Atypical infantile form of scimitar syndrome with bronchomalacia.

Journal: Interactive Cardiovascular And Thoracic Surgery
Published:
Abstract

A male infant presenting with severe heart failure and respiratory distress was diagnosed with a hypoplastic right lung, scimitar syndrome with pulmonary sequestration and multiple anomalous systemic arteries, left bronchomalacia, a large atrial septal defect and coarctation of the aorta. The infant underwent a successful combined treatment of surgical and transcatheter intervention, including coil embolization and endobronchial stenting.

Authors
Yoshihiro Oshima, Ikuo Hashimoto, Chikashi Shimazu, Fukiko Ichida