医学
视神经炎
髓鞘少突胶质细胞糖蛋白
葡萄膜炎
背景(考古学)
免疫学
多发性硬化
抗体
病理
皮肤病科
眼科
实验性自身免疫性脑脊髓炎
生物
古生物学
作者
Sudarshini Ramanathan,Clare L. Fraser,Sarah R. Curnow,Mona Ghaly,Richard J. Leventer,Jeannette Lechner‐Scott,Andrew Henderson,Stephen Reddel,Russell C. Dale,Fabienne Brilot
摘要
Background and purpose Antibodies to myelin oligodendrocyte glycoprotein (MOG) have been identified in both children and adults with demyelination, with a strong association with bilateral or recurrent optic neuritis (ON). However, the full clinical spectrum of this newly described condition is unknown. We sought to describe non‐ON inflammatory ophthalmological presentations such as uveitis and optic perineuritis in the context of MOG antibody seropositivity. Methods Using a live cell‐based assay analysed by flow cytometry, we identified seropositive patients referred for MOG antibody testing in Australasia between 2014 and 2017. We identified four MOG antibody‐positive patients with non‐ON inflammatory ophthalmological presentations and present their detailed clinical information in this case series. Results Three patients had uveitis either in association with, or remote from, ON. One patient had optic perineuritis and peripheral ulcerative keratitis. We describe the presentation, examination, investigation findings and clinical course of these four patients. Conclusions Recognition of these novel clinical associations may expand the clinical spectrum of MOG antibody‐associated presentations. An expedited diagnosis may guide the management of these complex patients.
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