Primary hypothyroidism: uncommon presentation with reversible dilated cardiomyopathy in a young subject

authors:

avatar Siva Kota , avatar Sruti Jammula , avatar Lalit Meher , avatar Kirtikumar Modi , avatar Sunil Kota , *


How To Cite? Kota S, Jammula S, Meher L, Modi K, Kota S. Primary hypothyroidism: uncommon presentation with reversible dilated cardiomyopathy in a young subject. Int J Endocrinol Metab. 2012;10(1): 440-443. https://doi.org/10.5812/ijem.2382.

Abstract

 
Most patients with dilated cardiomyopathy have a poor prognosis that is associated with progressive and irreversible myocardial dysfunction. Rarely, a reversible metabolic etiology that is amenable to specific therapy is identified. Thyroid hormones have many effects on the heart. Although cardiac output is reduced in hypothyroidism, heart failure is relatively rare due to the lower demand for peripheral oxygen delivery. We report a 14-year-old girl who presented with dilated cardiomyopathy (DCM) and was determined to have primary hypothyroidism, for whom cardiac function improved significantly after levothyroxine replacement therapy. Our case underscores the necessity of thyroid function testing to examine the etiology of nonischemic DCM, even in young subjects.
Please cite this paper as:
Kumar Kota S, Tripathy PR, Krishna Kota S, Jammula S, Kumar Meher L, Modi KD, Primary Hypothyroidism: Uncommon Presentation With Reversible Dilated Cardiomyopathy in a Young Subject. Int J Endocrinol Metab. 2012;10(1): 440-3. DOI: 10.5812/ijem.2382
                                                                      Copyright © 2012 Kowsar M. P. Co. All rights reserved.
 

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