Suppr超能文献

以复发性脑血管意外为表现的前激肽释放酶缺乏症:病例报告及文献复习

Prekallikrein deficiency presenting as recurrent cerebrovascular accident: case report and review of the literature.

作者信息

Bojanini Esteban Uribe, Loaiza-Bonilla Arturo, Pimentel Agustin

机构信息

Division of Hematology and Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, 1475 NW 12th Ave Suite 3300, Miami, FL 33136, USA.

出版信息

Case Rep Hematol. 2012;2012:723204. doi: 10.1155/2012/723204. Epub 2012 Aug 16.

Abstract

We report the case of a woman with history of hypertension and hyperlipidemia presenting with recurrent episodes consistent clinically with cerebrovascular accidents (CVA), and MRI changes suggestive of ischemia versus vasculitis as their cause. No anatomical neurological, rheumatic, cardioembolic, or arteriosclerotic etiologies could be determined by extensive workup. Incidentally, the patient was found to have prolonged activated Partial Thromboplastin Time (aPTT) and a normal Prothrombin Time (PT); further testing revealed a prekallikrein deficiency. Since no other cause for the CVAs was established, and other prothrombotic states were ruled out, it is proposed that they are clinical manifestations derived from the prekallikrein deficiency, which in a patient with known cardiovascular risk factors could lead to thrombotic complications such as stroke.

摘要

我们报告了一名有高血压和高脂血症病史的女性病例,其反复出现临床上与脑血管意外(CVA)相符的发作,且MRI表现提示缺血或血管炎为病因。通过广泛检查未发现解剖学上的神经、风湿、心源性栓塞或动脉硬化病因。偶然发现该患者活化部分凝血活酶时间(aPTT)延长而凝血酶原时间(PT)正常;进一步检查显示前激肽释放酶缺乏。由于未确定CVA的其他病因,且排除了其他血栓前状态,因此推测这些发作是前激肽释放酶缺乏导致的临床表现,在已知有心血管危险因素的患者中可能导致血栓形成并发症,如中风。

相似文献

4
Prekallikrein deficiency.前激肽释放酶缺乏症
J Pediatr Oncol Nurs. 2013 Jul-Aug;30(4):198-204. doi: 10.1177/1043454213487436. Epub 2013 Apr 29.
6
Prekallikrein deficiency in a dog.一只狗的前激肽释放酶缺乏症。
J Vet Med Sci. 2011 Jan;73(1):107-11. doi: 10.1292/jvms.10-0207. Epub 2010 Aug 23.
9
[An elderly case of congenital prekallikrein deficiency].[一例先天性前激肽释放酶缺乏症老年病例]
Nihon Ronen Igakkai Zasshi. 2009 Jul;46(4):348-51. doi: 10.3143/geriatrics.46.348.

引用本文的文献

本文引用的文献

1
Severe prekallikrein deficiency due to a homozygous Trp499Stop nonsense mutation.
Blood Coagul Fibrinolysis. 2011 Jun;22(4):337-9. doi: 10.1097/MBC.0b013e3283444ddb.
2
Congenital prekallikrein deficiency.先天性激肽原缺乏症。
Expert Rev Hematol. 2010 Dec;3(6):685-95. doi: 10.1586/ehm.10.69.

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