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Conception and diagnostic criteria for autoimmune gastritis Shu Hoteya 1 1Department of Gastroenterology, Toranomon Hospital, Tokyo, Japan Keyword: autoimmune gastritis , corpus-dominant advanced atrophy , anti-parietal cell antibody pp.790-795
Published Date 2026/7/25
DOI https://doi.org/10.24479/endo.0000002745
  • Abstract
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 With the declining prevalence of Helicobacter pylori infection and the widespread use of eradication therapy, gastrointestinal endoscopic practice has entered an era in which diseases arising in H. pylori-negative gastric mucosa must be properly recognized. Autoimmune gastritis (AIG), once considered a rare disorder, is increasingly identified during screening endoscopy and diagnostic workup for gastric neoplasms. However, its endoscopic appearance varies depending on disease stage, often making diagnosis challenging for endoscopists.

 AIG is characterized by immune-mediated destruction of parietal cells, leading to oxyntic gland atrophy, hypergastrinemia, and an increased risk of gastric adenocarcinoma and gastric neuroendocrine neoplasms. Traditionally, a unified diagnostic system for AIG had been lacking. In 2023, the Japan Gastroenterological Endoscopy Society proposed diagnostic criteria based on a combination of endoscopic findings, histopathological features, and serological autoimmune markers.

 This review outlines the disease concept and pathophysiology of AIG and summarizes the newly proposed Japanese diagnostic criteria, with particular emphasis on endoscopic features relevant to daily practice. Understanding stage-specific endoscopic findings and integrating them with pathological and serological information are essential in order for endoscopists to appropriately diagnose and manage AIG in the era of H. pylori-negative gastric disease.


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電子版ISSN 印刷版ISSN 0915-3217 東京医学社

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