• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

多囊肾病中的自发性冠状动脉夹层。

Spontaneous coronary artery dissection in polycystic kidney disease.

机构信息

Department of General Medicine, Diakonessenhuis, Utrecht, The Netherlands.

Department of Cardiology, Diakonessenhuis, Utrecht, The Netherlands.

出版信息

Clin Kidney J. 2012 Feb;5(1):44-6. doi: 10.1093/ndtplus/sfr158. Epub 2012 Jan 28.

DOI:10.1093/ndtplus/sfr158
PMID:26069747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4400459/
Abstract

Little is known about the association between autosomal-dominant polycystic kidney disease (ADPKD) and coronary artery dissection (CAD). We suggest that the genetic disorder in ADPKD is the main cause of instable artery vasculature. Our case also shows that CAD can be missed in the acute phase. Therefore, we recommend additional investigation in patients with ADPKD presenting with acute chest pain. We report a case of a patient who developed a myocardial infarction due to a spontaneous dissection of the left anterior descending coronary artery. ADPKD was diagnosed during the additional investigation. The patient received medical management.

摘要

关于常染色体显性遗传性多囊肾病（ADPKD）与冠状动脉夹层（CAD）之间的关联知之甚少。我们认为，ADPKD 的遗传疾病是动脉血管不稳定的主要原因。我们的病例还表明，CAD 在急性期可能会被漏诊。因此，我们建议对出现急性胸痛的 ADPKD 患者进行额外的检查。我们报告了一例因左前降支冠状动脉自发性夹层导致心肌梗死的患者。在进一步检查中诊断出 ADPKD。患者接受了药物治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee2/4400459/f8a3ab94f416/ndtplussfr158f02_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee2/4400459/a50b9f410d3c/ndtplussfr158f01_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee2/4400459/f8a3ab94f416/ndtplussfr158f02_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee2/4400459/a50b9f410d3c/ndtplussfr158f01_ht.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee2/4400459/f8a3ab94f416/ndtplussfr158f02_ht.jpg

相似文献

1
Spontaneous coronary artery dissection in polycystic kidney disease.多囊肾病中的自发性冠状动脉夹层。
Clin Kidney J. 2012 Feb;5(1):44-6. doi: 10.1093/ndtplus/sfr158. Epub 2012 Jan 28.
2
Spontaneous coronary artery dissection: One more extrarenal manifestation of autosomal dominant polycystic kidney disease?自发性冠状动脉夹层：常染色体显性遗传性多囊肾病的又一种肾外表现？
J Nephrol. 2009 May-Jun;22(3):414-6.
3
Spontaneous coronary artery dissection in a woman with polycystic kidney disease.一名患有多囊肾病的女性发生自发性冠状动脉夹层。
Am J Kidney Dis. 2009 Mar;53(3):518-21. doi: 10.1053/j.ajkd.2008.08.027. Epub 2008 Nov 6.
4
Spontaneous coronary dissection should not be ignored in patients with chest pain in autosomal dominant polycystic kidney disease: A case report.常染色体显性多囊肾病患者胸痛时不应忽视自发性冠状动脉夹层：一例报告
World J Clin Cases. 2021 May 6;9(13):3095-3101. doi: 10.12998/wjcc.v9.i13.3095.
5
Spontaneous coronary artery dissection in a patient with hereditary polycystic kidney disease and a recent liver transplant: a case report.一名患有遗传性多囊肾病且近期接受肝移植患者的自发性冠状动脉夹层：病例报告
Eur Heart J Case Rep. 2019 Dec;3(4):1-5. doi: 10.1093/ehjcr/ytz216. Epub 2019 Dec 13.
6
Spontaneous coronary artery dissection in a patient with autosomal dominant polycystic kidney disease: a case report.常染色体显性多囊肾病患者的自发性冠状动脉夹层：一例报告
J Med Case Rep. 2016 Mar 10;10:62. doi: 10.1186/s13256-016-0832-8.
7
Autosomal dominant polycystic kidney disease and coronary artery dissection or aneurysm: a systematic review.常染色体显性多囊肾病与冠状动脉夹层或动脉瘤：一项系统综述
Ren Fail. 2016;38(4):493-502. doi: 10.3109/0886022X.2016.1144209. Epub 2016 Feb 18.
8
A Spontaneous Extracranial Internal Carotid Artery Dissection with Autosomal Dominant Polycystic Kidney Disease: A Case Report and Literature Review.常染色体显性多囊肾病并发自发性颅外颈内动脉夹层：病例报告及文献复习。
Medicina (Kaunas). 2022 May 20;58(5):679. doi: 10.3390/medicina58050679.
9
Spontaneous Coronary Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease: A Systematic Review of the Literature.常染色体显性多囊肾病患者的自发性冠状动脉夹层：文献系统综述
J Pers Med. 2024 Jun 29;14(7):702. doi: 10.3390/jpm14070702.
10
Computed tomography angiographic demonstration of an unexpected left main coronary artery dissection in a patient with polycystic kidney disease.计算机断层血管造影显示多囊肾病患者左主干冠状动脉意外夹层。
J Thorac Imaging. 2011 Feb;26(1):W4-6. doi: 10.1097/RTI.0b013e3181dc2a53.

