Does this optic neuritis patient have neuromyelitis optica? An approach to optic neuritis in the context of neuromyelitis optica

被引:1
|
作者
Burton, Jodie M. [1 ,2 ,3 ,4 ]
Costello, Fiona [1 ,2 ,3 ,5 ]
机构
[1] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[2] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB, Canada
[3] Univ Calgary, Calgary, AB, Canada
[4] Univ Calgary, Dept Community Hlth Sci, Calgary, AB, Canada
[5] Univ Calgary, Dept Surg Ophthalmol, Calgary, AB, Canada
关键词
aquaporin-4; demyelinating disease; Devic's disease; immunosuppression; myelopathy; neuromyelitis optica; neuromyelitis optica spectrum disorder; NMO-IgG; optic neuritis; rituximab;
D O I
10.1586/17469899.2014.922874
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Optic neuritis is a common presentation of demyelinating disease, most often associated with multiple sclerosis, and typically associated with a relatively good recovery and prognosis. However, when optic neuritis is the heralding event of neuromyelitis optica (NMO), it is much more likely to be the start of a devastating and disabling chronic disease with a reduced lifespan. Early recognition of NMO is the best chance a patient has of avoiding life-altering disability, as relapse prevention is essentially disability prevention because this disease, unlike MS, does not really have a progressive component. The following review was written to assist the clinician, particularly the ophthalmologist, in assessing optic neuritis in evaluating and recognizing the potential NMO patient.
引用
收藏
页码:205 / 216
页数:12
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