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Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis
OBJECTIVES: The goal of this study was to analyze the clinical and magnetic resonance imaging (MRI) characteristics of autoimmune encephalitis (AE) and viral encephalitis (VE) at the initial stage of onset. METHODS: This study was a retrospective analysis of the clinical manifestations, laboratory t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taibah University
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926194/ https://www.ncbi.nlm.nih.gov/pubmed/36817222 http://dx.doi.org/10.1016/j.jtumed.2022.09.016 |
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author | Tan, Yongming Liu, Meng He, Laichang |
author_facet | Tan, Yongming Liu, Meng He, Laichang |
author_sort | Tan, Yongming |
collection | PubMed |
description | OBJECTIVES: The goal of this study was to analyze the clinical and magnetic resonance imaging (MRI) characteristics of autoimmune encephalitis (AE) and viral encephalitis (VE) at the initial stage of onset. METHODS: This study was a retrospective analysis of the clinical manifestations, laboratory tests, electroencephalogram examination, imaging examinations, and treatment outcomes of 24 VE patients and 20 AE patients. RESULTS: The onset age was significantly younger in the VE group than in the AE group, mainly occurring in adolescents (P < 0.05). The proportions of fever, headache, and vomiting were higher in the VE group than in the AE group (P < 0.05), and there were few manifestations of central hypoventilation. The incidence of abnormal myocardial enzymes was significantly higher in the VE group than in the AE group (P < 0.05). There was no significant difference in electroencephalogram test results between the VE and AE groups. Regarding magnetic resonance imaging (MRI), the proportion of single lesion involving a single lobe or multiple asymmetries involving the limbic system in the VE group was higher than that in the AE group (P < 0.05). The incidence of lesion enhancement in the VE group was higher than that in the AE group. Meanwhile, diffusion-weighted imaging sequence was more sensitive than T2 liquid-attenuated inversion recovery sequence in the detection, efficacy evaluation, and follow-up review of the AE and VE groups. CONCLUSION: The onset age of VE is younger, and the clinical symptoms of AE and VE differ with statistical significance. MRI can objectively reflect the imaging characteristics of both groups. Combining early clinical manifestations with imaging manifestations can facilitate early diagnosis and treatment, and improve the prognosis. |
format | Online Article Text |
id | pubmed-9926194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taibah University |
record_format | MEDLINE/PubMed |
spelling | pubmed-99261942023-02-16 Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis Tan, Yongming Liu, Meng He, Laichang J Taibah Univ Med Sci Original Article OBJECTIVES: The goal of this study was to analyze the clinical and magnetic resonance imaging (MRI) characteristics of autoimmune encephalitis (AE) and viral encephalitis (VE) at the initial stage of onset. METHODS: This study was a retrospective analysis of the clinical manifestations, laboratory tests, electroencephalogram examination, imaging examinations, and treatment outcomes of 24 VE patients and 20 AE patients. RESULTS: The onset age was significantly younger in the VE group than in the AE group, mainly occurring in adolescents (P < 0.05). The proportions of fever, headache, and vomiting were higher in the VE group than in the AE group (P < 0.05), and there were few manifestations of central hypoventilation. The incidence of abnormal myocardial enzymes was significantly higher in the VE group than in the AE group (P < 0.05). There was no significant difference in electroencephalogram test results between the VE and AE groups. Regarding magnetic resonance imaging (MRI), the proportion of single lesion involving a single lobe or multiple asymmetries involving the limbic system in the VE group was higher than that in the AE group (P < 0.05). The incidence of lesion enhancement in the VE group was higher than that in the AE group. Meanwhile, diffusion-weighted imaging sequence was more sensitive than T2 liquid-attenuated inversion recovery sequence in the detection, efficacy evaluation, and follow-up review of the AE and VE groups. CONCLUSION: The onset age of VE is younger, and the clinical symptoms of AE and VE differ with statistical significance. MRI can objectively reflect the imaging characteristics of both groups. Combining early clinical manifestations with imaging manifestations can facilitate early diagnosis and treatment, and improve the prognosis. Taibah University 2022-10-11 /pmc/articles/PMC9926194/ /pubmed/36817222 http://dx.doi.org/10.1016/j.jtumed.2022.09.016 Text en © 2022 [The Author/The Authors] https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Tan, Yongming Liu, Meng He, Laichang Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis |
title | Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis |
title_full | Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis |
title_fullStr | Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis |
title_full_unstemmed | Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis |
title_short | Clinical and MRI differential analysis of autoimmune encephalitis and viral encephalitis |
title_sort | clinical and mri differential analysis of autoimmune encephalitis and viral encephalitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926194/ https://www.ncbi.nlm.nih.gov/pubmed/36817222 http://dx.doi.org/10.1016/j.jtumed.2022.09.016 |
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