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Sickle cell disease and HIV: A case highlighting management challenges for children in a resource-limited setting

机译:镰状细胞病和艾滋病毒:一个案例突出资源有限环境下儿童的管理挑战

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Sickle cell disease (SCD) is a genetic disorder resulting from a mutation in the hemoglobin (Hb) gene. Sickle cell disease results in chronic anemia and a variety of acute and chronic complications that can lead to early mortality. A child with both SCD and HIV presents a management challenge, particularly in a resource-limited setting. In this case report, we describe the case of an 18-month-old Kenyan girl with SCD and HIV who developed a severe hypersensitivity reaction to first-line antiretroviral therapy (ART). Selecting an appropriate drug substitute for a child with SCD and HIV presents a management dilemma when the available options have problematic side effect profiles or are inaccessible or inappropriate according to national guidelines. The challenges in choosing an appropriate ART regimen for a child with SCD and HIV highlight the lack of data and scarcity of treatment options for pediatric patients.
机译:镰状细胞病(SCD)是由血红蛋白(Hb)基因突变导致的遗传性疾病。镰状细胞病导致慢性贫血以及各种急性和慢性并发症,可导致早期死亡。患有SCD和HIV的儿童面临管理方面的挑战,尤其是在资源有限的环境中。在此病例报告中,我们描述了一个患有SCD和HIV的18个月大肯尼亚女孩的情况,该女孩对一线抗逆转录病毒疗法(ART)产生了严重的超敏反应。根据国家指南,当可用的选择方案有不良副作用或难以获得或不合适时,为患有SCD和HIV的儿童选择合适的药物替代品会带来管理难题。为患有SCD和HIV的儿童选择合适的抗逆转录病毒治疗方案所面临的挑战凸显了缺乏数据和针对儿科患者的治疗选择不足。

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