Department of General Medicine, Center Hospital of the National Center for Global Health and Medicine, Japan.
Department of Genomic Medicine, Center Hospital of the National Center for Global Health and Medicine, Japan.
Intern Med. 2023 Feb 15;62(4):553-557. doi: 10.2169/internalmedicine.9259-22. Epub 2022 Jul 29.
Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder of the vasculature, characterized by epistaxis, telangiectasia and arteriovenous malformations in multiple organs. We herein report a 49-year-old woman with a history of early-onset myocardial infarction and intracranial aneurysms, in whom we incidentally detected multiple hepatic vascular abnormalities. We subsequently diagnosed her with HHT after discovering gastrointestinal telangiectases and a pulmonary arteriovenous fistula along with a history of recurrent epistaxis. Whole-exome sequencing revealed a novel pathogenic variant in SMAD4, a relatively rare causative gene for HHT. This case highlights the fact that HHT patients may present with asymptomatic liver lesions.
遗传性出血性毛细血管扩张症(HHT)是一种血管遗传疾病,其特征是鼻出血、毛细血管扩张和多个器官的动静脉畸形。本文报告了一例 49 岁女性,有早发心肌梗死和颅内动脉瘤病史,在此期间我们偶然发现其存在多种肝脏血管异常。随后,我们发现其存在胃肠道毛细血管扩张和肺动静脉瘘,并伴有反复发作的鼻出血,最终诊断为 HHT。全外显子组测序显示 SMAD4 中存在一种新的致病性变异,SMAD4 是 HHT 相对罕见的致病基因。该病例强调了 HHT 患者可能存在无症状性肝脏病变。