Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report
Autor(a) principal: | |
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Data de Publicação: | 2013 |
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=S0365-05962013000300448 |
Resumo: | Behçet's disease is a chronic inflammatory disease of unknown aetiology, characterized by recurrent oral and genital aphthous ulcerations, uveitis, skin lesions and other multisystem affections associated with vasculitis. Different types of vessels, predominantly veins, can be affected in Behçet's disease. The frequency of vascular lesions in Behçet's disease, such as superficial and deep venous thromboses, arterial aneurysms and occlusions, ranges between 7-29%. Budd-Chiari syndrome is a rare and serious complication of Behçet's disease and implies thrombosis of the hepatic veins and/or the intrahepatic or suprahepatic inferior vena cava. We report a case of a 25-year-old man with Behçet's disease that developed Budd-Chiari syndrome. The correlation of dermatological, pathological and imaging studies confirmed the diagnosis. |
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Anais brasileiros de dermatologia (Online) |
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Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case reportBehcet diseaseBudd-Chiari SyndromeThrombosisBehçet's disease is a chronic inflammatory disease of unknown aetiology, characterized by recurrent oral and genital aphthous ulcerations, uveitis, skin lesions and other multisystem affections associated with vasculitis. Different types of vessels, predominantly veins, can be affected in Behçet's disease. The frequency of vascular lesions in Behçet's disease, such as superficial and deep venous thromboses, arterial aneurysms and occlusions, ranges between 7-29%. Budd-Chiari syndrome is a rare and serious complication of Behçet's disease and implies thrombosis of the hepatic veins and/or the intrahepatic or suprahepatic inferior vena cava. We report a case of a 25-year-old man with Behçet's disease that developed Budd-Chiari syndrome. The correlation of dermatological, pathological and imaging studies confirmed the diagnosis.Sociedade Brasileira de Dermatologia2013-06-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000300448Anais Brasileiros de Dermatologia v.88 n.3 2013reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20131930info:eu-repo/semantics/openAccessBittencourt,Maraya de Jesus SemblanoDias,Carolina MoraesLage,Thaiane LimaBarros,Renata SilvaPaz,Otavio Augusto GomesVieira,Waldonio de Britoeng2013-06-26T00:00:00Zoai:scielo:S0365-05962013000300448Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2013-06-26T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report |
title |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report |
spellingShingle |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report Bittencourt,Maraya de Jesus Semblano Behcet disease Budd-Chiari Syndrome Thrombosis |
title_short |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report |
title_full |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report |
title_fullStr |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report |
title_full_unstemmed |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report |
title_sort |
Behçet disease in association with Budd-Chiari syndrome and multiple thrombosis - Case report |
author |
Bittencourt,Maraya de Jesus Semblano |
author_facet |
Bittencourt,Maraya de Jesus Semblano Dias,Carolina Moraes Lage,Thaiane Lima Barros,Renata Silva Paz,Otavio Augusto Gomes Vieira,Waldonio de Brito |
author_role |
author |
author2 |
Dias,Carolina Moraes Lage,Thaiane Lima Barros,Renata Silva Paz,Otavio Augusto Gomes Vieira,Waldonio de Brito |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Bittencourt,Maraya de Jesus Semblano Dias,Carolina Moraes Lage,Thaiane Lima Barros,Renata Silva Paz,Otavio Augusto Gomes Vieira,Waldonio de Brito |
dc.subject.por.fl_str_mv |
Behcet disease Budd-Chiari Syndrome Thrombosis |
topic |
Behcet disease Budd-Chiari Syndrome Thrombosis |
description |
Behçet's disease is a chronic inflammatory disease of unknown aetiology, characterized by recurrent oral and genital aphthous ulcerations, uveitis, skin lesions and other multisystem affections associated with vasculitis. Different types of vessels, predominantly veins, can be affected in Behçet's disease. The frequency of vascular lesions in Behçet's disease, such as superficial and deep venous thromboses, arterial aneurysms and occlusions, ranges between 7-29%. Budd-Chiari syndrome is a rare and serious complication of Behçet's disease and implies thrombosis of the hepatic veins and/or the intrahepatic or suprahepatic inferior vena cava. We report a case of a 25-year-old man with Behçet's disease that developed Budd-Chiari syndrome. The correlation of dermatological, pathological and imaging studies confirmed the diagnosis. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-06-01 |
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=S0365-05962013000300448 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000300448 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20131930 |
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.88 n.3 2013 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_ |
1752126418687361024 |