36岁男性HIV感染者进行性多灶性脑白质病免疫重建炎症综合征(PML IRIS

Jon Stewart Dy
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摘要

进行性多灶性白质脑病-免疫重建炎症综合征(PMLIRIS)是在开始抗逆转录病毒治疗(ART)后出现或加重的亚急性神经功能缺损。这是由于严重的神经炎症与重建免疫能力。大约25%的HIV和PML患者发展为IRIS。PML-IRIS治疗的临床试验缺乏,只有有限的证据支持使用调查性治疗,如皮质类固醇和马拉维洛克。我们报告一个36岁的菲律宾男性,已知高血压和诊断为艾滋病毒,谁提出了记忆问题。在开始抗逆转录病毒治疗后的第3周,他最终被视为PML-IRIS病例。患者接受了一个疗程的静脉地塞米松、口服甲氟喹和静脉免疫球蛋白治疗,并继续进行抗逆转录病毒治疗。本例患者的临床结果显示症状整体改善,神经功能缺损无恶化。
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Unmasking the truth Progressive multifocal leukoencephalopathy immune reconstitution inflammatory syndrome PML IRIS in a 36 year old male with HIV
Progressive Multifocal Leukoencephalopathy – Immune Reconstitution Inflammatory Syndrome (PMLIRIS) is the subacute onset of neurological deficits that appeared or was exacerbated after initiation antiretroviral therapy (ART) for treatment of PML. It is due to severe neuroinflammation with re-establishment of immuncompetence. Approximately 25% of patients with HIV and PML develop IRIS. Clinical trials on the treatment of PML-IRIS is lacking with only limited evidence supporting the use of investigative therapies such as corticosteroids and Maraviroc. We report a case of a 36-year old Filipino male, known hypertensive and diagnosed with HIV, who presented with memory problems. He was eventually treated as a case of PML-IRIS on the 3rd week after initiation of ART. He was treated with a course of intravenous Dexamethasone, oral Mefloquine and intravenous immunoglobulin, and ART was continued. Clinical outcome in our patient shows an overall improvement of symptoms and no deterioration of neurologic deficits.
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