Friend or Foe: Factor XII Deficiency Discovered Incidentally during Management of NSTEMI.

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2023-01-01 DOI:10.1155/2023/5926340
Patrick J Beck, John Benfield, Joshua Morales
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Abstract

Factor XII (FXII) deficiency is a rare coagulopathy that typically goes undiagnosed due to the lack of abnormal bleeding or thrombosis. However, the accompanying prolonged activated partial thromboplastin time (aPTT) can create difficulties with maintaining therapeutic anticoagulation in the setting of acute coronary syndrome (ACS). Here, we present the case of a 52-year-old man presenting with chest pain and diagnosed with an NSTEMI but also found with a prolonged baseline aPTT ultimately secondary to FXII deficiency. Here, we discuss the diagnostic work-up of an isolated prolonged aPTT to identify possible etiologies, such as FXII deficiency, and ultimately inform ACS management.

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朋友还是敌人:在非stemi治疗过程中偶然发现的因子12缺乏。
因子XII (FXII)缺乏症是一种罕见的凝血病,通常由于缺乏异常出血或血栓而无法诊断。然而,在急性冠状动脉综合征(ACS)的情况下,伴随的延长的活化部分凝血活素时间(aPTT)会给维持治疗性抗凝造成困难。在这里,我们报告了一名52岁男性的病例,其表现为胸痛,诊断为非stemi,但也发现基线aPTT延长,最终继发于FXII缺乏。在这里,我们讨论了一个孤立的延长aPTT的诊断工作,以确定可能的病因,如FXII缺乏,并最终告知ACS管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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0.00%
发文量
51
审稿时长
13 weeks
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