Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.16/2182
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degois.publication.issue4pt_PT
degois.publication.locationUnited States of Americapt_PT
degois.publication.titleDermatology Online Journalpt_PT
dc.relation.publisherversionhttp://escholarship.org/uc/item/4493x33gpt_PT
dc.contributor.authorMota, F.-
dc.contributor.authorMachado, S.-
dc.contributor.authorMoreno, F.-
dc.contributor.authorBarbosa, T.-
dc.contributor.authorSelores, M.-
dc.date.accessioned2017-09-04T18:42:15Z-
dc.date.available2017-09-04T18:42:15Z-
dc.date.issued2017-04-15-
dc.identifier.citationDermatol Online J. 2017 Apr 15;23(4)pt_PT
dc.identifier.issn1087-2108-
dc.identifier.urihttp://hdl.handle.net/10400.16/2182-
dc.description.abstractInfantile 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.pt_PT
dc.language.isoengpt_PT
dc.publisherUniversity of California, Davispt_PT
dc.rightsopenAccesspt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectinfantile myofibromatosispt_PT
dc.subjectmesenchymal tumorpt_PT
dc.subjectinfancypt_PT
dc.titleInfantile myofibromatosis - a clinical and pathological diagnostic challengept_PT
dc.typearticlept_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.peerreviewedyespt_PT
degois.publication.volume23pt_PT
dc.identifier.doipii: 13030/qt4493x33gpt_PT
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SAP - Artigos publicados em revistas indexadas na Medline
SD - Artigos publicados em revistas indexadas na Medline

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