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Acute pulmonary thromboembolism caused by factor V Leiden mutation in South Korea: A case report

机译:V因子莱顿突变在韩国引起的急性肺血栓栓塞症:一例报道

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Rationale: Although Factor V Leiden (FVL) mutation is a major cause of inherited thrombophilia in Western populations; the mutation is extremely rare in Asia. Patient concerns: Here we report a case of a 28-year old Korean woman admitted to our hospital with extensive pulmonary embolism. Diagnosis: She was heterozygous for FVL mutation up on evaluation, and screening for asymptomatic family members also revealed heterozygous FVL mutation for her mother. Interventions: Enoxaparin 1 mg/kg was initiated, followed by rivaroxaban 15 mg every 12 hours. Outcomes: The patient showed improvement in both subjective dyspnea and right ventricular dysfunction and was successfully discharged after five hospital days. Lessons: FVL mutation screening may be considered in Asian patients with thrombophilia of uncertain etiology in the future.
机译:理由:尽管因子V莱顿(FVL)突变是西方人群遗传性血栓形成的主要原因;这种突变在亚洲极为罕见。病人担忧:在这里,我们报道了一名28岁的韩国妇女因广泛的肺栓塞入院。诊断:经过评估,她的FVL突变是杂合的,对无症状家庭成员的筛查也显示出母亲的FVL杂合。干预措施:开始使用依诺肝素1 mg / kg,然后每12小时服用一次利伐沙班15 mg。结果:该患者主观呼吸困难和右心室功能障碍均得到改善,并在住院五天后成功出院。经验教训:将来可能在病因不明的亚洲血栓形成患者中考虑FVL突变筛查。

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