单侧肺不发育、食管裂孔疝和房室间隔缺损：一种罕见的先天性异常组合。
Unilateral lung agenesis, hiatal hernia and atrioventricular septal defect: a rare combination of congenital anomalies.
作者信息
Gorla Sudheer R, Fernandez-Sanchez Josaura, Garg Ashish, Swaminathan Sethuraman
机构信息
Division of Cardiology, Department of Pediatrics, University of Miami Miller School of Medicine, Miami, Florida, USA.
出版信息
BMJ Case Rep. 2018 May 12;2018:bcr-2018-224382. doi: 10.1136/bcr-2018-224382.
Unilateral lung agenesis is a relatively rare congenital anomaly with a reported incidence of 1 in 15 000 births. It is frequently associated with other congenital malformations. Some of the sequelae of lung agenesis are potentially life-threatening. Here, we report a case of left lung agenesis in association with hiatal hernia and atrioventricular septal defect, a rare combination of anomalies which have not been described previously in the literature.
单侧肺不发育是一种相对罕见的先天性异常，据报道其发病率为15000例出生中有1例。它常与其他先天性畸形相关。肺不发育的一些后遗症可能危及生命。在此，我们报告一例左肺不发育合并食管裂孔疝和房室间隔缺损的病例，这种罕见的异常组合在以前的文献中尚未有描述。
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