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Successful staged neonatal repair of tetralogy of Fallot with long-segment hypoplasia of the aorta.

作者信息

Lu Jimmy C, Shah Sanket S, Owens Sonal T, Dorfman Adam L, Vedre Ameeth, Goble Monica M, Hirsch Jennifer C, Charpie John R

机构信息

Congenital Heart Center, University of Michigan, Ann Arbor, MI 48109-5204, USA.

出版信息

Pediatr Cardiol. 2010 Jan;31(1):124-7. doi: 10.1007/s00246-009-9547-6. Epub 2009 Sep 26.

DOI:10.1007/s00246-009-9547-6
PMID:19784693
Abstract

We describe an extremely rare combination of tetralogy of Fallot (TOF), right-sided cervical aortic arch with long-segment hypoplasia, and other vascular anomalies. A two-stage surgical approach included aortic arch reconstruction followed by right ventricular muscle bundle division and ventricular septal defect closure a few weeks later. The initial clinical presentation, perioperative course, and imaging studies are presented along with a review of the relevant literature. This is the first report of successful neonatal repair of TOF with long-segment hypoplasia of the aorta.

摘要

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本文引用的文献

1
Tetralogy of Fallot with atypical coarctation of the aorta and carotid arterial stenosis due to fibromuscular dysplasia.
Cardiol Young. 2007 Dec;17(6):689-90. doi: 10.1017/S1047951107001618. Epub 2007 Nov 1.
2
Absence of the left common carotid artery with cervical origin of the right subclavian artery.左颈总动脉缺如，右锁骨下动脉起源于颈部。
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3
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4
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Coarctation co-existing with tetralogy of Fallot and pulmonary atresia.主动脉缩窄与法洛四联症及肺动脉闭锁并存。
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Tetralogy of Fallot and coarctation of the aorta: successful repair in an infant.
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Hemodynamic considerations in the development of narrowing of the aorta.主动脉缩窄发展过程中的血流动力学因素
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10
Interrupted aortic arch with tetralogy of Fallot. A report of an unsuccessful surgically treated case.法洛四联症合并主动脉弓中断。1例手术治疗失败病例报告。
J Cardiovasc Surg (Torino). 1991 Jul-Aug;32(4):541-3.