Cargando…
Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report
BACKGROUND: Anti–N-methyl-D-aspartate receptor immunoglobulin G antibodies directed against the GluN1 subunit are considered highly specific for anti-N-methyl-D-aspartate receptor encephalitis, a severe clinical syndrome characterized by seizures, psychiatric symptoms, orofacial dyskinesia and auton...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307172/ https://www.ncbi.nlm.nih.gov/pubmed/25539977 http://dx.doi.org/10.1186/1756-0500-7-948 |
_version_ | 1782354413503905792 |
---|---|
author | Waschbisch, Anne Kallmünzer, Bernd Schwab, Stefan Gölitz, Philipp Vincent, Angela Lee, De-Hyung Linker, Ralf A |
author_facet | Waschbisch, Anne Kallmünzer, Bernd Schwab, Stefan Gölitz, Philipp Vincent, Angela Lee, De-Hyung Linker, Ralf A |
author_sort | Waschbisch, Anne |
collection | PubMed |
description | BACKGROUND: Anti–N-methyl-D-aspartate receptor immunoglobulin G antibodies directed against the GluN1 subunit are considered highly specific for anti-N-methyl-D-aspartate receptor encephalitis, a severe clinical syndrome characterized by seizures, psychiatric symptoms, orofacial dyskinesia and autonomic dysfunction. CASE PRESENTATION: Here we report a 33 year old Caucasian male patient with clinically definite multiple sclerosis who was found to be positive for anti-N-methyl-D-aspartate receptor antibodies. Rituximab therapy was initiated. On the 18 months follow-up visit the patient was found to be clinically stable, without typical signs of anti-N-methyl-D-aspartate receptor encephalitis. CONCLUSION: Our findings add to the growing evidence for a possible association between anti-N-methyl-D-aspartate receptor encephalitis and demyelinating diseases. |
format | Online Article Text |
id | pubmed-4307172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43071722015-01-28 Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report Waschbisch, Anne Kallmünzer, Bernd Schwab, Stefan Gölitz, Philipp Vincent, Angela Lee, De-Hyung Linker, Ralf A BMC Res Notes Case Report BACKGROUND: Anti–N-methyl-D-aspartate receptor immunoglobulin G antibodies directed against the GluN1 subunit are considered highly specific for anti-N-methyl-D-aspartate receptor encephalitis, a severe clinical syndrome characterized by seizures, psychiatric symptoms, orofacial dyskinesia and autonomic dysfunction. CASE PRESENTATION: Here we report a 33 year old Caucasian male patient with clinically definite multiple sclerosis who was found to be positive for anti-N-methyl-D-aspartate receptor antibodies. Rituximab therapy was initiated. On the 18 months follow-up visit the patient was found to be clinically stable, without typical signs of anti-N-methyl-D-aspartate receptor encephalitis. CONCLUSION: Our findings add to the growing evidence for a possible association between anti-N-methyl-D-aspartate receptor encephalitis and demyelinating diseases. BioMed Central 2014-12-23 /pmc/articles/PMC4307172/ /pubmed/25539977 http://dx.doi.org/10.1186/1756-0500-7-948 Text en © Waschbisch et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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 Waschbisch, Anne Kallmünzer, Bernd Schwab, Stefan Gölitz, Philipp Vincent, Angela Lee, De-Hyung Linker, Ralf A Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report |
title | Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report |
title_full | Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report |
title_fullStr | Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report |
title_full_unstemmed | Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report |
title_short | Demyelinating disease and anti-N-methyl-D-aspartate receptor immunoglobulin G antibodies: a case report |
title_sort | demyelinating disease and anti-n-methyl-d-aspartate receptor immunoglobulin g antibodies: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307172/ https://www.ncbi.nlm.nih.gov/pubmed/25539977 http://dx.doi.org/10.1186/1756-0500-7-948 |
work_keys_str_mv | AT waschbischanne demyelinatingdiseaseandantinmethyldaspartatereceptorimmunoglobulingantibodiesacasereport AT kallmunzerbernd demyelinatingdiseaseandantinmethyldaspartatereceptorimmunoglobulingantibodiesacasereport AT schwabstefan demyelinatingdiseaseandantinmethyldaspartatereceptorimmunoglobulingantibodiesacasereport AT golitzphilipp demyelinatingdiseaseandantinmethyldaspartatereceptorimmunoglobulingantibodiesacasereport AT vincentangela demyelinatingdiseaseandantinmethyldaspartatereceptorimmunoglobulingantibodiesacasereport AT leedehyung demyelinatingdiseaseandantinmethyldaspartatereceptorimmunoglobulingantibodiesacasereport AT linkerralfa demyelinatingdiseaseandantinmethyldaspartatereceptorimmunoglobulingantibodiesacasereport |