dc.creatorZeferino L.C.
dc.creatorRabelo-Santos S.H.
dc.creatorVilla L.L.
dc.creatorSarian L.O.
dc.creatorCosta M.C.
dc.creatorDo Amaral Westin M.C.
dc.creatorDe Angelo-Andrade L.A.L.
dc.creatorDerchain S.
dc.date2011
dc.date2015-06-30T20:38:28Z
dc.date2015-11-26T14:52:26Z
dc.date2015-06-30T20:38:28Z
dc.date2015-11-26T14:52:26Z
dc.date.accessioned2018-03-28T22:04:30Z
dc.date.available2018-03-28T22:04:30Z
dc.identifier
dc.identifierEuropean Journal Of Obstetrics Gynecology And Reproductive Biology. , v. 159, n. 1, p. 160 - 164, 2011.
dc.identifier3012115
dc.identifier10.1016/j.ejogrb.2011.05.023
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-81855194297&partnerID=40&md5=688d7e2677dd389d9f4b477ea716c83f
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/108745
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/108745
dc.identifier2-s2.0-81855194297
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1254820
dc.descriptionObjective: This study analyzed whether HPV (human papillomavirus) testing contributes towards defining histological abnormalities in women with atypical glandular cells (AGC) diagnosed at cervical cytology. Study design: One hundred and eight women with conventional cervical cancer screening smears suggestive of AGC not otherwise specified (AGC-NOS) and favor neoplastic (AGC-FN) were consecutively enrolled. All women underwent colposcopic examinations and biopsy was performed according to the cytopathologic and/or colposcopic abnormalities present. All specimens were tested for high risk HPV genotypes by Roche's polymerase chain reaction reverse line blot assay. The chi-square test was used to evaluate the association between HPV findings and a diagnosis of high-grade pre-invasive or invasive disease (CIN 2 or worse) taking negative tests or CIN 1 as a reference. Odds ratios (OR) with their respective 95% confidence intervals (95%CI) were used to evaluate the magnitude of the association between HPV testing and CIN 2 or worse. Sensitivity, specificity and their respective 95% confidence intervals (95%CI), positive predictive values (PPV) and negative predictive values (NPV) were also calculated. Results: Final diagnosis revealed a negative outcome in 80 cases (74%), cervical epithelial neoplasia 1 (CIN 1) in 13 cases (12%), CIN 2 or worse in 12 cases (11%) and glandular neoplasia in 3 (3%) cases. The overall detection rate of HPV was 21% (23/108). Neoplasia was significantly associated with positive HPV-DNA in women with AGC-NOS (OR = 15.21; 95%CI: 2.64-87.50); however, there was no significant association between a histological diagnosis of neoplasia and HPV positivity in women with AGC-FN (OR = 3.00; 95%CI: 0.36-24.92). The sensitivity, specificity, positive predictive value and negative predictive value of HPV-DNA testing for the detection of CIN 2 or worse in women with AGC-NOS were 71%, 86%, 29% and 97%, respectively. In women with AGC-FN, these values were 50%, 75%, 66% and 60%, respectively. Conclusions: HPV testing at the time of colposcopy for patients with AGC in whom no colposcopic abnormality is found may be a powerful ancillary tool for identifying women at a high risk of underlying significant cervical lesions. © 2011 Elsevier Ireland Ltd. All rights reserved.
dc.description159
dc.description1
dc.description160
dc.description164
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dc.languageen
dc.publisher
dc.relationEuropean Journal of Obstetrics Gynecology and Reproductive Biology
dc.rightsfechado
dc.sourceScopus
dc.titleValue Of Hpv-dna Test In Women With Cytological Diagnosis Of Atypical Glandular Cells (agc)
dc.typeArtículos de revistas


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