Stewart-Treves Syndrome of the Lower Extremity

AbstractStewart-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. Despi...

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Main Authors: Rossana Ruth Garcia da Veiga, Bianca Angelina Macêdo do Nascimento, Alessandra Haber Carvalho, Arival Cardoso de Brito, Maraya de Jesus Semblano Bittencourt
Format: Article
Language:English
Published: Sociedade Brasileira de Dermatologia 2015-06-01
Series:Anais Brasileiros de Dermatologia
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700232&tlng=en
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author Rossana Ruth Garcia da Veiga
Bianca Angelina Macêdo do Nascimento
Alessandra Haber Carvalho
Arival Cardoso de Brito
Maraya de Jesus Semblano Bittencourt
author_facet Rossana Ruth Garcia da Veiga
Bianca Angelina Macêdo do Nascimento
Alessandra Haber Carvalho
Arival Cardoso de Brito
Maraya de Jesus Semblano Bittencourt
author_sort Rossana Ruth Garcia da Veiga
collection DOAJ
description AbstractStewart-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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spelling doaj.art-7e9586a2ad944d0d889bdb361ec820c02022-12-21T19:35:45ZengSociedade Brasileira de DermatologiaAnais Brasileiros de Dermatologia0365-05962015-06-01903 suppl 123223410.1590/abd1806-4841.20153926Stewart-Treves Syndrome of the Lower ExtremityRossana Ruth Garcia da VeigaBianca Angelina Macêdo do NascimentoAlessandra Haber CarvalhoArival Cardoso de BritoMaraya de Jesus Semblano BittencourtAbstractStewart-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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700232&tlng=enLymphedemaNeoplasms, vascular tissueSarcoma
spellingShingle Rossana Ruth Garcia da Veiga
Bianca Angelina Macêdo do Nascimento
Alessandra Haber Carvalho
Arival Cardoso de Brito
Maraya de Jesus Semblano Bittencourt
Stewart-Treves Syndrome of the Lower Extremity
Anais Brasileiros de Dermatologia
Lymphedema
Neoplasms, vascular tissue
Sarcoma
title 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_short Stewart-Treves Syndrome of the Lower Extremity
title_sort stewart treves syndrome of the lower extremity
topic Lymphedema
Neoplasms, vascular tissue
Sarcoma
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700232&tlng=en
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AT alessandrahabercarvalho stewarttrevessyndromeofthelowerextremity
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