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Successful balloon valvuloplasty using direct puncture of the heart for pentalogy of Cantrell with complete ectopia cordis, low birth weight, single ventricle and severe pulmonary stenosis

Published online by Cambridge University Press:  12 October 2020

Toshikatsu Tanaka*
Affiliation:
Department of Cardiology, Kobe Children’s Hospital, 1-6-7, Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo650-0047, Japan
Shingo Kubo
Affiliation:
Department of Cardiology, Kobe Children’s Hospital, 1-6-7, Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo650-0047, Japan
Naoya Kamei
Affiliation:
Department of Cardiology, Kobe Children’s Hospital, 1-6-7, Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo650-0047, Japan
*
Author for correspondence: T. Tanaka, MD, Department of Cardiology, Kobe Children’s Hospital, 1-6-7, Minatojima-minamimachi, Chuo-ku, Kobe, Hyogo650-0047, Japan. Tel: +81-78-945-7300; Fax: 81-78-302-1023. E-mail: [email protected]

Abstract

We present a 31 gestational weeks’ premature baby whose fetal echocardiogram showed ectopia cordis, single ventricle and severe pulmonary stenosis. At 31 gestational weeks, an emergency caesarean section was performed, and his birth weight was 1756 g, SpO2 was 80% on 100% O2. Epicardial echocardiogram showed double inlet right ventricle, severe valvular pulmonary stenosis and no ductus arteriosus. The risk of surgery was very high, so we decided to perform balloon valvuloplasty by direct puncture of the heart. We punctured the apex of the ventricle using a 16-gauge needle under echo guidance, advanced the guidewire to the pulmonary artery and performed balloon valvuloplasty. Soon after the procedure, the cyanosis improved dramatically. This is the first report of a transcatheter procedure performed by direct puncture of the heart for ectopia cordis with complex congenital heart disease.

Type
Brief Report
Copyright
© The Author(s), 2020. Published by Cambridge University Press

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References

Gabriel, A, Donnelly, J, Kuc, A, et al. Ectopia cordis: a rare congenital anomaly. Clin Anat 2014; 27: 11931199.CrossRefGoogle ScholarPubMed
Cantrell, JR, Haller, JA, Ravitch, MM. A syndrome of congenital defects involving the abdominal wall, sternum, diaphragm, pericardium and heart. Surg Gynecol Obset 1958; 7: 602614.Google Scholar
Tongsong, T, Wanapirak, C, Sirivatanapa, P, Wongtrangan, S. Prenatal sonographic diagnosis of ectopia cordis. J Clin Ultrasound 1999; 27 440445.3.0.CO;2-6>CrossRefGoogle ScholarPubMed
O’Gorman, CS, Tortoriello, TA, McMahon, CJ. Outcome of children with pentalogy of Cantrell following cardiac surgery. Pediatr Cardiol 2009; 30: 426430 CrossRefGoogle ScholarPubMed
McMahon, CJ, Walsh, KP. Transcatheter right ventricular outflow tract stent implantation in a child with pentalogy of Cantrell, double outlet right ventricle, and severe pulmonary stenosis. Catheter Cardiovasc Interv 2013; 82: 11641167.CrossRefGoogle Scholar
Galeczka, M, Fiszer, R, Knop, MT, et al. Successful atrial septal defect transcatheter closure in a patient with pentalogy of Cantrell and ectopia cordis. Postepy Kardiol Interwencyjnej 2019; 15: 247250.Google Scholar
Schmitz, C, Esmailzadeh, B, Herberg, U et al. Hybrid procedures can reduce the risk of congenital cardiovascular surgery. Eur J Cardiothorac Surg 2008; 34: 718725.CrossRefGoogle ScholarPubMed