Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature.
Identifieur interne : 002326 ( PubMed/Corpus ); précédent : 002325; suivant : 002327Lymphangiosarcoma 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 [ 1600-0560 ] ; 2012.
English descriptors
- KwdEn :
- Aged, Filariasis (complications), Filariasis (pathology), Filariasis (therapy), Hemangiosarcoma (etiology), Hemangiosarcoma (parasitology), Hemangiosarcoma (pathology), Hemangiosarcoma (therapy), Humans, Male, Skin Neoplasms (etiology), Skin Neoplasms (parasitology), Skin Neoplasms (pathology), Skin Neoplasms (therapy), Time Factors.
- MESH :
- complications : Filariasis.
- etiology : Hemangiosarcoma, Skin Neoplasms.
- parasitology : Hemangiosarcoma, Skin Neoplasms.
- pathology : Filariasis, Hemangiosarcoma, Skin Neoplasms.
- therapy : Filariasis, Hemangiosarcoma, Skin Neoplasms.
- Aged, Humans, Male, Time Factors.
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.
DOI: 10.1111/j.1600-0560.2011.01785.x
PubMed: 22211335
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Jambhekar</name></author></analytic><series><title level="j">Journal of cutaneous pathology</title><idno type="eISSN">1600-0560</idno><imprint><date when="2012" type="published">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Filariasis (complications)</term><term>Filariasis (pathology)</term><term>Filariasis (therapy)</term><term>Hemangiosarcoma (etiology)</term><term>Hemangiosarcoma (parasitology)</term><term>Hemangiosarcoma (pathology)</term><term>Hemangiosarcoma (therapy)</term><term>Humans</term><term>Male</term><term>Skin Neoplasms (etiology)</term><term>Skin Neoplasms (parasitology)</term><term>Skin Neoplasms (pathology)</term><term>Skin Neoplasms (therapy)</term><term>Time Factors</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Filariasis</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="parasitology" xml:lang="en"><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Filariasis</term><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Filariasis</term><term>Hemangiosarcoma</term><term>Skin Neoplasms</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Humans</term><term>Male</term><term>Time Factors</term></keywords></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.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22211335</PMID><DateCreated><Year>2012</Year><Month>01</Month><Day>03</Day></DateCreated><DateCompleted><Year>2012</Year><Month>05</Month><Day>01</Day></DateCompleted><DateRevised><Year>2012</Year><Month>09</Month><Day>27</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1600-0560</ISSN><JournalIssue CitedMedium="Internet"><Volume>39</Volume><Issue>1</Issue><PubDate><Year>2012</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Journal of cutaneous pathology</Title><ISOAbbreviation>J. Cutan. Pathol.</ISOAbbreviation></Journal><ArticleTitle>Lymphangiosarcoma arising after 33 years within a background of chronic filariasis: a case report with review of literature.</ArticleTitle><Pagination><MedlinePgn>52-5</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1600-0560.2011.01785.x</ELocationID><Abstract><AbstractText>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.</AbstractText><CopyrightInformation>Copyright © 2011 John Wiley & Sons A/S.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Krishnamoorthy</LastName><ForeName>Naveen</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>Department of Pathology, Tata Memorial Hospital, Mumbai, India.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Viswanathan</LastName><ForeName>Seethalakshmi</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Rekhi</LastName><ForeName>Bharat</ForeName><Initials>B</Initials></Author><Author ValidYN="Y"><LastName>Jambhekar</LastName><ForeName>Nirmala A</ForeName><Initials>NA</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Cutan Pathol</MedlineTA><NlmUniqueID>0425124</NlmUniqueID><ISSNLinking>0303-6987</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="CommentIn"><RefSource>J Cutan Pathol. 2012 Aug;39(8):813</RefSource><PMID Version="1">22575002</PMID></CommentsCorrections></CommentsCorrectionsList><MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005368" MajorTopicYN="N">Filariasis</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName><QualifierName UI="Q000469" MajorTopicYN="N">parasitology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName><QualifierName UI="Q000469" MajorTopicYN="N">parasitology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>1</Month><Day>4</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>1</Month><Day>4</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2012</Year><Month>5</Month><Day>2</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">22211335</ArticleId><ArticleId IdType="doi">10.1111/j.1600-0560.2011.01785.x</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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