</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Cutaneous Pathology</title></titleInfo><titleInfo type="abbreviated"><title>J Cutan Pathol</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Case Report</topic></subject><identifier type="ISSN">0303-6987</identifier><identifier type="eISSN">1600-0560</identifier><identifier type="DOI">10.1111/(ISSN)1600-0560</identifier><identifier type="PublisherID">CUP</identifier><part><date>2013</date><detail type="volume"><caption>vol.</caption><number>40</number></detail><detail type="issue"><caption>no.</caption><number>12</number></detail><extent unit="pages"><start>1059</start><end>1062</end><total>4</total></extent></part></relatedItem><identifier type="istex">D4EA5C723196CCF27BF3340577107CE2599821FF</identifier><identifier type="DOI">10.1111/cup.12225</identifier><identifier type="ArticleID">CUP12225</identifier><accessCondition type="use and reproduction" contentType="copyright">© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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