Moon-Grady Anita J, Moore Phillip, Azakie Anthony
Pediatric Heart Center, UCSF Benioff Children's Hospital, University of California San Francisco, San Francisco, CA 94143-0117, USA.
Pediatr Cardiol. 2011 Feb;32(2):211-4. doi: 10.1007/s00246-010-9841-3. Epub 2010 Nov 24.
We report a patient who presented during fetal life with severe aortic stenosis, left-ventricular dysfunction, and endocardial fibroelastosis (evolving hypoplastic left heart syndrome). Management involved in utero and postnatal balloon aortic valvuloplasty for partial relief of obstruction and early postnatal hybrid stage I palliation until recovery of left-ventricular systolic function had occurred. The infant subsequently had successful conversion to a biventricular circulation by combining resection of endocardial fibroelastosis with single-stage Ross-Konno, aortic arch reconstruction, hybrid takedown, and pulmonary artery reconstruction.
我们报告了一名胎儿期出现严重主动脉瓣狭窄、左心室功能障碍和心内膜弹力纤维增生症(演变中的左心发育不全综合征)的患者。治疗包括在子宫内和出生后进行球囊主动脉瓣成形术以部分缓解梗阻,并在出生后早期进行混合I期姑息治疗,直至左心室收缩功能恢复。该婴儿随后通过将心内膜弹力纤维增生症切除术与单阶段Ross-Konno手术、主动脉弓重建、混合拆除和肺动脉重建相结合,成功转变为双心室循环。