青少年限制性心肌病罕见病例

Archit Dahiya , Deepesh Agarwal , Naveen Gupta , Harsh Wardhan , Jai Chowdhary
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摘要

限制性心肌病(RCM)是一种罕见的心肌病,其特征是由于心肌硬度增加而导致心室充盈受损。在印度,RCM常见于年轻人,地方性心内膜纤维化见于相当数量的病例。我们报告一个15岁的男孩谁提出了这样一个可治疗的原因心力衰竭。在二维超声心动图上,我们观察到限制性心肌病(RCM)和严重的二尖瓣和三尖瓣反流的迹象。RCM是一种罕见的心肌病,通常与预后不良有关。基因检查显示髓系肿瘤伴嗜酸性粒细胞增多。嗜酸性心肌病是一种罕见的报告实体。
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Unusual case of restrictive cardiomyopathy in young

Restrictive cardiomyopathy (RCM) is an uncommon form of cardiomyopathy and is characterized by impaired ventricular filling due to increased myocardial stiffness. In India, RCM is frequently observed in the young and endemic endomyocardial fibrosis is seen in a significant number of cases. We report a case of 15-year-old boy who presented with such a treatable cause of heart failure. On 2D Echocardiography we observed signs of restrictive cardiomyopathy (RCM) and severe mitral and tricuspid regurgitation. RCM is an uncommon form of cardiomyopathy and is usually associated with a poor prognosis. Genetic workup revealed myeloid neoplasm with eosinophilia. Eosinophilic cardiomyopathy is an infrequently reported entity.

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