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A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics
BACKGROUND: Segmental zoster paresis (SZP) of limbs, characterized by focal weakness of extremity, is recognized as a rare complication of herpes zoster (HZ). The following study analyzes the clinical characteristics and data from electromyography and MRI scans in patients with motor weakness after...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102897/ https://www.ncbi.nlm.nih.gov/pubmed/30131076 http://dx.doi.org/10.1186/s12883-018-1130-4 |
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author | Liu, Ying Wu, Bing-Yun Ma, Zhen-Shen Xu, Juan-Juan Yang, Bing Li, Heng Duan, Rui-Sheng |
author_facet | Liu, Ying Wu, Bing-Yun Ma, Zhen-Shen Xu, Juan-Juan Yang, Bing Li, Heng Duan, Rui-Sheng |
author_sort | Liu, Ying |
collection | PubMed |
description | BACKGROUND: Segmental zoster paresis (SZP) of limbs, characterized by focal weakness of extremity, is recognized as a rare complication of herpes zoster (HZ). The following study analyzes the clinical characteristics and data from electromyography and MRI scans in patients with motor weakness after zoster infection. METHODS: One thousand three hundred ninety-three patients from our database (Shandong Provincial Qianfoshan Hospital) suffering from HZ were retrospectively reviewed from June 2015 to July 2017. Patients who fulfilled the diagnostic criteria for SZP were included in the analysis. The clinical characteristics, as well as electromyography findings and MRI scans were analyzed. RESULTS: SZP was present in 0.57% of patients with HZ (8/1393). The average age of symptom onset in 8 SZP patients was 69 years old (SD: 13, range 47–87). The severity of muscle weakness ranged from mild to severe. The electrophysiological testing revealed the characteristics of axonopathy. Radiculopathy (2/8), plexopathy (2/8), radiculoplexopathy (3/8) and combined radiculopathy and mononeuropathy (1/8) were also identified. MRI revealed hyperintensity of the affected spinal dorsal horns, nerve roots or peripheral nerves. CONCLUSIONS: SZP is associated with obvious limb weakness, nerve axons lesions and localization to nerve roots, plexus or peripheral nerves. |
format | Online Article Text |
id | pubmed-6102897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61028972018-08-27 A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics Liu, Ying Wu, Bing-Yun Ma, Zhen-Shen Xu, Juan-Juan Yang, Bing Li, Heng Duan, Rui-Sheng BMC Neurol Research Article BACKGROUND: Segmental zoster paresis (SZP) of limbs, characterized by focal weakness of extremity, is recognized as a rare complication of herpes zoster (HZ). The following study analyzes the clinical characteristics and data from electromyography and MRI scans in patients with motor weakness after zoster infection. METHODS: One thousand three hundred ninety-three patients from our database (Shandong Provincial Qianfoshan Hospital) suffering from HZ were retrospectively reviewed from June 2015 to July 2017. Patients who fulfilled the diagnostic criteria for SZP were included in the analysis. The clinical characteristics, as well as electromyography findings and MRI scans were analyzed. RESULTS: SZP was present in 0.57% of patients with HZ (8/1393). The average age of symptom onset in 8 SZP patients was 69 years old (SD: 13, range 47–87). The severity of muscle weakness ranged from mild to severe. The electrophysiological testing revealed the characteristics of axonopathy. Radiculopathy (2/8), plexopathy (2/8), radiculoplexopathy (3/8) and combined radiculopathy and mononeuropathy (1/8) were also identified. MRI revealed hyperintensity of the affected spinal dorsal horns, nerve roots or peripheral nerves. CONCLUSIONS: SZP is associated with obvious limb weakness, nerve axons lesions and localization to nerve roots, plexus or peripheral nerves. BioMed Central 2018-08-21 /pmc/articles/PMC6102897/ /pubmed/30131076 http://dx.doi.org/10.1186/s12883-018-1130-4 Text en © The Author(s). 2018 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 | Research Article Liu, Ying Wu, Bing-Yun Ma, Zhen-Shen Xu, Juan-Juan Yang, Bing Li, Heng Duan, Rui-Sheng A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics |
title | A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics |
title_full | A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics |
title_fullStr | A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics |
title_full_unstemmed | A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics |
title_short | A retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics |
title_sort | retrospective case series of segmental zoster paresis of limbs: clinical, electrophysiological and imaging characteristics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102897/ https://www.ncbi.nlm.nih.gov/pubmed/30131076 http://dx.doi.org/10.1186/s12883-018-1130-4 |
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