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一名曾被诊断为扩张型心肌病的患者出现应激性心肌病的基底壁过度收缩:病例报告

Basal wall hypercontraction of Takotsubo cardiomyopathy in a patient who had been diagnosed with dilated cardiomyopathy: a case report.

作者信息

Ichihara Noboru, Fujita Shuichi, Kanzaki Yumiko, Fujisaka Tomohiro, Ozeki Michishige, Ishizaka Nobukazu

机构信息

Department of Cardiology, Osaka Medical College, Takatsuki-shi Daigaku-machi 2-7, Osaka, 569-8686, Japan.

出版信息

BMC Cardiovasc Disord. 2017 Dec 12;17(1):293. doi: 10.1186/s12872-017-0730-z.

Abstract

BACKGROUND

Takotsubo cardiomyopathy is characterized by the basal hypercontractility and apical ballooning of the left ventriculum and T-wave inversion in the electrocardiogram. It has been suggested that Takotsubo cardiomyopathy might underlie the pathogenesis of persistent cardiac dysfunction; however, few reports are present demonstrating the advent of Takotsubo cardiomyopathy in patients with idiopathic cardiomyopathy.

CASE PRESENTATION

A 64-year-old women was admitted due to dyspnea on effort and lower extremity edema. She had been diagnosed with idiopathic dilated cardiomyopathy 2.5 years before owing to the reduced left ventricular ejection fraction (24%), normal coronary artery, and interstitial fibrosis of the myocardial samples. On admission, her electrocardiogram showed giant negative T wave in II, III, aVF, and precordial leads. Echocardiography showed dyskinesis of the left ventricular apex and hypercontraction of the basal wall, which had not been observed in the previous examinations. Coronary angiography showed normal coronary arteries, and apical ballooning and basal hypercontractility was confirmed by left ventriculography. On day 15 of admission, contraction of apical wall was recovered, and basal hypercontraction was disappeared.

CONCLUSION

The present case is the first report demonstrating appearance the transient basal wall hypercontraction along with the advent of Takotsubo cardiomyopathy in a patient diagnosed with dilated cardiomyopathy. Whether such findings are indicative of fair prognosis and have the utility of understanding the pathogenesis of dilated cardiomyopathy needs further investigation.

摘要

背景

应激性心肌病的特征为左心室基底段收缩功能亢进、心尖部气球样变以及心电图T波倒置。有人提出应激性心肌病可能是持续性心脏功能障碍发病机制的基础;然而,很少有报告表明特发性心肌病患者会出现应激性心肌病。

病例报告

一名64岁女性因劳力性呼吸困难和下肢水肿入院。2.5年前,她因左心室射血分数降低(24%)、冠状动脉正常以及心肌样本间质纤维化被诊断为特发性扩张型心肌病。入院时,她的心电图显示II、III、aVF导联及胸前导联出现巨大负向T波。超声心动图显示左心室心尖部运动障碍和基底段心肌过度收缩,这在之前的检查中未被观察到。冠状动脉造影显示冠状动脉正常,左心室造影证实有心尖部气球样变和基底段心肌过度收缩。入院第15天,心尖部心肌收缩恢复,基底段心肌过度收缩消失。

结论

本病例是首例报告,显示在一名诊断为扩张型心肌病的患者中出现了应激性心肌病,伴有短暂的基底段心肌过度收缩。这些发现是否预示良好预后以及对理解扩张型心肌病的发病机制是否有用,尚需进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/241b/5728071/8d95dbc43b65/12872_2017_730_Fig1_HTML.jpg

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