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A case of mitochondrial cardiomyopathy with restrictive transmitral filling pattern.

作者信息

Otsui Kazunori, Inoue Nobutaka, Tamagawa Anna, Onishi Kazuo

机构信息

Department of Cardiovascular Medicine, Kobe Rosai Hospital, Kobe, Japan.

出版信息

Int Med Case Rep J. 2012 Apr 13;5:19-22. doi: 10.2147/IMCRJ.S30336. Print 2012.

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.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab5/3658249/ba09c330e2c0/imcrj-5-019Fig1.jpg

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本文引用的文献

1
Multisystem manifestations of mitochondrial disorders.
J Neurol. 2009 May;256(5):693-710. doi: 10.1007/s00415-009-5028-3. Epub 2009 Mar 1.
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Rapid progression of cardiomyopathy in mitochondrial diabetes.
Jpn Circ J. 1999 Feb;63(2):130-2. doi: 10.1253/jcj.63.130.

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