Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature
Identifieur interne : 006575 ( Istex/Corpus ); précédent : 006574; suivant : 006576Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature
Auteurs : Naveen Krishnamoorthy ; Seethalakshmi Viswanathan ; Bharat Rekhi ; Nirmala A. JambhekarSource :
- Journal of Cutaneous Pathology [ 0303-6987 ] ; 2012-01.
Abstract
Cutaneous angiosarcoma or lymphangiosarcoma represents an uncommon aggressive tumor known to arise on a background of chronic lymphedema secondary to various etiologies, principally following surgery or irradiation. There have been rarely reported cases of angiosarcoma following infective conditions that eventuate with lymphatic stasis. We report a case of angiosarcoma arising after 33 years within a background of filariasis. Awareness of this association can lead to early diagnosis and appropriate treatment of this potentially fatal malignant tumor. Krishnamoorthy N, Viswanathan S, Rekhi B, Jambhekar NA. Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature.
Url:
DOI: 10.1111/j.1600-0560.2011.01785.x
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Jambhekar</name><affiliation><mods:affiliation>Department of Pathology, Tata Memorial Hospital, Mumbai, India</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">39</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="52">52</biblScope><biblScope unit="page" to="55">55</biblScope><biblScope unit="page-count">4</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2012-01">2012-01</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" xml:lang="en">Cutaneous angiosarcoma or lymphangiosarcoma represents an uncommon aggressive tumor known to arise on a background of chronic lymphedema secondary to various etiologies, principally following surgery or irradiation. There have been rarely reported cases of angiosarcoma following infective conditions that eventuate with lymphatic stasis. We report a case of angiosarcoma arising after 33 years within a background of filariasis. Awareness of this association can lead to early diagnosis and appropriate treatment of this potentially fatal malignant tumor. Krishnamoorthy N, Viswanathan S, Rekhi B, Jambhekar NA. Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>lymphangiosarcoma</json:string><json:string>lymphedema</json:string><json:string>angiosarcoma</json:string><json:string>chronic lymphedema</json:string><json:string>lariasis</json:string><json:string>lymphatic</json:string><json:string>sarcoma</json:string><json:string>larial</json:string><json:string>nodule</json:string><json:string>amputation</json:string><json:string>cutaneous</json:string><json:string>metastasis</json:string><json:string>endothelium</json:string><json:string>sordillo</json:string><json:string>larial lymphedema</json:string><json:string>multiple nodules</json:string><json:string>case report</json:string><json:string>seethalakshmi viswanathan</json:string><json:string>tumor cells</json:string><json:string>total extent</json:string><json:string>tata memorial hospital</json:string><json:string>knee amputation</json:string><json:string>extensive skin</json:string><json:string>john wiley sons</json:string><json:string>lymphatic differentiation</json:string><json:string>results program</json:string><json:string>soft tissue sarcoma</json:string><json:string>early diagnosis</json:string><json:string>cutan pathol</json:string><json:string>lower extremity</json:string><json:string>larial origin</json:string><json:string>chronic lymphatic stasis</json:string><json:string>skeletal muscle</json:string></teeft></keywords><author><json:item><name>Naveen Krishnamoorthy</name><affiliations><json:string>Department of Pathology, Tata Memorial Hospital, Mumbai, India</json:string></affiliations></json:item><json:item><name>Seethalakshmi Viswanathan</name><affiliations><json:string>Department of Pathology, Tata Memorial Hospital, Mumbai, India</json:string><json:string>E-mail: drseetha.v@gmail.com</json:string></affiliations></json:item><json:item><name>Bharat Rekhi</name><affiliations><json:string>Department of Pathology, Tata Memorial Hospital, Mumbai, India</json:string></affiliations></json:item><json:item><name>Nirmala A. 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Tel: +91 22 24177270
Fax: +91 22 24125556
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Tel: +91 22 24177270
Fax: +91 22 24125556
e‐mail: <email>drseetha.v@gmail.com</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CUP.CUP1785.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Accepted for publication March 12, 2011</unparsedEditorialHistory><countGroup><count type="figureTotal" number="5"></count><count type="tableTotal" number="1"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="14"></count></countGroup><titleGroup><title type="main">Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature</title><title type="shortAuthors">Krishnamoorthy et al.</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>Naveen</givenNames><familyName>Krishnamoorthy</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1" corresponding="yes"><personName><givenNames>Seethalakshmi</givenNames><familyName>Viswanathan</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a1"><personName><givenNames>Bharat</givenNames><familyName>Rekhi</familyName></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a1"><personName><givenNames>Nirmala A.</givenNames><familyName>Jambhekar</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="IN"><unparsedAffiliation>Department of Pathology, Tata Memorial Hospital, Mumbai, India</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">chronic lymphedema</keyword><keyword xml:id="k2">cutaneous angiosarcoma</keyword><keyword xml:id="k3">filariasis</keyword><keyword xml:id="k4">lymphangiosarcoma</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><p>Cutaneous angiosarcoma or lymphangiosarcoma represents an uncommon aggressive tumor known to arise on a background of chronic lymphedema secondary to various etiologies, principally following surgery or irradiation. 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There have been rarely reported cases of angiosarcoma following infective conditions that eventuate with lymphatic stasis. We report a case of angiosarcoma arising after 33 years within a background of filariasis. Awareness of this association can lead to early diagnosis and appropriate treatment of this potentially fatal malignant tumor. Krishnamoorthy N, Viswanathan S, Rekhi B, Jambhekar NA. Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature.</abstract><subject lang="en"><genre>keywords</genre><topic>chronic lymphedema</topic><topic>cutaneous angiosarcoma</topic><topic>filariasis</topic><topic>lymphangiosarcoma</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Cutaneous Pathology</title></titleInfo><genre type="journal">journal</genre><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>2012</date><detail type="volume"><caption>vol.</caption><number>39</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>52</start><end>55</end><total>4</total></extent></part></relatedItem><identifier type="istex">D8CD98B85302936C0BFF5C69114949275B782828</identifier><identifier type="DOI">10.1111/j.1600-0560.2011.01785.x</identifier><identifier type="ArticleID">CUP1785</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2011 John Wiley & Sons A/S</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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