抗磷脂抗体在镰状细胞病患者血栓形成的作用

IF 0.7 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
A. Petrungaro, E. Quartarone, L. Rigoli, P. Sciarrone
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引用次数: 0

摘要

镰状细胞病(SCD)是非洲、加勒比和地中海国家常见的遗传性疾病。SCD是一种血液学疾病,由β-珠蛋白基因的一个明显的点突变引起,该突变产生异常的血红蛋白S,导致缺氧条件下红细胞镰状坏死。SCD患者表现出“高凝状态”,导致严重静脉和动脉血栓性血管事件的风险增加。在此,我们报告一例严重的血栓并发症的SCD患者谁显示高抗磷脂抗体(APA)水平在血管闭塞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prothrombotic role of antiphospholipid antibodies in a patient with sickle cell disease
Sickle cell disease (SCD) is a common inherited condition in African, Caribbean, and Mediterranean countries. SCD is a hematologic disorder caused by a well-characterized point mutation in the β-globin gene, which produces an abnormal hemoglobin S that results in the sickling of red blood cells in deoxygenated conditions. Patients with SCD display a “hypercoagulation state” leading to an increased risk of severe venous and arterial thrombotic vascular events. Herein we report a case of severe thrombotic complications in a patient with SCD who showed high antiphospholipid antibodies (APA) levels during vascular occlusions.
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来源期刊
AIMS Medical Science
AIMS Medical Science MEDICINE, RESEARCH & EXPERIMENTAL-
自引率
14.30%
发文量
20
审稿时长
12 weeks
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