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Differential Diseases of Gastric Neuroendocrine Tumors(NETs):X-ray/endoscopic Diagnosis Yasuhiko Maruyama 1 , Shigeto Yoshii 1 , Masanobu Kageoka 1 , Akihiko Ohata 1 , Tomohiro Terai 1 , Hironori Hoshino 1 , Keisuke Inagaki 1 , Wataru Inui 1 , Kodai Baba 1 , Takumi Maruyama 1 , Kenji Koda 2 , Tomoyo Yasuda 3 , Satoshi Baba 4 1Department of Gastroenterology, Fujieda Municipal General Hospital, Fujieda, Japan 2Department of Pathology, Fujieda Municipal General Hospital, Fujieda, Japan 3Department of Pathology, Shizuoka Prefectural Hospital Organization, Shizuoka, Japan 4Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan Keyword: neuroendocrine tumor , neuroendocrine neoplasia , Type I NET , autoimmune gastritis , Type III NET pp.673-686
Published Date 2024/5/25
DOI https://doi.org/10.11477/mf.1403203620
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 Gastric NETs(neuroendocrine tumors)are epithelial tumors that arise from enterochromaffin-like cells in the deep mucosal layer and are generally recognized as yellowish-white to reddish subepithelial lesions. However, endoscopic findings vary slightly depending on factors such as the state of atrophy of the background mucosa, the tumor size, and the distance to the tumor surface. Tumors that are not exposed to the mucosal surface, such as NETs and fundic gland-type adenocarcinoma, also induce superficial crypt epithelium changes, such as foveal enlargement, elongation, and vascular dilation. This aids in diagnosis especially when differentiating it from subepithelial lesions that arise from the shallow submucosal layer. Among AIGs, AIG associated with Rindi type I NET presents with high serum gastrin levels and severe atrophy. The difference in background atrophy between the small lesions of Rindi type I and type III NETs was believed to influence the morphology of the findings.


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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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