Alteraciones adquiridas de la coagulación

A.C. Leal Ferrero, A. Mendoza Martínez, C.I. Morellón Peña, V. Jiménez Yuste
{"title":"Alteraciones adquiridas de la coagulación","authors":"A.C. Leal Ferrero,&nbsp;A. Mendoza Martínez,&nbsp;C.I. Morellón Peña,&nbsp;V. Jiménez Yuste","doi":"10.1016/j.med.2024.11.012","DOIUrl":null,"url":null,"abstract":"<div><div>Acquired coagulation disorders are those that occur alongside and develop as a part of hematological, neoplastic, autoimmune, cardiovascular, or hepatic diseases; though they can also originate spontaneously. They usually manifest as a deficit of a coagulation factor or as global hemostasis impairment. Given its variable pathophysiology, the clinical phenotype ranges from mild hemorrhagic symptoms to potentially lethal hemorrhagic manifestations. In most situations, treatment involves addressing the underlying medical condition and includes supportive care to prevent or treat hemorrhagic manifestations.</div></div>","PeriodicalId":100912,"journal":{"name":"Medicine - Programa de Formación Médica Continuada Acreditado","volume":"14 22","pages":"Pages 1299-1308"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine - Programa de Formación Médica Continuada Acreditado","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0304541224002981","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Acquired coagulation disorders are those that occur alongside and develop as a part of hematological, neoplastic, autoimmune, cardiovascular, or hepatic diseases; though they can also originate spontaneously. They usually manifest as a deficit of a coagulation factor or as global hemostasis impairment. Given its variable pathophysiology, the clinical phenotype ranges from mild hemorrhagic symptoms to potentially lethal hemorrhagic manifestations. In most situations, treatment involves addressing the underlying medical condition and includes supportive care to prevent or treat hemorrhagic manifestations.
获得性凝血改变
获得性凝血障碍是与血液、肿瘤、自身免疫、心血管或肝脏疾病同时发生和发展的疾病;尽管它们也可以自发产生。它们通常表现为凝血因子缺陷或全身性止血障碍。鉴于其可变的病理生理,临床表型范围从轻微的出血症状到潜在的致命出血表现。在大多数情况下,治疗包括解决潜在的医疗状况,包括支持性护理,以预防或治疗出血表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
0.30
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