Stewart-Treves Syndrome after Bilateral Mastectomy and Radiotherapy for Breast Carcinoma: Case Report.
Identifieur interne : 001107 ( PubMed/Curation ); précédent : 001106; suivant : 001108Stewart-Treves Syndrome after Bilateral Mastectomy and Radiotherapy for Breast Carcinoma: Case Report.
Auteurs : Arzu Ta Demir [Turquie] ; Hatice Karaman [Turquie] ; Dilek Ünal [Turquie] ; Hasan Mutlu [Turquie]Source :
- Journal of breast health (2013) [ 2149-1976 ] ; 2015.
Abstract
Stewart-Treves syndrome is an angiosarcoma that occurs because of chronic lymphedema, which in most cases is a complication after mastectomy with axillary node dissection and postoperative radiation. Prognosis for this rare tumor is poor. The best therapy is early and radical excision. Chronic lymphedema seems to be an important pathogenic factor. We report a 59-year-old patient with chronic lymphedema and lymphangiosarcoma of the left upper limb who had a left modified radical mastectomy with axillary node dissection and postoperative radiation nine years ago. Additionally, the patient underwent a right modified radical mastectomy with axillary node dissection and postoperative radiation one year ago. In this report, we present a case of Stewart-Treves syndrome after the patient was operated for bilateral breast carcinoma, a review of literature, and principles of treatment.
DOI: 10.5152/tjbh.2015.1604
PubMed: 28331699
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Prognosis for this rare tumor is poor. The best therapy is early and radical excision. Chronic lymphedema seems to be an important pathogenic factor. We report a 59-year-old patient with chronic lymphedema and lymphangiosarcoma of the left upper limb who had a left modified radical mastectomy with axillary node dissection and postoperative radiation nine years ago. Additionally, the patient underwent a right modified radical mastectomy with axillary node dissection and postoperative radiation one year ago. In this report, we present a case of Stewart-Treves syndrome after the patient was operated for bilateral breast carcinoma, a review of literature, and principles of treatment.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">28331699</PMID><DateCreated><Year>2017</Year><Month>03</Month><Day>23</Day></DateCreated><DateRevised><Year>2017</Year><Month>04</Month><Day>03</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Print">2149-1976</ISSN><JournalIssue CitedMedium="Print"><Volume>11</Volume><Issue>2</Issue><PubDate><Year>2015</Year><Month>Apr</Month></PubDate></JournalIssue><Title>Journal of breast health (2013)</Title><ISOAbbreviation>J Breast Health (2013)</ISOAbbreviation></Journal><ArticleTitle>Stewart-Treves Syndrome after Bilateral Mastectomy and Radiotherapy for Breast Carcinoma: Case Report.</ArticleTitle><Pagination><MedlinePgn>92-94</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.5152/tjbh.2015.1604</ELocationID><Abstract><AbstractText>Stewart-Treves syndrome is an angiosarcoma that occurs because of chronic lymphedema, which in most cases is a complication after mastectomy with axillary node dissection and postoperative radiation. Prognosis for this rare tumor is poor. The best therapy is early and radical excision. Chronic lymphedema seems to be an important pathogenic factor. We report a 59-year-old patient with chronic lymphedema and lymphangiosarcoma of the left upper limb who had a left modified radical mastectomy with axillary node dissection and postoperative radiation nine years ago. Additionally, the patient underwent a right modified radical mastectomy with axillary node dissection and postoperative radiation one year ago. In this report, we present a case of Stewart-Treves syndrome after the patient was operated for bilateral breast carcinoma, a review of literature, and principles of treatment.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Taşdemir</LastName><ForeName>Arzu</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Department of Pathology, Kayseri Training and Research Hospital, Kayseri, Turkey.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Karaman</LastName><ForeName>Hatice</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Department of Pathology, Kayseri Training and Research Hospital, Kayseri, Turkey.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ünal</LastName><ForeName>Dilek</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Department of Oncology, Kayseri Training and Research Hospital, Kayseri, Turkey.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mutlu</LastName><ForeName>Hasan</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Department of Radiation Oncology, Kayseri Training and Research Hospital, Kayseri, Turkey.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>04</Month><Day>01</Day></ArticleDate></Article><MedlineJournalInfo><Country>Turkey</Country><MedlineTA>J Breast Health (2013)</MedlineTA><NlmUniqueID>101699515</NlmUniqueID><ISSNLinking>2149-1976</ISSNLinking></MedlineJournalInfo><CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Breast J. 2006 Nov-Dec;12(6):536-43</RefSource><PMID Version="1">17238983</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Cases J. 2009 Sep 01;2:6887</RefSource><PMID Version="1">19918554</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Dermatopathol. 1987 Oct;9(5):406-12</RefSource><PMID Version="1">3120612</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Cir Esp. 2005 Dec;78(6):382-4</RefSource><PMID Version="1">16420866</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Am J Med. 1960 Jun;28:1008-12</RefSource><PMID Version="1">14444271</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Ann Surg. 1967 Aug;166(2):245-53</RefSource><PMID Version="1">6029576</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 Clin Oncol. 2006 Mar 20;24(9):1477-8</RefSource><PMID Version="1">16549844</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Clin Orthop Relat Res. 1995 Nov;(320):135-41</RefSource><PMID Version="1">7586817</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>Am J Dermatopathol. 1991 Oct;13(5):488-92</RefSource><PMID Version="1">1951986</PMID></CommentsCorrections><CommentsCorrections RefType="Cites"><RefSource>Presse Med. 2010 Dec;39(12):1305-8</RefSource><PMID Version="1">20970956</PMID></CommentsCorrections></CommentsCorrectionsList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Bilateral breast cancer</Keyword><Keyword MajorTopicYN="N">angiosarcoma</Keyword><Keyword MajorTopicYN="N">chronic lymphedema</Keyword></KeywordList><CoiStatement>Conflict of Interest: No conflict of interest was declared by the authors.</CoiStatement></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2014</Year><Month>01</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2014</Year><Month>01</Month><Day>15</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2017</Year><Month>3</Month><Day>24</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2015</Year><Month>1</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2015</Year><Month>1</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">28331699</ArticleId><ArticleId IdType="doi">10.5152/tjbh.2015.1604</ArticleId><ArticleId IdType="pii">jbh-11-2-92</ArticleId><ArticleId IdType="pmc">PMC5351494</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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