Tatari Hassan, Dehaki Maziar Gholampour, Omrani Gholamreza, Ghaheri Hafez, Al-Dairy Alwaleed, Mortezaeian Hojjat
1 Department of Cardiovascular Surgery, Division of Congenital Cardiac Surgery, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.
2 Alzahra Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Asian Cardiovasc Thorac Ann. 2018 Nov;26(9):704-706. doi: 10.1177/0218492317692467. Epub 2017 Jan 29.
Quadricuspid aortic valve is a rare anomaly, and most patients require surgery for aortic regurgitation in the 5th or 6th decades of life; only a few cases of aortic valve repair in childhood have been reported. A 3-year-old boy was scheduled for ventricular septal defect closure and aortic valve repair. Quadricuspid aortic valve was an incidental finding at operation; it was repaired by joining the left anterior and right anterior cusps. At the 9-month follow-up, the patient had no more than mild aortic regurgitation. We emphasize the importance of detecting this anomaly, especially in children with aortic valve regurgitation.
四叶式主动脉瓣是一种罕见的先天性心脏畸形,大多数患者在50或60岁时因主动脉瓣反流需要进行手术;仅有少数儿童期主动脉瓣修复的病例报道。一名3岁男孩计划进行室间隔缺损修补和主动脉瓣修复手术。术中意外发现四叶式主动脉瓣;通过将左前叶和右前叶瓣叶连接进行修复。术后9个月随访,患者仅有轻度主动脉瓣反流。我们强调检测这种畸形的重要性,尤其是对于有主动脉瓣反流的儿童。