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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/69643
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dc.contributor.authorRodrigues, Paulo Antônio-
dc.contributor.authorKobayasi, Shoiti-
dc.contributor.authorRodrigues, Maria Aparecida Marchesan-
dc.date.accessioned2014-05-27T11:22:28Z-
dc.date.accessioned2016-10-25T18:23:49Z-
dc.date.available2014-05-27T11:22:28Z-
dc.date.available2016-10-25T18:23:49Z-
dc.date.issued2007-05-01-
dc.identifierhttp://dx.doi.org/10.1590/S0102-86502007000300009-
dc.identifier.citationActa Cirurgica Brasileira, v. 22, n. 3, p. 210-214, 2007.-
dc.identifier.issn0102-8650-
dc.identifier.issn1678-2674-
dc.identifier.urihttp://hdl.handle.net/11449/69643-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69643-
dc.description.abstractPurpose: to investigate if combining VT to DGR through the pylorus can modulate the biological behavior of PL induced by DGR and to verify if TV alone can induce morphologic lesions in the gastric mucosa. Methods: 62 male Wistar rats were assigned to four groups: 1 - Control (CT) gastrotomy; 2 - Troncular Vagotomy (TV) plus gastrotomy; 3 - Duodenogastric reflux through the pylorus (R) and 4 - Troncular vagotomy plus DGR (RTV). The animals were killed at the 54 week of the experiment. DGR was obtained by anastomosing a proximal jejunal loop to the anterior gastric wall. TV was performed through isolation and division of the vagal trunks. Gastrotomy consisted of 1 cm incision at the anterior gastric wall. PL were analyzed gross and histologically in the antral mucosa, at the gastrojejunal stoma and at the squamous portion of the gastric mucosa. Results: Groups R and RTV developed exophytic lesions in the antral mucosa (R=90.9%; RTV=100%) and at the gastrojejunal stoma (R=54.54%; RTV=63.63%). Histologically they consisted of proliferative benign lesions, without cellular atypias, diagnosed as adenomatous hyperplasia. Both groups exposed to DGR presented squamous hyperplasia at the squamous portion of the gastric mucosa (R= 54.5%; RTV= 45.4%). TV, alone, did not induce gross or histological alterations in the gastric mucosa. TV did note change the morphologic pattern of the proliferative lesions induced by DGR. Conclusions: DGR induces the development of PL in the pyloric mucosa and at the gastrojejunal stoma. TV does not change the morphologic pattern of the proliferative lesions induced by DGR. TV alone is not able to induce morphologic lesions in the gastric mucosa.en
dc.format.extent210-214-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectDuodenogastric reflux-
dc.subjectHyperplasia-
dc.subjectRats-
dc.subjectVagotomy, truncal-
dc.subjectadenoma-
dc.subjectanastomosis-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectanimal tissue-
dc.subjectbiological activity-
dc.subjectcell structure-
dc.subjectcontrol group-
dc.subjectcontrolled study-
dc.subjectduodenogastric reflux-
dc.subjectexperimental study-
dc.subjecthistopathology-
dc.subjecthyperplasia-
dc.subjectincision-
dc.subjectjejunum-
dc.subjectmale-
dc.subjectmorphology-
dc.subjectnonhuman-
dc.subjectpylorus-
dc.subjectrat-
dc.subjectstoma-
dc.subjectstomach lesion-
dc.subjectstomach mucosa-
dc.subjectstomach wall-
dc.subjectsurgical technique-
dc.subjectvagotomy-
dc.subjectvagus nerve-
dc.subjectWistar rat-
dc.subjectAdenocarcinoma-
dc.subjectAnastomosis, Surgical-
dc.subjectAnimals-
dc.subjectDisease Models, Animal-
dc.subjectDuodenogastric Reflux-
dc.subjectGastric Mucosa-
dc.subjectGastrostomy-
dc.subjectHumans-
dc.subjectJejunum-
dc.subjectMale-
dc.subjectPylorus-
dc.subjectRats, Wistar-
dc.subjectStomach-
dc.subjectStomach Neoplasms-
dc.subjectVagotomy, Truncal-
dc.titleDoes troncular vagotomy modify the proliferative gastric lesions induced in rats by duodenogastric reflux?en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Surgery and Orthopedics Botucatu Medical School UNESP-
dc.description.affiliationDepartment of Pathology Botucatu Medical School UNESP-
dc.description.affiliationFaculdade de Medicina de Botucatu-UNESP Departamento de Cirurgia e Ortopedia, 18618-970 Botucatu - SP-
dc.description.affiliationUnespDepartment of Surgery and Orthopedics Botucatu Medical School UNESP-
dc.description.affiliationUnespDepartment of Pathology Botucatu Medical School UNESP-
dc.description.affiliationUnespFaculdade de Medicina de Botucatu-UNESP Departamento de Cirurgia e Ortopedia, 18618-970 Botucatu - SP-
dc.identifier.doi10.1590/S0102-86502007000300009-
dc.identifier.scieloS0102-86502007000300009-
dc.identifier.wosWOS:000258573100009-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-34250185380.pdf-
dc.relation.ispartofActa Cirúrgica Brasileira-
dc.identifier.scopus2-s2.0-34250185380-
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