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首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Comparison of Colposcopic Biopsy Results of Patients Who have Cytomorphological Normal but HPV 16-18 or Other High-Risk HPV Subtypes Positive
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Comparison of Colposcopic Biopsy Results of Patients Who have Cytomorphological Normal but HPV 16-18 or Other High-Risk HPV Subtypes Positive

机译:细胞形态学正常但HPV 16-18或其他高危HPV亚型阳性患者的阴道镜活检结果比较

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Objective: Current guidelines suggest annual co-test follow-up in non-16/18 high-risk HPV positive patients withoutabnormal cytologic findings. Considering the relatively high false-negative rates of cervical cytology, a follow-up periodof one year might constitute an additional risk for development of cervical malignancies in these patients. The currentstudy aims to evaluate colposcopic biopsy results of cytologically normal patients detected to carry high risk HPV byscreening tests. Materials and Methods: A total of 160 patients with normal cervical cytology and high-risk HPVsubtypes who underwent colposcopic examination were included in the study. Patients were divided into two groupsaccording to their HPV results: HPV 16-18 and other types (non-16/18 high-risk subtypes). ECC, cervical biopsy, LEEP/conization results were analyzed for both groups. Histopathological results of the groups were compared in terms of≤LSIL, HSIL and cervical cancer rates. Results: Cervical biopsy results in the “16-18” group were assessed as HSILin 40 (48.2%) patients, LSIL in 6 patients (7.2%) and normal in 37 (44.6%) patients. ECC results revealed HSIL in9 (10.8%) patients and LSIL in 1 (1.2%) patient. Nineteen out of 42 patients who underwent LEEP/conization hadHSIL (surgical margin positivity was reported in 4 cases), while 3 patients had LSIL. None of the cases had cervicalcarcinoma. Conclusion: The present study detected that 15.6% of women infected with non-16/18 high-risk HPVsubgroups developed ≥HSIL lesions. Although this rate seems lower than HPV 16-18 group, it is still too high to beoverlooked. In conclusion, we suggest further clinical trials with larger number of patients to be conducted on this topic.
机译:目的:目前的指南建议对未发生细胞学异常的非16/18高危HPV阳性患者进行年度联合测试随访。考虑到子宫颈细胞学的假阴性率相对较高,一年的随访期可能构成这些患者子宫颈恶性肿瘤发展的额外风险。本研究旨在通过筛查测试评估被检测为携带高危HPV的细胞学正常患者的阴道镜活检结果。资料与方法:本研究共纳入160例接受阴道镜检查的宫颈细胞学正常且高危HPV亚型的患者。根据他们的HPV结果将患者分为两组:HPV 16-18和其他类型(非16/18高风险亚型)。分析了两组的ECC,宫颈活检,LEEP /检查结果。比较各组的组织病理学结果,其≤LSIL,HSIL和子宫颈癌的发生率。结果:“ 16-18”组的宫颈活检结果被评估为HSIL 40例(48.2%),LSIL 6例(7.2%),正常37例(44.6%)。 ECC结果显示9例(10.8%)患者为HSIL,1例(1.2%)患者为LSIL。在接受LEEP /超声检查的42例患者中,有19例患有HSIL(4例报告有手术切缘阳性),而3例患有LSIL。所有病例均无宫颈癌。结论:本研究发现,感染非16/18高危HPV亚组的女性中有15.6%发生了≥HSIL病变。尽管这个比率似乎低于HPV 16-18组,但仍然太高而不能被忽视。总之,我们建议对该主题进行更多患者的进一步临床试验。

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