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Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review

BACKGROUND: Overlap syndromes of anti-NMDA receptor encephalitis and MOG-mediated demyelination have been reported. In this case we provide a long-term longitudinal follow-up of clinical and imaging characteristics as well as of antibody dynamics. CASE PRESENTATION: We report a 32-year-old male pati...

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Autores principales: Berek, Klaus, Grams, Astrid, Uprimny, Christian, Prieschl, Manuela, Ramberger, Melanie, Unterberger, Iris, Deisenhammer, Florian, Reindl, Markus, Hegen, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667590/
https://www.ncbi.nlm.nih.gov/pubmed/36384491
http://dx.doi.org/10.1186/s12883-022-02974-x
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author Berek, Klaus
Grams, Astrid
Uprimny, Christian
Prieschl, Manuela
Ramberger, Melanie
Unterberger, Iris
Deisenhammer, Florian
Reindl, Markus
Hegen, Harald
author_facet Berek, Klaus
Grams, Astrid
Uprimny, Christian
Prieschl, Manuela
Ramberger, Melanie
Unterberger, Iris
Deisenhammer, Florian
Reindl, Markus
Hegen, Harald
author_sort Berek, Klaus
collection PubMed
description BACKGROUND: Overlap syndromes of anti-NMDA receptor encephalitis and MOG-mediated demyelination have been reported. In this case we provide a long-term longitudinal follow-up of clinical and imaging characteristics as well as of antibody dynamics. CASE PRESENTATION: We report a 32-year-old male patient who presented with psychosis, decreased consciousness and movement disorders and was tested positive for anti-NMDA receptor antibodies. Forty-four months after symptom onset and diagnosis of autoimmune encephalitis, he suffered from relapse. At this time, the patient developed anti-MOG and anti-Caspr2 antibodies. Treatment with plasmapheresis, steroids and rituximab eventually led to substantial clinical and radiological improvement. Anti-Caspr2 antibodies persisted, anti-NMDA receptor antibodies decreased, while anti-MOG antibodies turned negative again. CONCLUSION: We provide long-term longitudinal follow-up of a patient with anti-NMDA receptor encephalitis who developed triple antibody positivity at the time of relapse. Antibody dynamics were associated with clinical disease course. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-022-02974-x.
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spelling pubmed-96675902022-11-17 Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review Berek, Klaus Grams, Astrid Uprimny, Christian Prieschl, Manuela Ramberger, Melanie Unterberger, Iris Deisenhammer, Florian Reindl, Markus Hegen, Harald BMC Neurol Case Report BACKGROUND: Overlap syndromes of anti-NMDA receptor encephalitis and MOG-mediated demyelination have been reported. In this case we provide a long-term longitudinal follow-up of clinical and imaging characteristics as well as of antibody dynamics. CASE PRESENTATION: We report a 32-year-old male patient who presented with psychosis, decreased consciousness and movement disorders and was tested positive for anti-NMDA receptor antibodies. Forty-four months after symptom onset and diagnosis of autoimmune encephalitis, he suffered from relapse. At this time, the patient developed anti-MOG and anti-Caspr2 antibodies. Treatment with plasmapheresis, steroids and rituximab eventually led to substantial clinical and radiological improvement. Anti-Caspr2 antibodies persisted, anti-NMDA receptor antibodies decreased, while anti-MOG antibodies turned negative again. CONCLUSION: We provide long-term longitudinal follow-up of a patient with anti-NMDA receptor encephalitis who developed triple antibody positivity at the time of relapse. Antibody dynamics were associated with clinical disease course. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12883-022-02974-x. BioMed Central 2022-11-16 /pmc/articles/PMC9667590/ /pubmed/36384491 http://dx.doi.org/10.1186/s12883-022-02974-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Berek, Klaus
Grams, Astrid
Uprimny, Christian
Prieschl, Manuela
Ramberger, Melanie
Unterberger, Iris
Deisenhammer, Florian
Reindl, Markus
Hegen, Harald
Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review
title Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review
title_full Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review
title_fullStr Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review
title_full_unstemmed Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review
title_short Anti-NMDA receptor encephalitis and MOG-associated demyelination – a case report with long-term follow-up and a systematic review
title_sort anti-nmda receptor encephalitis and mog-associated demyelination – a case report with long-term follow-up and a systematic review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667590/
https://www.ncbi.nlm.nih.gov/pubmed/36384491
http://dx.doi.org/10.1186/s12883-022-02974-x
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