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Natalizumab-related progressive multifocal leukoencephalopathy-immune reconstitution inflammatory syndrome: a case report highlighting clinical and mrI features

机译:纳他珠单抗相关的进行性多灶性白质脑病-免疫重建炎性综合征:突出临床和MRI特征的病例报告

摘要

Multiple sclerosis (MS) patients treated with natalizumab often face the uncommon but severe complication of developing progressive multifocal leukoencephalopathy (PML). PML may be further complicated by immune reconstitution inflammatory syndrome (IRIS) after the removal of the drug. Since both PML and IRIS are associated with high morbidity and mortality rates, early clinical and radiological diagnosis of these complications is of paramount importance. Here, we report a case of an adult male patient who was diagnosed with PML after receiving natalizumab therapy for 6 years for the treatment of MS. Upon cessation of natalizumab, he presented with a paradoxical worsening of clinical and radiological findings consistent with an inflammatory brain injury due to IRIS. He was treated with high dose corticosteroid therapy followed by a gradual improvement in clinical and imaging findings. This article illustrates the magnetic resonance imaging (MRI) features of natalizumab-associated PML-IRIS, along with a brief overview of its clinical features, complications and management strategies.
机译:用那他珠单抗治疗的多发性硬化症(MS)患者通常面临发展性进行性多灶性白质脑病(PML)的罕见但严重的并发症。移除药物后,免疫重建炎症综合症(IRIS)可能会使PML更加复杂。由于PML和IRIS均与高发病率和高死亡率相关,因此对这些并发症的早期临床和影像学诊断至关重要。在这里,我们报告了一名成年男性患者的病例,该患者在接受那他珠单抗治疗6年以治疗MS后被诊断为PML。停用那他珠单抗后,他的临床和影像学发现与IRIS引起的炎性脑损伤相矛盾,呈现出自相矛盾的恶化。他接受了大剂量皮质类固醇激素治疗,随后临床和影像学检查结果逐渐好转。本文阐述了那他珠单抗相关的PML-IRIS的磁共振成像(MRI)特征,并对其临床特征,并发症和治疗策略进行了简要概述。

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