二尖瓣脱垂合并心肌功能障碍和家族性肥厚性心肌病1例。

Journal of cardiography Pub Date : 1986-03-01
T Kumaki, Y Yokota, K Okamoto, A Takarada, T Seo, N Maehashi, S Toyama, H Fukuzaki
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摘要

这是一个报告的患者二尖瓣脱垂(MVP)和心肌内膜活检的心肌异常,其亲属是肥厚性心肌病(HCM)。一名19岁女子因心脏杂音入院。左胸骨边界第三肋间隙可听到收缩期射血杂音,标准12导联心电图显示II、III和aVF导联ST-T波改变。超声心动图显示二尖瓣前小叶脱垂,但未见左室肥厚。心内膜活检显示心肌轻度肥大和紊乱。家庭研究显示,她的母亲没有高血压病史,但鼻中隔肥厚不对称。她的妹妹在超声心动图上有轻微的室间隔肥大,她的组织病理学结果提示HCM的诊断。该病例在临床上被认为是MVP,但如其母亲所见的左心室肥厚可能在未来发生。
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[Mitral valve prolapse with myocardial disarrangement and familial hypertrophic cardiomyopathy: a case report].

This is a report of a patient with mitral valve prolapse (MVP) and myocardial abnormalities on endomyocardial biopsy in whose relatives hypertrophic cardiomyopathy (HCM) was identified. A 19-year-old woman was admitted to our hospital for evaluation of a heart murmur. A systolic ejection murmur was audible in the third intercostal space at the left sternal border, and a standard 12-lead electrocardiogram showed ST-T wave changes in leads II, III and aVF. Echocardiography revealed prolapse of the anterior leaflet of the mitral valve, but no left ventricular hypertrophy. Endomyocardial biopsy disclosed mild hypertrophy and disarrangement of the myocardium. The family study revealed asymmetrical septal hypertrophy in her mother, who had no history of hypertension. Her younger sister had mild hypertrophy of the interventricular septum on echocardiography, and her histopathological findings suggested a diagnosis of HCM. This case was clinically regarded as MVP, but development of left ventricular hypertrophy as noted in her mother may occur in the future.

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