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Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report

BACKGROUND: Autoimmune encephalitis (AE) with multiple auto-antibodies is of great clinical significance because its complex clinical manifestations and atypical imaging increase the difficulty of diagnosis, differential diagnosis and treatment, which may aggravate the disease, increase the recurren...

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Autores principales: Xie, Yi, Wen, Jia, Zhao, Zhihua, Liu, Hongbo, Xie, Nanchang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626930/
https://www.ncbi.nlm.nih.gov/pubmed/34836497
http://dx.doi.org/10.1186/s12883-021-02460-w
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author Xie, Yi
Wen, Jia
Zhao, Zhihua
Liu, Hongbo
Xie, Nanchang
author_facet Xie, Yi
Wen, Jia
Zhao, Zhihua
Liu, Hongbo
Xie, Nanchang
author_sort Xie, Yi
collection PubMed
description BACKGROUND: Autoimmune encephalitis (AE) with multiple auto-antibodies is of great clinical significance because its complex clinical manifestations and atypical imaging increase the difficulty of diagnosis, differential diagnosis and treatment, which may aggravate the disease, increase the recurrence rate and mortality. The coexistence of anti-Leucinie-rich Glioma Inactivated 1 (LGI1) and anti-γ-aminobutyric acid-beta-receptor 1 (GABA(B)R1) has not been published before. CASE PRESENTATION: We herein present the case of a 60-year-old man with slow response, behavioral changes, psychosis and sleep disorders. Laboratory test included serum hyponatremia, positive serum LGI1 and GABA(B)R1 antibodies using transfected cell-based assays. Electroencephalogram exhibited moderate diffusion abnormality. The patient responded well to steroid impulse treatment and sodium supplement therapy, and did not recur during the follow-up. CONCLUSIONS: Here we report the first AE characterized by positive LGI1 and GABA(B)R1 antibodies, as well as summarizing AE with multiple auto-antibodies reported so far, hopefully to provide experience for clinical practice.
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spelling pubmed-86269302021-11-29 Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report Xie, Yi Wen, Jia Zhao, Zhihua Liu, Hongbo Xie, Nanchang BMC Neurol Case Report BACKGROUND: Autoimmune encephalitis (AE) with multiple auto-antibodies is of great clinical significance because its complex clinical manifestations and atypical imaging increase the difficulty of diagnosis, differential diagnosis and treatment, which may aggravate the disease, increase the recurrence rate and mortality. The coexistence of anti-Leucinie-rich Glioma Inactivated 1 (LGI1) and anti-γ-aminobutyric acid-beta-receptor 1 (GABA(B)R1) has not been published before. CASE PRESENTATION: We herein present the case of a 60-year-old man with slow response, behavioral changes, psychosis and sleep disorders. Laboratory test included serum hyponatremia, positive serum LGI1 and GABA(B)R1 antibodies using transfected cell-based assays. Electroencephalogram exhibited moderate diffusion abnormality. The patient responded well to steroid impulse treatment and sodium supplement therapy, and did not recur during the follow-up. CONCLUSIONS: Here we report the first AE characterized by positive LGI1 and GABA(B)R1 antibodies, as well as summarizing AE with multiple auto-antibodies reported so far, hopefully to provide experience for clinical practice. BioMed Central 2021-11-27 /pmc/articles/PMC8626930/ /pubmed/34836497 http://dx.doi.org/10.1186/s12883-021-02460-w Text en © The Author(s) 2021 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
Xie, Yi
Wen, Jia
Zhao, Zhihua
Liu, Hongbo
Xie, Nanchang
Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report
title Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report
title_full Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report
title_fullStr Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report
title_full_unstemmed Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report
title_short Autoimmune encephalitis with coexistent LGI1 and GABA(B)R1 antibodies: case report
title_sort autoimmune encephalitis with coexistent lgi1 and gaba(b)r1 antibodies: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626930/
https://www.ncbi.nlm.nih.gov/pubmed/34836497
http://dx.doi.org/10.1186/s12883-021-02460-w
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