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Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality?
BACKGROUND: Bickerstaff’s encephalitis (BE) is an acute post-infectious demyelinating disease with albuminocytological dissociation. A chronic form has rarely been described previously. CASE PRESENTATION: A 44-year-old man was hospitalized for drowsiness, cognitive complaint limb weakness, ataxia an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040113/ https://www.ncbi.nlm.nih.gov/pubmed/24885623 http://dx.doi.org/10.1186/1471-2377-14-99 |
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author | Renaud, Mathilde Aupy, Jérôme Camuset, Guillaume Collongues, Nicolas Chanson, Jean-Baptiste de Seze, Jérôme Blanc, Frédéric |
author_facet | Renaud, Mathilde Aupy, Jérôme Camuset, Guillaume Collongues, Nicolas Chanson, Jean-Baptiste de Seze, Jérôme Blanc, Frédéric |
author_sort | Renaud, Mathilde |
collection | PubMed |
description | BACKGROUND: Bickerstaff’s encephalitis (BE) is an acute post-infectious demyelinating disease with albuminocytological dissociation. A chronic form has rarely been described previously. CASE PRESENTATION: A 44-year-old man was hospitalized for drowsiness, cognitive complaint limb weakness, ataxia and sensory disturbance after diarrhea. Neuropsychological evaluation showed slowing, memory and executive function impairment, while analysis of the CSF showed albuminocytological dissociation. Immunologic tests showed positive anti-ganglioside antibodies (anti-GM1 IgM, anti-GD1a IgG and anti-GD1b IgM). Brain MRI was normal but SPECT showed bilateral temporal and frontal hypoperfusion. Outcome under immunoglobulin treatment (IVIG) was favorable with an initial improvement but was marked by worsening after a few weeks. Consequently, the patient was treated with IVIG every 2 months due to the recurrence of symptoms after 6 weeks. CONCLUSION: This case raises the question of the existence of a chronic form of BE with cognitive impairment, in the same way as chronic inflammatory demyelinating polyneuropathy is considered to be a chronic form of Guillain–Barré syndrome. |
format | Online Article Text |
id | pubmed-4040113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40401132014-06-01 Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality? Renaud, Mathilde Aupy, Jérôme Camuset, Guillaume Collongues, Nicolas Chanson, Jean-Baptiste de Seze, Jérôme Blanc, Frédéric BMC Neurol Case Report BACKGROUND: Bickerstaff’s encephalitis (BE) is an acute post-infectious demyelinating disease with albuminocytological dissociation. A chronic form has rarely been described previously. CASE PRESENTATION: A 44-year-old man was hospitalized for drowsiness, cognitive complaint limb weakness, ataxia and sensory disturbance after diarrhea. Neuropsychological evaluation showed slowing, memory and executive function impairment, while analysis of the CSF showed albuminocytological dissociation. Immunologic tests showed positive anti-ganglioside antibodies (anti-GM1 IgM, anti-GD1a IgG and anti-GD1b IgM). Brain MRI was normal but SPECT showed bilateral temporal and frontal hypoperfusion. Outcome under immunoglobulin treatment (IVIG) was favorable with an initial improvement but was marked by worsening after a few weeks. Consequently, the patient was treated with IVIG every 2 months due to the recurrence of symptoms after 6 weeks. CONCLUSION: This case raises the question of the existence of a chronic form of BE with cognitive impairment, in the same way as chronic inflammatory demyelinating polyneuropathy is considered to be a chronic form of Guillain–Barré syndrome. BioMed Central 2014-05-06 /pmc/articles/PMC4040113/ /pubmed/24885623 http://dx.doi.org/10.1186/1471-2377-14-99 Text en Copyright © 2014 Renaud et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Renaud, Mathilde Aupy, Jérôme Camuset, Guillaume Collongues, Nicolas Chanson, Jean-Baptiste de Seze, Jérôme Blanc, Frédéric Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality? |
title | Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality? |
title_full | Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality? |
title_fullStr | Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality? |
title_full_unstemmed | Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality? |
title_short | Chronic Bickerstaff’s encephalitis with cognitive impairment, a reality? |
title_sort | chronic bickerstaff’s encephalitis with cognitive impairment, a reality? |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4040113/ https://www.ncbi.nlm.nih.gov/pubmed/24885623 http://dx.doi.org/10.1186/1471-2377-14-99 |
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