肺动脉干扩张导致左冠状动脉主干外源性受压,导致缺血症状

R. Bhoil, S. Sood, Sabina Bhoil, Anshul Chamail, R. Sood
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引用次数: 4

摘要

左冠状动脉压迫综合征是一种罕见的疾病,其特征是主动脉和肺动脉主干之间的左中动脉压迫。它通常与先天性心脏缺陷有关。心脏64层MDCT提供了一种无创和准确的方法来评估整个心脏周期内LMCA的动态压迫程度,其相对于左Valsalva窦的角度和肺部病理描述,使其成为怀疑左冠状动脉压迫患者的有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extrinsic compression of left main coronary artery due to dilated pulmonary trunk resulting in ischaemic symptoms
Left coronary artery compression syndrome is an uncommon entity and characterized by compression of the LMCA in-between the aorta and an enlarged main pulmonary arterial trunk. It is usually associated with a congenital cardiac defect. Cardiac 64-slice MDCT provides a non-invasive and an accurate method for assessing the degree of dynamic LMCA compression throughout the cardiac cycle, its angulation relative to the left sinus of Valsalva and depiction of pulmonary pathology, making it a valuable tool in the workup of patients suspected of left coronary artery compression.
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