Syndrome in question

Detalhes bibliográficos
Autor(a) principal: Rosmaninho, A.
Data de Publicação: 2016
Outros Autores: Carvalho, S., Oujo, E., Horta, M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.16/2074
Resumo: Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification, is a rare disorder. It may go unrecognized if few lesions are observed. We present a case of segmental neurofibromatosis in a 28 year-old patient who presented with multiple papules and nodules distributed in dermatomal fashion on the trunk. The histopathological examination of the lesions revealed a non-encapsulated, well-circumscribed spindle cell neoplasm, which was consistent with neurofibromas.
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spelling Syndrome in questionNeurofibromaNeurofibromatosissegmentar neurofibromatosisNeurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification, is a rare disorder. It may go unrecognized if few lesions are observed. We present a case of segmental neurofibromatosis in a 28 year-old patient who presented with multiple papules and nodules distributed in dermatomal fashion on the trunk. The histopathological examination of the lesions revealed a non-encapsulated, well-circumscribed spindle cell neoplasm, which was consistent with neurofibromas.Sociedade Brasileira de DermatologiaRepositório Científico do Centro Hospitalar Universitário de Santo AntónioRosmaninho, A.Carvalho, S.Oujo, E.Horta, M.2017-04-24T14:12:21Z2016-042016-04-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/2074engAn Bras Dermatol. 2016 Apr;91(2):245-7.0365-059610.1590/abd1806-4841.20164231info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-10-20T10:59:00Zoai:repositorio.chporto.pt:10400.16/2074Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:38:21.167185Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Syndrome in question
title Syndrome in question
spellingShingle Syndrome in question
Rosmaninho, A.
Neurofibroma
Neurofibromatosis
segmentar neurofibromatosis
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 Rosmaninho, A.
author_facet Rosmaninho, A.
Carvalho, S.
Oujo, E.
Horta, M.
author_role author
author2 Carvalho, S.
Oujo, E.
Horta, M.
author2_role author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Centro Hospitalar Universitário de Santo António
dc.contributor.author.fl_str_mv Rosmaninho, A.
Carvalho, S.
Oujo, E.
Horta, M.
dc.subject.por.fl_str_mv Neurofibroma
Neurofibromatosis
segmentar neurofibromatosis
topic Neurofibroma
Neurofibromatosis
segmentar neurofibromatosis
description Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification, is a rare disorder. It may go unrecognized if few lesions are observed. We present a case of segmental neurofibromatosis in a 28 year-old patient who presented with multiple papules and nodules distributed in dermatomal fashion on the trunk. The histopathological examination of the lesions revealed a non-encapsulated, well-circumscribed spindle cell neoplasm, which was consistent with neurofibromas.
publishDate 2016
dc.date.none.fl_str_mv 2016-04
2016-04-01T00:00:00Z
2017-04-24T14:12:21Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.16/2074
url http://hdl.handle.net/10400.16/2074
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv An Bras Dermatol. 2016 Apr;91(2):245-7.
0365-0596
10.1590/abd1806-4841.20164231
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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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 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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