Mabrouki Fatima Zahra, Aziouaz Faiza, Sekhsoukh Rachid, Yassine Mebrouk
Ophthalmology, Mohammed VI University Hospital of Oujda/Faculty of Medicine and Pharmacy of Oujda, Oujda, MAR.
Neurology, Mohammed VI University Hospital of Oujda/Faculty of Medicine and Pharmacy of Oujda, Oujda, MAR.
Cureus. 2021 Aug 31;13(8):e17588. doi: 10.7759/cureus.17588. eCollection 2021 Aug.
Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is an autoimmune disease of the central nervous system characterized by positive GFAP autoantibody. The most common are encephalitis, meningoencephalitis or meningoencephalomyelitis. Antibodies in cerebrospinal fluid (CSF) against GFAP are biomarkers and expressed in most cases with autoimmune GFAP astrocytopathy. Diagnosis by biopsy is not common practice and has been rarely performed in the literature. This is the particularity of our reported case of autoimmune GFAP astrocytopathy presented as opticopyramidal syndrome, all paraclinical investigations were normal, only the biopsy allowed the diagnosis.
自身免疫性胶质纤维酸性蛋白(GFAP)星形细胞病是一种中枢神经系统自身免疫性疾病,其特征为GFAP自身抗体呈阳性。最常见的是脑炎、脑膜脑炎或脑膜脑脊髓炎。脑脊液(CSF)中针对GFAP的抗体是生物标志物,在大多数自身免疫性GFAP星形细胞病病例中均有表达。通过活检进行诊断并不常见,文献中也很少进行。这就是我们报告的以视锥综合征形式出现的自身免疫性GFAP星形细胞病病例的特殊性,所有辅助检查均正常,只有活检才能确诊。