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Characterization of the cellular component of polymorphous low-grade adenocarcinoma by immunohistochemistry and electron microscopy

dc.contributor.authorAraujo, V
dc.contributor.authorSousa, S.
dc.contributor.authorJaeger, M.
dc.contributor.authorJaeger, R.
dc.contributor.authorLoyola, A.
dc.contributor.authorCrivelini, M.
dc.contributor.authorAraujo, N.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:24:31Z
dc.date.available2014-05-20T15:24:31Z
dc.date.issued1999-03-01
dc.description.abstractIn order to characterize the cellular component of the polymorphous low-grade adenocarcinoma (PLGA) of the salivary gland, a morphological and immunohistochemical study was carried out. Thirty cases of PLGA were studied by light microscopy and immunohistochemistry and five cases by transmission electron microscopy (TEM). The expression of cytokeratins (CKs) 7,8,10,13,14,18,19, vimentin and muscle-specific actin (MSA) was investigated through the streptavidin-biotin method. The majority of tumor cells stained for vimentin, CKs 8,18 and 7. CK 14 was positive in most cells of the papillary and trabecular sub-types. Although the expression of CKs 8,18 and 14 varied among the tumors sub-types, a straight relationship between each histologic pattern and the CK expression could not be delineated. MSA was reactive in only three tumors while CKs 10 and 13 were not detected in any tumor studied. The absence of MSA and the expression of CKs 8,18 and 7, in most of the tumor cells, lead to the hypothesis that myoepithelial cells are not the major cellular component of the PLGA. TEM revealed cells exhibiting microvilli and variable amounts of secretory granules, some of them suggesting an excretory activity. The presence of CKs 8, 18 and 7, added to the secretory granules, indicates that PLGA originates from cells located at the acinar-intercalated duct junction. (C) 1999 Elsevier B.V. Ltd. All rights reserved.en
dc.description.affiliationUniv São Paulo, Sch Dent, Fac Odontol, BR-05508900 São Paulo, Brazil
dc.description.affiliationUniversidade Federal de Uberlândia (UFU), Sch Dent, Uberlandia, MG, Brazil
dc.description.affiliationPaulista State Univ, Sch Dent, Aracatuba, Brazil
dc.description.affiliationUnespPaulista State Univ, Sch Dent, Aracatuba, Brazil
dc.format.extent164-172
dc.identifierhttp://dx.doi.org/10.1016/S1368-8375(98)00102-X
dc.identifier.citationOral Oncology. Oxford: Pergamon-Elsevier B.V., v. 35, n. 2, p. 164-172, 1999.
dc.identifier.doi10.1016/S1368-8375(98)00102-X
dc.identifier.issn0964-1955
dc.identifier.urihttp://hdl.handle.net/11449/35123
dc.identifier.wosWOS:000079090100007
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofOral Oncology
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectsalivary gland tumorspt
dc.subjectpolymorphous low-grade adenocarcinomapt
dc.subjectintermediate filamentspt
dc.subjectactinpt
dc.subjectimmunohistochemistrypt
dc.subjecttransmission electron microscopypt
dc.titleCharacterization of the cellular component of polymorphous low-grade adenocarcinoma by immunohistochemistry and electron microscopyen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.departmentPatologia e Propedêutica Clínica - FOApt

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