Case for diagnosis

Detalhes bibliográficos
Autor(a) principal: Boza, Juliana Catucci
Data de Publicação: 2014
Outros Autores: Dorn, Timótio Volnei, Oliveira, Fabiana Bazanella de, Bakos, Renato Marchiori
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/131327
Resumo: Abstract: The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions. Lesions occur in different organs and can lead to hemorrhage in the lungs, digestive tract and brain. We describe the case of a patient with cutaneous manifestations and severe impairment of the digestive tract. It is important for the dermatologist to recognize this syndrome, since the cutaneous lesions may play a key role in diagnosis.
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spelling Boza, Juliana CatucciDorn, Timótio VolneiOliveira, Fabiana Bazanella deBakos, Renato Marchiori2015-12-24T02:39:28Z20140365-0596http://hdl.handle.net/10183/131327000979376Abstract: The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions. Lesions occur in different organs and can lead to hemorrhage in the lungs, digestive tract and brain. We describe the case of a patient with cutaneous manifestations and severe impairment of the digestive tract. It is important for the dermatologist to recognize this syndrome, since the cutaneous lesions may play a key role in diagnosis.application/pdfengAnais brasileiros de dermatologia. Rio de Janeiro. Vol. 89, n. 6 (2014), p. 999-1001.DiagnósticoEpistaxeTelangiectasiaTelangiectasia hemorrágica hereditáriaDiagnosisEpistaxisTelangiectasiaHereditary hemorrhagicTelangiectasisCase for diagnosisinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000979376.pdf000979376.pdfTexto completo (inglês)application/pdf107573http://www.lume.ufrgs.br/bitstream/10183/131327/1/000979376.pdf5557dde318580649e20da7a386a621b8MD51TEXT000979376.pdf.txt000979376.pdf.txtExtracted Texttext/plain7746http://www.lume.ufrgs.br/bitstream/10183/131327/2/000979376.pdf.txt0813ea9513b69918b916f572113e1db7MD52THUMBNAIL000979376.pdf.jpg000979376.pdf.jpgGenerated Thumbnailimage/jpeg1964http://www.lume.ufrgs.br/bitstream/10183/131327/3/000979376.pdf.jpge33b652e3cff9233b1e33fa4b64eaeccMD5310183/1313272021-09-18 04:52:44.574762oai:www.lume.ufrgs.br:10183/131327Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-09-18T07:52:44Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Case for diagnosis
title Case for diagnosis
spellingShingle Case for diagnosis
Boza, Juliana Catucci
Diagnóstico
Epistaxe
Telangiectasia
Telangiectasia hemorrágica hereditária
Diagnosis
Epistaxis
Telangiectasia
Hereditary hemorrhagic
Telangiectasis
title_short Case for diagnosis
title_full Case for diagnosis
title_fullStr Case for diagnosis
title_full_unstemmed Case for diagnosis
title_sort Case for diagnosis
author Boza, Juliana Catucci
author_facet Boza, Juliana Catucci
Dorn, Timótio Volnei
Oliveira, Fabiana Bazanella de
Bakos, Renato Marchiori
author_role author
author2 Dorn, Timótio Volnei
Oliveira, Fabiana Bazanella de
Bakos, Renato Marchiori
author2_role author
author
author
dc.contributor.author.fl_str_mv Boza, Juliana Catucci
Dorn, Timótio Volnei
Oliveira, Fabiana Bazanella de
Bakos, Renato Marchiori
dc.subject.por.fl_str_mv Diagnóstico
Epistaxe
Telangiectasia
Telangiectasia hemorrágica hereditária
topic Diagnóstico
Epistaxe
Telangiectasia
Telangiectasia hemorrágica hereditária
Diagnosis
Epistaxis
Telangiectasia
Hereditary hemorrhagic
Telangiectasis
dc.subject.eng.fl_str_mv Diagnosis
Epistaxis
Telangiectasia
Hereditary hemorrhagic
Telangiectasis
description Abstract: The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions. Lesions occur in different organs and can lead to hemorrhage in the lungs, digestive tract and brain. We describe the case of a patient with cutaneous manifestations and severe impairment of the digestive tract. It is important for the dermatologist to recognize this syndrome, since the cutaneous lesions may play a key role in diagnosis.
publishDate 2014
dc.date.issued.fl_str_mv 2014
dc.date.accessioned.fl_str_mv 2015-12-24T02:39:28Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/131327
dc.identifier.issn.pt_BR.fl_str_mv 0365-0596
dc.identifier.nrb.pt_BR.fl_str_mv 000979376
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Anais brasileiros de dermatologia. Rio de Janeiro. Vol. 89, n. 6 (2014), p. 999-1001.
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