Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in an Adult

被引：1

作者：

Nazli, Yunus ^{[1
]}

Aksoy, Omer Nuri ^{[1
]}

Korkmaz, Kemal ^{[2
]}

Akkaya, Ismail Olgun ^{[1
]}

Colak, Necmettin ^{[1
]}

机构：

[1] Univ Turgut Ozal, Fac Med, Ankara, Turkey

[2] Numune Res & Training Hosp, Dept Cardiovasc Surg, Ankara, Turkey

来源：

JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE | 2013年 / 4卷

关键词：

Congenital Heart Defect; Coronary Artery Bypass Grafting;

D O I：

10.4328/JCAM.2501

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Anomalous origin of the left main coronary artery from the pulmonary artery (ALCAPA), also known as Garland-Bland-White syndrome, is an extremely rare but potentially fatal congenital cardiovascular anomaly and it often exists as an isolated condition. We report an unusual case of a 32 years-old patient with ALCAPA presenting with chest pain and dyspnea who underwent surgical correction of this rare anomaly. This anomaly was simply repaired by the combination of LMCA ligation and coronary artery bypass grafting.

引用

页码：446 / 448

页数：3

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