法洛氏三部曲:一种罕见的先天性心脏病

Li Juan, Neerusha Kaisbain, Kim Heng Shee
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引用次数: 0

摘要

背景:先天性心脏病约占活产儿的1%。法洛三联症是一种罕见的先天性心脏病,包括肺动脉瓣狭窄、房间隔缺损和右心室肥厚。病例:我们描述了一个病人,他在体格检查中偶然发现全收缩期杂音,最终在经胸超声心动图上被诊断为严重的肺狭窄和大房间隔缺损。探讨经皮房间隔缺损封堵联合球囊瓣膜成形术治疗法洛三联症的治疗方案。结论:虽然法洛三联是一种罕见的先天性心脏病,但我们需要警惕识别这种组合,因为早期经皮经导管治疗或手术矫正可以预防长期有害的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trilogy of fallot: a rare congenital heart disease
Background: Congenital heart diseases occur in around 1% of the liveborn. Trilogy of Fallot is a rare congenital heart disease comprising of pulmonary valve stenosis, atrial septal defect, and right ventricular hypertrophy. Case: We describe a patient who has incidental findings of pansystolic murmur during physical examination and was ultimately diagnosed with severe pulmonary stenosis with large atrial septal defect on transthoracic echocardiography. Possible management plan was discussed with patient including combined percutaneous atrial septal defect occlusion and pulmonary balloon valvuloplasty in treating Trilogy of Fallot. Conclusion: Although the Trilogy of Fallot is a rare congenital heart disease, we need to be vigilant to identify this combination as the early treatment with percutaneous transcatheter or surgical correction can prevent long term deleteriously complications.
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