Dhanapalaratnam Roshan, Markoulli Maria, Krishnan Arun V
Prince of Wales Clinical School, University of New South Wales Sydney, Sydney, Australia.
School of Optometry and Vision Science, University of New South Wales Sydney, Sydney, Australia.
Clin Exp Optom. 2022 Jan;105(1):3-12. doi: 10.1080/08164622.2021.1947745. Epub 2021 Aug 4.
Multiple sclerosis (MS) is a neurological inflammatory disorder known to attack the heavily myelinated regions of the nervous system including the optic nerves, cerebellum, brainstem and spinal cord. This review will discuss the clinical manifestations and investigations for MS and other similar neurological inflammatory disorders affecting vision, as well as the effects of MS treatments on vision. Assessment of visual pathways is critical, considering MS can involve multiple components of the visual pathway, including optic nerves, uvea, retina and occipital cortex. Optical coherence tomography is increasingly being recognised as a highly sensitive tool in detecting subclinical optic nerve changes. Magnetic resonance imaging (MRI) is critical in MS diagnosis and in predicting long-term disability. Optic neuritis in MS involves unilateral vision loss, with characteristic pain on eye movement. The visual loss in neuromyelitis optica spectrum disorder tends to be more severe with preferential altitudinal field loss, chiasmal and tract lesions are also more common. Other differential diagnoses include chronic relapsing inflammatory optic neuropathy and giant cell arteritis. Leber's hereditary optic neuropathy affects young males and visual loss tends to be painless and subacute, typically involving both optic nerves. MS lesions in the vestibulocerebellum, brainstem, thalamus and basal ganglia may lead to abnormalities of gaze, saccades, pursuit and nystagmus which can be identified on eye examination. Medial longitudinal fasciculus lesions can cause another frequent presentation of MS, internuclear ophthalmoplegia, with failure of ipsilateral eye adduction and contralateral eye abduction nystagmus. Treatments for MS include high-dose corticosteroids for acute relapses and disease-modifying medications for relapse prevention. These therapies may also have adverse effects on vision, including central serous retinopathy with corticosteroid therapy and macular oedema with fingolimod.
多发性硬化症(MS)是一种神经炎性疾病,已知会侵袭神经系统中髓鞘丰富的区域,包括视神经、小脑、脑干和脊髓。本综述将讨论MS以及其他影响视力的类似神经炎性疾病的临床表现和检查,以及MS治疗对视力的影响。鉴于MS可累及视觉通路的多个组成部分,包括视神经、葡萄膜、视网膜和枕叶皮质,因此对视觉通路的评估至关重要。光学相干断层扫描越来越被认为是检测亚临床视神经变化的高度敏感工具。磁共振成像(MRI)在MS诊断和预测长期残疾方面至关重要。MS中的视神经炎涉及单侧视力丧失,眼球运动时伴有特征性疼痛。视神经脊髓炎谱系障碍中的视力丧失往往更严重,伴有优先性的海拔视野缺损,视交叉和视束病变也更常见。其他鉴别诊断包括慢性复发性炎性视神经病变和巨细胞动脉炎。Leber遗传性视神经病变影响年轻男性,视力丧失往往无痛且呈亚急性,通常累及双侧视神经。前庭小脑、脑干、丘脑和基底神经节中的MS病变可能导致注视、扫视、跟踪和眼球震颤异常,这些异常可通过眼部检查发现。内侧纵束病变可导致MS的另一种常见表现,即核间性眼肌麻痹,患侧眼球内收失败和对侧眼球外展性眼球震颤。MS的治疗包括用于急性复发的大剂量皮质类固醇和用于预防复发的疾病修正药物。这些疗法也可能对视力产生不利影响,包括皮质类固醇治疗引起的中心性浆液性视网膜病变和芬戈莫德引起的黄斑水肿。