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Transcatheter therapy of anomalous systemic venous drainage

Part of: Interventional Cardiology

Published online by Cambridge University Press:  20 December 2017

Shahnawaz M. Amdani ,
Thomas J. Forbes  and
Daisuke Kobayashi
Shahnawaz M. Amdani
Affiliation:
Carman and Ann Adams Department of Pediatrics, Division of Pediatric Cardiology, Children’s Hospital of Michigan, Wayne State University School of Medicine, Detroit, Michigan, United States of America
Thomas J. Forbes
Affiliation:
Carman and Ann Adams Department of Pediatrics, Division of Pediatric Cardiology, Children’s Hospital of Michigan, Wayne State University School of Medicine, Detroit, Michigan, United States of America
Daisuke Kobayashi*
Affiliation:
Carman and Ann Adams Department of Pediatrics, Division of Pediatric Cardiology, Children’s Hospital of Michigan, Wayne State University School of Medicine, Detroit, Michigan, United States of America
*
Correspondence to: D. Kobayashi, Division of Pediatric Cardiology, Children’s Hospital of Michigan, Carman and Ann Adams Department of Pediatrics, Wayne State University School of Medicine, 3901 Beaubien Blvd., Detroit, MI 48201-2119, United States of America. Tel: +1 313 745 5481; Fax: +1 313 993 0894; E-mail: [email protected]
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Abstract

Anomalous drainage of the right superior caval vein into the left atrium is a rare congenital anomaly that causes cyanosis and occult infection owing to right-to-left shunting. Transcatheter management of this anomaly is unique and rarely reported. We report a 32-year-old man with a history of brain abscess, who was diagnosed with an anomalous right superior caval vein draining to the left atrium; right upper pulmonary vein and right middle pulmonary vein draining into the inferior portion of the right superior caval vein; and a left superior caval vein draining into the right atrium through the coronary sinus without a bridging vein. Pre-procedural planning was guided by three-dimensional printed model. The right superior caval vein was occluded with a 16-mm Amplatzer muscular Ventricular Septal Defect occluder inferior to the azygous vein, but superior to the entries of right upper and middle pulmonary veins. This diverted the right superior caval vein flow to the inferior caval vein system through the azygos vein in a retrograde manner and allowed the right upper pulmonary vein and right middle pulmonary vein flow to drain into the left atrium normally, achieving exclusion of right-to-left shunting and allowing normal drainage of pulmonary veins into the left atrium. At the 6-month follow-up, his saturation improved from 93 to 97% with no symptoms of superior caval vein syndrome.

Keywords

Amplatzer muscular Ventricular Septal Defect occluderanomalous venous drainagethree-dimensional printed model
Type
Brief Report
Information
Cardiology in the Young , Volume 28 , Issue 3 , March 2018 , pp. 502 - 506
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Copyright
© Cambridge University Press 2017 

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References

1. Park, HM, Smith, ET, Silberstein, EB. Isolated right superior vena cava draining into left atrium diagnosed by radionuclide angiocardiography. J Nucl Med 1973; 14: 240–242.Google ScholarPubMed
2. Baggett, C, Skeen, SJ, Gantt, DS, Trotter, BR, Birkemeier, KL. Isolated right superior vena cava drainage into the left atrium diagnosed noninvasively in the peripartum period. Tex Heart Inst J 2009; 36: 611.Google Scholar
3. Braudo, MI, Beanlands, DS, Trusler, G. Anomalous drainage of the right superior vena cava into the left atrium. Can Med Assoc J 1968; 99: 715.Google ScholarPubMed
4. Alpert, BS, Rao, PS, Moore, HV, Covitz, W. Surgical correction of anomalous right superior vena cava to the left atrium. J Thorac Cardiovasc Surg 1981; 82: 301.CrossRefGoogle Scholar
5. Raghib, G, Ruttenberg, HD, Anderson, RC, Amplatz, K, Adams, P, Edwards, JE. Termination of left superior vena cava in left atrium, atrial septal defect, and absence of coronary sinus. Circulation. 1965; 31: 906–918.CrossRefGoogle ScholarPubMed
6. Mazzucco, A, Bortolotti, U, Stellin, G, Gallucci, V. Anomalies of the systemic venous return: a review. J Card Surg 1990; 5: 122–133.Google Scholar
7. Ezekowitz, MD, Alderson, PO, Bulkley, BH, Dwyer, PN, Watkins, L, Lappe, DL, et al. Isolated drainage of the superior vena cava into the left atrium in a 52-year-old man: a rare congenital malformation in the adult presenting with cyanosis, polycythemia, and an unsuccessful lung scan. Circulation 1978; 58: 751–756.Google Scholar
8. Leventhal, AR, Shah, AH, Crean, AM, Osten, M, Horlick, E, Benson, L. Percutaneous correction of right superior vena cava to left atrium. JACC Cardiovasc Interv 2015; 8: e221–e222.CrossRefGoogle ScholarPubMed
9. Giannopoulos, AA, Mitsouras, D, Yoo, SJ, Liu, PP, Chatzizisis, YS, Rybicki, FJ. Applications of 3D printing in cardiovascular diseases. Nat Rev Cardiol. 2016; 13: 701–718.CrossRefGoogle ScholarPubMed
10. Yoo, SJ, Thabit, O, Kim, EK, Ide, H, Yim, D, Dragulescu, A, Seed, M, Grosse-Wortmann, L, van Arsdell, G. 3D printing in medicine of congenital heart diseases. 3D Print Med 2015; 2: 3.CrossRefGoogle ScholarPubMed