Pula John H, Kattah Jorge C, Keung Bonnie, Wang Huaping, Daily Jennifer
Department of Neurology, NorthShore University Health System Glenview, IL 60026, USA.
Department of Neurology, University of Illinois College of Medicine at Peoria, USA.
J Neurol Sci. 2014 Oct 15;345(1-2):209-12. doi: 10.1016/j.jns.2014.07.049. Epub 2014 Jul 28.
Neuomyelitis optica, sarcoid, and multiple sclerosis can all cause optic neuritis. Further means of distinguishing the causes of optic neuritis among these etiologies would be valuable for the clinician.
This is a retrospective, cohort study from a single university based hospital and neuro-ophthalmology clinic. Blinded interpretation of orbit MRIs was performed on patients with acute optic neuritis from multiple sclerosis (n=25), sarcoid (n=5) and neuromyelitis optica spectrum disorder (n=6).
A length of >40 mm anterior visual pathway enhancement distinguished neuromyelitis optica spectrum disorder from multiple sclerosis (p=0.0376). No statistically significant differences were found for presence of pain or papillitis, however there was a trend for bilateral involvement and chiasmal involvement in neuromyelitis optica spectrum disorder compared to multiple sclerosis.
In acute optic neuritis, enhancing anterior visual pathway lesion length >40 mm helps differentiate neuromyelitis optica spectrum disorder from multiple sclerosis. This degree of involvement can be considered longitudinally extensive optic neuritis. Further characterization is necessary as this degree of enhancement occurs in other clinical syndromes besides neuromyelitis optica.
视神经脊髓炎、结节病和多发性硬化均可导致视神经炎。对于临床医生而言,进一步区分这些病因所致视神经炎的方法将很有价值。
这是一项来自单一大学附属医院和神经眼科诊所的回顾性队列研究。对来自多发性硬化(n = 25)、结节病(n = 5)和视神经脊髓炎谱系障碍(n = 6)的急性视神经炎患者的眼眶MRI进行盲法解读。
前视觉通路强化长度>40 mm可将视神经脊髓炎谱系障碍与多发性硬化区分开来(p = 0.0376)。在疼痛或视乳头炎的存在方面未发现统计学上的显著差异,然而与多发性硬化相比,视神经脊髓炎谱系障碍存在双侧受累和视交叉受累的趋势。
在急性视神经炎中,前视觉通路强化病变长度>40 mm有助于区分视神经脊髓炎谱系障碍与多发性硬化。这种受累程度可被视为纵向广泛的视神经炎。由于除视神经脊髓炎外,其他临床综合征也会出现这种强化程度,因此需要进一步进行特征描述。