LymphedemaV1, PubMed, Corpus, bibRecord, 003B06

[Stewart-Treves syndrome].

Identifieur interne : 003B06 ( PubMed/Corpus ); précédent : 003B05; suivant : 003B07

[Stewart-Treves syndrome].

Auteurs : Miguel Echenique-Elizondo ; Ana Tuneu-Valls ; José Zubizarreta ; Carmen Lobo

Source :

Cirugia espanola [ 0009-739X ] ; 2005.

RBID : pubmed:16420866

English descriptors

KwdEn :
- Adult, Aged, Female, Follow-Up Studies, Humans, Lymphangiosarcoma (diagnosis), Lymphangiosarcoma (therapy), Male, Middle Aged, Syndrome.
MESH :
- diagnosis : Lymphangiosarcoma.
- therapy : Lymphangiosarcoma.
- Adult, Aged, Female, Follow-Up Studies, Humans, Male, Middle Aged, Syndrome.

Abstract

Lymphangiosarcoma is an uncommon vascular tumor that usually develops in longstanding lymphedema. We gathered the cases of lymphangioma observed in a hospital and attempted to analyze their characteristics: age, sex, localization, treatment and follow-up data. We studied five cases: three cases of Stewart-Treves syndrome after mastectomy and radiotherapy and two cases that developed in patients with late-onset congenital lymphedema. There were four women and one man. Radical surgery was performed in four patients. The techniques employed were: above-knee amputation (one patient), hip disarticulation (one patient), scapulo-humeral disarticulation (two patients) and gemcitabine and radiotherapy in one patient with metastatic disease at diagnosis. Three patients died in the first 14 months of follow-up, while two are disease free after 46 and 86 months respectively. This study confirms the poor prognosis of patients with Steward-Treves syndrome.

