Case for diagnosis
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Anais brasileiros de dermatologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000300521 |
Resumo: | Degos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unknown etiology characterized by infarcts in the dermis, gastrointestinal tract, central nervous system, and other organs. It is characterized by papules, which become umbilicated and evolve with a depressed porcelain-white central area, with an erythematous halo with telangiectasias. Histological findings include wedge-shaped dermoepidermal necrosis and blood vessel thrombosis. Approximately 50-60% of patients with systemic symptoms die within 2-3 years, most due to gastrointestinal perforation. We report a typical case, with lethal outcome, in a 45-year-old woman. |
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Anais brasileiros de dermatologia (Online) |
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Case for diagnosisComplement C5Malignant atrophic papulosisVascular diseasesDegos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unknown etiology characterized by infarcts in the dermis, gastrointestinal tract, central nervous system, and other organs. It is characterized by papules, which become umbilicated and evolve with a depressed porcelain-white central area, with an erythematous halo with telangiectasias. Histological findings include wedge-shaped dermoepidermal necrosis and blood vessel thrombosis. Approximately 50-60% of patients with systemic symptoms die within 2-3 years, most due to gastrointestinal perforation. We report a typical case, with lethal outcome, in a 45-year-old woman.Sociedade Brasileira de Dermatologia2014-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000300521Anais Brasileiros de Dermatologia v.89 n.3 2014reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20142863info:eu-repo/semantics/openAccessLima,Lourenço de AzevedoHaddad,Natacha de Carvalho MelloLima,Ricardo BarbosaD'Acri,Antonio MacedoMartins,Carlos Joséeng2015-10-19T00:00:00Zoai:scielo:S0365-05962014000300521Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2015-10-19T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Case for diagnosis |
title |
Case for diagnosis |
spellingShingle |
Case for diagnosis Lima,Lourenço de Azevedo Complement C5 Malignant atrophic papulosis Vascular diseases |
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 |
Lima,Lourenço de Azevedo |
author_facet |
Lima,Lourenço de Azevedo Haddad,Natacha de Carvalho Mello Lima,Ricardo Barbosa D'Acri,Antonio Macedo Martins,Carlos José |
author_role |
author |
author2 |
Haddad,Natacha de Carvalho Mello Lima,Ricardo Barbosa D'Acri,Antonio Macedo Martins,Carlos José |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Lima,Lourenço de Azevedo Haddad,Natacha de Carvalho Mello Lima,Ricardo Barbosa D'Acri,Antonio Macedo Martins,Carlos José |
dc.subject.por.fl_str_mv |
Complement C5 Malignant atrophic papulosis Vascular diseases |
topic |
Complement C5 Malignant atrophic papulosis Vascular diseases |
description |
Degos disease, also known as malignant atrophic papulosis, is a rare occlusive vasculopathy of unknown etiology characterized by infarcts in the dermis, gastrointestinal tract, central nervous system, and other organs. It is characterized by papules, which become umbilicated and evolve with a depressed porcelain-white central area, with an erythematous halo with telangiectasias. Histological findings include wedge-shaped dermoepidermal necrosis and blood vessel thrombosis. Approximately 50-60% of patients with systemic symptoms die within 2-3 years, most due to gastrointestinal perforation. We report a typical case, with lethal outcome, in a 45-year-old woman. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-06-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000300521 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962014000300521 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20142863 |
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.89 n.3 2014 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_ |
1752126419800948736 |