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A case report of adalimumab-associated optic neuritis

机译:阿达木单抗相关性视神经炎一例

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To describe a case of retrobulbar optic neuritis that presented within 3?weeks of adalimumab treatment initiation. This index case was evaluated with visual field testing, brain magnetic resonance imaging, lumbar puncture, and laboratory evaluation, and treated with intravenous methylprednisolone followed by a steroid taper. Our patient made a full visual recovery, but was found to have extensive T2/FLAIR foci of hyperintensities that enhanced and had restricted diffusion on magnetic resonance imaging (MRI). Six months later, these demyelinating lesions still persisted and our patient was initiated on immunomodulatory treatment. With the extensive burden of disease at presentation and persistence of lesions on follow-up MRI, this unusual case seems to suggest an unmasking of an underlying demyelinating process by adalimumab. The clinician should be mindful of this association and monitor for any manifestations and treat appropriately.
机译:描述在阿达木单抗治疗开始后3周内出现的球后视神经炎。该指数病例通过视野测试,脑磁共振成像,腰椎穿刺和实验室评估进行评估,并先后静脉注射甲基泼尼松龙和类固醇锥度治疗。我们的患者完全恢复了视力,但发现其广泛的T2 / FLAIR高强度病灶增强了磁共振成像(MRI)的扩散,并限制了扩散。六个月后,这些脱髓鞘病变仍持续存在,我们的患者开始接受免疫调节治疗。由于存在广泛的疾病负担,并且在后续的MRI检查中病灶持续存在,这种不寻常的病例似乎表明阿达木单抗揭示了潜在的脱髓鞘过程。临床医生应注意这种关联,并监测任何表现并适当治疗。

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