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Arrhythmogenic Right Ventricular Cardiomyopathy in a 20-year-old Woman with Systemic Sclerosis

机译:一名20岁系统性硬化症妇女的心律失常性右室心肌病

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A 20-year-old Japanese woman with systemic sclerosis was evaluated for the progressive aggravation of chest pain, palpitations and dyspnea. Cardiac magnetic resonance imaging revealed diffuse wall thinning, segmental dyskinesis and late gadolinium enhancement of the right ventricular (RV) myocardium. Cardiac catheterization demonstrated no pulmonary hypertension. 24-hour electrocardiography monitoring showed non-sustained ventricular tachycardia (VT). Pulseless VT was induced via programmed ventricular stimulation. An endomyocardial biopsy of the right side of the interventricular septum was performed, the histological specimen of which demonstrated massive myocardial atrophy and fibro-fatty replacement with predominant fibrotic changes. The patient was ultimately diagnosed with arrhythmogenic RV cardiomyopathy.
机译:评估了一名20岁的系统性硬化症的日本女性的胸痛,心和呼吸困难的进行性加重。心脏磁共振成像显示右心室(RV)心肌弥漫性壁变薄,节段性运动障碍和晚期ado增强。心脏导管检查未显示肺动脉高压。 24小时心电图监测显示非持续性室性心动过速(VT)。通过程序性心室刺激诱发无脉性室速。进行了室间隔右侧的心肌内膜活检,其组织学标本显示大量心肌萎缩和纤维脂肪替代,并伴有明显的纤维化改变。该患者最终被诊断出患有心律失常性RV心肌病。

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