Karatza Ageliki, Mylonas Konstantinos S, Tzifa Aphrodite
Department of Pediatrics, Division of Pediatric Cardiology, General University Hospital of Patras, Patras, Greece.
Department of Pediatric Cardiology and Adult Congenital Heart Disease, Mitera Children's Hospital, Athens, Greece.
Cardiol Young. 2019 Sep;29(9):1208-1210. doi: 10.1017/S1047951119001707. Epub 2019 Aug 5.
We present the case of a 3-year-old boy with bicuspid aortic valve, aortic coarctation, and left ventricular non-compaction. The diagnosis was made post-natally with ultrasonography and was verified by cardiac MRI. Aortic coarctation was initially repaired surgically. At age 3 months, recoarctation and heart failure developed. Balloon angioplasty was performed with immediate improvement. At age 3 years, the patient remains asymptomatic and normotensive.
我们报告一例患有二叶式主动脉瓣、主动脉缩窄和左心室心肌致密化不全的3岁男孩。出生后通过超声心动图做出诊断，并经心脏磁共振成像证实。主动脉缩窄最初通过手术修复。3个月大时，出现再缩窄和心力衰竭。进行了球囊血管成形术，症状立即改善。3岁时，患者仍无症状且血压正常。
