Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement

Detalhes bibliográficos
Autor(a) principal: Gontijo,João Renato Vianna
Data de Publicação: 2017
Outros Autores: Pinto,Jackson Machado, Paula,Maysa Carla de
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=S0365-05962017000500731
Resumo: Abstract: Systemic light chain amiloydosis is a rare disease. Due to its typical cutaneous lesions, dermatologists play an essential role in its diagnosis. Clinical manifestations vary according to the affected organ and are often unspecific. Definitive diagnosis is achieved through biopsy. We report a patient with palpebral amyloidosis, typical bilateral ecchymoses and cardiac involvement, without plasma cell dyscrasia or lymphomas. The patient died shortly after the diagnosis.
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spelling Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvementAmyloidosisAmyloidPlaque, amyloidEcchymosisPurpuraAbstract: Systemic light chain amiloydosis is a rare disease. Due to its typical cutaneous lesions, dermatologists play an essential role in its diagnosis. Clinical manifestations vary according to the affected organ and are often unspecific. Definitive diagnosis is achieved through biopsy. We report a patient with palpebral amyloidosis, typical bilateral ecchymoses and cardiac involvement, without plasma cell dyscrasia or lymphomas. The patient died shortly after the diagnosis.Sociedade Brasileira de Dermatologia2017-10-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962017000500731Anais Brasileiros de Dermatologia v.92 n.5 2017reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20176958info:eu-repo/semantics/openAccessGontijo,João Renato ViannaPinto,Jackson MachadoPaula,Maysa Carla deeng2017-11-14T00:00:00Zoai:scielo:S0365-05962017000500731Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2017-11-14T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false
dc.title.none.fl_str_mv Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
title Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
spellingShingle Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
Gontijo,João Renato Vianna
Amyloidosis
Amyloid
Plaque, amyloid
Ecchymosis
Purpura
title_short Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
title_full Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
title_fullStr Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
title_full_unstemmed Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
title_sort Case for diagnosis. Systemic light chain amyloidosis with cutaneous involvement
author Gontijo,João Renato Vianna
author_facet Gontijo,João Renato Vianna
Pinto,Jackson Machado
Paula,Maysa Carla de
author_role author
author2 Pinto,Jackson Machado
Paula,Maysa Carla de
author2_role author
author
dc.contributor.author.fl_str_mv Gontijo,João Renato Vianna
Pinto,Jackson Machado
Paula,Maysa Carla de
dc.subject.por.fl_str_mv Amyloidosis
Amyloid
Plaque, amyloid
Ecchymosis
Purpura
topic Amyloidosis
Amyloid
Plaque, amyloid
Ecchymosis
Purpura
description Abstract: Systemic light chain amiloydosis is a rare disease. Due to its typical cutaneous lesions, dermatologists play an essential role in its diagnosis. Clinical manifestations vary according to the affected organ and are often unspecific. Definitive diagnosis is achieved through biopsy. We report a patient with palpebral amyloidosis, typical bilateral ecchymoses and cardiac involvement, without plasma cell dyscrasia or lymphomas. The patient died shortly after the diagnosis.
publishDate 2017
dc.date.none.fl_str_mv 2017-10-01
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=S0365-05962017000500731
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962017000500731
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/abd1806-4841.20176958
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.92 n.5 2017
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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