ANOMALOUS ORIGIN OF THE LEFT MAIN PULMONARY-ARTERY FROM THE ASCENDING AORTA ASSOCIATED WITH DIGEORGE-SYNDROME

被引：36

作者：

DODO, H

ALEJOS, JC

PERLOFF, JK

LAKS, H

DRINKWATER, DC

WILLIAMS, RG

机构：

[1] UNIV CALIF LOS ANGELES,DEPT MED,LOS ANGELES,CA 90024

[2] UNIV CALIF LOS ANGELES,DEPT SURG,LOS ANGELES,CA 90024

[3] UNIV CALIF LOS ANGELES,DIV MED CARDIOL,LOS ANGELES,CA

[4] UNIV CALIF LOS ANGELES,DEPT PEDIAT CARDIOL,LOS ANGELES,CA

[5] UNIV CALIF LOS ANGELES,DIV CARDIOTHORAC SURG,LOS ANGELES,CA

[6] UNIV CALIF LOS ANGELES,CTR ADULT CONGENITAL HEART DIS,LOS ANGELES,CA

来源：

AMERICAN JOURNAL OF CARDIOLOGY | 1995年 / 75卷 / 17期

关键词：

D O I：

10.1016/S0002-9149(99)80788-7

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We place on record 2 infants with the DiGeorge syndrome and anomalous origin of the left pulmonary artery from the ascending aorta. We postulate that: (1) embryogenesis of anomalous origin of the left pulmonary artery from the ascending aorta might be due to the persistent fifth aortic arch connecting both arterial systems; (2) an anomalous pulmonary artery arising from the ascending aorta is part of the aortic arch abnormality accompanied by normal conotruncal septation; and (3) in the DiGeorge syndrome, cardiac anomalies that originate from the conotruncus or aortic arch, or both, may have the same embryologic mechanisms. © 1995 Excerpta Medica, Inc. All rights reserved.

引用

页码：1294 / 1295

页数：2

共 6 条

[1] TRICUSPID AND PULMONARY ATRESIA WITH COARCTATION OF THE AORTA - A RARE COMBINATION POSSIBLY EXPLAINED BY PERSISTENCE OF THE 5TH AORTIC-ARCH WITH A SYSTEMIC-TO-PULMONARY ARTERIAL CONNECTION [J].