南达科他州罕见的出血性疾病组合:一个病例报告。

Q4 Medicine
Dallas Petroff, David Ring
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引用次数: 0

摘要

血友病A是一种凝血障碍,由于因子VIII缺乏,导致出血时间延长。获得性血友病A是由免疫系统攻击因子VIII引起的,通常发生在生命后期。Leiden因子V是一种基因突变,主要在静脉中引起异常血凝块形成。这种突变是遗传的,增加了凝血的风险。这些情况的结合是极其罕见的。任何出血性疾病患者的正确管理是必要的外科病例,以防止灾难。我们提出一个手术病例涉及血友病a和因子V莱顿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Combination of Bleeding Disorders in South Dakota: A Case Report.

Hemophilia A is a clotting disorder due to factor VIII deficiency, leading to prolonged bleeding. Acquired hemophilia A results from the immune system attacking factor VIII, typically occurring later in life. Factor V Leiden is a genetic mutation causing abnormal blood clot formation, primarily in veins. This mutation is inheritable and increases the risk of clotting. A combination of these conditions is extremely rare. Correct management of a patient with any bleeding disorder is imperative for a surgical case to prevent catastrophe. We present a surgical case involving both hemophilia A and Factor V Leiden.

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CiteScore
0.50
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