Bové T, Goldstein J P, Viart P, Deuvaert F E
Department of Cardiac Surgery, Hôpital des Enfants Reine Fabiola, Brussels, Belgium.
Ann Thorac Surg. 1997 Aug;64(2):561-2. doi: 10.1016/S0003-4975(97)00558-4.
We report on a 2-month-old infant with the unusual association of an upper sternal defect and tetralogy of Fallot. Surgical correction of the cardiac disease consisted of closing the ventricular septal defect and relief of the right ventricular outflow tract by infundibuloplasty. The already less compliant bony thorax of the infant made direct approximation of the upper sternal defect only possible with adjuvant bilateral chondrotomies. Sternal cleft repair is advised during the very first weeks of life, during which complete correction of the rarely associated tetralogy of Fallot can be successfully performed.
我们报告了一名2个月大的婴儿,其患有罕见的上位胸骨缺损与法洛四联症合并症。心脏病的手术矫正包括闭合室间隔缺损以及通过漏斗部成形术缓解右心室流出道梗阻。婴儿本就顺应性较差的骨性胸廓使得仅通过双侧软骨切开术辅助才能直接闭合上位胸骨缺损。建议在出生后的最初几周内进行胸骨裂修复,在此期间可成功完成很少合并的法洛四联症的完全矫正。