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Mult Scler Int. 2013;2013:398259. doi: 10.1155/2013/398259. Epub 2013 Jan 27.
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Brain abnormalities in neuromyelitis optica spectrum disorder.视神经脊髓炎谱系障碍中的脑异常
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Altered topological organization of white matter structural networks in patients with neuromyelitis optica.视神经脊髓炎患者脑白质结构网络拓扑组织的改变。
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No MRI evidence of cortical lesions in neuromyelitis optica.视神经脊髓炎中无皮质病变的 MRI 证据。
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White matter volume is decreased in the brain of patients with neuromyelitis optica.视神经脊髓炎患者的脑白质体积减少。
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Diffuse and heterogeneous T2-hyperintense lesions in the splenium are characteristic of neuromyelitis optica.胼胝体弥散和不均匀的 T2 高信号病变是视神经脊髓炎的特征。
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Hypothermia, hypotension, hypersomnia, and obesity associated with hypothalamic lesions in a patient positive for the anti-aquaporin 4 antibody: a case report and literature review.抗水通道蛋白4抗体阳性患者下丘脑病变相关的体温过低、低血压、嗜睡和肥胖:病例报告及文献综述
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Magnetic resonance imaging of optic neuritis in patients with neuromyelitis optica versus multiple sclerosis.视神经炎患者的磁共振成像:视神经脊髓炎与多发性硬化症的比较。
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视神经脊髓炎的传统与先进成像技术

Conventional and advanced imaging in neuromyelitis optica.

作者信息

Barnett Y, Sutton I J, Ghadiri M, Masters L, Zivadinov R, Barnett M H

机构信息

From the Sydney Neuroimaging Analysis Centre (Y.B., M.H.B.), Sydney, AustraliaBrain and Mind Research Institute (Y.B., M.G., L.M., M.H.B.), University of Sydney, Sydney, AustraliaDepartment of Medical Imaging and Neurology (Y.B., I.J.S.), St Vincent's Hospital, Sydney, Australia.

Department of Medical Imaging and Neurology (Y.B., I.J.S.), St Vincent's Hospital, Sydney, Australia.

出版信息

AJNR Am J Neuroradiol. 2014 Aug;35(8):1458-66. doi: 10.3174/ajnr.A3592. Epub 2013 Jun 13.

DOI:10.3174/ajnr.A3592
PMID:23764723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7964440/
Abstract

Myelitis and optic neuritis are prototypic clinical presentations of both multiple sclerosis and neuromyelitis optica. Once considered a subtype of multiple sclerosis, neuromyelitis optica, is now known to have a discrete pathogenesis in which antibodies to the water channel, aquaporin 4, play a critical role. Timely differentiation of neuromyelitis optica from MS is imperative, determining both prognosis and treatment strategy. Early, aggressive immunosuppression is required to prevent the accrual of severe disability in neuromyelitis optica; conversely, MS-specific therapies may exacerbate the disease. The diagnosis of neuromyelitis optica requires the integration of clinical, MR imaging, and laboratory data, but current criteria are insensitive and exclude patients with limited clinical syndromes. Failure to recognize the expanding spectrum of cerebral MR imaging patterns associated with aquaporin 4 antibody seropositivity adds to diagnostic uncertainty in some patients. We present the state of the art in conventional and nonconventional MR imaging in neuromyelitis optica and review the place of neuroimaging in the diagnosis, management, and research of the condition.

摘要

脊髓炎和视神经炎是多发性硬化症和视神经脊髓炎的典型临床表现。视神经脊髓炎曾被认为是多发性硬化症的一种亚型,现在已知其具有独特的发病机制,其中水通道蛋白4抗体起着关键作用。及时区分视神经脊髓炎和多发性硬化症至关重要,这决定了预后和治疗策略。在视神经脊髓炎中,需要早期积极的免疫抑制来预防严重残疾的累积;相反,针对多发性硬化症的疗法可能会使病情恶化。视神经脊髓炎的诊断需要综合临床、磁共振成像和实验室数据,但目前的标准不敏感,会排除临床综合征有限的患者。未能认识到与水通道蛋白4抗体血清阳性相关的脑磁共振成像模式范围不断扩大,增加了一些患者的诊断不确定性。我们介绍了视神经脊髓炎传统和非传统磁共振成像的最新情况,并回顾了神经影像学在该疾病的诊断、管理和研究中的地位。