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Interactive Cardiovascular and Thoracic Surgery 2:298-300(2003)
© 2003 European Association of Cardio-Thoracic Surgery

Case report - Congenital

Atypical infantile form of scimitar syndrome with bronchomalacia

Yoshihiro Oshimaa,b,*, Ikuo Hashimotoa,b, Chikashi Shimazua,b and Fukiko Ichidaa,b

a Department of Surgery (I), Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama 930-0194, Japan
b Department of Pediatrics, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama 930-0194, Japan

* Corresponding author. Tel.: +81-076-434-2281; fax: +81-076-434-5032
oshima{at}ms.toyama-mpu.ac.jp

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.

Key Words: Scimitar; Bronchomalacia; Endobronchial stenting




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V. L. Vida, S. Speggiorin, M. A. Padalino, G. Crupi, C. Marcelletti, L. Zannini, A. Frigiola, A. Varrica, D. Di Carlo, R. Di Donato, et al.
The scimitar syndrome: an Italian multicenter study.
Ann. Thorac. Surg., August 1, 2009; 88(2): 440 - 444.
[Abstract] [Full Text] [PDF]


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