Stewart-Treves syndrome as a rare complication of a hereditary lymphedema.
Identifieur interne : 004034 ( PubMed/Curation ); précédent : 004033; suivant : 004035Stewart-Treves syndrome as a rare complication of a hereditary lymphedema.
Auteurs : H R Dürr [Allemagne] ; C. Pellengahr ; A. Nerlich ; A. Baur ; M. Maier ; V. JanssonSource :
- VASA. Zeitschrift fur Gefasskrankheiten [ 0301-1526 ] ; 2004.
Descripteurs français
- KwdFr :
- Adulte, Amputation chirurgicale, Antigènes CD31 (analyse), Biopsie, Femelle, Gènes dominants, Humains, Imagerie par résonance magnétique, Invasion tumorale (anatomopathologie), Issue fatale, Jambe (anatomopathologie), Lymphangiosarcome (), Lymphangiosarcome (anatomopathologie), Lymphangiosarcome (diagnostic), Lymphoedème (), Lymphoedème (anatomopathologie), Lymphoedème (diagnostic), Lymphoedème (génétique), Peau (anatomopathologie), Prédisposition génétique à une maladie (génétique), Syndrome, Tumeurs cutanées (), Tumeurs cutanées (anatomopathologie), Tumeurs cutanées (diagnostic), Tumeurs des tissus mous (), Tumeurs des tissus mous (anatomopathologie), Tumeurs des tissus mous (diagnostic), Évolution de la maladie.
- MESH :
- analyse : Antigènes CD31.
- anatomopathologie : Invasion tumorale, Jambe, Lymphangiosarcome, Lymphoedème, Peau, Tumeurs cutanées, Tumeurs des tissus mous.
- diagnostic : Lymphangiosarcome, Lymphoedème, Tumeurs cutanées, Tumeurs des tissus mous.
- génétique : Lymphoedème, Prédisposition génétique à une maladie.
- Adulte, Amputation chirurgicale, Biopsie, Femelle, Gènes dominants, Humains, Imagerie par résonance magnétique, Issue fatale, Lymphangiosarcome, Lymphoedème, Syndrome, Tumeurs cutanées, Tumeurs des tissus mous, Évolution de la maladie.
English descriptors
- KwdEn :
- Adult, Amputation, Antigens, CD31 (analysis), Biopsy, Disease Progression, Fatal Outcome, Female, Genes, Dominant, Genetic Predisposition to Disease (genetics), Humans, Leg (pathology), Lymphangiosarcoma (diagnosis), Lymphangiosarcoma (pathology), Lymphangiosarcoma (surgery), Lymphedema (complications), Lymphedema (diagnosis), Lymphedema (genetics), Lymphedema (pathology), Magnetic Resonance Imaging, Neoplasm Invasiveness (pathology), Skin (pathology), Skin Neoplasms (diagnosis), Skin Neoplasms (pathology), Skin Neoplasms (surgery), Soft Tissue Neoplasms (diagnosis), Soft Tissue Neoplasms (pathology), Soft Tissue Neoplasms (surgery), Syndrome.
- MESH :
- chemical , analysis : Antigens, CD31.
- complications : Lymphedema.
- diagnosis : Lymphangiosarcoma, Lymphedema, Skin Neoplasms, Soft Tissue Neoplasms.
- genetics : Genetic Predisposition to Disease, Lymphedema.
- pathology : Leg, Lymphangiosarcoma, Lymphedema, Neoplasm Invasiveness, Skin, Skin Neoplasms, Soft Tissue Neoplasms.
- surgery : Lymphangiosarcoma, Skin Neoplasms, Soft Tissue Neoplasms.
- Adult, Amputation, Biopsy, Disease Progression, Fatal Outcome, Female, Genes, Dominant, Humans, Magnetic Resonance Imaging, Syndrome.
Abstract
Lymphangiosarcoma (LAS) may occur as a rare complication of primary lymphedema. A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.
DOI: 10.1024/0301-1526.33.S65.42
PubMed: 15061047
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A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">15061047</PMID><DateCreated><Year>2004</Year><Month>04</Month><Day>05</Day></DateCreated><DateCompleted><Year>2004</Year><Month>08</Month><Day>26</Day></DateCompleted><DateRevised><Year>2012</Year><Month>10</Month><Day>19</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0301-1526</ISSN><JournalIssue CitedMedium="Print"><Volume>33</Volume><Issue>1</Issue><PubDate><Year>2004</Year><Month>Feb</Month></PubDate></JournalIssue><Title>VASA. Zeitschrift fur Gefasskrankheiten</Title><ISOAbbreviation>VASA</ISOAbbreviation></Journal><ArticleTitle>Stewart-Treves syndrome as a rare complication of a hereditary lymphedema.</ArticleTitle><Pagination><MedlinePgn>42-5</MedlinePgn></Pagination><Abstract><AbstractText>Lymphangiosarcoma (LAS) may occur as a rare complication of primary lymphedema. A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Dürr</LastName><ForeName>H R</ForeName><Initials>HR</Initials><AffiliationInfo><Affiliation>Department of Orthopaedics and Orthopaedic Surgery, Ludwig-Maximilians-University Munich, Germany. hans_roland.duerr@med.uni-muenchen.de</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Pellengahr</LastName><ForeName>C</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Nerlich</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Baur</LastName><ForeName>A</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Maier</LastName><ForeName>M</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Jansson</LastName><ForeName>V</ForeName><Initials>V</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Vasa</MedlineTA><NlmUniqueID>0317051</NlmUniqueID><ISSNLinking>0301-1526</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D019408">Antigens, CD31</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000671" MajorTopicYN="N">Amputation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019408" MajorTopicYN="N">Antigens, CD31</DescriptorName><QualifierName UI="Q000032" 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MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="Y">complications</QualifierName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008279" MajorTopicYN="N">Magnetic Resonance Imaging</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009361" MajorTopicYN="N">Neoplasm Invasiveness</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012867" MajorTopicYN="N">Skin</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012983" MajorTopicYN="N">Soft Tissue Neoplasms</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2004</Year><Month>4</Month><Day>6</Day><Hour>5</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2004</Year><Month>8</Month><Day>27</Day><Hour>5</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2004</Year><Month>4</Month><Day>6</Day><Hour>5</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">15061047</ArticleId><ArticleId IdType="doi">10.1024/0301-1526.33.S65.42</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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