Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-23T07:15:05.290Z Has data issue: false hasContentIssue false
  • English
  • Français

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.
Get access Rights & Permissions [Opens in a new window]

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

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

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