左心室不压实的不同临床表现:附3例报告

M. Bolognesi, D. Bolognesi
{"title":"左心室不压实的不同临床表现:附3例报告","authors":"M. Bolognesi, D. Bolognesi","doi":"10.13172/2052-0077-2-5-629","DOIUrl":null,"url":null,"abstract":"Abstract Introduction Left ventricular non-compaction is a morphological abnormality of exces-sive trabeculation of the left ventricle, and often, but not always, complicated by cardioembolism, arrhythmias and ventricular dysfunction. Since its irst mention in the 1980s, left ventricular non-compaction cardiomyopathy has gained increasing awareness and atten-tion. Thirty or more years of research and an ever-increasing number of published articles have improved our understanding of this rare cardiomyo-pathy, yet many issues remain unre-solved. In particular, the phenotypic and clinical expression of the same genetic cardiomyopathy assumes dif-ferent forms depending on the type of subjects involved. These case reports describe the different clinical evolu-tions of the same cardiomyopathy inde-pendently of the anatomical substrate and illustrate two aspects of the same disease in different types of patients. Case report Isolated left ventricular non-com-paction cardiomyopathy has been observed both as a sporadic and a familiar form, but newly diagnosed patients have been stratiied for symp-toms found at the time of diagnosis.","PeriodicalId":19393,"journal":{"name":"OA Case Reports","volume":"10 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2013-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The different clinical scenarios of left ventricular non-compaction: report of three cases\",\"authors\":\"M. Bolognesi, D. Bolognesi\",\"doi\":\"10.13172/2052-0077-2-5-629\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Introduction Left ventricular non-compaction is a morphological abnormality of exces-sive trabeculation of the left ventricle, and often, but not always, complicated by cardioembolism, arrhythmias and ventricular dysfunction. Since its irst mention in the 1980s, left ventricular non-compaction cardiomyopathy has gained increasing awareness and atten-tion. Thirty or more years of research and an ever-increasing number of published articles have improved our understanding of this rare cardiomyo-pathy, yet many issues remain unre-solved. In particular, the phenotypic and clinical expression of the same genetic cardiomyopathy assumes dif-ferent forms depending on the type of subjects involved. These case reports describe the different clinical evolu-tions of the same cardiomyopathy inde-pendently of the anatomical substrate and illustrate two aspects of the same disease in different types of patients. Case report Isolated left ventricular non-com-paction cardiomyopathy has been observed both as a sporadic and a familiar form, but newly diagnosed patients have been stratiied for symp-toms found at the time of diagnosis.\",\"PeriodicalId\":19393,\"journal\":{\"name\":\"OA Case Reports\",\"volume\":\"10 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"OA Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.13172/2052-0077-2-5-629\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"OA Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.13172/2052-0077-2-5-629","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

左室不压实是左室过度小梁的形态学异常,通常但并非总是合并心栓塞、心律失常和心室功能障碍。自20世纪80年代首次被提及以来,左室非压实性心肌病越来越受到人们的关注和重视。三十多年的研究和越来越多的发表文章提高了我们对这种罕见心肌病的理解,但许多问题仍未解决。特别是,相同的遗传性心肌病的表型和临床表现根据所涉及的受试者类型而呈现不同的形式。这些病例报告描述了同一种心肌病独立于解剖学基础的不同临床演变,并说明了不同类型患者同一种疾病的两个方面。孤立性左室非紧张性心肌病是一种散发性和常见的形式,但新诊断的患者已根据诊断时发现的症状进行分层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The different clinical scenarios of left ventricular non-compaction: report of three cases
Abstract Introduction Left ventricular non-compaction is a morphological abnormality of exces-sive trabeculation of the left ventricle, and often, but not always, complicated by cardioembolism, arrhythmias and ventricular dysfunction. Since its irst mention in the 1980s, left ventricular non-compaction cardiomyopathy has gained increasing awareness and atten-tion. Thirty or more years of research and an ever-increasing number of published articles have improved our understanding of this rare cardiomyo-pathy, yet many issues remain unre-solved. In particular, the phenotypic and clinical expression of the same genetic cardiomyopathy assumes dif-ferent forms depending on the type of subjects involved. These case reports describe the different clinical evolu-tions of the same cardiomyopathy inde-pendently of the anatomical substrate and illustrate two aspects of the same disease in different types of patients. Case report Isolated left ventricular non-com-paction cardiomyopathy has been observed both as a sporadic and a familiar form, but newly diagnosed patients have been stratiied for symp-toms found at the time of diagnosis.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信