摘要
自身免疫性胶质纤维酸性蛋白星形细胞病(GFAP-A)是一种新型自身免疫性星形细胞病,临床少见,常被误诊。该文分析了2例GFAP-A患者的临床及MRI表现,以期提高对该病的临床诊断能力。
Autoimmune glial fibrillary acidic protein astrocytopathy(GFAP-A)is a novel autoimmune astrocytopathy,which is rare in clinical practice and often misdiagnosed.The clinical and MRI findings of 2 patients with GFAP-A were studied in this paper in order to improve the capacity of clinical diagnostic of the disease.
作者
黄波涛
黄聪
HUANG Bo-tao;HUANG Cong(Department of Radiology,Houjie Hospital Affiliated Guangdong Medical University,Dongguan 523945,China;Department of Radiology,the 926 Hospital of PLA,Kaiyuan 661699,China)
出处
《广东医科大学学报》
2022年第4期478-480,共3页
Journal of Guangdong Medical University
关键词
自身免疫性星形细胞病
胶质纤维酸性蛋白
抗体
磁共振成像
autoimmune astrocytopathy
glial fibrillary acidic protein
antibody
magnetic resonance imaging
