Kim Alice, Saffra Norman
Division of Ophthalmology, Maimonides Medical Center, 902 49th Street, Brooklyn, NY, 11219, USA,
J Ophthalmic Inflamm Infect. 2012 Sep;2(3):145-7. doi: 10.1007/s12348-011-0058-2. Epub 2012 Jan 24.
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.
描述1例在开始使用阿达木单抗治疗后3周内出现的球后视神经炎病例。
对该索引病例进行了视野测试、脑磁共振成像、腰椎穿刺和实验室评估,并先给予静脉注射甲泼尼龙,随后逐渐减量使用类固醇。
我们的患者视力完全恢复,但在磁共振成像(MRI)上发现有广泛的T2/液体衰减反转恢复序列(FLAIR)高信号灶,这些病灶有强化且扩散受限。6个月后,这些脱髓鞘病变仍然存在,我们的患者开始接受免疫调节治疗。
鉴于该病例在就诊时疾病负担较重且在随访MRI上病变持续存在,这个不寻常的病例似乎提示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,并监测任何表现并进行适当治疗。