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妇科细胞学中的人乳头瘤病毒(HPV):从分子生物学到临床检测

Human papillomaviruses (HPV) in gynaecological cytology: from molecular biology to clinical testing.

作者信息

Herrington C S

机构信息

Nuffield Department of Pathology, John Radcliffe Hospital, Oxford, UK.

出版信息

Cytopathology. 1995 Jun;6(3):176-89. doi: 10.1111/j.1365-2303.1995.tb00471.x.

Abstract

Molecular epidemiological and pathological studies show that different HPV types are associated with different cervical lesions allowing classification of the viruses into types associated with 'high', 'intermediate' and 'low' risk of cervical neoplasia. However, HPV infection often regresses and, where it is associated with neoplasia, is an early event. This suggests that other factors are involved in the carcinogenic process, and there is some mechanistic basis for the interaction of epidemiologically defined factors with HPV infection in the process of cervical carcinogenesis. With the refinement of techniques for HPV detection in clinical material, HPV testing is now a realistic possibility, but how this should be performed and in what clinical situation(s) is still uncertain. Particular areas of interest are: (i) the assessment of patients with borderline cytological changes or mild dyskaryosis; and (ii) the definition of those patients at greater risk of invasive disease. Clinical trials are needed before the utility of HPV testing can be properly assessed.

摘要

分子流行病学和病理学研究表明,不同的人乳头瘤病毒(HPV)类型与不同的宫颈病变相关,从而可将这些病毒分为与宫颈肿瘤形成“高”、“中”和“低”风险相关的类型。然而,HPV感染通常会自行消退,并且在与肿瘤形成相关的情况下,这是一个早期事件。这表明其他因素也参与了致癌过程,并且在宫颈癌发生过程中,流行病学定义的因素与HPV感染之间的相互作用存在一些机制基础。随着临床材料中HPV检测技术的完善,HPV检测现在已成为一种现实的可能性,但应如何进行检测以及在何种临床情况下进行检测仍不确定。特别感兴趣的领域是:(i)对细胞学变化处于临界状态或轻度核异质的患者进行评估;以及(ii)确定那些患浸润性疾病风险更高的患者。在能够正确评估HPV检测的效用之前,需要进行临床试验。

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