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Tetralogy of Fallot associated with scimitar syndrome

Published online by Cambridge University Press:  19 August 2008

Nawal Azhari ,
Fadel Al-Fadley  and
Ziad R. Bulbul
Nawal Azhari
Affiliation:
King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Fadel Al-Fadley
Affiliation:
King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Ziad R. Bulbul*
Affiliation:
King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
*
Ziad R. Bulbul, MD, Section of Pediatric Cardiology, Department of Cardiovascular Diseases (MBC 16), P.O. Box 3354, Riyadh, 11211, Kingdom of Saudi Arabia. Tel: 00-966-1 464-7272 ext 32056; Fax: 00-966-1 442-7482.
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Abstract

We present a case of tetralogy of Fallot associated with Scimitar syndrome. The patient was an 11-month old female who underwent successfully total repair of her lesion, including rerouting of the anomalous pulmonary vein to the left atrium. The diagnosis was suspected from the chest x-ray and echocardiography, and confirmed by angiography. To the best of our knowledge only 2 additional cases have previously been reported.

Keywords

Tetralogy of Fallotscimitar Syndromelung hypoplasia
Type
Brief Reports
Information
Cardiology in the Young , Volume 10 , Issue 1 , January 2000 , pp. 70 - 72
Copyright
Copyright © Cambridge University Press 2000

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References

1.Chassinat, R. Observation d' anomalies anatomiques remarqualbies de l'appareil circulatoires, avec heparocele congen itale, n'agent donne lieu pendant la vie a aucum symptome parriculier. Arch Gen Med 1836; 11: 80–91.Google Scholar
2.Cooper, G. Case of malformation of the thoracic viscera consisting of imperfect development of right lung, and trans position of the heart. London Med Gazette 1836; 18: 600–602.Google Scholar
3.Kiely, B, Filler, J, Stone, S, Doyle, EF. Syndrome of anomalous venous drainage of the right lung to the inferior vena cava. Am J Cardiol 20: 102–116.Google Scholar
4.Gikonyo, DK. Scimitar syndrome in Neonates: Report of Four Cases and Review of the literature. Pediatr Cardiol 1986; 6(4)193–197.Google Scholar
5.Jue, KL, Amplatz, K, Adams, P Jr, Anderson, RC. Anomalies of great vessels associated with lung hypoplasia: the scimitar syndrome. Am J Dis Child 1966; 111: 35–44.Google Scholar
6.Shibuya, K, Smallhorn, JE, McCrindle, BW. Echocardiographic Clues and accuracy in the diagnosis of scimitar syndrome. J Am Soc Echocardiog 1996; 9(2): 174–181.Google Scholar