Abstract

BackgroundPartial anomalous pulmonary venous return is a rare congenital cardiac anomaly that usually involves the right pulmonary vein and an atrial septal defect. Isolated partial anomalous pulmonary venous return with an intact atrial septum is even rarer, and this condition is usually treated surgically in younger patients. We describe isolated partial anomalous pulmonary venous return in a 65-year-old woman who was treated by caval division with pericardial patch baffling through a surgically created atrial septal defect and reconstruction of the superior vena cava using a prosthetic graft.Case presentationA 65-year-old Asian woman who presented with exertional dyspnea was diagnosed with isolated partial anomalous pulmonary venous return. The surgical indications and strategy were controversial because of the rarity of this pathology. She had an indication for surgery because she was symptomatic and had a high ratio of pulmonary to systemic blood flow. We considered that surgical procedures should avoid postoperative stenosis of a reconstructed flow tract, sinus node dysfunction, and thrombogenesis. We created a caval division with pericardial patch baffling through a surgically created atrial septal defect and reconstructed the superior vena cava using a prosthetic graft for the isolated partial anomalous pulmonary venous return. She has since remained free of exertional dyspnea, arrhythmia, and thrombotic complications. This surgical strategy is safe and effective for treating isolated partial anomalous pulmonary venous return in older symptomatic adults.ConclusionsThe long-term outcome of surgical repair of partial anomalous pulmonary venous return with an intact atrial septum in our patient, a symptomatic 65-year-old woman, was excellent.

Highlights

  • Partial anomalous pulmonary venous return is a rare congenital cardiac anomaly that usually involves the right pulmonary vein and an atrial septal defect

  • A concurrent pressure study revealed oxygen step-up in gas sampling between the superior vena cava (SVC) and right atrium (RA) with a pulmonary blood flow/systemic blood flow ratio (Qp/Qs) of 2.07, even though pulmonary artery pressure was normal in the pressure study and the atrial septum was intact on echocardiography

  • Contrast-enhanced computed tomography (CT) revealed that the right upper pulmonary vein (RUPV) flowed into the SVC (Fig. 1) without any other congenital heart conditions, including an atrial septal defect (ASD) and a dilated RA and right ventricle (RV)

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Summary

Conclusions

We surgically repaired PAPVR with an intact atrial septum using caval division with pericardial patch baffling, a surgically created ASD, and SVC reconstruction using a prosthetic graft in a symptomatic older adult with an excellent long-term outcome. Ethical guidelines for medical and health research involving human subjects. 2014. http://www.lifescience.mext.go.jp/files/pdf/n1500_01.pdf

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