一例罕见的非缺血性扩张型心肌病表现为包涵体肌炎

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摘要

包涵体肌炎是50岁以后最常见的炎症性肌病。与多肌炎和皮肌炎不同,包涵体肌炎与扩张型心肌病等心脏病无关,而多肌炎和皮肌炎的心脏受累相对常见。我们报告一个57岁的2型糖尿病患者在治疗中,入院急性充血性心力衰竭的观察。临床旁检查显示为包涵体肌炎合并心衰和扩张型心肌病,在治疗心衰的同时给予皮质类固醇和免疫抑制剂大剂量治疗,这种态度改善了患者的症状和生活质量。本研究的目的是强调诊断和早期治疗合并心血管症状的肌炎的重要性,尤其是扩张型心肌病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Non-Ischemic Dilated Cardiomyopathy Revealing Inclusion Body Myositis
Inclusion body myositis is the most common inflammatory myopathy after age 50. Unlike polymyositis and dermatomyositis, in which cardiac involvement is relatively common, current evidence indicates that inclusion body myositis is not associated with cardiac disease such as dilated cardiomyopathy. We report the observation of a 57-year-old patient known to be type 2 diabetic under treatment, admitted with acute congestive heart failure. the paraclinical examinations carried out were in favor of inclusion body myositis complicated by heart failure and dilated cardiomyopathy, the patient was treated with boluses of corticosteroids and immunosuppressants as well as treatment of heart failure, this attitude has improved his symptoms as well as his quality of life. The interest of this work is to underline the importance of diagnosis and early treatment in the management of myositis complicated by cardiovascular manifestations, particularly dilated cardiomyopathy.
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