Publicação: Characterization of the cellular component of polymorphous low-grade adenocarcinoma by immunohistochemistry and electron microscopy
dc.contributor.author | Araujo, V | |
dc.contributor.author | Sousa, S. | |
dc.contributor.author | Jaeger, M. | |
dc.contributor.author | Jaeger, R. | |
dc.contributor.author | Loyola, A. | |
dc.contributor.author | Crivelini, M. | |
dc.contributor.author | Araujo, N. | |
dc.contributor.institution | Universidade de São Paulo (USP) | |
dc.contributor.institution | Universidade Federal de Uberlândia (UFU) | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-20T15:24:31Z | |
dc.date.available | 2014-05-20T15:24:31Z | |
dc.date.issued | 1999-03-01 | |
dc.description.abstract | In 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.affiliation | Univ São Paulo, Sch Dent, Fac Odontol, BR-05508900 São Paulo, Brazil | |
dc.description.affiliation | Universidade Federal de Uberlândia (UFU), Sch Dent, Uberlandia, MG, Brazil | |
dc.description.affiliation | Paulista State Univ, Sch Dent, Aracatuba, Brazil | |
dc.description.affiliationUnesp | Paulista State Univ, Sch Dent, Aracatuba, Brazil | |
dc.format.extent | 164-172 | |
dc.identifier | http://dx.doi.org/10.1016/S1368-8375(98)00102-X | |
dc.identifier.citation | Oral Oncology. Oxford: Pergamon-Elsevier B.V., v. 35, n. 2, p. 164-172, 1999. | |
dc.identifier.doi | 10.1016/S1368-8375(98)00102-X | |
dc.identifier.issn | 0964-1955 | |
dc.identifier.uri | http://hdl.handle.net/11449/35123 | |
dc.identifier.wos | WOS:000079090100007 | |
dc.language.iso | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation.ispartof | Oral Oncology | |
dc.rights.accessRights | Acesso restrito | pt |
dc.source | Web of Science | |
dc.subject | salivary gland tumors | pt |
dc.subject | polymorphous low-grade adenocarcinoma | pt |
dc.subject | intermediate filaments | pt |
dc.subject | actin | pt |
dc.subject | immunohistochemistry | pt |
dc.subject | transmission electron microscopy | pt |
dc.title | Characterization of the cellular component of polymorphous low-grade adenocarcinoma by immunohistochemistry and electron microscopy | en |
dc.type | Artigo | pt |
dcterms.license | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dcterms.rightsHolder | Elsevier B.V. | |
dspace.entity.type | Publication | |
relation.isOrgUnitOfPublication | 8b3335a4-1163-438a-a0e2-921a46e0380d | |
relation.isOrgUnitOfPublication.latestForDiscovery | 8b3335a4-1163-438a-a0e2-921a46e0380d | |
unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatuba | pt |
unesp.department | Patologia e Propedêutica Clínica - FOA | pt |
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