Arboleda Miguel, Niño de Guzman Iván, Ticona Eva, Morales Gabriela, Gloria Edgard, Obregon Plinio, Lora Alfredo, Ganiku María, Adrianzen Manuel, Falcon Liana
Instituto Nacional del Corazón, Departamento de Cardiopediatría (ESSALUD), Lima, Peru.
Arq Bras Cardiol. 2004 Dec;83(6):519-21; 516-8. doi: 10.1590/s0066-782x2004001800010. Epub 2005 Jan 7.
The anomalous origin of the right pulmonary artery (AORPA) from the ascending aorta is a rare congenital malformation. We describe an infant who underwent a surgical correction with direct anastomosis between the right pulmonary artery and the pulmonary trunk. Eighteen months later, the patient remains asymptomatic, and no significant residual stenosis was detected on angioresonance.
右肺动脉起源于升主动脉的异常(AORPA)是一种罕见的先天性畸形。我们描述了一名婴儿,其接受了右肺动脉与肺动脉干直接吻合的手术矫正。18个月后,患者仍无症状,血管造影未检测到明显的残余狭窄。