El Louali Fedoua, Azagoh-Kouadio Richard, Kammache Issam, Fouilloux Virginie, Kreitmann Bernard, Fraisse Alain
Cardiologie Pédiatrique, Hôpital de la Timone-Enfants, 264 rue St Pierre, 13385, Marseille Cedex 05, France.
Pediatr Cardiol. 2013 Feb;34(2):438-40. doi: 10.1007/s00246-012-0282-z. Epub 2012 Apr 4.
A right ventricular outflow tract stent was implanted in a 1-month-old (3.5 kg) baby boy with tetralogy of Fallot and worsening cyanosis to relieve infundibular and pulmonary valve stenosis in the setting of well-developed pulmonary artery branches. This management allowed a symmetric and optimal growth of the pulmonary artery branches, with right and left pulmonary arteries measuring 7-mm (z-score, +1.3 SD) and 7.3-mm (z-score, +1.7 SD), respectively, 3 months after stent implantation. No signs of pulmonary overcirculation developed, and complete surgical repair was performed at the age of 6 months.
一名1个月大（3.5千克）患有法洛四联症且发绀加重的男婴植入了右心室流出道支架，以缓解在肺动脉分支发育良好情况下的漏斗部和肺动脉瓣狭窄。这种处理方式使肺动脉分支得以对称且最佳地生长，支架植入3个月后，右肺动脉和左肺动脉分别为7毫米（Z值，+1.3标准差）和7.3毫米（Z值，+1.7标准差）。未出现肺循环过度的迹象，患儿在6个月大时接受了完全性手术修复。
