ヤマモト　アヤコ   Yamamoto Ayako   山本　章子    所属   その他 その他    職種   嘱託医師
論文種別	症例報告
言語種別	英語
査読の有無	査読なし
表題	A case of early autoimmune gastritis with characteristic endoscopic findings.
掲載誌名	正式名：Clinical journal of gastroenterology 略　 称：Clin J Gastroenterol ISSNコード：18657265/18657265
掲載区分	国外
巻・号・頁	14(3),pp.718-724
著者・共著者	KISHINO Maiko†, YAO Kenshi, HASHIMOTO Hiroshi, NITTA Hiroko, KURE Rie, YAMAMOTO Ayako, YAMAMOTO Kana, NONAKA KoKoichi, NAKAMURA Shinichi, TOKUSHIGE Katsutoshi
発行年月	2021/06
概要	Significant atrophic gastritis in the fundic gland region is a well-known endoscopic finding observed in autoimmune gastritis (AIG). The endoscopic features of early AIG have not been reported. Iron deficiency, vitamin B12 deficiency, anemia, or neurological symptoms may not be observed in the early stages of AIG, and it may thus be difficult to diagnose early AIG based on clinical findings. We treated a 50-year-old Japanese female whose condition was suspected to be early AIG. The endoscopic findings showed normal gastric pyloric gland mucosa, and diffuse reddened and edematous gastric fundic gland mucosa. Pathologically, local infiltration of lymphocytes and decrease of parietal cells was present in a deep part of the gastric fundic gland mucosa. Blood tests showed that the titer of parietal cell antibody (PCA) was 1:320 and the gastrin level was 820 pg/ml. We determined that the patient had AIG because she also had Hashimoto's disease, the PCA titer was high, the serum gastrin level was slightly increased, and inflammation was observed only in the gastric body on the endoscopic images. To the best of our knowledge, this is the first case report of endoscopic findings that suggest early AIG, before atrophic changes were observed.
DOI	10.1007/s12328-021-01351-4
PMID	33566307