From the Departments of Radiology (E.B.)
Statistics (J.K.), Hacettepe University Faculty of Medicine, Ankara, Turkey.
AJNR Am J Neuroradiol. 2019 Apr;40(4):726-731. doi: 10.3174/ajnr.A6003. Epub 2019 Mar 7.
Differentiating pediatric-onset neuromyelitis optica spectrum disorder from acute disseminated encephalomyelitis could be challenging, especially in cases presenting with only brain manifestations. Our purpose was to investigate brain MR imaging features that may help distinguish these 2 entities.
We retrospectively examined initial brain MR imaging studies of 10 patients with pediatric-onset neuromyelitis optica spectrum disorder (female/male ratio, 7:3) and 10 patients with acute disseminated encephalomyelitis (female/male ratio, 2:8). The mean age of the patients was 10.3 ± 5.6 and 8.7 ± 5.3 years, respectively. Brain lesions were evaluated with respect to location, extent, expansion, T1 hypointensity, contrast enhancement/pattern, and diffusion characteristics. The χ test (Yates or Fisher exact χtests) was used to compare differences between groups.
Cerebral subcortical ± juxtacortical and pons ± middle cerebellar peduncle were the most frequent locations involved in both neuromyelitis optica spectrum disorder ( = 5 and 4, respectively) and acute disseminated encephalomyelitis ( = 9 and 7, respectively). Thalamic lesions were more frequent in acute disseminated encephalomyelitis ( = .020) and were detected only in 1 patient with neuromyelitis optica spectrum disorder. None of the patients with neuromyelitis optica spectrum disorder had hypothalamic, internal capsule, or cortical lesions. The internal capsule involvement was found to be significantly different between groups ( = .033). There was no significant difference in terms of extent, expansion, T1 hypointensity, contrast enhancement/pattern, and diffusion characteristics.
Although there is a considerable overlap in brain MR imaging findings, thalamic and internal capsule involvement could be used to differentiate pediatric-onset neuromyelitis optica spectrum disorder from acute disseminated encephalomyelitis.
儿童发病的视神经脊髓炎谱系疾病与急性播散性脑脊髓炎的鉴别可能具有挑战性,尤其是在仅表现为脑部症状的情况下。我们的目的是研究有助于区分这两种疾病的脑 MRI 影像学特征。
我们回顾性分析了 10 例儿童发病的视神经脊髓炎谱系疾病(男女比例为 7:3)和 10 例急性播散性脑脊髓炎(男女比例为 2:8)患者的初始脑 MRI 研究。患者的平均年龄分别为 10.3 ± 5.6 岁和 8.7 ± 5.3 岁。评估脑病变的位置、范围、扩展、T1 低信号、对比增强/模式和弥散特征。使用 χ2 检验(Yates 或 Fisher 确切概率 χ2 检验)比较组间差异。
皮质下/皮质旁和脑桥/中脑小脑脚是视神经脊髓炎谱系疾病(分别为 5 例和 4 例)和急性播散性脑脊髓炎(分别为 9 例和 7 例)最常见的病变部位。丘脑病变在急性播散性脑脊髓炎中更为常见( =.020),仅在 1 例视神经脊髓炎谱系疾病患者中发现。视神经脊髓炎谱系疾病患者无一例存在下丘脑、内囊或皮质病变。两组内囊受累情况差异有统计学意义( =.033)。在病变范围、扩展、T1 低信号、对比增强/模式和弥散特征方面,两组间无显著差异。
尽管脑 MRI 影像学表现有很大的重叠,但丘脑和内囊受累可用于鉴别儿童发病的视神经脊髓炎谱系疾病与急性播散性脑脊髓炎。