Diffuse systemic sclerosis with bullous lesions without systemic manifestations
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=S0365-05962013000800078 |
Resumo: | Here, we describe an atypical case of systemic sclerosis in its diffuse cutaneous form with acute and rapid progression of the cutaneous condition, without any systemic manifestations and the infrequent formation of bullae, showing the importance of diagnosis and early treatment in such cases. This case also shows that special measures should be taken for bullous cutaneous lesions and ulcerations resulting from serious sclerosis, which are entry points and increase morbidity and risk of death. Other prognostic factors include age, ESR and renal and pulmonary involvement. Capillaroscopies can be useful predictors of greater severity of systemic scleroderma, revealing a greater link with systemic, rather than cutaneous, involvement. |
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Anais brasileiros de dermatologia (Online) |
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Diffuse systemic sclerosis with bullous lesions without systemic manifestationsConnective tissue diseasesScleroderma, diffuseScleroderma, systemicSkin diseases, vesiculobullousSkin and connective tissue diseasesHere, we describe an atypical case of systemic sclerosis in its diffuse cutaneous form with acute and rapid progression of the cutaneous condition, without any systemic manifestations and the infrequent formation of bullae, showing the importance of diagnosis and early treatment in such cases. This case also shows that special measures should be taken for bullous cutaneous lesions and ulcerations resulting from serious sclerosis, which are entry points and increase morbidity and risk of death. Other prognostic factors include age, ESR and renal and pulmonary involvement. Capillaroscopies can be useful predictors of greater severity of systemic scleroderma, revealing a greater link with systemic, rather than cutaneous, involvement.Sociedade Brasileira de Dermatologia2013-12-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000800078Anais Brasileiros de Dermatologia v.88 n.6 suppl.1 2013reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20132160info:eu-repo/semantics/openAccessMacedo,Paula Renaux Wanderley CarattaMota,Amanda Nascimento Cavalleiro de MacedoGripp,Alexandre CarlosAlves,Maria de Fatima Guimarães ScotelaroKlumb,Evandro Mendeseng2014-06-16T00:00:00Zoai:scielo:S0365-05962013000800078Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2014-06-16T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false |
dc.title.none.fl_str_mv |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations |
title |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations |
spellingShingle |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations Macedo,Paula Renaux Wanderley Caratta Connective tissue diseases Scleroderma, diffuse Scleroderma, systemic Skin diseases, vesiculobullous Skin and connective tissue diseases |
title_short |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations |
title_full |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations |
title_fullStr |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations |
title_full_unstemmed |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations |
title_sort |
Diffuse systemic sclerosis with bullous lesions without systemic manifestations |
author |
Macedo,Paula Renaux Wanderley Caratta |
author_facet |
Macedo,Paula Renaux Wanderley Caratta Mota,Amanda Nascimento Cavalleiro de Macedo Gripp,Alexandre Carlos Alves,Maria de Fatima Guimarães Scotelaro Klumb,Evandro Mendes |
author_role |
author |
author2 |
Mota,Amanda Nascimento Cavalleiro de Macedo Gripp,Alexandre Carlos Alves,Maria de Fatima Guimarães Scotelaro Klumb,Evandro Mendes |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Macedo,Paula Renaux Wanderley Caratta Mota,Amanda Nascimento Cavalleiro de Macedo Gripp,Alexandre Carlos Alves,Maria de Fatima Guimarães Scotelaro Klumb,Evandro Mendes |
dc.subject.por.fl_str_mv |
Connective tissue diseases Scleroderma, diffuse Scleroderma, systemic Skin diseases, vesiculobullous Skin and connective tissue diseases |
topic |
Connective tissue diseases Scleroderma, diffuse Scleroderma, systemic Skin diseases, vesiculobullous Skin and connective tissue diseases |
description |
Here, we describe an atypical case of systemic sclerosis in its diffuse cutaneous form with acute and rapid progression of the cutaneous condition, without any systemic manifestations and the infrequent formation of bullae, showing the importance of diagnosis and early treatment in such cases. This case also shows that special measures should be taken for bullous cutaneous lesions and ulcerations resulting from serious sclerosis, which are entry points and increase morbidity and risk of death. Other prognostic factors include age, ESR and renal and pulmonary involvement. Capillaroscopies can be useful predictors of greater severity of systemic scleroderma, revealing a greater link with systemic, rather than cutaneous, involvement. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-12-01 |
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=S0365-05962013000800078 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000800078 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/abd1806-4841.20132160 |
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.6 suppl.1 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_ |
1752126419133005824 |