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一个关于腺瘤性结肠息肉病基因启动子 1B 中未报道点突变的病例,该突变与胃腺癌和胃近端息肉病有关。

A case of an unreported point mutation in promoter 1B of the adenomatous polyposis coli gene, which is responsible for gastric adenocarcinoma and proximal polyposis of the stomach.

机构信息

Department of Palliative Medicine, National Cancer Hospital East, 6-5-1 Kashiwanoha, Kashiwa-Shi, Chiba, 277-8577, Japan.

Department of Gastroenterology, Kanagawa Cancer Center, Yokohama, Kanagawa, Japan.

出版信息

Clin J Gastroenterol. 2024 Aug;17(4):602-606. doi: 10.1007/s12328-024-01964-5. Epub 2024 Apr 18.

Abstract

A 35-year-old woman of Asian descent with epigastralgia was referred to our hospital. Esophagogastroduodenoscopy revealed gastric cancer in the upper body and carpeting fundic gland polyposis in the fornix and body. Computed tomography revealed no metastases. Total colonoscopy and capsule endoscopy revealed no polyposis, except in the stomach. The patient was diagnosed with advanced gastric cancer and underwent open total gastrectomy. We speculated that her gastric cancer was a hereditary tumor due to its early onset and accompanying fundic gland polyposis. Germline multi-gene panel testing identified a single-nucleotide variant, c.-191 T > G, in exon 1B of the adenomatous polyposis coli gene, which can cause gastric adenocarcinoma and proximal polyposis of the stomach. To our knowledge, this is the first manuscript to report the variant (c.-191 T > G) in promoter 1B of the adenomatous polyposis coli gene, which is related to a predisposition to gastric adenocarcinoma and proximal polyposis of the stomach.

摘要

一位 35 岁的亚裔女性因上腹痛就诊于我院。食管胃十二指肠镜检查显示胃体上部胃癌和穹窿及体部胃底腺息肉病。计算机断层扫描未发现转移。全结肠镜和胶囊内镜检查除胃部外,未见息肉。患者被诊断为晚期胃癌,行开放性全胃切除术。我们推测她的胃癌是一种遗传性肿瘤,因为其发病早且伴有胃底腺息肉病。种系多基因panel 检测在腺瘤性结肠息肉病基因的 1B 外显子中发现了一个单核苷酸变异 c.-191T>G,可导致胃腺癌和胃近端息肉病。据我们所知,这是第一篇报道腺瘤性结肠息肉病基因启动子 1B 中 c.-191T>G 变异与胃腺癌和胃近端息肉病易感性相关的论文。

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