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Cytology and high risk HPV HPV testing in cervical cancer screening program: Outcome of 3‐year follow‐up in an academic institute

机译:宫颈癌筛查计划中的细胞学和高风险HPV HPV检测:学术研究所的3年后续行动的结果

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摘要

Background Combination of cervical cytology and high‐risk human papillomavirus (HR‐HPV) testing, co‐testing, has been increasingly used in screening cervical cancers. The present study summarized the outcome of co‐testing by reviewing 3‐year clinical and pathological follow‐up information. Methods Patients were retrospectively identified via computerized search and were grouped based on the cytologic diagnosis and HR‐HPV status as negative for intraepithelial lesion or malignancy (NILM)/HPV–, NILM/HPV+, atypical squamous cells of undetermined significance (ASC‐US)/HPV–, ASC‐US/HPV+, low grade squamous intraepithelial lesion (LSIL)/HPV–, LSIL/HPV+, atypical squamous cells, cannot exclude high grade squamous intraepithelial lesion (ASC‐H)/HPV–, ASC‐H/HPV+, high grade squamous intraepithelial lesion (HSIL)/HPV–, and HSIL/HPV+. The patients' pertinent past medical history and follow‐up information were analyzed. Results During 3‐year follow‐up period, histologically proven HSIL was found in 5 of 1565 (0.3%) patients with NILM/HPV–, 7 of 141 (5.0%) with NILM/HPV+, 2 of 502 (0.4%) with ASC‐US/HPV–, 30 of 274 (10.9%) with ASC‐US/HPV+, 1 of 81 (1.2%) with LSIL/HPV–, 28 of 159 (17.6%) with LSIL/HPV+, 3 of 18 (16.7%) with ASC‐H/HPV–, 34 of 69 (49.3%) with ASC‐H/HPV+, 7 of 7 (100%) with HSIL/HPV–, and 35 of 56 (62.5%) HSIL/HPV+. In reviewing 12 HSIL cases that were originally diagnosed as NILM, 7 remained as NILM, and the other 5 were reclassified as 1 HSIL, 1 ASC‐H, and 3 ASC‐US, respectively. In 18 HSIL cases with negative HR‐HPV, 12 patients had a prior history of positive HR‐HPV testing and/or positive p16 IHC stain in the follow‐up cervical biopsy. Conclusion HR‐HPV testing plays an important role in cervical cancer screening by identifying HSIL in patients with ASC‐US, LSIL, and NILM. Co‐testing is an optimal method to identifying the patients with higher risk for developing cervical abnormalities.
机译:背景技术宫颈细胞学和高风险的人乳头瘤病毒(HR-HPV)测试,共同测试越来越多地用于筛查宫颈癌。本研究通过审查3年临床和病理后续信息来总结了共同测试的结果。方法通过计算机化搜索回顾性鉴定患者,并根据细胞学诊断和HR-HPV状态分组为阴性上皮病变或恶性肿瘤(NILM)/ HPV-,NILM / HPV +,非典型鳞状细胞的阴性(ASC-US) / HPV-,ASC-US / HPV +,低等级鳞状上皮内病变(LSIL)/ HPV-,LSIL / HPV +,非典型鳞状细胞,不能排除高级鳞状上皮内病变(ASC-H)/ HPV-,ASC-H / HPV +,高级鳞状上皮内病变(HSIL)/ HPV-和HSIL / HPV +。分析了患者相关的过去的病史和后续信息。结果在3年的随访期间,组织学证明HSIL在1565(0.3%)含有Nilm / HPV-,71(5.0%)的患者中的5名中发现,其中含有尼霉/ HPV +,2502(0.4%) ASC-US / HPV-,274(10.9%)的ASC-US / HPV +,1,其中81(1.2%),LSIL / HPV-,28 of 159(17.6%),LSIL / HPV +,18个( 16.7%)ASC-H / HPV-,34&69(49.3%),ASC-H / HPV +,7分,7(100%),HSIL / HPV-和35个,共56例(62.5%)HSIL / HPV +。在审查最初被诊断为Nilm的HSIL病例中,7仍然是尼尔,另外5分别被重新分类为1 HSIL,1 ASC-H和3 ASC-US。在18个HSIL病例中,具有负HR-HPV,12例患者在后续宫颈活组织检查中具有阳性HR-HPV测试和/或阳性P16 IHC染色的历史。结论HR-HPV检测在宫颈癌筛查中发挥着重要作用,通过鉴定ASC-US,LSIL和NILM患者。共同测试是鉴定患有患者患有颈部异常的患者的最佳方法。

著录项

  • 来源
    《Diagnostic cytopathology》 |2018年第1期|共6页
  • 作者单位

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

    The Department of Pathology and Laboratory MedicineMedical University of South CarolinaCharleston;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学;
  • 关键词

    cervical cancer; cervical cytology; co‐testing; HR‐HPV; Pap smear;

    机译:宫颈癌;宫颈细胞学;共同测试;HR-HPV;PAP涂抹;

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