Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-10T08:01:40.251Z Has data issue: false hasContentIssue false
  • English
  • Français

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 ,
Sezen Ugan Atik  and
Helen Bornaun
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: sezenugan@hotmail.com
Get access Rights & Permissions [Opens in a new window]

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.

Keywords

Scimitar syndrometranscatheter correctionpartial anomalous pulmonary venous connection
Type
Brief Report
Information
Cardiology in the Young , Volume 27 , Issue 8 , October 2017 , pp. 1627 - 1629
Check for updates
Copyright
© Cambridge University Press 2017 

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. Wang, CC, Wu, ET, Chen, SJ, et al. Scimitar syndrome: incidence, treatment, and prognosis. Eur J Pediatr 2008; 167: 155–160.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: 997–999.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: 330–335.Google Scholar
4. Kasarala, G, Fiore, A, Schowengerdt, K, Jureidini, S. Partial anomalous pulmonary venous return: transcatheter repair. Pediatr Cardiol 2011; 32: 1238–1240.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: 357–360.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: 1212–1216.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: 192–195.3.0.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: 265–269.Google Scholar
9. Gao, YA, Burrows, PE, Benson, LN, Rabinovitch, M, Freedom, RM. Scimitar syndrome in infancy. J Am Coll Cardiol 1993; 22: 873–882.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: 671–678.CrossRefGoogle ScholarPubMed