Hostname: page-component-cd9895bd7-gbm5v Total loading time: 0 Render date: 2024-12-27T15:20:20.874Z Has data issue: false hasContentIssue false
  • English
  • Français

Thoracoscopic treatment of left-to-right shunt in a child with scimitar syndrome

Part of: Surgery

Published online by Cambridge University Press:  11 September 2017

Zafer Dokumcu Open the ORCID record for Zafer Dokumcu [Opens in a new window] ,
Emre Divarci  and
Ata Erdener
Zafer Dokumcu*
Affiliation:
Department of Pediatric Surgery, Ege Universitesi Tip Fakultesi, Izmir, Turkey
Emre Divarci
Affiliation:
Department of Pediatric Surgery, Ege Universitesi Tip Fakultesi, Izmir, Turkey
Ata Erdener
Affiliation:
Department of Pediatric Surgery, Ege Universitesi Tip Fakultesi, Izmir, Turkey
*
Correspondence to: Z. Dokumcu, Department of Pediatric Surgery, Ege Universitesi Tip Fakultesi, Bornova, Izmir 35100, Turkey. Tel: +90 232 390 2800; Fax: +90 232 390 2802; E-mail: zdokumcu@gmail.com
Get access Rights & Permissions [Opens in a new window]

Abstract

Scimitar syndrome represents a rare variant of partial anomalous pulmonary venous connection with right lung hypoplasia, dextrocardia, and concomitant airway-vessel abnormalities. Surgical correction is preferred in symptomatic patients or in patients with increased left-to-right shunt. In this report, the first case of scimitar syndrome with dual arterial supply and venous drainage to be treated with thoracoscopic approach is presented.

Keywords

Scimitar syndromepulmonary anomalous venous returnpulmonary malinosculationthoracoscopychild
Type
Brief Report
Information
Cardiology in the Young , Volume 28 , Issue 1 , January 2018 , pp. 159 - 162
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. Sade, RM, Clouse, M, Ellis, FH. The spectrum of pulmonary sequestration. Ann Thorac Surg 1974; 18: 644–658.Google Scholar
2. Bo, I, Carvalho, JS, Cheasty, E, et al. Variants of the scimitar syndrome. Cardiol Young 2016; 26: 941–947.Google Scholar
3. Clements, BS, Warner, JO. Pulmonary sequestration and related congenital bronchopulmonary-vascular malformations: nomenclature and classification based on anatomical and embryological considerations. Thorax 1987; 42: 401–408.Google Scholar
4. Irodi, A, Prabhu, SM, John, RA, et al. Congenital bronchopulmonary vascular malformations, “sequestration” and beyond. Indian J Radiol Imaging 2015; 25: 35–43.Google ScholarPubMed
5. Cicek, S, Arslan, AH, Ugurlucan, M, et al. Scimitar syndrome: the curved Turkish Sabre. Semin Thorac Cardiovasc Surg Pediatr Card Surg Ann 2014; 17: 56–61.CrossRefGoogle ScholarPubMed
6. Hall, SM, Hislop, AA, Haworth, SG. Origin, differentiation, and maturation of human pulmonary veins. Am J Respir Cell Mol Biol 2002; 26: 333–340.CrossRefGoogle ScholarPubMed
7. Fuchigami, T, Gabe, A, Takahashi, K, et al. Thoracoscopic surgery for partial anomalous pulmonary venous connection with dual drainage. J Card Surg 2015; 30: 764–766.CrossRefGoogle ScholarPubMed
8. Guneyli, S, Cinar, C, Bozkaya, H, et al. Application of the Amplatzer vascular plug to various vascular lesions. Diagn Interv Radiol 2014; 20: 155–159.Google Scholar
9. Katre, R, Burns, SK, Murillo, H, et al. Anomalous pulmonary venous connections. Semin Ultrasound CT MR, 33: 485–499.CrossRefGoogle Scholar
10. Uthaman, B, Abushaban, L, Al-Qbandi, M, et al. The impact of interruption of anomalous systemic arterial supply on scimitar syndrome presenting during infancy. Catheter Cardiovasc Interv 2008; 71: 671–678.CrossRefGoogle ScholarPubMed