Suppr超能文献

[儿童心肌病]

[Cardiomyopathy in children].

作者信息

Malcić I, Barisić N

机构信息

Zavod za kardiologiju i reumatologiju, Klinika za djecje bolesti Rebro.

出版信息

Lijec Vjesn. 1992 May-Aug;114(5-8):161-5.

PMID:1343052
Abstract

Cardiomyopathies (CMP) are rare diseases in childhood. There are three different types (dilated, hypertrophic and restrictive). Exact epidemiologic drawing are not well-known, and the numerous nosologic problems still exist. The basic classification distinguishes primary (not well-knows cause) and secondary CMP (cardiac changes have been developed as any influence of the well-known diseases of the cardiovascular system). Dilated forms make 55%, hypertrophic 40% and restrictive only 5% of all CMP. The tendency of this paper is introduce the knowledge of new approaches to cardiomyopathies, the definition of which was taken at 1983. The mean consideration includes etiology and therapeutic approach of different types of CMP. The chapter on dilated CMP was mainly aimed to discuss their development after virus myocarditis, immunologic processes and complicated therapeutic treatment (different in acute, subacute and chronic phase). The purpose of this paper is to call the attention on the CMP in children, as the main problem in pediatric cardiology after congenital heart diseases.

摘要

心肌病(CMP)在儿童时期是罕见疾病。有三种不同类型(扩张型、肥厚型和限制型)。确切的流行病学情况尚不明确,众多疾病分类问题依然存在。基本分类区分原发性(病因不明)和继发性CMP(心脏变化是由已知心血管系统疾病的任何影响所导致)。在所有CMP中,扩张型占55%,肥厚型占40%,限制型仅占5%。本文的倾向是介绍心肌病新方法的知识,其定义于1983年确定。主要内容包括不同类型CMP的病因和治疗方法。关于扩张型CMP的章节主要旨在讨论其在病毒性心肌炎后的发展、免疫过程以及复杂的治疗(在急性期、亚急性期和慢性期有所不同)。本文的目的是引起对儿童CMP的关注,因为它是先天性心脏病之后儿科心脏病学中的主要问题。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验