Syndrome in question

Detalhes bibliográficos
Autor(a) principal: Pousa,Catharina Maria Freire de Lucena
Data de Publicação: 2015
Outros Autores: Lavorato,Fernanda Guedes, Rehfeldt,Fernanda Valente, Mann,Danielle, Alves,Maria de Fátima Gonçalves Scotelaro
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=S0365-05962015000500759
Resumo: AbstractMuir-Torre syndrome is a rare genodermatosis characterized by the occurrence of at least one sebaceous tumor associated with visceral neoplasia, but with no predisposing factors. The sebaceous neoplasm may appear before, during or after the diagnosis of colorectal cancer. As it is regarded as a subtype of nonpolyposis hereditary colorectal cancer, it is important to evaluate the patient's first-degree relatives. The clinical course of the neoplasm is usually more indolent and the syndrome has a good prognosis. We report the case of a patient who, after a ten-year diagnosis of colorectal cancer, presented with multiple sebaceous neoplasms.
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spelling Syndrome in questionSebaceous gland neoplasmsColorectal neoplasms, hereditary nonpolyposisSkin NeoplasmsSyndromeMuir-Torre SyndromeAbstractMuir-Torre syndrome is a rare genodermatosis characterized by the occurrence of at least one sebaceous tumor associated with visceral neoplasia, but with no predisposing factors. The sebaceous neoplasm may appear before, during or after the diagnosis of colorectal cancer. As it is regarded as a subtype of nonpolyposis hereditary colorectal cancer, it is important to evaluate the patient's first-degree relatives. The clinical course of the neoplasm is usually more indolent and the syndrome has a good prognosis. We report the case of a patient who, after a ten-year diagnosis of colorectal cancer, presented with multiple sebaceous neoplasms.Sociedade Brasileira de Dermatologia2015-10-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000500759Anais Brasileiros de Dermatologia v.90 n.5 2015reponame:Anais brasileiros de dermatologia (Online)instname:Sociedade Brasileira de Dermatologia (SBD)instacron:SBD10.1590/abd1806-4841.20153193info:eu-repo/semantics/openAccessPousa,Catharina Maria Freire de LucenaLavorato,Fernanda GuedesRehfeldt,Fernanda ValenteMann,DanielleAlves,Maria de Fátima Gonçalves Scotelaroeng2015-11-05T00:00:00Zoai:scielo:S0365-05962015000500759Revistahttp://www.anaisdedermatologia.org.br/https://old.scielo.br/oai/scielo-oai.phpabd@sbd.org.br||revista@sbd.org.br1806-48410365-0596opendoar:2015-11-05T00:00Anais brasileiros de dermatologia (Online) - Sociedade Brasileira de Dermatologia (SBD)false
dc.title.none.fl_str_mv Syndrome in question
title Syndrome in question
spellingShingle Syndrome in question
Pousa,Catharina Maria Freire de Lucena
Sebaceous gland neoplasms
Colorectal neoplasms, hereditary nonpolyposis
Skin Neoplasms
Syndrome
Muir-Torre Syndrome
title_short Syndrome in question
title_full Syndrome in question
title_fullStr Syndrome in question
title_full_unstemmed Syndrome in question
title_sort Syndrome in question
author Pousa,Catharina Maria Freire de Lucena
author_facet Pousa,Catharina Maria Freire de Lucena
Lavorato,Fernanda Guedes
Rehfeldt,Fernanda Valente
Mann,Danielle
Alves,Maria de Fátima Gonçalves Scotelaro
author_role author
author2 Lavorato,Fernanda Guedes
Rehfeldt,Fernanda Valente
Mann,Danielle
Alves,Maria de Fátima Gonçalves Scotelaro
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pousa,Catharina Maria Freire de Lucena
Lavorato,Fernanda Guedes
Rehfeldt,Fernanda Valente
Mann,Danielle
Alves,Maria de Fátima Gonçalves Scotelaro
dc.subject.por.fl_str_mv Sebaceous gland neoplasms
Colorectal neoplasms, hereditary nonpolyposis
Skin Neoplasms
Syndrome
Muir-Torre Syndrome
topic Sebaceous gland neoplasms
Colorectal neoplasms, hereditary nonpolyposis
Skin Neoplasms
Syndrome
Muir-Torre Syndrome
description AbstractMuir-Torre syndrome is a rare genodermatosis characterized by the occurrence of at least one sebaceous tumor associated with visceral neoplasia, but with no predisposing factors. The sebaceous neoplasm may appear before, during or after the diagnosis of colorectal cancer. As it is regarded as a subtype of nonpolyposis hereditary colorectal cancer, it is important to evaluate the patient's first-degree relatives. The clinical course of the neoplasm is usually more indolent and the syndrome has a good prognosis. We report the case of a patient who, after a ten-year diagnosis of colorectal cancer, presented with multiple sebaceous neoplasms.
publishDate 2015
dc.date.none.fl_str_mv 2015-10-01
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=S0365-05962015000500759
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962015000500759
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/abd1806-4841.20153193
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.90 n.5 2015
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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