Right pulmonary artery originating from the ascending aorta with tetralogy of fallot and pulmonary atresia

被引:0
|
作者
Rorris, Filippos-Paschalis [1 ]
Kanakis, Meletios [1 ]
Samanidis, George [2 ]
Tsoutsinos, Alexandros [3 ]
Lioulias, Achilleas [1 ]
Bobos, Dimitrios [1 ]
机构
[1] Onassis Cardiac Surg Ctr, Dept Paediat Cardiol & Adult Congenital Heart Dis, Athens, Greece
[2] Onassis Cardiac Surg Ctr, Dept Adult Cardiac Surg 1, 356 Leoforos Suggrou, Athens 17674, Greece
[3] Onassis Cardiac Surg Ctr, Dept Paediat Cardiol & Adult Congenital Heart Dis, Athens, Greece
来源
CLINICAL CASE REPORTS | 2024年 / 12卷 / 08期
关键词
congenital heart defect; Hemitruncus; pulmonary artery from ascending aorta; pulmonary atresia;
D O I
10.1002/ccr3.9232
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Key Clinical MessageAnomalous origin of right pulmonary artery from the ascending aorta is a rare congenital heart malformation that results in early infant mortality. These patients are at risk for the early development of significant pulmonary hypertension. The surgical management during the early period of life is imperative.AbstractAnomalous pulmonary artery originating from the ascending aorta (often called hemitruncus) is a rare congenital cardiac defect requiring immediate management in the neonatal period. We report a case of a rare variant of anomalous right pulmonary artery originating from the ascending aorta in combination with pulmonary atresia and tetralogy of Fallot. The above-mentioned combination makes the surgical management of such cardiac defect exceedingly demanding.
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页数:2
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