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Atypical infantile form of scimitar syndrome with bronchomalacia.

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.
AuthorsYoshihiro Oshima, Ikuo Hashimoto, Chikashi Shimazu, Fukiko Ichida
JournalInteractive cardiovascular and thoracic surgery (Interact Cardiovasc Thorac Surg) Vol. 2 Issue 3 Pg. 298-300 (Sep 2003) ISSN: 1569-9285 [Electronic] England
PMID17670052 (Publication Type: Journal Article)

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