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本文引用的文献

1
Reproducibility of endocervical curettage diagnoses.宫颈内膜刮片诊断的可重复性。
Obstet Gynecol. 2011 Aug;118(2 Pt 1):240-248. doi: 10.1097/AOG.0b013e318223552d.
2
Detection of cervical cancer and its precursors by endocervical curettage in 13,115 colposcopically guided biopsy examinations.经阴道镜引导的 13115 例宫颈活检中,经宫颈管搔刮术检测宫颈癌及其前体病变。
Am J Obstet Gynecol. 2010 Nov;203(5):481.e1-9. doi: 10.1016/j.ajog.2010.06.048. Epub 2010 Aug 30.
3
Evidence for frequent regression of cervical intraepithelial neoplasia-grade 2.宫颈上皮内瘤变2级频繁消退的证据。
Obstet Gynecol. 2009 Jan;113(1):18-25. doi: 10.1097/AOG.0b013e31818f5008.
4
Risk assessment to guide the prevention of cervical cancer.指导宫颈癌预防的风险评估。
J Low Genit Tract Dis. 2008 Jan;12(1):1-7. doi: 10.1097/lgt.0b013e31815ea58b.
5
2006 consensus guidelines for the management of women with cervical intraepithelial neoplasia or adenocarcinoma in situ.2006年宫颈上皮内瘤变或原位腺癌女性管理共识指南
J Low Genit Tract Dis. 2007 Oct;11(4):223-39. doi: 10.1097/LGT.0b013e318159408b.
6
Histopathologic extent of cervical intraepithelial neoplasia 3 lesions in the atypical squamous cells of undetermined significance low-grade squamous intraepithelial lesion triage study: implications for subject safety and lead-time bias.意义不明确的非典型鳞状细胞-低级别鳞状上皮内病变分流研究中宫颈上皮内瘤变3级病变的组织病理学范围:对受试者安全性和领先时间偏倚的影响
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7
A critical evaluation of the endocervical curettage.宫颈管搔刮术的批判性评估。
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宫颈管搔刮术与宫颈活检后发现 CIN1 时高级别组织病理学诊断的比较风险。

Comparative risk of high-grade histopathology diagnosis after a CIN 1 finding in endocervical curettage versus cervical biopsy.

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20892-7234, USA.

出版信息

J Low Genit Tract Dis. 2013 Apr;17(2):137-41. doi: 10.1097/LGT.0b013e3182630c41.

DOI:10.1097/LGT.0b013e3182630c41
PMID:23343702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3608705/
Abstract

OBJECTIVE

No evidence-based clinical management recommendations exist for women with an endocervical curettage (ECC) cervical intraepithelial neoplasia grade 1 (CIN 1) result when the concurrent cervical biopsy is not high-grade. For women with these pathologic findings, we assessed their short-term risk of high-grade histopathologic diagnosis in the Calgary Health Region where ECC was routinely performed.

MATERIALS AND METHODS

We analyzed pathology and colposcopy reports from 1,902 referral colposcopies where both ECC and biopsies were normal or CIN 1. We calculated the short-term risk of CIN 2 or more severe (CIN 2+) detected 12 to 24 months after colposcopy. Pearson χ tests or Fisher exact tests were used to compare risks of a CIN 2+ diagnosis between combinations of test results and strata of risk factors.

RESULTS

The short-term risk of CIN 2+ was the same after a CIN 1 biopsy and CIN 1 ECC (4.9% of 1,389 vs 5.0% of 359, respectively, p = .37). Compared with low-grade referral cytology, the risk of CIN 2+ after high-grade cytology was elevated significantly for CIN 1 ECC (13.3% vs 3.3%, p < .01) and nonsignificantly for CIN 1 biopsy (7.1% vs 4.6%, p = .12).

CONCLUSIONS

After low-grade cytology, the short-term risk of a high-grade histologic diagnosis in women with either CIN 1 ECC or biopsy is equivalent, suggesting similar management. A CIN 1 ECC may warrant different management in the context of high-grade referral cytology.

摘要

目的

对于宫颈活检未见高级别病变的宫颈内膜上皮内瘤变 1 级(CIN1)患者,目前尚无基于循证的临床管理推荐意见。对于这些病理发现的患者,我们评估了她们在卡尔加里卫生区(常规行内膜刮宫术)短期内出现高级别组织学诊断的风险。

材料与方法

我们分析了 1902 例转诊阴道镜检查的病理和阴道镜报告,这些患者的内膜刮宫术和活检均正常或为 CIN1。我们计算了阴道镜检查后 12 至 24 个月内 CIN2 或更高级别病变(CIN2+)的短期风险。使用 Pearson χ 检验或 Fisher 确切概率检验比较不同检查结果组合和危险因素分层之间的 CIN2+诊断风险。

结果

CIN1 活检和内膜刮宫术的 CIN2+短期风险相同(1389 例中为 4.9%,359 例中为 5.0%,p=.37)。与低级别转诊细胞学相比,高级别细胞学患者的 CIN2+风险显著升高,内膜刮宫术(13.3% vs. 3.3%,p <.01),活检(7.1% vs. 4.6%,p=.12)无显著升高。

结论

低级别细胞学检查后,内膜刮宫术或活检诊断为 CIN1 的患者短期内出现高级别组织学诊断的风险相当,提示管理方法相似。在高级别转诊细胞学的情况下,内膜刮宫术可能需要不同的管理。