臨牀消化器内科 Vol.19 No.5(2)


特集名 H.pylori陰性上部消化管疾患 -- 21世紀の疾病構造の推移を念頭に
題名 H.pylori陰性萎縮性胃炎・腸上皮化生
発刊年月 2004年 05月
著者 今津 浩喜 藤田保健衛生大学外科
著者 宇山 一朗 藤田保健衛生大学外科
著者 小森 義之 藤田保健衛生大学外科
著者 桜井 洋一 藤田保健衛生大学外科
著者 落合 正宏 藤田保健衛生大学外科
【 要旨 】 萎縮性胃炎およびこれに伴う腸上皮化生は加齢よりもH.pylori感染がその発生と進展に大きく関与することが明らかになったが,少数ながらH.pylori陰性の萎縮性胃炎,腸上皮化生も認められる.その頻度は萎縮性胃炎4~18%,腸上皮化生2~6.2%程度と報告され,これらは組織学的にはH.pylori陽性例に比較して萎縮の程度は軽いと報告されている.成因は薬剤性,喫煙,飲酒など体外因子やA型胃炎,炎症性腸疾患や肝硬変,慢性腎不全などの全身疾患の合併および胃切除後状態などがあり,このうちA型胃炎と残胃炎に関してはほかと比較し高頻度で発癌を認めるとされている.残胃炎のうち,gastritis cystica polyposa (GCP) が認められる症例ではとくに吻合部を中心とした残胃粘膜における細胞回転の亢進や遺伝子変異などが報告され,残胃発癌における前癌状態としての十二指腸液逆流の存在が注目されている.
Theme H.pylori Negative Upper Gastroenterological Diseases; Increasing of Their Incidence in the 21st Century
Title Helicobacter pylori Negative Atrophic Gastritis and Intestinal Metaplasia
Author Hiroki Imazu Department of Surgery, Fujita Health University School of Medicine
Author Ichiro Uyama Department of Surgery, Fujita Health University School of Medicine
Author Yoshiyuki Komori Department of Surgery, Fujita Health University School of Medicine
Author Yoichi Sakurai Department of Surgery, Fujita Health University School of Medicine
Author Masahiro Ochiai Department of Surgery, Fujita Health University School of Medicine
[ Summary ] It is well known that atrophic changes and intestinal metaplasia of the gastric mucosa were caused more often by Helicobacter pylori (H.pylori) infection rather than aging, and negative cases are very rare. It has been reported that atrophic changes, without H.pylori infection, are seen only in 4 to 18% of cases and intestinal metaplasia without H.pylori infection was also observed in 2 to 6.2% of cases. In these cases, histological atrophy was milder in comparison with positive cases. Some of the factors (environmental, habitual, type A gastritis, complications from systemic diseases, e.g. inflammatory bowel disease, liver cirrhosis, chronic renal failure, etc., including post gasterectomy states) have been suggested as causes of H.pylori negative gastritis. Especially, patients with type A gastritis and remnant gastritis were at high risk for developing gastric carcinoma. Acceleration of the cell cycle and gene mutations of the remnant epithelium at the anastomotic site, caused by regurgitation of duodenal juice, were reported.
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