Myocardial steatosis: An autopsy-discovered case

A. Ouédraogo, W. N. Ramdé, F. Ido, I. Savadogo, R. A. Ouédraogo, S. Ouattara, Aïda S Ouedraogo, Wyc Nikiema
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Abstract

Introduction: Myocardial steatosis, a poorly documented pathology, is characterized by the accumulation of abnormal amounts of triglycerides in the cardiomyocytes. Myocardial steatosis is generally asymptomatic, but it can be the cause of heart failure. It is primarily of hypoxic or metabolic origin. Case Report: We report a case of postmortem diagnosis in a 53-year-old male patient, without known his pathological history, who was a victim of sudden death from abdominal pain. The autopsy revealed diffuse atheromatous cardiac, aortic, and hepatic lesions. Conclusion: It is very common for myocardial steatosis to be diagnosed postmortem due to its nonspecific symptomatology. The risk of mortality and morbidity could be reduced through a healthy lifestyle and regular biological examination to identify risk factors.
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心肌脂肪变性:尸检发现一例
简介:心肌脂肪变性是一种文献很少的病理,其特征是心肌细胞中甘油三酯的异常积累。心肌脂肪变性通常是无症状的,但它可能是心力衰竭的原因。主要是缺氧或代谢所致。病例报告:我们报告一例53岁男性患者尸检诊断,不知道他的病理病史,谁是受害者猝死腹痛。尸检显示弥漫性心脏动脉粥样硬化,主动脉和肝脏病变。结论:心肌脂肪变性因其非特异性症状,尸检诊断非常常见。通过健康的生活方式和定期进行生物检查以确定危险因素,可以降低死亡和发病的风险。
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