2012
DOI: 10.1590/s1679-45082012000400013
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Comparative study of the results from conventional cervico-vaginal oncotic cytology and liquid-based cytology

Abstract: Liquid-based cytology had a better performance to diagnose atypical cells and the cytohistological concordance was higher than in the conventional cytology.

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Cited by 16 publications
(17 citation statements)
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“…A number of non-FDA-approved methods have been developed for use outside of the USA. These include LiquiPrep [4], Turbitec [5], PapSpin [6], TACAS [7,8], Siriraj-LBC [9], DNA-Citoliq (Digene) [10], GluCyte [11], and some other devices [12,13]. Specimen materials collected in the preservation medium are routinely used for cell blocks, which can provide additional diagnostic information, including architectural pattern, immunocytochemistry (ICC) and special stains.…”
Section: Introductionmentioning
confidence: 99%
“…A number of non-FDA-approved methods have been developed for use outside of the USA. These include LiquiPrep [4], Turbitec [5], PapSpin [6], TACAS [7,8], Siriraj-LBC [9], DNA-Citoliq (Digene) [10], GluCyte [11], and some other devices [12,13]. Specimen materials collected in the preservation medium are routinely used for cell blocks, which can provide additional diagnostic information, including architectural pattern, immunocytochemistry (ICC) and special stains.…”
Section: Introductionmentioning
confidence: 99%
“…Several authors have demonstrated and confirmed the advantages of ThinPrep in relation to CP for cervical exams ( 8 , 22 - 25 ). ThinPrep has been referred to as the method of superior performance because it provides better cellular representation, with increased sensitivity for the detection of lesions, compared with conventional methodology ( 5 , 8 , 14 , 24 - 28 ). Several authors have shown that this greater diagnostic sensitivity applies to high-grade and glandular lesions ( 26 - 28 ).…”
Section: Discussionmentioning
confidence: 90%
“…Approved in 1996 by the United States Food and Drug Administration, ThinPrep was introduced as an alternative to using the conventional method, with the purpose of improving the screening of atypical cells, cervical cancer, or its precursor lesions [low-grade squamous intraepithelial lesions (LSIL) and high-grade squamous intraepithelial lesions (HSIL)]. The aim was to improve sensitivity, because it permits the use of a monolayer of cells to facilitate the diagnosis by the cytopathologist, with better cellular preservation and the possibility to carry out molecular biology testing, making possible, for example, HPV and Chlamydia trachomatis DNA detection ( 4 , 8 - 12 ). This technique has been widely adopted and is gradually replacing the CP in control programs of cervical cancer in some countries ( 13 , 14 ).…”
Section: Introductionmentioning
confidence: 99%
“…The majority of subjects had healthy cervix and vagina. Totally, 35 (95%) women had postmenopausal changes on per speculum examination, like cervix flushed with vagina (19), narrowing of vagina (12), and senile vaginitis (10). It was observed that Pap smear reported 14.3% inadequate smears in women with postmenopausal changes and 5% inadequate smears in women without postmenopausal changes.…”
Section: Resultsmentioning
confidence: 99%