From the Neuroimmunology Program (T.A.), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)-Hospital Clinic, University of Barcelona, Barcelona, Spain.
Neurology Department (T.A.), Neuroimmunology Unit, Sant Joan de Deu Children's Hospital, University of Barcelona, Barcelona, Spain.
AJNR Am J Neuroradiol. 2024 Jun 7;45(6):769-772. doi: 10.3174/ajnr.A8220.
While classic brain MR imaging features of Alexander disease have been well-documented, lesional patterns can overlap with other leukodystrophies, especially in the early stages of the disease or in milder phenotypes. We aimed to assess the utility of a new neuroimaging sign to help increase the diagnostic specificity of Alexander disease.
A peculiar bilateral symmetric hyperintense signal on T2-weighted images affecting the medulla oblongata was identified in an index patient with type I Alexander disease. Subsequently, 5 observers performed a systematic MR imaging review for this pattern by examining 55 subjects with Alexander disease and 74 subjects with other leukodystrophies. Interobserver agreement was assessed by the κ index. Sensitivity, specificity, and receiver operating characteristic curves were determined.
The identified pattern was present in 87% of subjects with Alexander disease and 14% of those without Alexander disease leukodystrophy ( < .001), 3 with vanishing white matter, 4 with adult polyglucosan body disease, and 3 others. It was found equally in both type I and type II Alexander disease (28/32, 88% versus 18/21, 86%; = .851) and in subjects with unusual disease features (2/2). Sensitivity (87.3%; 95% CI, 76.0%-93.7%), specificity (86.5%; 95% CI, 76.9%-92.5%), and interobserver agreement (κ index = 0.82) were high.
The identified pattern in the medulla oblongata, called the chipmunk sign due to its resemblance to the face of this rodent, is extremely common in subjects with Alexander disease and represents a diagnostic tool that can aid in early diagnosis, especially in subjects with otherwise atypical MR imaging findings and/or clinical features.
尽管经典的脑磁共振成像(MRI)特征已被充分记录在案,但病变模式可能与其他脑白质营养不良重叠,尤其是在疾病的早期阶段或更轻微的表型中。我们旨在评估一种新的神经影像学征象在帮助提高脑白质营养不良的诊断特异性方面的效用。
在 1 名 1 型亚历山大病患者中,我们发现一种独特的双侧对称的脑桥延髓高信号在 T2 加权图像上,随后 5 名观察者通过检查 55 名亚历山大病患者和 74 名其他脑白质营养不良患者,对这种模式进行了系统的 MRI 回顾。观察者间的一致性通过κ指数进行评估。灵敏度、特异性和接受者操作特征曲线被确定。
在 87%的亚历山大病患者中发现了这种模式,而在没有亚历山大病脑白质营养不良的患者中仅发现了 14%(<0.001),其中 3 例为脑桥小脑萎缩,4 例为成年型多系统脑白质营养不良,还有 3 例其他疾病。它在 1 型和 2 型亚历山大病中同样存在(28/32,88%与 18/21,86%; = .851),也存在于不常见的疾病特征的患者中(2/2)。灵敏度(87.3%;95%可信区间,76.0%-93.7%)、特异性(86.5%;95%可信区间,76.9%-92.5%)和观察者间的一致性(κ指数=0.82)都很高。
这种脑桥延髓的模式被称为花栗鼠征,因其类似于这种啮齿动物的面部而得名,在亚历山大病患者中非常常见,是一种有助于早期诊断的诊断工具,特别是在那些磁共振成像表现和/或临床特征不典型的患者中。