Endomyocardial fibrosis related sudden cardiac death; two autopsied case-reports from Egypt

心肌纤维化 医学 尸检 心源性猝死 死因 病因学 猝死 心室 限制性心肌病 心内膜 纤维化 心肌病 心脏病学 疾病 内科学 病理 心力衰竭
作者
Nora Fawzy Fnon,Hanan Hosny Hassan,Shaimaa A. Shehata,Khadiga M. Abdelrahman,Mahrous A. Ibrahim
出处
期刊:Legal Medicine [Elsevier]
卷期号:62: 102221-102221
标识
DOI:10.1016/j.legalmed.2023.102221
摘要

Endomyocardial fibrosis (EMF) is an idiopathic tropical disorder that is characterized by the development of restrictive cardiomyopathy. Neglected EMF can cause sudden cardiac death (SCD) in adults. Conclusive diagnosis of EMF depends on autopsy after death. In an effort to attract the interest of the community for this rare disease, we report two cases of SCD that were diagnosed as EMF during autopsy in Egypt. Both cases were thoroughly investigated with emphasis on death circumstances and post-mortem anatomical and histopathological findings. The two cases were for adult males presented with SCD following a quarrel with a negative medical history and family history regarding cardiac diseases. No trauma or drug abuse. The autopsy revealed hypertrophied hearts, thick fibrosed endocardium, patchy myocardial fibrosis, and filling of the apex by fibrosis and calcifications. In one of them, there was a huge mural thrombus reaching the level of the mitral valve that totally occluded the cavity of the left ventricle. Histopathologically, fibrosis was confirmed, and no eosinophils were detected. In contrast to previously reported cases in Egypt, the left ventricle was solely affected. Despite the rarity of the disease outside the tropics, the frequency of EMF cases is more likely to be more than the number of reported cases. EMF should be considered as possible cause of SCD during autopsy. Further studies are needed to clarify the etiology and epidemiology of EMF.

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