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胃上皮癌前病变和病灶的处理(MAPS II):欧洲胃肠道内镜学会(ESGE)、欧洲幽门螺杆菌和微生物研究组(EHMSG)、欧洲病理学会(ESP)和葡萄牙消化内镜学会(SPED)指南更新 2019 年。

Management of epithelial precancerous conditions and lesions in the stomach (MAPS II): European Society of Gastrointestinal Endoscopy (ESGE), European Helicobacter and Microbiota Study Group (EHMSG), European Society of Pathology (ESP), and Sociedade Portuguesa de Endoscopia Digestiva (SPED) guideline update 2019.

机构信息

Gastroenterology Department, Portuguese Oncology Institute of Porto, Portugal.

Center for Research in Health Technologies and Information Systems (CINTESIS), Faculty of Medicine, Porto, Portugal.

出版信息

Endoscopy. 2019 Apr;51(4):365-388. doi: 10.1055/a-0859-1883. Epub 2019 Mar 6.

DOI:10.1055/a-0859-1883
PMID:30841008
Abstract

Patients with chronic atrophic gastritis or intestinal metaplasia (IM) are at risk for gastric adenocarcinoma. This underscores the importance of diagnosis and risk stratification for these patients. High definition endoscopy with chromoendoscopy (CE) is better than high definition white-light endoscopy alone for this purpose. Virtual CE can guide biopsies for staging atrophic and metaplastic changes and can target neoplastic lesions. Biopsies should be taken from at least two topographic sites (antrum and corpus) and labelled in two separate vials. For patients with mild to moderate atrophy restricted to the antrum there is no evidence to recommend surveillance. In patients with IM at a single location but with a family history of gastric cancer, incomplete IM, or persistent gastritis, endoscopic surveillance with CE and guided biopsies may be considered in 3 years. Patients with advanced stages of atrophic gastritis should be followed up with a high quality endoscopy every 3 years. In patients with dysplasia, in the absence of an endoscopically defined lesion, immediate high quality endoscopic reassessment with CE is recommended. Patients with an endoscopically visible lesion harboring low or high grade dysplasia or carcinoma should undergo staging and treatment. eradication heals nonatrophic chronic gastritis, may lead to regression of atrophic gastritis, and reduces the risk of gastric cancer in patients with these conditions, and it is recommended. eradication is also recommended for patients with neoplasia after endoscopic therapy. In intermediate to high risk regions, identification and surveillance of patients with precancerous gastric conditions is cost-effective.

摘要

患有慢性萎缩性胃炎或肠上皮化生(IM)的患者存在胃腺癌风险。这凸显了对这些患者进行诊断和风险分层的重要性。与单纯高清白光内镜相比,高清内镜联合染色内镜(CE)在这方面效果更好。虚拟 CE 可引导活检以对萎缩性和化生改变进行分期,并可针对肿瘤性病变。活检应至少取自两个解剖部位(胃窦和胃体),并分别标记在两个单独的小瓶中。对于局限于胃窦且萎缩程度较轻的患者,没有证据推荐进行监测。对于局限于胃窦且有胃癌家族史、不完全 IM 或持续性胃炎的患者,可考虑在 3 年内进行 CE 内镜监测和引导活检。对于处于晚期萎缩性胃炎的患者,应每 3 年进行一次高质量的内镜随访。对于存在异型增生的患者,如果内镜未发现病变,建议立即行 CE 检查进行高质量内镜再评估。对于存在低级别或高级别异型增生或癌的内镜可见病变的患者,应进行分期和治疗。根除可治愈非萎缩性慢性胃炎,可能导致萎缩性胃炎的消退,并降低此类患者的胃癌风险,因此建议进行根除治疗。对于内镜治疗后的肿瘤患者,也建议进行根除治疗。在中高危地区,对具有癌前胃部疾病的患者进行识别和监测具有成本效益。

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