一例罕见的法洛四联症-肺动脉闭锁合并右肺动脉缺如及左肺动脉起自升主动脉的病例。
A rare case of tetralogy of Fallot-pulmonary atresia with absent right pulmonary artery and anomalous origin of left pulmonary artery from ascending aorta.
作者信息
Nagulakonda Sravan, Ojha Vineeta, Malhi Amarinder Singh, Balaji Arvind, Singh Resham, Jagia Priya
机构信息
Department of Cardiovascular Radiology & Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India.
Department of Cardiology, All India Institute of Medical Sciences, New Delhi, India.
出版信息
J Card Surg. 2022 Jun;37(6):1718-1719. doi: 10.1111/jocs.16455. Epub 2022 Mar 26.
We report a case of a 5-year-old child with tetralogy of Fallot-pulmonary atresia with anomalous origin of left pulmonary artery from ascending aorta and right lung supplied by collateral arteries. This case highlights the role of preoperative CT angiography in differentiating this entity from a common arterial trunk with discontinuous pulmonary arteries.
我们报告一例5岁法洛四联症合并肺动脉闭锁的患儿，其左肺动脉起自升主动脉且右肺由侧支动脉供血。该病例突出了术前CT血管造影在鉴别此病变与伴有肺动脉中断的共同动脉干方面的作用。
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