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A case of mitochondrial cardiomyopathy with restrictive transmitral filling pattern

机译:线粒体心肌病伴有局限性充盈型的一例

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Abstract: A 61-year-old diabetic woman with a mitochondrial A3243G mutation was hospitalized for evaluation of breathlessness, general fatigue, and leg edema. Chest radiography revealed cardiomegaly with massive pleural effusion. Serum lactate, pyruvate, and brain natriuretic peptide concentrations were elevated. Transthoracic echocardiography revealed a restrictive pattern of transmitral flow, although systolic function of the left ventricle was only mildly impaired. Based on these findings and her clinical course, the patient was diagnosed with right-sided heart failure caused by mitochondrial cardiomyopathy associated with a restrictive transmitral filling pattern. Treatment with furosemide, enalapril, and eplerenone was effective, and improvement in her symptoms was associated with amelioration of transthoracic echocardiographic findings and a reduction in serum brain natriuretic peptide levels. Previous reports have indicated heterogeneity in the clinical features of mitochondrial cardiomyopathy in patients carrying the A3243G mutation; the present case highlights the substantial variability in the clinical features of this disease.
机译:摘要:一名患有线粒体A3243G突变的61岁糖尿病妇女因住院评估呼吸困难,总体疲劳和腿部水肿而入院。胸部X线摄片显示心脏肥大并伴有大量胸腔积液。血清乳酸,丙酮酸和脑钠肽浓度升高。经胸超声心动图检查显示出传输血流受限,尽管左心室的收缩功能仅受到轻度损害。根据这些发现和她的临床历程,该患者被诊断为由线粒体心肌病引起的右侧心力衰竭,并伴有限制性的传输性充盈。速尿,依那普利和依普利农的治疗有效,其症状改善与经胸超声心动图检查结果改善和血清脑钠肽水平降低有关。先前的报道表明,携带A3243G突变的患者线粒体心肌病的临床特征存在异质性。本病例强调了该疾病临床特征的实质性变异。

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