| CASE REPORT OF A 6-WEEK-OLD BOY WITH BLAND- WHITE-GARLAND SYNDROME |
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| 作者姓名： | 杨晓东 STEIN Joerg-Ingolf |
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| 作者单位： | [1]Department of Cardiology, Shanghai Children Hospital of Shanghai Jiaotong University, Shanghai 200040, China [2]Department of pediatrics cardiology, Innsbruck Medical University, Innsbruck A-6020, Austria |
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| 摘 要： | Bland-White-Garland syndrome is a rare syndrome with anomalous origin of the left coronary artery （ LCA ） arising from the pulmonary artery, resulting in left ventricular failure. It could occur shortly after birth. We here reported the case of a 6-week-old boy with aortostenosis. Coronary angiography revealed an anomalous LCA arising from the pulmonary artery. Representation of a prominent right coronary artery （ RCA ） delivered numerous collateral vessels to the LCA area, The patient underwent a correction operation with translocation of the LCA and re-implantation into the ascending aorta. One month after operation, clear decrease in the expanded ventricle was noted with an increase in the contractibility.
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| 关 键 词： | 冠状动脉 不规则 肺动脉 失效 |
CASE REPORT OF A 6-WEEK-OLD BOY WITH BLAND-WHITE-GARLAND SYNDROME |
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| YANG Xiao-dong,STEIN Joerg-Ingolf.CASE REPORT OF A 6-WEEK-OLD BOY WITH BLAND- WHITE-GARLAND SYNDROME[J].Journal of Shanghai Second Medical University(Foreign Language Edition),2008,20(1):64-66,70. |
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| Authors: | YANG Xiao-dong STEIN Joerg-Ingolf |
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| Institution: | [1]Department of Cardiology, Shanghai Children Hospital of Shanghai Jiaotong University, Shanghai 200040, China; [2]Department of pediatrics cardiology, Innsbruck Medical University, Innsbruck A-6020, Austria |
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| Abstract: | Bland-White-Garland syndrome is a rare syndrome with anomalous origin of the left coronary artery (LCA) arising from the pulmonary artery, resulting in left ventricular failure. It could occur shortly after birth. We here reported the case of a 6-week-old boy with aortostenosis. Coronary angiography revealed an anomalous LCA arising from the pulmonary artery. Representation of a prominent right coronary artery (RCA) delivered numerous collateral vessels to the LCA area. The patient underwent a correction operation with translocation of the LCA and re-implantation into the ascending aorta. One month after operation, clear decrease in the expanded ventricle was noted with an increase in the contractibility. |
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| Keywords: | Bland-White-Garland syndrome left coronary artery anomaly |
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