Notoya Genso, Niikura Ryota, Yamada Atsuo, Ochi Masanori, Kawai Takashi, Koike Kazuhiko
Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Gastroenterological Endoscopy, Tokyo Medical University, Tokyo, Japan.
Case Rep Gastroenterol. 2021 Sep 23;15(3):819-824. doi: 10.1159/000519004. eCollection 2021 Sep-Dec.
Heyde's syndrome, which is caused by aortic stenosis and subsequent acquired von Willebrand factor deficiency, is a gastrointestinal bleeding disease. Gastrointestinal bleeding develops in patients with Heyde's syndrome, which may have a different prognosis from general gastrointestinal bleeding; thus, it is important to understand the clinical course. We report a 76-year-old Japanese female who underwent aortic mechanical valve replacement 1 year ago and presented with recurrent gastrointestinal bleeding in angiodysplasia of the sigmoid colon. Endoscopic interventions achieved hemostasis. However, 6 rebleeding events occurred due to a sigmoid colon ulcer and gastric and jejunal angiodysplasia 7 years after first hemostasis. The patient underwent multiple endoscopic hemostatic procedures (upper, lower, and balloon-assisted endoscopy) and repeated transfusions (total of 394 units of red blood cells). The intensive treatment contributed to the survival time of 10 years. In addition, we performed a literature review of the prognosis of patients with Heyde's syndrome.
海德综合征是一种胃肠道出血疾病,由主动脉瓣狭窄及随后获得性血管性血友病因子缺乏引起。海德综合征患者会出现胃肠道出血,其预后可能与一般胃肠道出血不同;因此,了解其临床病程很重要。我们报告一名76岁的日本女性,她1年前接受了主动脉机械瓣膜置换术,之后出现乙状结肠血管发育异常导致的反复胃肠道出血。内镜干预实现了止血。然而,首次止血7年后,由于乙状结肠溃疡以及胃和空肠血管发育异常,发生了6次再出血事件。该患者接受了多次内镜止血手术(上消化道、下消化道及气囊辅助内镜检查)并反复输血(共394单位红细胞)。强化治疗使患者存活了10年。此外,我们还对海德综合征患者的预后进行了文献综述。