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首页> 外文期刊>Archives of Clinical and Experimental Surgery >Tricuspid Valve Repair for a Patient with Congenital Isolated Severe Tricuspid Regurgitation
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Tricuspid Valve Repair for a Patient with Congenital Isolated Severe Tricuspid Regurgitation

机译:先天性重度三尖瓣关闭不全患者三尖瓣修复

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Severe tricuspid regurgitation commonly results from left-sided heart disease and secondary pulmonary hypertension, while isolated tricuspid regurgitation requiring surgical intervention is extremely rare. We describe a case of an 81-year-old man presenting with congenital isolated severe tricuspid regurgitation due to annular dilatation and tricuspid valve leaflet dysfunction. Echocardiography revealed enlargement of the right atrium and dilatation of the tricuspid annulus. Significant downward displacement of the tricuspid septal leaflet (>10mm) suggesting Ebstein's abnormality was not seen. Right cardiac catheterization confirmed elevated right atrial pressure, and no left-to-right shunt was detected at the right atrium. Upon surgery, severe annular dilatation of the tricuspid valve with a deformed anterior tricuspid leaflet was visualized. Tricuspid annuloplasty with a prosthetic ring and tricuspid repair was successfully performed with subsequent resolution of the patient's condition.
机译:严重的三尖瓣关闭不全通常是由左侧心脏病和继发性肺动脉高压引起的,而需要手术干预的孤立的三尖瓣关闭不全非常罕见。我们描述了一个因环扩张和三尖瓣瓣叶功能不全而导致的先天性孤立性严重三尖瓣关闭不全的81岁男子的病例。超声心动图显示右心房扩大和三尖瓣环扩张。三尖瓣间隔小叶明显向下移位(> 10mm),表明未观察到Ebstein异常。右心导管检查证实右心房压力升高,并且在右心房未检测到从左到右的分流。手术后,可见三尖瓣严重的环形扩张以及变形的三尖瓣前瓣。具有假体环的三尖瓣瓣环成形术和三尖瓣修复术成功完成,随后患者情况得以缓解。

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