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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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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. |
format | Online Article Text |
id | pubmed-8482051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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