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首页> 外文期刊>Cytopathology >European guidelines for quality assurance in cervical cancer screening: recommendations for clinical management of abnormal cervical cytology, part 1.
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European guidelines for quality assurance in cervical cancer screening: recommendations for clinical management of abnormal cervical cytology, part 1.

机译:欧洲宫颈癌筛查质量保证指南:宫颈细胞学异常的临床管理建议,第1部分。

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摘要

The current paper presents the first part of Chapter 6 of the second edition of the European Guidelines for Quality Assurance in Cervical Cancer Screening. It provides guidance on how to manage women with abnormal cervical cytology. Throughout this article the Bethesda system is used for cervical cytology terminology, as the European guidelines have recommended that all systems should at least be translated into that terminology while cervical intraepithelial neoplasia (CIN) is used for histological biopsies (Cytopathology 2007; 18:213-9). A woman with a high-grade cytological lesion, a repeated low-grade lesion or with an equivocal cytology result and a positive human papillomavirus (HPV) test should be referred for colposcopy. The role of the colposcopist is to identify the source of the abnormal cells and to make an informed decision as to whether or not any treatment is required. If a patient requires treatment the colposcopist will decide which is the most appropriate method of treatment for each individual woman. The colposcopist should also organize appropriate follow-up for each woman seen. Reflex testing for high-risk HPV types of women with atypical squamous cells (ASC) of undetermined significance with referral for colposcopy of women who test positive is a first option. Repeat cytology is a second possibility. Direct referral to a gynaecologist should be restricted to special circumstances. Follow-up of low-grade squamous intraepithelial lesion is more difficult because currently there is no evidence to support any method of management as being optimal; repeat cytology and colposcopy are options, but HPV testing is not sufficiently selective, unless for older women. Women with high-grade squamous intraepithelial lesion (HSIL) or atypical squamous cells, cannot exclude HSIL (ASC-H) should be referred without triage. Women with glandular lesions require particular attention. In a subsequent issue of Cytopathology, the second part of Chapter 6 will be presented, with recommendations for managementand treatment of histologically confirmed intraepithelial neoplasia and guidance for follow-up of special cases such as women who are pregnant, postmenopausal or immunocompromised.
机译:本文介绍了《欧洲宫颈癌筛查质量保证指南》第二版第6章的第一部分。它为如何处理宫颈细胞学异常的妇女提供指导。在整篇文章中,Bethesda系统用于宫颈细胞学术语,因为欧洲指南建议所有系统至少应翻译成该术语,而宫颈上皮内瘤变(CIN)用于组织活检(Cytopathology 2007; 18:213- 9)。阴道镜检查应选择具有高度细胞病变,反复低度病变或细胞学检查结果不明确,人乳头瘤病毒(HPV)检测阳性的女性。阴道镜专家的作用是识别异常细胞的来源,并就是否需要任何治疗做出明智的决定。如果患者需要治疗,那么阴道镜专家将决定哪种方法最适合每个女性。阴道镜专家还应为每个看到的妇女组织适当的随访。对于具有非确定意义的非典型鳞状细胞(ASC)的高风险HPV类型女性进行反射测试,并转诊接受阴道镜检查阳性的女性是首选。重复细胞学检查是第二种可能性。直接转诊给妇科医生应仅限于特殊情况。低度鳞状上皮内病变的随访更加困难,因为目前尚无证据支持任何治疗方法都是最佳的。可以重复进行细胞学检查和阴道镜检查,但是HPV检测的选择性不够,除非是老年妇女。患有高度鳞状上皮内病变(HSIL)或不能排除HSIL(ASC-H)的非典型鳞状细胞的女性应进行分流。患有腺体病变的女性需要特别注意。在随后的细胞病理学杂志中,将介绍第6章的第二部分,并就组织学上证实的上皮内瘤形成的治疗和治疗建议以及对孕妇,绝经后或免疫功能低下的特殊病例的随访提供指导。

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