Stewart-Treves Syndrome of the Lower Extremity
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , |
Tipo de documento: | Relatório |
Idioma: | eng |
Título da fonte: | Anais brasileiros de dermatologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700232 |
Resumo: | Abstract Stewart-Treves syndrome is a rare cutaneous angiosarcoma that develops in long-standing chronic lymphedema. Though most commonly this angiosarcoma is a result of post mastectomy lymphoedema, it also develops in Milroy disease, idiopathic, congenital, traumatic and filarial lymphoedema. Despite the rarity of this syndrome and its poor prognosis, early diagnosis associated with radical surgery can provide improved survival. We report a case of angiosarcoma in the lower limb in a patient with chronic lymphedema associated with history of repeated erysipela episodes. |
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Anais brasileiros de dermatologia (Online) |
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Stewart-Treves Syndrome of the Lower ExtremityLymphedemaNeoplasms, vascular tissueSarcomaAbstract Stewart-Treves syndrome is a rare cutaneous angiosarcoma that develops in long-standing chronic lymphedema. Though most commonly this angiosarcoma is a result of post mastectomy lymphoedema, it also develops in Milroy disease, idiopathic, congenital, traumatic and filarial lymphoedema. Despite the rarity of this syndrome and its poor prognosis, early diagnosis associated with radical surgery can provide improved survival. We report a case of angiosarcoma in the lower limb in a patient with chronic lymphedema associated with history of repeated erysipela episodes.Sociedade Brasileira de Dermatologia2015-06-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700232Anais Brasileiros de Dermatologia v.90 n.3 suppl.1 2015reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20153926info:eu-repo/semantics/openAccessVeiga,Rossana Ruth Garcia daNascimento,Bianca Angelina Macêdo doCarvalho,Alessandra HaberBrito,Arival Cardoso deBittencourt,Maraya de Jesus Semblanoeng2015-11-19T00:00:00Zoai:scielo:S0365-05962015000700232Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2015-11-19T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Stewart-Treves Syndrome of the Lower Extremity |
title |
Stewart-Treves Syndrome of the Lower Extremity |
spellingShingle |
Stewart-Treves Syndrome of the Lower Extremity Veiga,Rossana Ruth Garcia da Lymphedema Neoplasms, vascular tissue Sarcoma |
title_short |
Stewart-Treves Syndrome of the Lower Extremity |
title_full |
Stewart-Treves Syndrome of the Lower Extremity |
title_fullStr |
Stewart-Treves Syndrome of the Lower Extremity |
title_full_unstemmed |
Stewart-Treves Syndrome of the Lower Extremity |
title_sort |
Stewart-Treves Syndrome of the Lower Extremity |
author |
Veiga,Rossana Ruth Garcia da |
author_facet |
Veiga,Rossana Ruth Garcia da Nascimento,Bianca Angelina Macêdo do Carvalho,Alessandra Haber Brito,Arival Cardoso de Bittencourt,Maraya de Jesus Semblano |
author_role |
author |
author2 |
Nascimento,Bianca Angelina Macêdo do Carvalho,Alessandra Haber Brito,Arival Cardoso de Bittencourt,Maraya de Jesus Semblano |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Veiga,Rossana Ruth Garcia da Nascimento,Bianca Angelina Macêdo do Carvalho,Alessandra Haber Brito,Arival Cardoso de Bittencourt,Maraya de Jesus Semblano |
dc.subject.por.fl_str_mv |
Lymphedema Neoplasms, vascular tissue Sarcoma |
topic |
Lymphedema Neoplasms, vascular tissue Sarcoma |
description |
Abstract Stewart-Treves syndrome is a rare cutaneous angiosarcoma that develops in long-standing chronic lymphedema. Though most commonly this angiosarcoma is a result of post mastectomy lymphoedema, it also develops in Milroy disease, idiopathic, congenital, traumatic and filarial lymphoedema. Despite the rarity of this syndrome and its poor prognosis, early diagnosis associated with radical surgery can provide improved survival. We report a case of angiosarcoma in the lower limb in a patient with chronic lymphedema associated with history of repeated erysipela episodes. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-06-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/report |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
report |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700232 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700232 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20153926 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Dermatologia |
dc.source.none.fl_str_mv |
Anais Brasileiros de Dermatologia v.90 n.3 suppl.1 2015 reponame:Anais brasileiros de dermatologia (Online) instname:Sociedade Brasileira de Dermatologia (SBD) instacron:SBD |
instname_str |
Sociedade Brasileira de Dermatologia (SBD) |
instacron_str |
SBD |
institution |
SBD |
reponame_str |
Anais brasileiros de dermatologia (Online) |
collection |
Anais brasileiros de dermatologia (Online) |
repository.name.fl_str_mv |
Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD) |
repository.mail.fl_str_mv |
abd@sbd.org.br||revista@sbd.org.br |
_version_ |
1752126420955430912 |