Stewart-Treves Syndrome: A Case Report and Review of Literature

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dc.contributor.authorAlbayati, Abbas
dc.contributor.authorEyupoglu, Atilla Adnan
dc.contributor.authorCologlu, Harun
dc.contributor.authorBal, Nebil
dc.contributor.authorErtas, Nilgun Markal
dc.contributor.orcID0000-0002-8605-9032en_US
dc.contributor.researcherIDAAO-4286-2020en_US
dc.date.accessioned2019-05-06T13:42:25Z
dc.date.available2019-05-06T13:42:25Z
dc.date.issued2018
dc.description.abstractStewart-Treves syndrome (STS) is defined as angiosarcoma arising in the setting of chronic lymphedema. It is typically presented in breast cancer patients who underwent axillary dissection. A 79-year-old woman presented to our clinic with a wound that developed secondary to lymphedema. Pathologic examinations diagnosed the lesion as angiosarcoma. STS is a rare and deadly entity. It is hard to diagnose and has 10% mean survival rate for 5 years. We emphasize the importance of early diagnosis that can be a lifesaver.en_US
dc.identifier.endpage36en_US
dc.identifier.issn2528-8644
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-85044469536en_US
dc.identifier.startpage34en_US
dc.identifier.urihttp://www.turkjplastsurg.org/article.asp?issn=1300-6878;year=2018;volume=26;issue=1;spage=34;epage=36;aulast=Eyuboglu
dc.identifier.urihttp://hdl.handle.net/11727/3204
dc.identifier.volume26en_US
dc.identifier.wos000438219000009en_US
dc.language.isoengen_US
dc.relation.isversionof10.4103/tjps.tjps_18_18en_US
dc.relation.journalTURKISH JOURNAL OF PLASTIC SURGERYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAngiosarcomaen_US
dc.subjectBreast canceren_US
dc.subjectCancer diagnosisen_US
dc.subjectStewart-Treves syndromeen_US
dc.titleStewart-Treves Syndrome: A Case Report and Review of Literatureen_US
dc.typearticleen_US

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