一例维尔纳综合征患者通过微创心脏手术行主动脉瓣置换术。

IF 1.1 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Annals of Thoracic and Cardiovascular Surgery Pub Date : 2023-08-20 DOI:10.5761/atcs.cr.21-00214
Riki Sumiyoshi, Hideki Morita, Sho Kusadokoro, Kento Fujii, Hiroyuki Kawaura, Masakazu Aoki, Hiroshi Nagano
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引用次数: 0

摘要

沃纳氏综合征(WS)是一种表现为过早衰老的遗传性疾病。在本研究中,我们对一例出现主动脉狭窄的维尔纳综合征患者进行了微创心脏手术(MICS)-主动脉瓣置换术(AVR)。患者是一名49岁的日本男子,因运动时呼吸困难被送往急诊室。在超声心动图上,发现严重的主动脉狭窄,并计划手术。他的糖尿病控制不佳,为了避免发生胸骨骨髓炎的风险,他接受了MICS-AVR治疗,结果很好。主动脉瓣有硬化改变,基于年轻时主动脉瓣狭窄的发病、特征外观和各种衰老迹象,怀疑是遗传性疾病。基因检测导致WS的诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Patient with Werner's Syndrome Who Underwent Aortic Valve Replacement through Minimally Invasive Cardiac Surgery.

Werner's syndrome (WS) is a genetic disorder presenting with premature senility. In the present study, we performed minimally invasive cardiac surgery (MICS)-aortic valve replacement (AVR) on a patient with Werner's syndrome who presented with aortic stenosis. The patient, a 49-year-old Japanese man, was brought to the emergency room with dyspnea during exercise. On echocardiography, severe aortic stenosis was found and surgery was planned. He had poorly controlled diabetes mellitus and underwent MICS-AVR to avoid the risk of sternal osteomyelitis, which resulted in a good outcome. The aortic valve had sclerotic changes and a genetic disease was suspected based on the onset of aortic stenosis at a young age, characteristic appearance, and various signs of aging. Genetic testing led to the diagnosis of WS.

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来源期刊
Annals of Thoracic and Cardiovascular Surgery
Annals of Thoracic and Cardiovascular Surgery CARDIAC & CARDIOVASCULAR SYSTEMS-SURGERY
CiteScore
2.80
自引率
0.00%
发文量
56
审稿时长
4-8 weeks
期刊介绍: Information not localized
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