Rendu-Osler-Weber syndrome: dermatological approach

Detalhes bibliográficos
Autor(a) principal: Barbosa,Aline Blanco
Data de Publicação: 2015
Outros Autores: Hans Filho,Günter, Vicari,Carolina Faria dos Santos, Medeiros,Marcelo Zanolli, Couto,Daíne Vargas, Takita,Luiz Carlos
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=S0365-05962015000700226
Resumo: Abstract The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history. Recurrent bleeding, hypoxemia, congestive heart failure, portosystemic encephalopathy, and symptoms related to angiodysplasia of the central nervous system may occur. Since the treatment is based on supportive measures, early recognition is of utmost importance. This article reports the case of a 53-year-old male patient who presented telangiectasias on fingers, oral cavity and nasal mucosa for 10 years, with a history of recurrent epistaxis of varying severity since childhood. Mother, sister and daughter have similar lesions.
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spelling Rendu-Osler-Weber syndrome: dermatological approachEpistaxisGeneticsTelangiectasiahereditary hemorrhagicAbstract The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history. Recurrent bleeding, hypoxemia, congestive heart failure, portosystemic encephalopathy, and symptoms related to angiodysplasia of the central nervous system may occur. Since the treatment is based on supportive measures, early recognition is of utmost importance. This article reports the case of a 53-year-old male patient who presented telangiectasias on fingers, oral cavity and nasal mucosa for 10 years, with a history of recurrent epistaxis of varying severity since childhood. Mother, sister and daughter have similar lesions.Sociedade Brasileira de Dermatologia2015-06-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700226Anais Brasileiros de Dermatologia v.90 n.3 suppl.1 2015reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20152563info:eu-repo/semantics/openAccessBarbosa,Aline BlancoHans Filho,GünterVicari,Carolina Faria dos SantosMedeiros,Marcelo ZanolliCouto,Daíne VargasTakita,Luiz Carloseng2015-11-19T00:00:00Zoai:scielo:S0365-05962015000700226Revistahttp://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 Rendu-Osler-Weber syndrome: dermatological approach
title Rendu-Osler-Weber syndrome: dermatological approach
spellingShingle Rendu-Osler-Weber syndrome: dermatological approach
Barbosa,Aline Blanco
Epistaxis
Genetics
Telangiectasia
hereditary hemorrhagic
title_short Rendu-Osler-Weber syndrome: dermatological approach
title_full Rendu-Osler-Weber syndrome: dermatological approach
title_fullStr Rendu-Osler-Weber syndrome: dermatological approach
title_full_unstemmed Rendu-Osler-Weber syndrome: dermatological approach
title_sort Rendu-Osler-Weber syndrome: dermatological approach
author Barbosa,Aline Blanco
author_facet Barbosa,Aline Blanco
Hans Filho,Günter
Vicari,Carolina Faria dos Santos
Medeiros,Marcelo Zanolli
Couto,Daíne Vargas
Takita,Luiz Carlos
author_role author
author2 Hans Filho,Günter
Vicari,Carolina Faria dos Santos
Medeiros,Marcelo Zanolli
Couto,Daíne Vargas
Takita,Luiz Carlos
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Barbosa,Aline Blanco
Hans Filho,Günter
Vicari,Carolina Faria dos Santos
Medeiros,Marcelo Zanolli
Couto,Daíne Vargas
Takita,Luiz Carlos
dc.subject.por.fl_str_mv Epistaxis
Genetics
Telangiectasia
hereditary hemorrhagic
topic Epistaxis
Genetics
Telangiectasia
hereditary hemorrhagic
description Abstract The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history. Recurrent bleeding, hypoxemia, congestive heart failure, portosystemic encephalopathy, and symptoms related to angiodysplasia of the central nervous system may occur. Since the treatment is based on supportive measures, early recognition is of utmost importance. This article reports the case of a 53-year-old male patient who presented telangiectasias on fingers, oral cavity and nasal mucosa for 10 years, with a history of recurrent epistaxis of varying severity since childhood. Mother, sister and daughter have similar lesions.
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=S0365-05962015000700226
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000700226
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/abd1806-4841.20152563
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
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