血友病A的Emicizumab相关横纹肌溶解。

Clinical Hematology International Pub Date : 2020-10-07 eCollection Date: 2020-12-01 DOI:10.2991/chi.k.200924.001
Joseph A Wilson, Stephanie Hayden, Alexander Asamoah, Vivek R Sharma, David C Jennings, Ashok B Raj
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引用次数: 0

摘要

Emicizumab正日益成为A型血友病患者有或无抑制剂的一线治疗药物。横纹肌溶解是一种肌肉坏死和细胞内肌肉成分释放到循环中的综合征。肌酸激酶(CK)水平通常显著升高,肌肉疼痛和肌红蛋白尿可能存在。疾病的严重程度从血清肌酶无症状升高到与酶极端升高、电解质失衡、急性肾损伤和弥散性血管内凝血相关的危及生命的疾病不等。我们报告了一例非洲裔美国男性,患有严重的血友病a和因子VIII抑制剂史,持续使用emicizumab预防,并发有症状的高血凝症横纹肌溶解。迄今为止,尚无已知的横纹肌溶解与半珠单抗之间的联系。本报告揭示了半蜜单抗在适度运动后出现症状性横纹肌溶解的潜在副作用的可能性。
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Emicizumab Associated Rhabdomyolysis in Hemophilia A.

Emicizumab is increasingly the front-line treatment for patients with Hemophilia A with or without inhibitors. Rhabdomyolysis is a syndrome of muscle necrosis and release of intracellular muscle constituents into the circulation. Creatine kinase (CK) levels are typically markedly elevated, and muscle pain and myoglobinuria may be present. The severity of illness ranges from asymptomatic elevations in serum muscle enzymes to life-threatening disease associated with extreme enzyme elevations, electrolyte imbalances, acute kidney injury and disseminated intravascular coagulation. We present a case of an African American male with severe hemophilia A and history of factor VIII inhibitor, maintained on emicizumab prophylaxis, who developed rhabdomyolysis with a symptomatic hyperCKemia. To date, there is no known link between rhabdomyolysis to emicizumab. This report brings to light the possibility of symptomatic rhabdomyolysis as a potential side effect of emicizumab after moderate exertional activity.

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