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孤立性心室心肌致密化不全患儿的心肌缺血

Myocardial ischaemia in children with isolated ventricular non-compaction.

作者信息

Junga G, Kneifel S, Von Smekal A, Steinert H, Bauersfeld U

机构信息

Division of Cardiology, Children's University Hospital Zurich, Zurich, Switzerland.

出版信息

Eur Heart J. 1999 Jun;20(12):910-6. doi: 10.1053/euhj.1998.1398.

Abstract

AIMS

Isolated ventricular non-compaction is a rare congenital cardiomyopathy with a high morbidity and mortality due to malignant arrhythmias and pump failure. Areas affected by non-compaction are characterized by increased trabecularization and deep inter-trabecular spaces. We hypothesized perfusion defects in these areas and performed positron emission tomography to evaluate the myocardial perfusion in non-compacted areas.

METHODS AND RESULTS

Five children (age 10-14 years) with isolated ventricular non-compaction underwent positron emission tomography using N-13-ammonia as flow marker and intravenous dipyridamole for stress testing. Myocardial blood flow was quantified using the positron emission tomography time-activity curves in non-compacted areas and normal myocardium, which were diagnosed by echocardiography, magnetic resonance imaging, and angiography. Coronary angiography, performed in two children with extensive forms of left ventricular non-compaction, demonstrated normal coronary arteries. Myocardial blood flow measurements at rest and after dipyridamole application demonstrated 16-33% and 32-57% perfusion impairment, respectively, in non-compacted areas compared to normal myocardium. Areas of restricted myocardial perfusion corresponded well to the non-compacted areas, defined echographically and by magnetic resonance imaging.

CONCLUSION

Positron emission tomography demonstrates restricted myocardial perfusion and decreased flow reserve in areas of ventricular non-compaction in children. The myocardial perfusion defects in non-compacted areas may be the cause of myocardial damage and possibly form the basis of arrhythmias and pump failure.

摘要

目的

孤立性心室肌致密化不全是一种罕见的先天性心肌病,因恶性心律失常和泵衰竭导致高发病率和死亡率。受致密化不全影响的区域特征为小梁增多和小梁间间隙加深。我们推测这些区域存在灌注缺损,并进行正电子发射断层扫描以评估非致密化区域的心肌灌注情况。

方法与结果

5名(年龄10 - 14岁)孤立性心室肌致密化不全患儿接受了正电子发射断层扫描,使用N - 13 - 氨作为血流标记物,并静脉注射双嘧达莫进行负荷试验。利用正电子发射断层扫描时间 - 活性曲线对非致密化区域和正常心肌的心肌血流进行定量分析,这些区域通过超声心动图、磁共振成像和血管造影进行诊断。对两名患有广泛形式左心室致密化不全的患儿进行冠状动脉造影,结果显示冠状动脉正常。与正常心肌相比,静息状态和应用双嘧达莫后非致密化区域的心肌血流测量结果分别显示灌注受损16% - 33%和32% - 57%。心肌灌注受限区域与通过超声心动图和磁共振成像定义的非致密化区域高度吻合。

结论

正电子发射断层扫描显示儿童心室肌致密化不全区域心肌灌注受限且血流储备降低。非致密化区域的心肌灌注缺损可能是心肌损伤的原因,并且可能是心律失常和泵衰竭的基础。

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