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The diagnosis and assessment of an adult with anomalous origin of the left coronary artery from the pulmonary artery.

作者信息

Cowie M R, Mahmood S, Ell P J

机构信息

Cardiac Department, Whittington Hospital, London, UK.

出版信息

Eur J Nucl Med. 1994 Sep;21(9):1017-9. doi: 10.1007/BF00238130.

DOI:10.1007/BF00238130
PMID:7995280
Abstract

Anomalous origin of the left coronary artery from the pulmonary artery (the Bland-White-Garland syndrome) is a rare congenital cardiac defect which may present for the first time in adulthood. The recognition of this disorder, which produces widespread left ventricular ischaemia and the risk of sudden death, myocardial infarction and congestive heart failure, is important as the prognosis can be improved by surgical intervention. Thallium-201 scintigraphy has a useful role in demonstrating the widespread nature of the ischaemia of the left ventricle, whilst the diagnosis is confirmed at cardiac catheterisation.

摘要

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引用本文的文献

1
Bland-White-Garland syndrome and atrial septal defect - rare association and diagnostic challenge.布兰德-怀特-加兰综合征与房间隔缺损——罕见关联及诊断挑战。
Clin Res Cardiol. 2006 May;95(5):295-300. doi: 10.1007/s00392-006-0369-8. Epub 2006 Mar 8.

本文引用的文献

1
Anomalous origin of the left coronary artery from the pulmonary artery in an adult.成人左冠状动脉起源于肺动脉异常。
N Engl J Med. 1959 Nov 12;261:993-8. doi: 10.1056/NEJM195911122612003.
2
Thallium-20 1 myocardial imaging in young adults with anomalous left coronary artery arising from the pulmonary artery.
J Nucl Med. 1980 Nov;21(11):1076-9.
3
Anomalous origin of the left coronary artery from the pulmonary artery (Bland-White-Garland syndrome) in adult patients: long-term follow-up after surgery.成人患者左冠状动脉起源于肺动脉(布兰德-怀特-加兰综合征):手术后的长期随访
Am Heart J. 1983 Aug;106(2):381-8. doi: 10.1016/0002-8703(83)90207-7.
4
Anomalous origin of the left coronary artery from the pulmonary trunk. Its clinical spectrum, pathology, and pathophysiology, based on a review of 140 cases with seven further cases.左冠状动脉起源于肺动脉干异常。基于对140例病例及另外7例病例的回顾,阐述其临床谱、病理及病理生理学。
Circulation. 1968 Aug;38(2):403-25. doi: 10.1161/01.cir.38.2.403.