引用本文的文献

1
Genetics architecture of spontaneous coronary artery dissection in an Italian cohort.意大利队列中自发性冠状动脉夹层的遗传结构
Front Cardiovasc Med. 2024 Nov 25;11:1486273. doi: 10.3389/fcvm.2024.1486273. eCollection 2024.
2
Spontaneous Coronary Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease: A Systematic Review of the Literature.常染色体显性多囊肾病患者的自发性冠状动脉夹层：文献系统综述
J Pers Med. 2024 Jun 29;14(7):702. doi: 10.3390/jpm14070702.
3
Cardiovascular disease in women: A review of spontaneous coronary artery dissection.

本文引用的文献

1
Computed tomography angiographic demonstration of an unexpected left main coronary artery dissection in a patient with polycystic kidney disease.计算机断层血管造影显示多囊肾病患者左主干冠状动脉意外夹层。
J Thorac Imaging. 2011 Feb;26(1):W4-6. doi: 10.1097/RTI.0b013e3181dc2a53.
2
Polycystins and renovascular mechanosensory transduction.多囊蛋白和肾血管机械感觉转导。
Nat Rev Nephrol. 2010 Sep;6(9):530-8. doi: 10.1038/nrneph.2010.97. Epub 2010 Jul 13.
3
Spontaneous coronary artery dissection: a Western Denmark Heart Registry study.
女性心血管疾病：自发性冠状动脉夹层综述。
Medicine (Baltimore). 2022 Sep 23;101(38):e30433. doi: 10.1097/MD.0000000000030433.
4
Spontaneous coronary dissection should not be ignored in patients with chest pain in autosomal dominant polycystic kidney disease: A case report.常染色体显性多囊肾病患者胸痛时不应忽视自发性冠状动脉夹层：一例报告
World J Clin Cases. 2021 May 6;9(13):3095-3101. doi: 10.12998/wjcc.v9.i13.3095.
5
Spontaneous Coronary Artery Dissection: Insights on Rare Genetic Variation From Genome Sequencing.自发性冠状动脉夹层：全基因组测序揭示罕见遗传变异。
Circ Genom Precis Med. 2020 Dec;13(6):e003030. doi: 10.1161/CIRCGEN.120.003030. Epub 2020 Oct 30.
6
European Society of Cardiology, acute cardiovascular care association, SCAD study group: a position paper on spontaneous coronary artery dissection.欧洲心脏病学会、急性心血管护理协会、自发性冠状动脉夹层研究组：关于自发性冠状动脉夹层的立场文件。
Eur Heart J. 2018 Sep 21;39(36):3353-3368. doi: 10.1093/eurheartj/ehy080.
7
Spontaneous Coronary Artery Dissection: Current State of the Science: A Scientific Statement From the American Heart Association.自发性冠状动脉夹层：科学现状：美国心脏协会的科学声明。
Circulation. 2018 May 8;137(19):e523-e557. doi: 10.1161/CIR.0000000000000564. Epub 2018 Feb 22.
8
Spontaneous coronary artery dissection in a patient with autosomal dominant polycystic kidney disease: a case report.常染色体显性多囊肾病患者的自发性冠状动脉夹层：一例报告
J Med Case Rep. 2016 Mar 10;10:62. doi: 10.1186/s13256-016-0832-8.
自发性冠状动脉夹层：一项丹麦西部心脏注册研究。
Catheter Cardiovasc Interv. 2009 Nov 1;74(5):710-7. doi: 10.1002/ccd.22115.
4
Cardiovascular abnormalities in autosomal-dominant polycystic kidney disease.常染色体显性多囊肾病中的心血管异常
Nat Rev Nephrol. 2009 Apr;5(4):221-8. doi: 10.1038/nrneph.2009.13.
5
Analysis of the polycystins in aortic vascular smooth muscle cells.主动脉血管平滑肌细胞中多囊蛋白的分析。
J Am Soc Nephrol. 2003 Sep;14(9):2280-7. doi: 10.1097/01.asn.0000080185.38113.a3.
6
Pkd2 haploinsufficiency alters intracellular calcium regulation in vascular smooth muscle cells.多囊蛋白2单倍体不足改变血管平滑肌细胞内的钙调节。
Hum Mol Genet. 2003 Aug 1;12(15):1875-80. doi: 10.1093/hmg/ddg190.
7
Ventricular septal rupture caused by myocardial bridging.心肌桥导致的室间隔破裂
Ann Thorac Surg. 2001 Oct;72(4):1369-70. doi: 10.1016/s0003-4975(01)02562-0.
8
Survival after end-stage renal disease in autosomal dominant polycystic kidney disease: contribution of extrarenal complications to mortality.常染色体显性多囊肾病终末期肾病后的生存情况：肾外并发症对死亡率的影响
Am J Kidney Dis. 2001 Oct;38(4):777-84. doi: 10.1053/ajkd.2001.27720.
9
Vascular expression of polycystin.多囊蛋白的血管表达。
J Am Soc Nephrol. 1997 Apr;8(4):616-26. doi: 10.1681/ASN.V84616.
10
Autosomal dominant polycystic kidney disease.常染色体显性多囊肾病
N Engl J Med. 1993 Jul 29;329(5):332-42. doi: 10.1056/NEJM199307293290508.