Shah Shailja C, Piazuelo M Blanca, Kuipers Ernst J, Li Dan
Gastroenterology Section, Veterans Affairs San Diego Healthcare System, La Jolla, California; Division of Gastroenterology, University of California, San Diego, La Jolla, California.
Division of Gastroenterology, Hepatology, and Nutrition, Vanderbilt University Medical Center, Nashville, Tennessee.
Gastroenterology. 2021 Oct;161(4):1325-1332.e7. doi: 10.1053/j.gastro.2021.06.078. Epub 2021 Aug 26.
The purpose of this Clinical Practice Update Expert Review is to provide clinicians with guidance on the diagnosis and management of atrophic gastritis, a common preneoplastic condition of the stomach, with a primary focus on atrophic gastritis due to chronic Helicobacter pylori infection-the most common etiology-or due to autoimmunity. To date, clinical guidance for best practices related to the diagnosis and management of atrophic gastritis remains very limited in the United States, which leads to poor recognition of this preneoplastic condition and suboptimal risk stratification. In addition, there is heterogeneity in the definitions of atrophic gastritis, autoimmune gastritis, pernicious anemia, and gastric neoplasia in the literature, which has led to confusion in clinical practice and research. Accordingly, the primary objective of this Clinical Practice Update is to provide clinicians with a framework for the diagnosis and management of atrophic gastritis. By focusing on atrophic gastritis, this Clinical Practice Update is intended to complement the 2020 American Gastroenterological Association Institute guidelines on the management of gastric intestinal metaplasia. These recent guidelines did not specifically discuss the diagnosis and management of atrophic gastritis. Providers should recognize, however, that a diagnosis of intestinal metaplasia on gastric histopathology implies the diagnosis of atrophic gastritis because intestinal metaplasia occurs in underlying atrophic mucosa, although this is often not distinctly noted on histopathologic reports. Nevertheless, atrophic gastritis represents an important stage with distinct histopathologic alterations in the multistep cascade of gastric cancer pathogenesis.
The Best Practice Advice statements presented herein were developed from a combination of available evidence from published literature and consensus-based expert opinion. No formal rating of the strength or quality of the evidence was carried out. These statements are meant to provide practical advice to clinicians practicing in the United States. Best Practice Advice Statements BEST PRACTICE ADVICE 1: Atrophic gastritis is defined as the loss of gastric glands, with or without metaplasia, in the setting of chronic inflammation mainly due to Helicobacter pylori infection or autoimmunity. Regardless of the etiology, the diagnosis of atrophic gastritis should be confirmed by histopathology. BEST PRACTICE ADVICE 2: Providers should be aware that the presence of intestinal metaplasia on gastric histology almost invariably implies the diagnosis of atrophic gastritis. There should be a coordinated effort between gastroenterologists and pathologists to improve the consistency of documenting the extent and severity of atrophic gastritis, particularly if marked atrophy is present. BEST PRACTICE ADVICE 3: Providers should recognize typical endoscopic features of atrophic gastritis, which include pale appearance of gastric mucosa, increased visibility of vasculature due to thinning of the gastric mucosa, and loss of gastric folds, and, if with concomitant intestinal metaplasia, light blue crests and white opaque fields. Because these mucosal changes are often subtle, techniques to optimize evaluation of the gastric mucosa should be performed. BEST PRACTICE ADVICE 4: When endoscopic features of atrophic gastritis are present, providers should assess the extent endoscopically. Providers should obtain biopsies from the suspected atrophic/metaplastic areas for histopathological confirmation and risk stratification; at a minimum, biopsies from the body and antrum/incisura should be obtained and placed in separately labeled jars. Targeted biopsies should additionally be obtained from any other mucosal abnormalities. BEST PRACTICE ADVICE 5: In patients with histology compatible with autoimmune gastritis, providers should consider checking antiparietal cell antibodies and anti-intrinsic factor antibodies to assist with the diagnosis. Providers should also evaluate for anemia due to vitamin B-12 and iron deficiencies. BEST PRACTICE ADVICE 6: All individuals with atrophic gastritis should be assessed for H pylori infection. If positive, treatment of H pylori should be administered and successful eradication should be confirmed using nonserological testing modalities. BEST PRACTICE ADVICE 7: The optimal endoscopic surveillance interval for patients with atrophic gastritis is not well-defined and should be decided based on individual risk assessment and shared decision making. A surveillance endoscopy every 3 years should be considered in individuals with advanced atrophic gastritis, defined based on anatomic extent and histologic grade. BEST PRACTICE ADVICE 8: The optimal surveillance interval for individuals with autoimmune gastritis is unclear. Interval endoscopic surveillance should be considered based on individualized assessment and shared decision making. BEST PRACTICE ADVICE 9: Providers should recognize pernicious anemia as a late-stage manifestation of autoimmune gastritis that is characterized by vitamin B-12 deficiency and macrocytic anemia. Patients with a new diagnosis of pernicious anemia who have not had a recent endoscopy should undergo endoscopy with topographical biopsies to confirm corpus-predominant atrophic gastritis for risk stratification and to rule out prevalent gastric neoplasia, including neuroendocrine tumors. BEST PRACTICE ADVICE 10: Individuals with autoimmune gastritis should be screened for type 1 gastric neuroendocrine tumors with upper endoscopy. Small neuroendocrine tumors should be removed endoscopically, followed by surveillance endoscopy every 1-2 years, depending on the burden of neuroendocrine tumors. BEST PRACTICE ADVICE 11: Providers should evaluate for iron and vitamin B-12 deficiencies in patients with atrophic gastritis irrespective of etiology, especially if corpus-predominant. Likewise, in patients with unexplained iron or vitamin B-12 deficiency, atrophic gastritis should be considered in the differential diagnosis and appropriate diagnostic evaluation pursued. BEST PRACTICE ADVICE 12: In patients with autoimmune gastritis, providers should recognize that concomitant autoimmune disorders, particularly autoimmune thyroid disease, are common. Screening for autoimmune thyroid disease should be performed.
