From the Department of Neurology (N.A., A.E.G., S.S.M., N.V., J.D.S.).
Ataxia Center, Cognitive Behavioral Neurology Unit, Laboratory for Neuroanatomy and Cerebellar Neurobiology (N.A., A.E.G., J.D.S.).
AJNR Am J Neuroradiol. 2021 Jun;42(6):1073-1079. doi: 10.3174/ajnr.A7145. Epub 2021 May 13.
There are no validated imaging criteria for the diagnosis of progressive multifocal leukoencephalopathy in the cerebellum. Here we introduce the MR imaging shrimp sign, a cerebellar white matter lesion identifiable in patients with cerebellar progressive multifocal leukoencephalopathy, and we evaluate its sensitivity and specificity.
We first identified patients with progressive multifocal leukoencephalopathy seen at Massachusetts General Hospital between 1998 and 2019 whose radiology reports included the term "cerebellum." Drawing on a priori knowledge, 2 investigators developed preliminary diagnostic criteria for the shrimp sign. These criteria were revised and validated in 2 successive stages by 4 additional blinded investigators. After defining the MR imaging shrimp sign, we assessed its sensitivity, specificity, positive predictive value, and negative predictive value.
We identified 20 patients with cerebellar progressive multifocal leukoencephalopathy: 16 with definite progressive multifocal leukoencephalopathy (mean, 46.4 [SD, 9.2] years of age; 5 women), and 4 with possible progressive multifocal leukoencephalopathy (mean, 45.8 [SD, 8.5] years of age; 1 woman). We studied 40 disease controls (mean, 43.6 [SD, 21.0] years of age; 16 women) with conditions known to affect the cerebellar white matter. We defined the MR imaging shrimp sign as a T2- and FLAIR-hyperintense, T1-hypointense, discrete cerebellar white matter lesion abutting-but-sparing the dentate nucleus. MR imaging shrimp sign sensitivity was 0.85; specificity, 1; positive predictive value, 1; and negative predictive value, 0.93. The shrimp sign was also seen in fragile X-associated tremor ataxia syndrome, but radiographic and clinical features distinguished it from progressive multifocal leukoencephalopathy.
In the right clinical context, the MR imaging shrimp sign has excellent sensitivity and specificity for cerebellar progressive multifocal leukoencephalopathy, providing a new radiologic marker of the disease.
目前尚无经证实的小脑进行性多灶性白质脑病的影像学诊断标准。本研究介绍了一种磁共振成像(MRI)的“虾征”,这是一种可在小脑进行性多灶性白质脑病患者的小脑白质病变中识别的病变,我们评估了其敏感性和特异性。
我们首先确定了 1998 年至 2019 年期间在马萨诸塞州综合医院就诊的、放射学报告中包含“小脑”一词的进行性多灶性白质脑病患者。两名研究人员根据先验知识制定了“虾征”的初步诊断标准。这一标准在随后的两个阶段分别由 4 名额外的盲法研究人员进行了修订和验证。在定义 MRI 虾征后,我们评估了其敏感性、特异性、阳性预测值和阴性预测值。
我们共确定了 20 例小脑进行性多灶性白质脑病患者:16 例为明确的进行性多灶性白质脑病(平均年龄 46.4[标准差 9.2]岁;女性 5 例),4 例为可能的进行性多灶性白质脑病(平均年龄 45.8[标准差 8.5]岁;女性 1 例)。我们研究了 40 例已知影响小脑白质的疾病对照患者(平均年龄 43.6[标准差 21.0]岁;女性 16 例)。我们将 MRI 虾征定义为 T2 和液体衰减反转恢复(FLAIR)高信号、T1 低信号、边界清晰的小脑白质病变,毗邻但不累及齿状核。MRI 虾征的敏感性为 0.85,特异性为 1,阳性预测值为 1,阴性预测值为 0.93。“虾征”也见于脆性 X 相关震颤共济失调综合征,但影像学和临床特征可将其与进行性多灶性白质脑病区分开来。
在适当的临床背景下,MRI 虾征对小脑进行性多灶性白质脑病具有出色的敏感性和特异性,为该疾病提供了新的放射学标志物。