Colonoscopic surveillance in Lynch syndrome: guidelines in perspective

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Familial Cancer Pub Date : 2024-07-27 DOI:10.1007/s10689-024-00414-y
Joaquín Castillo-Iturra, Ariadna Sánchez, Francesc Balaguer
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引用次数: 0

Abstract

Lynch syndrome predisposes to a high risk of colorectal cancer and colonoscopy remains the primary preventive strategy. The prevention of colorectal cancer through colonoscopy relies on identifying and removing adenomas, the main precursor lesion. Nevertheless, colonoscopy is not an optimal strategy since post-colonoscopy colorectal cancer remains an important issue. In continuation of a 2021 journal review, the present article seeks to offer an updated perspective by examining relevant articles from the past 3 years. We place recent findings in the context of existing guidelines, with a specific focus on colonoscopy surveillance. Key aspects explored include colonoscopy quality standards, timing of initiation, and surveillance intervals. Our review provides a comprehensive analysis of adenoma-related insights in Lynch syndrome, delving into emerging technologies like virtual chromoendoscopy and artificial intelligence-assisted endoscopy. This review aims to contribute valuable insights into the topic of colonoscopy surveillance in Lynch syndrome.

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林奇综合征的结肠镜监测:透视指南
林奇综合征是结直肠癌的高发人群,结肠镜检查仍是主要的预防策略。通过结肠镜检查预防结肠直肠癌主要依靠识别和切除腺瘤这一主要前驱病变。然而,结肠镜检查并非最佳策略,因为结肠镜检查后的大肠癌仍然是一个重要问题。本文是 2021 年期刊综述的延续,旨在通过研究过去 3 年的相关文章,提供一个最新的视角。我们将最新研究结果置于现有指南的背景下,并特别关注结肠镜检查监测。探讨的主要方面包括结肠镜检查的质量标准、开始时间和监测间隔。我们的综述全面分析了林奇综合征中与腺瘤相关的见解,深入探讨了虚拟色内镜和人工智能辅助内镜等新兴技术。本综述旨在为林奇综合征结肠镜检查监测这一主题提供有价值的见解。
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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
期刊最新文献
A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic. Cascade genetic testing in hereditary cancer: exploring the boundaries of the Italian legal framework. Hereditary breast and ovarian cancer genetic testing in unselected patients: example of private supplementation of public healthcare service. BRCAIndica: a resource for ACMG/AMP classified BRCA1 and BRCA2 variants. Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome.
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