Avidan Olivia, Quesenberry Matthew
Internal Medicine Brown University.
Department of Hematology and Oncology, Rhode Island Hospital Brown University.
J Brown Hosp Med. 2023 Oct 1;2(4):85108. doi: 10.56305/001c.85108. eCollection 2023.
A 55 year old African American male with a medical history of diffuse large B-cell lymphoma (DLBCL) receiving chemotherapy presents for fatigue and dark red urine. Five days prior to this presentation, the patient was seen at his oncology clinic for progression of his cancer. The patient was started on a new chemotherapy regimen as well as rasburicase and allopurinol for hyperuricemia thought to be secondary to tumor lysis syndrome. Subsequent lab work indicated acute hemolytic anemia. Etiology was suspected to be hemolytic anemia triggered by rasburicase in the setting of undiagnosed G6PD deficiency. The patient recovered with supportive care including blood transfusions and cessation of rasburicase. G6PD deficiency is the most prevalent inherited erythrocyte disorder classically considered to impact populations in tropical Africa and Asia, however is estimated to impact approximately 10% of African American men. ¹⋅² This case exemplifies the importance of considering G6PD deficiency when administering medications that cause increased oxidative stress, such as rasburicase, in addition to the swift recognition and management of subsequent complications.
一名55岁的非裔美国男性,有弥漫性大B细胞淋巴瘤(DLBCL)病史,正在接受化疗,因疲劳和暗红色尿液前来就诊。在此次就诊前五天,该患者因癌症进展在肿瘤诊所就诊。患者开始接受新的化疗方案以及用于治疗继发于肿瘤溶解综合征的高尿酸血症的拉布立酶和别嘌醇。随后的实验室检查显示急性溶血性贫血。病因怀疑是在未诊断出葡萄糖-6-磷酸脱氢酶(G6PD)缺乏的情况下,由拉布立酶引发的溶血性贫血。患者通过包括输血和停用拉布立酶在内的支持性治疗得以康复。G6PD缺乏是最常见的遗传性红细胞疾病,传统上认为会影响热带非洲和亚洲的人群,但据估计约有10%的非裔美国男性受其影响。¹⋅² 本病例体现了在使用会增加氧化应激的药物(如拉布立酶)时考虑G6PD缺乏的重要性,以及对后续并发症的迅速识别和处理。