4.5 Article

Autoimmune glial fibrillary acidic protein astrocytopathy in children: a retrospective study

期刊

出版社

BMC
DOI: 10.1186/s40001-022-00641-y

关键词

Glial fibrillary acidic protein; Children; Magnetic resonance imaging; Cerebral spinal fluid examination; Virchow-Robin space

向作者/读者索取更多资源

This study retrospectively analyzed the clinical features of 11 pediatric patients with autoimmune GFAP astrocytopathy. The results showed that all patients presented with encephalitis and meningoencephalitis, accompanied by symptoms such as fever and headache for most patients. Cerebrospinal fluid analysis revealed elevated white blood cell counts, lactic dehydrogenase levels, protein levels, and slightly reduced glucose levels. Imaging findings showed abnormalities in the brain and spinal cord.
Objective To describe the clinical features of autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy in children. Method Data from 11 pediatric patients with autoimmune GFAP astrocytopathy were retrospectively analyzed. Results All of the patients showed encephalitis and meningoencephalitis or meningoencephalomyelitis with or without myelitis. 45.4% of the patients had fever, 27.3% headaches, 18.2% dizziness, 18.2% drowsiness, and 18.2% mental disorders. Cerebrospinal fluid (CSF) was detected in all patients. The white blood cell counts (WBC) (90.9%), lactic dehydrogenase levels (72.7%), protein level (36.4%), and adenosine deaminase activity (ADA) level (27.3%) were elevated, and the CSF glucose levels (72.7%) were slightly reduced. Nine patients (90%) were found to have brain abnormalities, of which five (50.0%) patients had abnormal symmetrical laminar patterns or line patterns hyperintensity lesions on T2-weighted and fluid-attenuated inversion recovery (FLAIR) images in the basal ganglia, hypothalamus, subcortical white matter and periventricular white matter. The linear radial enhancement pattern of the cerebral white matter was only seen in two patients, with the most common being abnormal enhancement of leptomeninges (50%). Five patients had longitudinally extensive spinal cord lesions. Conclusion The findings of pediatric patients with autoimmune GFAP astrocytopathy are different from previous reports.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据