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Transcatheter correction of Scimitar syndrome: occlusion of abnormal pulmonary venous drainage and vascular supply in an infant

Published online by Cambridge University Press:  16 May 2017

Levent Saltik
Affiliation:
Department of Pediatric Cardiology, Cerrahpaşa Medical Faculty, Istanbul University
Sezen Ugan Atik*
Affiliation:
Department of Pediatric Cardiology, Cerrahpaşa Medical Faculty, Istanbul University
Helen Bornaun
Affiliation:
Department of Pediatric Cardiology, Kanuni Sultan Süleyman Training and Research Hospital, İstanbul, Turkey
*
Correspondence to: S. Ugan Atik, Department of Pediatric Cardiology, Cerrahpaşa Medical Faculty, Istanbul University, İstanbul, Turkey. Tel: +90 506 367 21 88; Fax: +90 (212) 632 00 50; E-mail: [email protected]

Abstract

Treatment of Scimitar syndrome is usually surgical; however, if there is “dual drainage” – that is, one to the inferior caval vein and the other to the left atrium – it is possible to successfully treat this anomaly via a less-invasive transcatheter approach. We report a case of Scimitar syndrome in a 21-month-old, male infant successfully treated with transcatheter embolisation.

Type
Brief Report
Copyright
© Cambridge University Press 2017 

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References

1. Wang, CC, Wu, ET, Chen, SJ, et al. Scimitar syndrome: incidence, treatment, and prognosis. Eur J Pediatr 2008; 167: 155160.CrossRefGoogle ScholarPubMed
2. Tan, HC, Cranney, GB, French, BF, Chow, EK, Chow, F, Leung, DY. An unusual case of partial anomalous pulmonary venous drainage. J Am Soc Echocardiogr 2002; 15: 997999.Google Scholar
3. Forbess, LW, O’Laughlin, MP, Harrison, JK. Partially anomalous pulmonary venous connection: demonstration of dual drainage allowing nonsurgical correction. Cathet Cardiovasc Diagn 1998; 44: 330335.Google Scholar
4. Kasarala, G, Fiore, A, Schowengerdt, K, Jureidini, S. Partial anomalous pulmonary venous return: transcatheter repair. Pediatr Cardiol 2011; 32: 12381240.Google Scholar
5. Sarquella-Brugada, G, Prada, F, Mortera, C. Double venous drainage in scimitar syndrome. Ideal anatomy for percutaneous complete cure. Cardiol Young 2011; 21: 357360.CrossRefGoogle ScholarPubMed
6. Wilson, W, Horlick, E, Benson, L. Successful transcatheter occlusion of an anomalous pulmonary vein with dual drainage to the LA. Catheter Cardiovasc Interv 2015; 85: 12121216.Google Scholar
7. Mas, C, Goh, TH, Wilkinson, JL. New interventional therapeutic approach for dual drainage of the scimitar vein. Catheter Cardiovasc Interv 2000; 51: 192195.3.0.CO;2-V>CrossRefGoogle ScholarPubMed
8. Singh, H, Luthra, M, Bharadwaj, P, Kumar, R. Interventional rerouting of scimitar vein to LA using an Amplatzer vascular plug. Congenit Heart Dis 2007; 2: 265269.Google Scholar
9. Gao, YA, Burrows, PE, Benson, LN, Rabinovitch, M, Freedom, RM. Scimitar syndrome in infancy. J Am Coll Cardiol 1993; 22: 873882.CrossRefGoogle ScholarPubMed
10. Uthaman, B, Abushaban, L, Al-Qbandi, M, Rathinasamy, J. The impact of interruption of anomalous systemic arterial supply on scimitar syndrome presenting during infancy. Catheter Cardiovasc Interv 2008; 71: 671678.CrossRefGoogle ScholarPubMed