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一例2B型浆果综合征。

A case of berry syndrome type 2B.

作者信息

Mannelli Lorenzo, Mosca Ralph, Henry Gillian, Srichai-Parsia Monvadi Barbara

机构信息

Department of Radiology, New York University Langone Medical Center, New York, NY 10016, USA.

出版信息

Congenit Heart Dis. 2011 Jul-Aug;6(4):389-92. doi: 10.1111/j.1747-0803.2010.00476.x. Epub 2011 Mar 10.

Abstract

We present a case of a 34-day-old baby boy with congestive heart failure and differential cyanosis. Based on echocardiography and confirmed with computed tomography angiography, the following abnormalities were detected: aortopulmonary window, aortic origin of the right pulmonary artery, patent ductus arteriosus, and hypoplasia/coarctation of the aorta. No other congenital abnormalities were detected, and a diagnosis of Berry Syndrome type 2B was made. No preoperative cardiac catheterization or angiocardiography was needed. The patient underwent complete surgical repair of the aortopulmonary window and reconstruction of the hypoplastic aortic arch. This case highlights the value of cross-sectional imaging with computed tomography angiography in the evaluation of complex congenital heart disease.

摘要

我们报告一例34天大的男婴,患有充血性心力衰竭和差异性发绀。基于超声心动图并经计算机断层血管造影证实,检测到以下异常:主肺动脉窗、右肺动脉起源于主动脉、动脉导管未闭以及主动脉发育不全/缩窄。未检测到其他先天性异常,诊断为2B型贝里综合征。无需术前心脏导管插入术或心血管造影。患者接受了主肺动脉窗的完全手术修复和发育不全的主动脉弓重建。该病例突出了计算机断层血管造影横断面成像在评估复杂先天性心脏病中的价值。

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