本临床实践更新专家综述的目的是为临床医生提供有关萎缩性胃炎诊断和管理的指导,萎缩性胃炎是一种常见的胃癌前病变,主要关注由慢性幽门螺杆菌感染(最常见的病因)或自身免疫引起的萎缩性胃炎。迄今为止,在美国,与萎缩性胃炎诊断和管理相关的最佳实践临床指南仍然非常有限,这导致对这种癌前病变的认识不足以及风险分层不理想。此外,文献中萎缩性胃炎、自身免疫性胃炎、恶性贫血和胃肿瘤的定义存在异质性,这在临床实践和研究中造成了混乱。因此,本临床实践更新的主要目标是为临床医生提供一个萎缩性胃炎诊断和管理的框架。通过关注萎缩性胃炎,本临床实践更新旨在补充2020年美国胃肠病学会关于胃肠化生管理的指南。这些最新指南并未具体讨论萎缩性胃炎的诊断和管理。然而,临床医生应认识到,胃组织病理学上的肠化生诊断意味着萎缩性胃炎的诊断,因为肠化生发生在潜在的萎缩性黏膜中,尽管这在组织病理学报告中通常没有明确指出。尽管如此,萎缩性胃炎代表了胃癌发病多步骤级联中具有明显组织病理学改变的一个重要阶段。
本文提出的最佳实践建议声明是根据已发表文献中的现有证据和基于共识的专家意见相结合而制定的。未对证据的强度或质量进行正式评级。这些声明旨在为在美国执业的临床医生提供实用建议。最佳实践建议声明 最佳实践建议1:萎缩性胃炎定义为在主要由幽门螺杆菌感染或自身免疫引起的慢性炎症背景下胃腺的丧失,伴有或不伴有化生。无论病因如何,萎缩性胃炎的诊断均应通过组织病理学确认。 最佳实践建议2:临床医生应意识到,胃组织学上存在肠化生几乎总是意味着萎缩性胃炎的诊断。胃肠病学家和病理学家之间应共同努力,以提高记录萎缩性胃炎范围和严重程度的一致性,特别是在存在明显萎缩的情况下。 最佳实践建议3:临床医生应认识到萎缩性胃炎的典型内镜特征,包括胃黏膜外观苍白、由于胃黏膜变薄导致血管可见度增加以及胃皱襞消失,并且如果伴有肠化生,则有浅蓝色嵴和白色不透明区域。由于这些黏膜变化通常很细微,应采用优化胃黏膜评估的技术。 最佳实践建议4:当出现萎缩性胃炎的内镜特征时,临床医生应在内镜下评估范围。临床医生应从疑似萎缩/化生区域获取活检组织进行组织病理学确认和风险分层;至少应从胃体和胃窦/切迹获取活检组织,并放入单独标记的罐中。对于任何其他黏膜异常,还应进行靶向活检。 最佳实践建议5:对于组织学与自身免疫性胃炎相符的患者,临床医生应考虑检查抗壁细胞抗体和抗内因子抗体以辅助诊断。临床医生还应评估维生素B - 12和铁缺乏导致的贫血。 最佳实践建议6:所有萎缩性胃炎患者均应评估幽门螺杆菌感染。如果呈阳性,应进行幽门螺杆菌治疗,并使用非血清学检测方法确认成功根除。 最佳实践建议7:萎缩性胃炎患者的最佳内镜监测间隔尚未明确界定,应根据个体风险评估和共同决策来确定。对于根据解剖范围和组织学分级定义的重度萎缩性胃炎患者,应考虑每3年进行一次监测内镜检查。 最佳实践建议8:自身免疫性胃炎患者的最佳监测间隔尚不清楚。应根据个体化评估和共同决策考虑进行间隔内镜监测。 最佳实践建议9:临床医生应认识到恶性贫血是自身免疫性胃炎的晚期表现,其特征为维生素B - 12缺乏和大细胞性贫血。新诊断为恶性贫血且近期未进行内镜检查的患者应进行内镜检查并进行定位活检,以确认以胃体为主的萎缩性胃炎进行风险分层,并排除常见的胃肿瘤,包括神经内分泌肿瘤。 最佳实践建议10:自身免疫性胃炎患者应通过上消化道内镜检查筛查1型胃神经内分泌肿瘤。小的神经内分泌肿瘤应在内镜下切除,然后根据神经内分泌肿瘤的负担情况每1 - 2年进行一次监测内镜检查。 最佳实践建议11:无论病因如何,临床医生都应评估萎缩性胃炎患者的铁和维生素B - 12缺乏情况,特别是如果以胃体为主。同样,对于不明原因的铁或维生素B - 12缺乏患者,在鉴别诊断中应考虑萎缩性胃炎并进行适当的诊断评估。 最佳实践建议12:对于自身免疫性胃炎患者,临床医生应认识到合并自身免疫性疾病,特别是自身免疫性甲状腺疾病很常见。应进行自身免疫性甲状腺疾病的筛查。