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肺动脉瓣闭锁伴室间隔缺损及右肺侧支循环,伴发自升主动脉的异常左肺动脉。

Pulmonary atresia and ventricular septal defect with collaterals to right lung associated with anomalous left pulmonary artery from the ascending aorta.

机构信息

Department of Pediatrics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.

出版信息

Pediatr Radiol. 2010 Dec;40 Suppl 1:S72-6. doi: 10.1007/s00247-010-1832-2. Epub 2010 Sep 24.

Abstract

We present a 10-month-old boy with cyanosis. This is a rare case of pulmonary atresia, ventricular septal defect (VSD), major aorto-pulmonary collateral arteries (MAPCAs) to the right lung with absent native right pulmonary artery (RPA) in association with anomalous left pulmonary artery (LPA) from the ascending aorta (AAo). Echocardiography was unable to identify all of the cardiovascular abnormalities. Multidetector CT demonstrated all of these abnormalities and is the investigation of choice instead of cardiac catheterization.

摘要

我们呈现了一例 10 个月大的发绀男孩病例。这是一例罕见的肺动脉闭锁、室间隔缺损(VSD)伴右肺主要体肺侧支动脉(MAPCAs),而右肺动脉(RPA)缺如,同时伴发自升主动脉(AAo)的异常左肺动脉(LPA)。超声心动图未能识别所有心血管异常。多排 CT 显示了所有这些异常,是心脏导管检查的替代检查方法。

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