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经导管主动脉瓣植入术后海德综合征所致非典型胃黏膜出血消失

Disappearance of Atypical Gastric Mucosal Bleeding due to Heyde's Syndrome after Transcatheter Aortic Valve Implantation.

作者信息

Sugimoto Shinya, Takamura Takeshi

机构信息

Department of Gastroenterology, Ise Red Cross Hospital, Ise, Japan.

Department of Cardiology, Ise Red Cross Hospital, Ise, Japan.

出版信息

Case Rep Gastroenterol. 2022 Mar 28;16(1):165-170. doi: 10.1159/000522640. eCollection 2022 Jan-Apr.

Abstract

An 82-year-old man was admitted to our hospital due to dyspnea on exertion. Blood tests showed iron deficiency anemia, and echocardiography revealed severe aortic stenosis (AS). Considering the possibility of Heyde's syndrome, esophagogastroduodenoscopy was performed to confirm the presence or absence of gastrointestinal angiodysplasia. Endoscopy revealed multiple sites of mucosal bleeding in the stomach without angiodysplasia or mucosal erosion. Although it was an atypical endoscopic finding, we diagnosed gastric mucosal bleeding associated with Heyde's syndrome. Since no atypical blood vessels could be found, endoscopic treatment was not performed, and only transcatheter aortic valve implantation (TAVI) for aortic valve stenosis was performed. TAVI immediately improved the dyspnea on exertion, and follow-up endoscopy 4 months after TAVI showed the disappearance of the multifocal mucosal bleeding in the stomach. Heyde's syndrome is characterized by AS, acquired deficiency or dysfunction of von Willebrand factor, and gastrointestinal angiodysplasia; however, the exact diagnostic criteria have not been established. This is a case of mucosal bleeding due to Heyde's syndrome, without the typical endoscopic image of angiodysplasia. Cardiologists and gastroenterologists need to consider the possibility of Heyde's syndrome in AS patients with atypical gastrointestinal bleeding on endoscopy.

摘要

一名82岁男性因劳力性呼吸困难入院。血液检查显示缺铁性贫血,超声心动图显示严重主动脉瓣狭窄(AS)。考虑到黑德氏综合征的可能性,进行了食管胃十二指肠镜检查以确认是否存在胃肠道血管发育异常。内镜检查发现胃内多处黏膜出血,但无血管发育异常或黏膜糜烂。尽管这是一种非典型的内镜表现,但我们诊断为与黑德氏综合征相关的胃黏膜出血。由于未发现非典型血管,未进行内镜治疗,仅对主动脉瓣狭窄进行了经导管主动脉瓣植入术(TAVI)。TAVI立即改善了劳力性呼吸困难,TAVI术后4个月的随访内镜检查显示胃内多灶性黏膜出血消失。黑德氏综合征的特征是AS、血管性血友病因子获得性缺乏或功能障碍以及胃肠道血管发育异常;然而,确切的诊断标准尚未确立。这是一例因黑德氏综合征导致的黏膜出血病例,无血管发育异常的典型内镜图像。心脏病学家和胃肠病学家需要考虑在内镜检查发现非典型胃肠道出血的AS患者中存在黑德氏综合征的可能性。

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