Elarabi Ali Ibrahim, Leong Ming Chern, Alwi Mazeni
Paediatric and Congenital Heart Centre, Institut Jantung Negara, Kuala Lumpur, Malaysia.
Ann Pediatr Cardiol. 2017 May-Aug;10(2):203-205. doi: 10.4103/0974-2069.205157.
We report an 8-year-old male child with tetralogy of Fallot (TOF), who developed left pulmonary artery (LPA) atresia, following surgical repair of TOF and left pulmonary arterioplasty at the age of 6 years. He underwent successful radiofrequency recanalization and stenting of the LPA. The LPA exhibited satisfactory growth for 3 months, following recanalization and stenting.
我们报告一例患有法洛四联症(TOF)的8岁男性儿童,该患儿在6岁时接受TOF手术修复和左肺动脉成形术后发生左肺动脉(LPA)闭锁。他接受了成功的LPA射频再通和支架置入术。再通和支架置入术后,LPA在3个月内显示出令人满意的生长情况。