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Can non-collagenous proteins be employed for the differential diagnosis among fibrous dysplasia, cemento-osseous dysplasia and cemento-ossifying fibroma?

dc.contributor.authorVeltrini, Vanessa Cristina
dc.contributor.authorFigueira, Jéssica Araújo [UNESP]
dc.contributor.authorSantin, Gabriela Cristina
dc.contributor.authorde Sousa, Suzana Cantanhede Orsini Machado
dc.contributor.authorde Araújo, Ney Soares
dc.contributor.institutionState University of Maringa
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2019-10-06T16:30:25Z
dc.date.available2019-10-06T16:30:25Z
dc.date.issued2019-07-01
dc.description.abstractDifferential diagnosis among fibrous dysplasias, cemento-ossifying fibromas and cemento-osseous dysplasias is difficult, since there is considerable overlap of histologic features, but also extremely important, since they differ greatly in etiology, clinical behaviour, prognosis and terapeuthic approach. There is no data about the use of immunohistochemistry, a viable and accessible technique, for this purpose. The objective of this study was to investigate, comparatively, the immunohistochemical expression of major non-collagenous proteins (osteonectin [ON], osteopontin [OP], bone sialoprotein [BSP] and osteocalcin [OC]) of mineralized tissue extracellular matrix in 22 cases of fibrous dysplasias, 16 of cemento-ossifying fibromas and 16 of cemento-osseous dysplasias. ON maintained the same expression profile in all cases; the staining for OP was negative in fusiform cells producing cementoid globules and weak, as well as heterogeneous, in high mineralized matrixes; there was negativity for BSP in cementoid globules and in the fusiform cells that produce them, differently from the strong positive expression found in the majority of bone trabeculae and their peripheral cuboidal osteoblasts; and finally, the immuno-reactivity for OC was weak, except in cuboidal osteoblasts and osteocytes. We can conclude that the nature of mineralized structure and the cellular phenotype are much more responsible for variability in immunohistochemical profile than the type of lesion (fibrous dysplasias, cemento-ossifying fibromas and cemento-osseous dysplasias) which makes difficult, at least for a while, the use of these proteins with diagnosis purpose.en
dc.description.affiliationOral Pathology Discipline Dentistry Department State University of Maringa, Av. Mandacaru, 1550
dc.description.affiliationOral Oncology Center São Paulo State University (UNESP) School of Dentistry Rua José Bonifácio, 1193
dc.description.affiliationPediatric Dentistry Discipline Dentistry Department State University of Maringa, Av. Mandacaru, 1550
dc.description.affiliationOral Pathology Department School of Dentistry University of São Paulo, Av. Prof. Lineu Prestes, 2227
dc.description.affiliationUnespOral Oncology Center São Paulo State University (UNESP) School of Dentistry Rua José Bonifácio, 1193
dc.identifierhttp://dx.doi.org/10.1016/j.prp.2019.152450
dc.identifier.citationPathology Research and Practice, v. 215, n. 7, 2019.
dc.identifier.doi10.1016/j.prp.2019.152450
dc.identifier.issn1618-0631
dc.identifier.issn0344-0338
dc.identifier.scopus2-s2.0-85065660502
dc.identifier.urihttp://hdl.handle.net/11449/189118
dc.language.isoeng
dc.relation.ispartofPathology Research and Practice
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectBenign mesenchymal odontogenic tumours
dc.subjectBone sialoprotein
dc.subjectFibro-osseous lesions
dc.subjectOsteocalcin
dc.subjectOsteonectin
dc.subjectOsteopontin
dc.titleCan non-collagenous proteins be employed for the differential diagnosis among fibrous dysplasia, cemento-osseous dysplasia and cemento-ossifying fibroma?en
dc.typeArtigo
dspace.entity.typePublication

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