Mahimaiha Jayaranganath, Patra Soumya, Subramaniun Anand P, Sastry Usha Mandikal Kodanda Rama, Srinivasa Kikkeri Hemannasetty, Manjunath Cholenahally N
Department of cardiology, Sri Jayadeva Institute of Cardiovascular Sciences & Research, Bangalore, Karnataka, India.
Department of cardiology, Sri Jayadeva Institute of Cardiovascular Sciences & Research, Bangalore, Karnataka, India
World J Pediatr Congenit Heart Surg. 2014 Jul;5(3):481-3. doi: 10.1177/2150135114522277.
Coarctoplasty with stenting is often an effective strategy in cases of recoarctation following surgical repair. The potential benefit of coarctoplasty in a patient with Eisenmenger's syndrome is unknown. We describe the case of a 21-year-old male who presented with claudication of lower limbs. He was known to have congenital heart disease, consisting of ventricular septal defect, patent ductus arteriosus (PDA), and coarctation of the aorta. Coarctation repair and PDA ligation had been done at two months of age. At the time of presentation for evaluation of claudication, echocardiography revealed severe coarctation and evidence of Eisenmenger's syndrome. This patient subsequently underwent balloon angioplasty and stenting of coarctation without any increase in cyanosis.
支架置入缩窄成形术对于外科修复术后再缩窄的病例通常是一种有效的策略。缩窄成形术对艾森曼格综合征患者的潜在益处尚不清楚。我们描述了一名21岁男性患者,他出现下肢间歇性跛行。已知他患有先天性心脏病,包括室间隔缺损、动脉导管未闭(PDA)和主动脉缩窄。在两个月大时进行了缩窄修复和PDA结扎术。在因间歇性跛行前来评估时,超声心动图显示严重缩窄及艾森曼格综合征迹象。该患者随后接受了球囊血管成形术和缩窄部位的支架置入术,术后发绀未加重。