先天性四叶式主动脉瓣合并法洛四联症及肺动脉闭锁。
Congenital quadricuspid aortic valve with tetralogy of Fallot and pulmonary atresia.
作者信息
Suzuki Yasuyuki, Daitoku Kazuyuki, Minakawa Masahito, Fukui Kozo, Fukuda Ikuo
机构信息
Department of Surgery I, Hirosaki University School of Medicine, Aomori, Japan.
出版信息
Jpn J Thorac Cardiovasc Surg. 2006 Jan;54(1):44-6. doi: 10.1007/BF02743785.
We report the case of a 4-year-old girl who had quadricuspid aortic valve regurgitation with tetralogy of Fallot and pulmonary atresia. This combination is very uncommon. Aortic valve replacement was performed successfully due to aortic regurgitation which had progressed one year after the total repair. The dilated aortic annulus plus quadricuspid aortic valve may result in progressive aortic regurgitation for a short period.
我们报告了一名4岁女孩的病例，她患有四叶式主动脉瓣反流合并法洛四联症和肺动脉闭锁。这种组合非常罕见。由于在完全修复一年后主动脉反流有所进展，因此成功进行了主动脉瓣置换术。扩张的主动脉瓣环加上四叶式主动脉瓣可能会在短时间内导致进行性主动脉反流。
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