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Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report
BACKGROUND: Hashimoto’s encephalitis (HE) is a rare neurological complication of Hashimoto’s thyroiditis (HT), while limbic encephalitis (LE) is an autoimmune inflammatory disorder frequently associated with anti-neuronal antibodies. The glutamate receptor α-amino-3-hydroxy-5-methyl-4-isoxazole-prop...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320737/ https://www.ncbi.nlm.nih.gov/pubmed/28222692 http://dx.doi.org/10.1186/s12883-017-0823-4 |
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author | Zhu, Mingqin Yu, Xuefan Liu, Caiyun Duan, Chenchen Li, Chunxiao Zhu, Jie Zhang, Ying |
author_facet | Zhu, Mingqin Yu, Xuefan Liu, Caiyun Duan, Chenchen Li, Chunxiao Zhu, Jie Zhang, Ying |
author_sort | Zhu, Mingqin |
collection | PubMed |
description | BACKGROUND: Hashimoto’s encephalitis (HE) is a rare neurological complication of Hashimoto’s thyroiditis (HT), while limbic encephalitis (LE) is an autoimmune inflammatory disorder frequently associated with anti-neuronal antibodies. The glutamate receptor α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor (AMPAR) is important for synaptic transmission, memory, and learning. The etiology of HE remains unclear. We present a case of HE with antibodies to AMPAR2 both in the serum and cerebrospinal fluid. CASE PRESENTATION: The patient presented with progressive memory loss and subsequently went into a coma. Magnetic resonance imaging revealed temporal lobe and hippocampal lesions, while the electrocardiogram showed paroxysmal delta waves. Elevated serum levels of antibodies against thyroid globulin, thyroid peroxidase, and thyroid stimulating receptor were also noted. Ultrasonography showed enlargement of the thyroid gland. Therefore, the diagnosis was established as HE. Both the CSF and serum samples of the patient tested positive for antibodies to the cell-surface antigen AMPAR2. Intravenous injection of immunoglobulin followed by dexamethasone treatment resulted in recovery from the coma. Follow-up examination three months later showed some improvement of memory. To our knowledge, this is the first report on the detection of AMPAR2 antibodies in HE. CONCLUSIONS: Our findings suggest that antibodies to AMPAR2 may be involved in the pathogenesis of HE. Elevated levels of thyroid antibodies possibly cause immune dysfunction, leading to the production of anti-AMPAR2 antibodies that are detrimental to the neurons. We believe that encephalitis patients with thyroid abnormalities should undergo screening for anti-neuronal antibodies, and early immune therapy may improve prognosis. |
format | Online Article Text |
id | pubmed-5320737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53207372017-02-24 Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report Zhu, Mingqin Yu, Xuefan Liu, Caiyun Duan, Chenchen Li, Chunxiao Zhu, Jie Zhang, Ying BMC Neurol Case Report BACKGROUND: Hashimoto’s encephalitis (HE) is a rare neurological complication of Hashimoto’s thyroiditis (HT), while limbic encephalitis (LE) is an autoimmune inflammatory disorder frequently associated with anti-neuronal antibodies. The glutamate receptor α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor (AMPAR) is important for synaptic transmission, memory, and learning. The etiology of HE remains unclear. We present a case of HE with antibodies to AMPAR2 both in the serum and cerebrospinal fluid. CASE PRESENTATION: The patient presented with progressive memory loss and subsequently went into a coma. Magnetic resonance imaging revealed temporal lobe and hippocampal lesions, while the electrocardiogram showed paroxysmal delta waves. Elevated serum levels of antibodies against thyroid globulin, thyroid peroxidase, and thyroid stimulating receptor were also noted. Ultrasonography showed enlargement of the thyroid gland. Therefore, the diagnosis was established as HE. Both the CSF and serum samples of the patient tested positive for antibodies to the cell-surface antigen AMPAR2. Intravenous injection of immunoglobulin followed by dexamethasone treatment resulted in recovery from the coma. Follow-up examination three months later showed some improvement of memory. To our knowledge, this is the first report on the detection of AMPAR2 antibodies in HE. CONCLUSIONS: Our findings suggest that antibodies to AMPAR2 may be involved in the pathogenesis of HE. Elevated levels of thyroid antibodies possibly cause immune dysfunction, leading to the production of anti-AMPAR2 antibodies that are detrimental to the neurons. We believe that encephalitis patients with thyroid abnormalities should undergo screening for anti-neuronal antibodies, and early immune therapy may improve prognosis. BioMed Central 2017-02-21 /pmc/articles/PMC5320737/ /pubmed/28222692 http://dx.doi.org/10.1186/s12883-017-0823-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Zhu, Mingqin Yu, Xuefan Liu, Caiyun Duan, Chenchen Li, Chunxiao Zhu, Jie Zhang, Ying Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report |
title | Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report |
title_full | Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report |
title_fullStr | Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report |
title_full_unstemmed | Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report |
title_short | Hashimoto’s encephalitis associated with AMPAR2 antibodies: a case report |
title_sort | hashimoto’s encephalitis associated with ampar2 antibodies: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320737/ https://www.ncbi.nlm.nih.gov/pubmed/28222692 http://dx.doi.org/10.1186/s12883-017-0823-4 |
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