Stewart-Treves syndrome: a case report.
Identifieur interne : 001099 ( PubMed/Corpus ); précédent : 001098; suivant : 001100Stewart-Treves syndrome: a case report.
Auteurs : Anis Benmansour ; Saad Laanaz ; Abdeslam BougtabSource :
- The Pan African medical journal [ 1937-8688 ] ; 2014.
English descriptors
- KwdEn :
- MESH :
- adverse effects : Mastectomy.
- diagnosis : Hemangiosarcoma, Lymphangiosarcoma.
- pathology : Hemangiosarcoma, Lymphangiosarcoma.
- surgery : Breast Neoplasms.
- therapy : Hemangiosarcoma, Lymphangiosarcoma.
- Aged, Female, Humans.
Abstract
The Stewart-Treves syndrome was first described in 1948, it's an angiosarcoma developed on a longstanding lymphadenomatous limb, more often after radical mastectomy. Diagnosis is made on skin biopsy and the prognosis is poor when radical surgery can't be performed. We report the case on a Stewart-Treves syndrome in a sixty-six years old woman who underwent radical mastectomy for breast carcinoma ten years earlier. Surgery was not feasible at the time of diagnosis, and we lost touch of the patient even if chemotherapy was decided. Radical surgery is the best treatment to date for this rare disease. Conservative surgery with adjuvant radiotherapy is also possible. Systemic chemotherapy is reserved for locally advanced unresectable and metastatic forms. We advocate long term follow-up for every post mastectomy lymphedema to diagnosis this fatal disease when curable.
DOI: 10.11604/pamj.2014.19.2.4178
PubMed: 25574331
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pubmed:25574331Le document en format XML
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Diagnosis is made on skin biopsy and the prognosis is poor when radical surgery can't be performed. We report the case on a Stewart-Treves syndrome in a sixty-six years old woman who underwent radical mastectomy for breast carcinoma ten years earlier. Surgery was not feasible at the time of diagnosis, and we lost touch of the patient even if chemotherapy was decided. Radical surgery is the best treatment to date for this rare disease. Conservative surgery with adjuvant radiotherapy is also possible. Systemic chemotherapy is reserved for locally advanced unresectable and metastatic forms. We advocate long term follow-up for every post mastectomy lymphedema to diagnosis this fatal disease when curable.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25574331</PMID><DateCreated><Year>2015</Year><Month>01</Month><Day>09</Day></DateCreated><DateCompleted><Year>2015</Year><Month>09</Month><Day>03</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>20</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Electronic">1937-8688</ISSN><JournalIssue CitedMedium="Internet"><Volume>19</Volume><PubDate><Year>2014</Year></PubDate></JournalIssue><Title>The Pan African medical journal</Title><ISOAbbreviation>Pan Afr Med J</ISOAbbreviation></Journal><ArticleTitle>Stewart-Treves syndrome: a case report.</ArticleTitle><Pagination><MedlinePgn>2</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.11604/pamj.2014.19.2.4178</ELocationID><Abstract><AbstractText>The Stewart-Treves syndrome was first described in 1948, it's an angiosarcoma developed on a longstanding lymphadenomatous limb, more often after radical mastectomy. Diagnosis is made on skin biopsy and the prognosis is poor when radical surgery can't be performed. We report the case on a Stewart-Treves syndrome in a sixty-six years old woman who underwent radical mastectomy for breast carcinoma ten years earlier. Surgery was not feasible at the time of diagnosis, and we lost touch of the patient even if chemotherapy was decided. Radical surgery is the best treatment to date for this rare disease. Conservative surgery with adjuvant radiotherapy is also possible. Systemic chemotherapy is reserved for locally advanced unresectable and metastatic forms. We advocate long term follow-up for every post mastectomy lymphedema to diagnosis this fatal disease when curable.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Benmansour</LastName><ForeName>Anis</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Department of Surgical Oncology, National Institute of Oncology, Rabat, Morocco.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Laanaz</LastName><ForeName>Saad</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Department of Medical Oncology, National Institute of Oncology, Rabat, Morocco.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Bougtab</LastName><ForeName>Abdeslam</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Department of Surgical Oncology, National Institute of Oncology, Rabat, Morocco.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>09</Month><Day>01</Day></ArticleDate></Article><MedlineJournalInfo><Country>Uganda</Country><MedlineTA>Pan Afr Med J</MedlineTA><NlmUniqueID>101517926</NlmUniqueID></MedlineJournalInfo><SupplMeshList><SupplMeshName Type="Disease" UI="C537491">Stewart Treves syndrome</SupplMeshName></SupplMeshList><CitationSubset>IM</CitationSubset><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>J Korean Med Sci. 1988 Jun;3(2):83-8</RefSource><PMID Version="1">3267359</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Dermatol Surg Oncol. 1977 May-Jun;3(3):295-8</RefSource><PMID Version="1">874138</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Cancer. 1972 Aug;30(2):562-72</RefSource><PMID Version="1">5051679</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Sem Hop. 1983 Mar 10;59(10):687-94</RefSource><PMID Version="1">6304890</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Presse Med. 1960 Sep 24;68:1506-8</RefSource><PMID Version="1">13758174</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Pathol. 2010 Jan;176(1):34-9</RefSource><PMID Version="1">20008140</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Cancer. 1948 May;1(1):64-81</RefSource><PMID Version="1">18867440</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>J Am Acad Dermatol. 2012 Dec;67(6):1342-8</RefSource><PMID Version="1">22682884</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Nihon Hifuka Gakkai Zasshi. 1990 Sep;100(10):1029-39</RefSource><PMID Version="1">2266596</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Arch Pathol Lab Med. 1984 Feb;108(2):129-32</RefSource><PMID Version="1">6198997</PMID></CommentsCorrections></CommentsCorrectionsList><MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001943" MajorTopicYN="N">Breast Neoplasms</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006394" MajorTopicYN="N">Hemangiosarcoma</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></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="Q000628" MajorTopicYN="N">therapy</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008408" MajorTopicYN="N">Mastectomy</DescriptorName><QualifierName UI="Q000009" MajorTopicYN="Y">adverse effects</QualifierName></MeshHeading></MeshHeadingList><OtherID Source="NLM">PMC4282868</OtherID><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Stewart–Treves</Keyword><Keyword MajorTopicYN="N">angiosarcoma</Keyword><Keyword MajorTopicYN="N">syndrome</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2014</Year><Month>03</Month><Day>13</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2014</Year><Month>04</Month><Day>10</Day></PubMedPubDate><PubMedPubDate 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