Division of Gastroenterology and Nephrology, Faculty of Medicine, Tottori University, Japan.
Department of Pathology, Faculty of Medicine, Tottori University, Japan.
Intern Med. 2022 Sep 1;61(17):2587-2592. doi: 10.2169/internalmedicine.8701-21. Epub 2022 Feb 8.
Von Hippel-Lindau (VHL) disease is a rare inherited familial syndrome complicated with various neoplasms, including neuroendocrine tumors (NETs). We herein report the first case of multiple gastric NETs in a 45-year-old man with VHL. He had multiple gastric polyps, and several endoscopic resected lesions were diagnosed as NETs. The serum gastrin level was elevated because he was taking a proton pump inhibitor (PPI). We suspected that gastrin had played a role in the development of NETs, and the remaining polyps were followed up with discontinuation of the PPI. The NETs gradually reduced in size until they became hard to notice on endoscopy and have remained nearly invisible for over eight years.
希佩尔-林道(VHL)病是一种罕见的遗传性家族综合征,伴有多种肿瘤,包括神经内分泌肿瘤(NETs)。本文报告了首例 VHL 患者的多发胃 NETs。患者为 45 岁男性,存在多发胃息肉,数块内镜下切除标本诊断为 NETs。由于服用质子泵抑制剂(PPI),患者血清胃泌素水平升高。我们推测胃泌素在 NETs 的发生发展中起作用,停用 PPI 后其余息肉进行了随访。NETs 逐渐缩小,内镜下几乎难以察觉,至今已随访 8 年余,未见明显进展。