Infantile myofibromatosis - a clinical and pathological diagnostic challenge

Detalhes bibliográficos
Autor(a) principal: Mota, F.
Data de Publicação: 2017
Outros Autores: Machado, S., Moreno, F., Barbosa, T., Selores, 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/10400.16/2182
Resumo: Infantile myofibromatosis is a rare disorder of fibroblastic/myofibroblastic proliferation and represents the most frequent type of mesenchymal tumor in the neonatal period and primary infancy.Three clinical types have been described: solitary, multicentric, and generalized (with visceral involvement). A correct characterization of the histopathology is essential to diagnose these neoplasias in early infancy. We present a case of multicentric infantile myofibromatosis with regression over time.
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spelling Infantile myofibromatosis - a clinical and pathological diagnostic challengeinfantile myofibromatosismesenchymal tumorinfancyInfantile myofibromatosis is a rare disorder of fibroblastic/myofibroblastic proliferation and represents the most frequent type of mesenchymal tumor in the neonatal period and primary infancy.Three clinical types have been described: solitary, multicentric, and generalized (with visceral involvement). A correct characterization of the histopathology is essential to diagnose these neoplasias in early infancy. We present a case of multicentric infantile myofibromatosis with regression over time.University of California, DavisRepositório Científico do Centro Hospitalar Universitário de Santo AntónioMota, F.Machado, S.Moreno, F.Barbosa, T.Selores, M.2017-09-04T18:42:15Z2017-04-152017-04-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/2182engDermatol Online J. 2017 Apr 15;23(4)1087-2108pii: 13030/qt4493x33ginfo: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:RCAAP2023-10-20T10:59:28Zoai:repositorio.chporto.pt:10400.16/2182Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:38:25.267538Repositório 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 Infantile myofibromatosis - a clinical and pathological diagnostic challenge
title Infantile myofibromatosis - a clinical and pathological diagnostic challenge
spellingShingle Infantile myofibromatosis - a clinical and pathological diagnostic challenge
Mota, F.
infantile myofibromatosis
mesenchymal tumor
infancy
title_short Infantile myofibromatosis - a clinical and pathological diagnostic challenge
title_full Infantile myofibromatosis - a clinical and pathological diagnostic challenge
title_fullStr Infantile myofibromatosis - a clinical and pathological diagnostic challenge
title_full_unstemmed Infantile myofibromatosis - a clinical and pathological diagnostic challenge
title_sort Infantile myofibromatosis - a clinical and pathological diagnostic challenge
author Mota, F.
author_facet Mota, F.
Machado, S.
Moreno, F.
Barbosa, T.
Selores, M.
author_role author
author2 Machado, S.
Moreno, F.
Barbosa, T.
Selores, M.
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Centro Hospitalar Universitário de Santo António
dc.contributor.author.fl_str_mv Mota, F.
Machado, S.
Moreno, F.
Barbosa, T.
Selores, M.
dc.subject.por.fl_str_mv infantile myofibromatosis
mesenchymal tumor
infancy
topic infantile myofibromatosis
mesenchymal tumor
infancy
description Infantile myofibromatosis is a rare disorder of fibroblastic/myofibroblastic proliferation and represents the most frequent type of mesenchymal tumor in the neonatal period and primary infancy.Three clinical types have been described: solitary, multicentric, and generalized (with visceral involvement). A correct characterization of the histopathology is essential to diagnose these neoplasias in early infancy. We present a case of multicentric infantile myofibromatosis with regression over time.
publishDate 2017
dc.date.none.fl_str_mv 2017-09-04T18:42:15Z
2017-04-15
2017-04-15T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.16/2182
url http://hdl.handle.net/10400.16/2182
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Dermatol Online J. 2017 Apr 15;23(4)
1087-2108
pii: 13030/qt4493x33g
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv University of California, Davis
publisher.none.fl_str_mv University of California, Davis
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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