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Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review
INTRODUCTION: Autoantibodies to the alpha‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptor and N‐methyl‐d‐aspartate (NMDA) receptor are known to be the causes of autoimmune encephalitis particularly limbic encephalitis. The involvement of the peripheral nervous system is rarely rep...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607545/ https://www.ncbi.nlm.nih.gov/pubmed/28948076 http://dx.doi.org/10.1002/brb3.779 |
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author | Wei, Yi‐Chia Huang, Chin‐Chang Liu, Chi‐Hung Kuo, Hung‐Chou Lin, Jainn‐Jim |
author_facet | Wei, Yi‐Chia Huang, Chin‐Chang Liu, Chi‐Hung Kuo, Hung‐Chou Lin, Jainn‐Jim |
author_sort | Wei, Yi‐Chia |
collection | PubMed |
description | INTRODUCTION: Autoantibodies to the alpha‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptor and N‐methyl‐d‐aspartate (NMDA) receptor are known to be the causes of autoimmune encephalitis particularly limbic encephalitis. The involvement of the peripheral nervous system is rarely reported. METHODS: We analyzed the serial nerve conduction studies of a previously reported case of anti‐AMPA receptor encephalitis, who was presented with conscious disturbance and quadriplegia. Initial nerve conduction studies (NCS) revealed motor axonal polyneuropathy with active denervation. We also performed systematic review of similar cases with overlapped peripheral neuropathy and glutamate receptor encephalitis through Embase, PubMed, and MEDLINE. RESULTS: Follow‐up NCS of the patient with anti‐AMPA receptor encephalitis found reverse of the acute neuropathy, which was compatible with clinical recovery of quadriplegia. The systematic review identified 10 cases with overlapping peripheral neuropathy with anti‐AMPA or NMDA receptor encephalitis. Motor or sensorimotor neuropathies were more common than pure sensory neuropathies. Anti‐Hu, anti‐amphiphysin, or anti‐gnaglioside antibodies coexisted in some cases and might be associated with the peripheral symptoms. CONCLUSIONS: Both anti‐AMPA and anti‐NMDA receptor encephalitis could overlap with acute peripheral neuropathy. It is important to consider peripheral symptoms and perform diagnostic tests. |
format | Online Article Text |
id | pubmed-5607545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56075452017-09-25 Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review Wei, Yi‐Chia Huang, Chin‐Chang Liu, Chi‐Hung Kuo, Hung‐Chou Lin, Jainn‐Jim Brain Behav Original Research INTRODUCTION: Autoantibodies to the alpha‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptor and N‐methyl‐d‐aspartate (NMDA) receptor are known to be the causes of autoimmune encephalitis particularly limbic encephalitis. The involvement of the peripheral nervous system is rarely reported. METHODS: We analyzed the serial nerve conduction studies of a previously reported case of anti‐AMPA receptor encephalitis, who was presented with conscious disturbance and quadriplegia. Initial nerve conduction studies (NCS) revealed motor axonal polyneuropathy with active denervation. We also performed systematic review of similar cases with overlapped peripheral neuropathy and glutamate receptor encephalitis through Embase, PubMed, and MEDLINE. RESULTS: Follow‐up NCS of the patient with anti‐AMPA receptor encephalitis found reverse of the acute neuropathy, which was compatible with clinical recovery of quadriplegia. The systematic review identified 10 cases with overlapping peripheral neuropathy with anti‐AMPA or NMDA receptor encephalitis. Motor or sensorimotor neuropathies were more common than pure sensory neuropathies. Anti‐Hu, anti‐amphiphysin, or anti‐gnaglioside antibodies coexisted in some cases and might be associated with the peripheral symptoms. CONCLUSIONS: Both anti‐AMPA and anti‐NMDA receptor encephalitis could overlap with acute peripheral neuropathy. It is important to consider peripheral symptoms and perform diagnostic tests. John Wiley and Sons Inc. 2017-08-01 /pmc/articles/PMC5607545/ /pubmed/28948076 http://dx.doi.org/10.1002/brb3.779 Text en © 2017 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Wei, Yi‐Chia Huang, Chin‐Chang Liu, Chi‐Hung Kuo, Hung‐Chou Lin, Jainn‐Jim Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review |
title | Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review |
title_full | Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review |
title_fullStr | Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review |
title_full_unstemmed | Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review |
title_short | Peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: Case report and systematic literature review |
title_sort | peripheral neuropathy in limbic encephalitis with anti‐glutamate receptor antibodies: case report and systematic literature review |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607545/ https://www.ncbi.nlm.nih.gov/pubmed/28948076 http://dx.doi.org/10.1002/brb3.779 |
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