[Treatment of Stewart-Treves syndrome].
Identifieur interne : 006059 ( PubMed/Checkpoint ); précédent : 006058; suivant : 006060[Treatment of Stewart-Treves syndrome].
Auteurs : H. AmbergerSource :
- Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen [ 0009-4722 ] ; 1983.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- complications : Lymphedema.
- surgery : Breast Neoplasms, Hemangiosarcoma, Lymphangiosarcoma, Postoperative Complications, Skin Neoplasms, Soft Tissue Neoplasms.
- Aged, Female, Humans, Mastectomy, Middle Aged.
Abstract
The Stewart-Treves syndrome is the most dangerous complication of chronic lymphedema following mastectomy. Prognosis is poor. In the world literature 278 cases are described. At the Surgical Clinic of the University of Heidelberg 3 cases of Stewart-Treves syndrome have been treated so far. Decisive for the prognosis of this fast growing tumor of high malignancy is early detection and initiation of therapy. The only curative therapy seems to be radical surgery in the form of interthoracic scapular exarticulation of the arm at an early stage of this disease. Radio- and chemotherapy offer palliation in advanced tumor stage.
PubMed: 6684016
Affiliations:
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Amberger</name></author></analytic><series><title level="j">Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen</title><idno type="ISSN">0009-4722</idno><imprint><date when="1983" type="published">1983</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Breast Neoplasms (surgery)</term><term>Female</term><term>Hemangiosarcoma (surgery)</term><term>Humans</term><term>Lymphangiosarcoma (surgery)</term><term>Lymphedema (complications)</term><term>Mastectomy</term><term>Middle Aged</term><term>Postoperative Complications (surgery)</term><term>Skin Neoplasms (surgery)</term><term>Soft Tissue Neoplasms (surgery)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Complications postopératoires ()</term><term>Femelle</term><term>Humains</term><term>Hémangiosarcome ()</term><term>Lymphangiosarcome ()</term><term>Lymphoedème ()</term><term>Mastectomie</term><term>Sujet âgé</term><term>Tumeurs cutanées ()</term><term>Tumeurs des tissus mous ()</term><term>Tumeurs du sein ()</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Lymphedema</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Breast Neoplasms</term><term>Hemangiosarcoma</term><term>Lymphangiosarcoma</term><term>Postoperative Complications</term><term>Skin Neoplasms</term><term>Soft Tissue Neoplasms</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Female</term><term>Humans</term><term>Mastectomy</term><term>Middle Aged</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Complications postopératoires</term><term>Femelle</term><term>Humains</term><term>Hémangiosarcome</term><term>Lymphangiosarcome</term><term>Lymphoedème</term><term>Mastectomie</term><term>Sujet âgé</term><term>Tumeurs cutanées</term><term>Tumeurs des tissus mous</term><term>Tumeurs du sein</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The Stewart-Treves syndrome is the most dangerous complication of chronic lymphedema following mastectomy. Prognosis is poor. In the world literature 278 cases are described. At the Surgical Clinic of the University of Heidelberg 3 cases of Stewart-Treves syndrome have been treated so far. Decisive for the prognosis of this fast growing tumor of high malignancy is early detection and initiation of therapy. The only curative therapy seems to be radical surgery in the form of interthoracic scapular exarticulation of the arm at an early stage of this disease. Radio- and chemotherapy offer palliation in advanced tumor stage.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">6684016</PMID><DateCreated><Year>1983</Year><Month>10</Month><Day>08</Day></DateCreated><DateCompleted><Year>1983</Year><Month>10</Month><Day>08</Day></DateCompleted><DateRevised><Year>2006</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0009-4722</ISSN><JournalIssue CitedMedium="Print"><Volume>54</Volume><Issue>7</Issue><PubDate><Year>1983</Year><Month>Jul</Month></PubDate></JournalIssue><Title>Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen</Title><ISOAbbreviation>Chirurg</ISOAbbreviation></Journal><ArticleTitle>[Treatment of Stewart-Treves syndrome].</ArticleTitle><Pagination><MedlinePgn>487-9</MedlinePgn></Pagination><Abstract><AbstractText>The Stewart-Treves syndrome is the most dangerous complication of chronic lymphedema following mastectomy. Prognosis is poor. In the world literature 278 cases are described. At the Surgical Clinic of the University of Heidelberg 3 cases of Stewart-Treves syndrome have been treated so far. Decisive for the prognosis of this fast growing tumor of high malignancy is early detection and initiation of therapy. The only curative therapy seems to be radical surgery in the form of interthoracic scapular exarticulation of the arm at an early stage of this disease. Radio- and chemotherapy offer palliation in advanced tumor stage.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Amberger</LastName><ForeName>H</ForeName><Initials>H</Initials></Author></AuthorList><Language>ger</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D004740">English Abstract</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><VernacularTitle>Die Behandlung des Stewart-Treves-Syndrom.</VernacularTitle></Article><MedlineJournalInfo><Country>Germany</Country><MedlineTA>Chirurg</MedlineTA><NlmUniqueID>16140410R</NlmUniqueID><ISSNLinking>0009-4722</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001943" MajorTopicYN="N">Breast Neoplasms</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008204" MajorTopicYN="N">Lymphangiosarcoma</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008408" MajorTopicYN="N">Mastectomy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011183" MajorTopicYN="N">Postoperative Complications</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012878" MajorTopicYN="N">Skin Neoplasms</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012983" MajorTopicYN="N">Soft Tissue Neoplasms</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1983</Year><Month>7</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1983</Year><Month>7</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1983</Year><Month>7</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">6684016</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list></list><tree><noCountry><name sortKey="Amberger, H" sort="Amberger, H" uniqKey="Amberger H" first="H" last="Amberger">H. 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