Chartier Alexander R, Hillert Conor J, Gill Harpreet, Jha Pinky
Internal Medicine, Medical College of Wisconsin, Wauwatosa, USA.
Internal Medicine, Medical College of Wisconsin, Brookfield, USA.
Cureus. 2020 Jul 30;12(7):e9481. doi: 10.7759/cureus.9481.
Acquired factor V inhibitor (aFVi) is an exceptionally rare hematologic condition that can range from incidental laboratory abnormalities to life-threatening hemorrhage. Bovine thrombin was formerly the most common cause of this condition; however, the decreased use of bovine thrombin in surgical procedures has led to a shift in the cause of aFVi toward antibiotic use and malignancies. Here we present a case of an 80-year-old Caucasian female on long-term warfarin therapy who presented with epistaxis and an elevated international normalized ratio, and a history of cephalosporin antibiotic use. We review the published literature beginning in 2016 to identify the evolving causes of aFVi. Additionally, we propose that stress-mediated immune regulation may contribute to antibody formation, preventing the interaction between factor V and the damaged phospholipid membranes. This case highlights the evolving causes of aFVi and should prompt physicians to consider this diagnosis in coagulopathies that do not correct with traditional therapies.
获得性凝血因子V抑制剂(aFVi)是一种极为罕见的血液系统疾病,其表现范围从偶然的实验室异常到危及生命的出血。牛凝血酶曾是导致这种疾病的最常见原因;然而,外科手术中牛凝血酶使用的减少已导致aFVi的病因转向抗生素使用和恶性肿瘤。在此,我们报告一例80岁长期接受华法林治疗的白种女性病例,该患者出现鼻出血且国际标准化比值升高,并有头孢菌素类抗生素使用史。我们回顾了2016年以来发表的文献,以确定aFVi不断变化的病因。此外,我们提出应激介导的免疫调节可能有助于抗体形成,从而阻止凝血因子V与受损磷脂膜之间的相互作用。该病例突出了aFVi不断变化的病因,并应促使医生在传统治疗无法纠正的凝血病中考虑这一诊断。