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一种隐匿着具有重叠表型的罕见综合征的意外贫血。

An Unexpected Anemia Hiding a Rare Syndrome With Overlapping Phenotypes.

作者信息

Dal Buono Arianna, Poliani Laura, Repici Alessandro, Hassan Cesare, Bianchi Paolo

机构信息

Gastroenterology and Digestive Endoscopy Unit, Department of Gastroenterology, Humanitas Research Hospital, Rozzano (Milan), Italy.

Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.

出版信息

ACG Case Rep J. 2022 Nov 24;9(11):e00926. doi: 10.14309/crj.0000000000000926. eCollection 2022 Nov.

Abstract

Gastric polyposis is a rare endoscopic finding that can imply genetic syndromes predisposing to cancer development. Among the possible conditions associated with gastric polyposis and early onset gastric cancer (younger than 45 years) is juvenile polyposis syndrome. We present a clinical case of early onset gastric cancer associated with a frameshift mutation in the gene . Individuals carrying a pathogenic variant of this gene have a high risk of malignant transformation, especially of gastric cancer. Moreover, most of these patients present also with extraintestinal features of the hereditary hemorrhagic telangiectasia, and the first symptom prompting medical evaluation is anemia.

摘要

胃息肉病是一种罕见的内镜检查发现,可能提示存在易患癌症的遗传综合征。与胃息肉病和早发性胃癌(45岁以下)相关的可能病症之一是幼年性息肉病综合征。我们报告一例与该基因移码突变相关的早发性胃癌临床病例。携带该基因致病性变异的个体发生恶性转化的风险很高,尤其是患胃癌的风险。此外,这些患者中的大多数还表现出遗传性出血性毛细血管扩张症的肠外特征,促使进行医学评估的首发症状是贫血。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d766/9699651/9622c5a7d0fa/ac9-9-e00926-g001.jpg

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