PubMed: 16420866

Links to Exploration step

pubmed:16420866

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">[Stewart-Treves syndrome].</title>
<author><name sortKey="Echenique Elizondo, Miguel" sort="Echenique Elizondo, Miguel" uniqKey="Echenique Elizondo M" first="Miguel" last="Echenique-Elizondo">Miguel Echenique-Elizondo</name>
<affiliation><nlm:affiliation>Unidad Docente de Medicina, Facultad de Medicina, Universidad del País Vasco, San Sebastián, Guipúzcoa, Spain. gepecelm@sc.ehu.es</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Tuneu Valls, Ana" sort="Tuneu Valls, Ana" uniqKey="Tuneu Valls A" first="Ana" last="Tuneu-Valls">Ana Tuneu-Valls</name>
</author>
<author><name sortKey="Zubizarreta, Jose" sort="Zubizarreta, Jose" uniqKey="Zubizarreta J" first="José" last="Zubizarreta">José Zubizarreta</name>
</author>
<author><name sortKey="Lobo, Carmen" sort="Lobo, Carmen" uniqKey="Lobo C" first="Carmen" last="Lobo">Carmen Lobo</name>
</author>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">[Stewart-Treves syndrome].</title>
<author><name sortKey="Echenique Elizondo, Miguel" sort="Echenique Elizondo, Miguel" uniqKey="Echenique Elizondo M" first="Miguel" last="Echenique-Elizondo">Miguel Echenique-Elizondo</name>
<affiliation><nlm:affiliation>Unidad Docente de Medicina, Facultad de Medicina, Universidad del País Vasco, San Sebastián, Guipúzcoa, Spain. gepecelm@sc.ehu.es</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Tuneu Valls, Ana" sort="Tuneu Valls, Ana" uniqKey="Tuneu Valls A" first="Ana" last="Tuneu-Valls">Ana Tuneu-Valls</name>
</author>
<author><name sortKey="Zubizarreta, Jose" sort="Zubizarreta, Jose" uniqKey="Zubizarreta J" first="José" last="Zubizarreta">José Zubizarreta</name>
</author>
<author><name sortKey="Lobo, Carmen" sort="Lobo, Carmen" uniqKey="Lobo C" first="Carmen" last="Lobo">Carmen Lobo</name>
</author>
</analytic>
<series><title level="j">Cirugia espanola</title>
<idno type="ISSN">0009-739X</idno>
<imprint><date when="2005" type="published">2005</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Lymphangiosarcoma (diagnosis)</term>
<term>Lymphangiosarcoma (therapy)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Lymphangiosarcoma</term>
</keywords>
<keywords scheme="MESH" qualifier="therapy" xml:lang="en"><term>Lymphangiosarcoma</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Aged</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Syndrome</term>
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<front><div type="abstract" xml:lang="en">Lymphangiosarcoma is an uncommon vascular tumor that usually develops in longstanding lymphedema. We gathered the cases of lymphangioma observed in a hospital and attempted to analyze their characteristics: age, sex, localization, treatment and follow-up data. We studied five cases: three cases of Stewart-Treves syndrome after mastectomy and radiotherapy and two cases that developed in patients with late-onset congenital lymphedema. There were four women and one man. Radical surgery was performed in four patients. The techniques employed were: above-knee amputation (one patient), hip disarticulation (one patient), scapulo-humeral disarticulation (two patients) and gemcitabine and radiotherapy in one patient with metastatic disease at diagnosis. Three patients died in the first 14 months of follow-up, while two are disease free after 46 and 86 months respectively. This study confirms the poor prognosis of patients with Steward-Treves syndrome.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16420866</PMID>
<DateCreated><Year>2006</Year>
<Month>01</Month>
<Day>19</Day>
</DateCreated>
<DateCompleted><Year>2006</Year>
<Month>05</Month>
<Day>24</Day>
</DateCompleted>
<DateRevised><Year>2006</Year>
<Month>11</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0009-739X</ISSN>
<JournalIssue CitedMedium="Print"><Volume>78</Volume>
<Issue>6</Issue>
<PubDate><Year>2005</Year>
<Month>Dec</Month>
</PubDate>
</JournalIssue>
<Title>Cirugia espanola</Title>
<ISOAbbreviation>Cir Esp</ISOAbbreviation>
</Journal>
<ArticleTitle>[Stewart-Treves syndrome].</ArticleTitle>
<Pagination><MedlinePgn>382-4</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Lymphangiosarcoma is an uncommon vascular tumor that usually develops in longstanding lymphedema. We gathered the cases of lymphangioma observed in a hospital and attempted to analyze their characteristics: age, sex, localization, treatment and follow-up data. We studied five cases: three cases of Stewart-Treves syndrome after mastectomy and radiotherapy and two cases that developed in patients with late-onset congenital lymphedema. There were four women and one man. Radical surgery was performed in four patients. The techniques employed were: above-knee amputation (one patient), hip disarticulation (one patient), scapulo-humeral disarticulation (two patients) and gemcitabine and radiotherapy in one patient with metastatic disease at diagnosis. Three patients died in the first 14 months of follow-up, while two are disease free after 46 and 86 months respectively. This study confirms the poor prognosis of patients with Steward-Treves syndrome.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Echenique-Elizondo</LastName>
<ForeName>Miguel</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Unidad Docente de Medicina, Facultad de Medicina, Universidad del País Vasco, San Sebastián, Guipúzcoa, Spain. gepecelm@sc.ehu.es</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Tuneu-Valls</LastName>
<ForeName>Ana</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Zubizarreta</LastName>
<ForeName>José</ForeName>
<Initials>J</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lobo</LastName>
<ForeName>Carmen</ForeName>
<Initials>C</Initials>
</Author>
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<Language>spa</Language>
<PublicationTypeList><PublicationType UI="D004740">English Abstract</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
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<VernacularTitle>Síndrome de Stewart-Treves.</VernacularTitle>
</Article>
<MedlineJournalInfo><Country>Spain</Country>
<MedlineTA>Cir Esp</MedlineTA>
<NlmUniqueID>1254104</NlmUniqueID>
<ISSNLinking>0009-739X</ISSNLinking>
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<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
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<MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005500" MajorTopicYN="N">Follow-Up Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008204" MajorTopicYN="Y">Lymphangiosarcoma</DescriptorName>
<QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName>
<QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year>
<Month>1</Month>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">16420866</ArticleId>
<ArticleId IdType="pii">13082154</ArticleId>
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</record>

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[Stewart-Treves syndrome].

[Stewart-Treves syndrome].

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki