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Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy

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...

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Autores principales: Mabrouki, Fatima Zahra, Aziouaz, Faiza, Sekhsoukh, Rachid, Yassine, Mebrouk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482051/
https://www.ncbi.nlm.nih.gov/pubmed/34646641
http://dx.doi.org/10.7759/cureus.17588
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author Mabrouki, Fatima Zahra
Aziouaz, Faiza
Sekhsoukh, Rachid
Yassine, Mebrouk
author_facet Mabrouki, Fatima Zahra
Aziouaz, Faiza
Sekhsoukh, Rachid
Yassine, Mebrouk
author_sort Mabrouki, Fatima Zahra
collection PubMed
description 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.
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spelling pubmed-84820512021-10-12 Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy Mabrouki, Fatima Zahra Aziouaz, Faiza Sekhsoukh, Rachid Yassine, Mebrouk Cureus Neurology 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. Cureus 2021-08-31 /pmc/articles/PMC8482051/ /pubmed/34646641 http://dx.doi.org/10.7759/cureus.17588 Text en Copyright © 2021, Mabrouki et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurology
Mabrouki, Fatima Zahra
Aziouaz, Faiza
Sekhsoukh, Rachid
Yassine, Mebrouk
Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
title Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
title_full Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
title_fullStr Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
title_full_unstemmed Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
title_short Subacute Blindness Revealing an Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
title_sort subacute blindness revealing an autoimmune glial fibrillary acidic protein astrocytopathy
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482051/
https://www.ncbi.nlm.nih.gov/pubmed/34646641
http://dx.doi.org/10.7759/cureus.17588
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