1)海崎泰治,青柳裕之,宮永太門.特殊な組織型を呈する早期胃癌—カルチノイド・内分泌細胞癌.胃と腸 53:741-745, 2018
2)Rindi G, Luinetti O, Cornaggia M, et al. Three subtypes of gastric argyrophil carcinoid and the gastric neuroendocrine carcinoma:a clinicopathologic study. Gastroenterology 104:994-1006, 1993
3)海崎泰治.Rindiの分類(背景病変による分類).胃と腸 54:762-763, 2019
4)Ooi A, Ota M, Katsuda S, et al. An unusual case of multiple gastric carcinoids associated with diffuse endocrine cell hyperplasia and parietal cell hypertrophy. Endocr Pathol 6:229-237, 1995
5)Abraham SC, Carney JA, Ooi A, et al. Achlorhydria, parietal cell hyperplasia, and multiple gastric carcinoids:a new disorder. Am J Surg Pathol 29:969-975, 2005
6)Ishioka M, Hirasawa T, Kawachi H, et al. Enterochromaffin-like cell neuroendocrine tumor associated with parietal cell dysfunction. Gastrointest Endosc 90:841-845, 2019
7)Calvete O, Herraiz M, Reyes J, et al. A cumulative effect involving malfunction of the PTH1R and ATP4A genes explains a familial gastric neuroendocrine tumor with hypothyroidism and arthritis. Gastric Cancer 20:998-1003, 2017
8)Ihara Y, Umeno J, Hori Y. Type IV Gastric carcinoids in the stomach caused by ATP4A gene mutations. Clin Gastroenterol Hepatol 18:A22, 2020
9)Vaser R, Adusumalli S, Leng SN, et al. SIFT missense predictions for genomes. Nat Protoc 11:1-9, 2016
10)Adzhubei IA, Schmidt S, Peshkin L, et al. A method and server for predicting damaging missense mutations. Nat Methods 7:248-249, 2010
11)樋下徹哉,海崎泰治,細川治,他.A型胃炎をともなわない高ガストリン血症に合併した,微小多発胃カルチノイドの1例.日消誌 102:1275-1280, 2005
12)Hosoya Y, Satoh K, Hironaka M, et al. Multiple gastric carcinoids associated with parietal cell hyperplasia:intraoperative detection with a radiolabeled somatostatin analog. Gastric Cancer 11:123-126, 2008
13)Nakata K, Aishima S, Ichimiya H, et al. Unusual multiple gastric carcinoids with hypergastrinemia:report of a case. Surg Today 40:267-271, 2010
14)Calvete O, Reyes J, Zuñiga S, et al. Exome sequencing identifies ATP4A gene as responsible of an atypical familial type I gastric neuroendocrine tumour. Hum Mol Genet 24:2914-2922, 2015
15)森至弘,山田達也,江原一尚,他.多発性内分泌腫瘍症1型(MEN1)に伴うと考えられる多発胃神経内分泌腫瘍(NET)に対し腹腔鏡下胃全摘術(LTG)を施行した2例.癌と化療 44:1114-1116, 2017
16)Hirai R, Haruma K, Okada H, et al. A case of enterochromaffin-like cell neuroendocrine tumor associated with parietal cell dysfunction which was successfully treated with somatostatin analogue. Clin J Gastroenterol 15:363-367, 2022
17)Abe Y, Hatta W, Asonuma S, et al. Parietal cell dysfunction:a rare cause of gastric neuroendocrine neoplasm with achlorhydria and extreme hypergastrinemia. Intern Med 61:2441-2448, 2022
18)Shiroma S, Higuchi K, Ota H, et al. A rare case of an enterochromaffin-like neuroendocrine tumor associated with parietal cell dysfunction treated using endoscopic submucosal dissection. Clin J Gastroenterol 15:1041-1047, 2022
19)Maideen NMP. Adverse effects associated with long-term use of proton pump inhibitors. Chonnam Med J 59:115-127, 2023