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心肌病与心源性猝死的最新进展

Update on cardiomyopathies and sudden cardiac death.

作者信息

Rizzo Stefania, Carturan Elisa, De Gaspari Monica, Pilichou Kalliopi, Thiene Gaetano, Basso Cristina

机构信息

Cardiovascular Pathology, Department of Cardio-Thoracic-Vascular Sciences & Public Health and Azienda Ospedaliera, University of Padua Medical School, Padua, Italy.

出版信息

Forensic Sci Res. 2019 Aug 19;4(3):202-210. doi: 10.1080/20961790.2019.1631957. eCollection 2019.

Abstract

Sudden cardiac death (SCD) remains a leading mode of death in western countries. Since SCD can be the first and last clinical presentation of the underlying disease, autopsy could be the only medical examination available for early diagnosis and it should be performed according to the guidelines of the Association for European Cardiovascular Pathology. Although the vast majority of SCD are due to coronary artery disease, non-ischemic causes of SCD do exist and are prevalent in young people with structural (i.e. arrhythmogenic, hypertrophic and inflammatory cardiomyopathy) and non-structural (ion channel diseases) cardiomyopathies, accounting for up to one half of cases. A standardized autopsy protocol, in combination with blood sampling to ensure feasibility of postmortem molecular testing if needed, is mandatory. The pathologist is called to provide the correct diagnosis and to advice the relatives on the need of a cascade clinical and genetic screening in the presence of a heredo-familial disease.

摘要

心脏性猝死(SCD)仍是西方国家主要的死亡方式。由于SCD可能是潜在疾病的首发及唯一临床表现,尸检可能是早期诊断的唯一医学检查手段,应按照欧洲心血管病理学会的指南进行。虽然绝大多数SCD是由冠状动脉疾病引起的,但SCD的非缺血性病因确实存在,并且在患有结构性(即致心律失常性、肥厚性和炎性心肌病)和非结构性(离子通道疾病)心肌病的年轻人中很常见,占病例的一半。标准化的尸检方案,结合血样采集以确保必要时进行死后分子检测的可行性,是必不可少的。病理学家需要做出正确诊断,并在存在遗传家族性疾病时,就进行一系列临床和基因筛查的必要性向亲属提供建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7e9/6713087/d95812d4dcea/TFSR_A_1631957_F0001_C.jpg

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