早期诊断是成功治疗肺动脉高压的关键:晚期诊断2例(RCD代码:i1a .1)

Maryla Mianowana, Łukasz Siudak, P. Blaszczak
{"title":"早期诊断是成功治疗肺动脉高压的关键:晚期诊断2例(RCD代码:i1a .1)","authors":"Maryla Mianowana, Łukasz Siudak, P. Blaszczak","doi":"10.20418/JRCD.VOL4NO3.389","DOIUrl":null,"url":null,"abstract":"Pulmonary arterial hypertension is a rare disease of pulmonary circulation with poor prognosis if left untreated or diagnosed with delay. Active screening for the disease is not effective in the general population. However, in populations at increased risk for pulmonary arterial hypertension, all efforts should be taken to establish an early diagnosis. Here, we present 2 cases of late diagnosis. The first patient presented with a clear clinical picture, while the second case describes a patient in the at‐risk population who received treatment too late to obtain satisfactory results. We discuss the pitfalls which led to delayed diagnosis that finally resulted in treatment failure. JRCD 2019; 4 (3): 47-50.","PeriodicalId":37488,"journal":{"name":"Journal of Rare Cardiovascular Diseases","volume":"35 1","pages":"47-50"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Early diagnosis is crucial for successful treatment of pulmonary arterial hypertension: 2 cases of late diagnosis (RCD code: II 1A.1)\",\"authors\":\"Maryla Mianowana, Łukasz Siudak, P. Blaszczak\",\"doi\":\"10.20418/JRCD.VOL4NO3.389\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Pulmonary arterial hypertension is a rare disease of pulmonary circulation with poor prognosis if left untreated or diagnosed with delay. Active screening for the disease is not effective in the general population. However, in populations at increased risk for pulmonary arterial hypertension, all efforts should be taken to establish an early diagnosis. Here, we present 2 cases of late diagnosis. The first patient presented with a clear clinical picture, while the second case describes a patient in the at‐risk population who received treatment too late to obtain satisfactory results. We discuss the pitfalls which led to delayed diagnosis that finally resulted in treatment failure. JRCD 2019; 4 (3): 47-50.\",\"PeriodicalId\":37488,\"journal\":{\"name\":\"Journal of Rare Cardiovascular Diseases\",\"volume\":\"35 1\",\"pages\":\"47-50\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Rare Cardiovascular Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20418/JRCD.VOL4NO3.389\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Rare Cardiovascular Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20418/JRCD.VOL4NO3.389","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

肺动脉高压是一种罕见的肺循环疾病,如果不及时治疗或诊断迟缓,预后很差。这种疾病的主动筛查在一般人群中并不有效。然而,在肺动脉高压风险增加的人群中,应尽一切努力建立早期诊断。在此,我们报告2例晚期诊断。第一例患者的临床表现清晰,而第二例患者属于高危人群,因治疗太晚而未能获得满意的结果。我们讨论的陷阱,导致延误的诊断,最终导致治疗失败。JRCD 2019;4(3): 47-50。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Early diagnosis is crucial for successful treatment of pulmonary arterial hypertension: 2 cases of late diagnosis (RCD code: II 1A.1)
Pulmonary arterial hypertension is a rare disease of pulmonary circulation with poor prognosis if left untreated or diagnosed with delay. Active screening for the disease is not effective in the general population. However, in populations at increased risk for pulmonary arterial hypertension, all efforts should be taken to establish an early diagnosis. Here, we present 2 cases of late diagnosis. The first patient presented with a clear clinical picture, while the second case describes a patient in the at‐risk population who received treatment too late to obtain satisfactory results. We discuss the pitfalls which led to delayed diagnosis that finally resulted in treatment failure. JRCD 2019; 4 (3): 47-50.
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
Journal of Rare Cardiovascular Diseases
Journal of Rare Cardiovascular Diseases Medicine-Cardiology and Cardiovascular Medicine
自引率
0.00%
发文量
0
审稿时长
23 weeks
期刊介绍: Journal of Rare Cardiovascular Diseases (JRCD) is an international, quarterly issued, peer-reviewed, open access, online journal that keeps cardiologists and non-cardiologists up-to-date with rare disorders of the heart and vessels. The Journal publishes fine quality review articles, original, basic and clinical sciences research papers, either positive or negative, case reports and articles on public health issues in the field of rare cardiovascular diseases and orphan cardiovascular drugs. Topics of interest include, but are not limited to the following areas: (1) rare diseases of systemic circulation (2) rare diseases of pulmonary circulation (3) rare diseases of the heart (cardiomyopathies) (4) rare congenital cardiovascular diseases (5) rare arrhythmogenic disorders (6) cardiac tumors and cardiovascular diseases in malignancy (7) cardiovascular diseases in pregnancy (8) basic science (9) quality of life
期刊最新文献
Association of fibrinogen and D‑dimer levels with severity of acute coronary syndromes Journal of Rare Cardiovascular Diseases in EuroPub database An Extremely Rare Congenital Association: Uni- cuspid Aortic Valve with Left Ventricular Noncom- paction (RCD code: III-5A.1.o) Survival analysis of time to develop cardiovascular complications and its predictors among hypertensive patients treated in the Ayder Comprehensive Specialized Hospital, Ethiopia: a retrospective cohort study (RCD code: VIII) Autoimmune hepatitis induced by bosentan in a patient with pulmonary arterial hypertension (RCD code: II‐1A.1; VIII)
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1