林奇综合征上消化道镜检查中胃肠化生和幽门螺旋杆菌的发病率较低。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Familial Cancer Pub Date : 2024-03-01 Epub Date: 2024-01-31 DOI:10.1007/s10689-023-00354-z
Marya Pulaski, Michaela Dungan, Marina Weber, Gillain Constantino, Bryson W Katona
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引用次数: 0

摘要

林奇综合征(Lynch syndrome,LS)会增加罹患包括胃癌在内的多种癌症的风险。虽然一些现行指南建议在监测林奇综合征(Lynch Syndrome,LS)的上消化道癌症时进行经验性胃活检,但这些活检的结果以及胃肠化生(GIM)和幽门螺旋杆菌(HP)在林奇综合征中的流行率仍不清楚。在此,我们对 165 例连续接受上内镜监测的 LS 患者进行了分析,所有患者均接受了胃窦和胃体活检。在研究队列中,6.7% 接受过普遍活检的 LS 患者患有 GIM 和/或 HP(5.5% GIM,3.6% HP)。与单纯前胃活检相比,胃体活检并没有提高GIM/HP的识别率。在随后的监测中,有 2.2% 之前未进行过 GIM 检查的患者被检测出 GIM,这可能是新出现的 GIM,也可能是之前的上内镜检查因取样错误而漏检的 GIM。这些研究结果支持将至少基线胃窦活检作为在LS进行的所有标准监测上内镜检查的常规组成部分。
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Low prevalence of gastric intestinal metaplasia and Helicobacter pylori on surveillance upper endoscopy in Lynch syndrome.

Lynch syndrome (LS) increases the risk of numerous different cancers including gastric cancer. While some current guidelines recommend empiric gastric biopsies be performed during upper gastrointestinal cancer surveillance in Lynch syndrome (LS), the yield of these biopsies and the prevalence of gastric intestinal metaplasia (GIM) and Helicobacter pylori (HP) in LS remains unknown. Herein we analyze 165 consecutive individuals with LS who underwent upper endoscopic surveillance with biopsies of the gastric antrum and body being performed universally in all individuals. Of the study cohort, 6.7% of universally biopsied individuals with LS had GIM and/or HP (5.5% GIM, 3.6% HP). Biopsies of the gastric body did not increase rates of GIM/HP identification compared to antral biopsies alone. GIM was detected on subsequent surveillance in 2.2% of individuals without prior GIM, which may represent either newly developed GIM or GIM that was missed on a prior upper endoscopy due to sampling error. These findings support inclusion of at least baseline gastric antrum biopsies as a routine component of all standard surveillance upper endoscopies performed in LS.

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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
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