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Spinal segmental myoclonus as an unusual presentation of multiple sclerosis

BACKGROUND: Unusual presentations of multiple sclerosis (MS) at onset may post a diagnostic dilemma to the treating neurologists. Spinal myoclonus is rare in MS and may lead to perform extensive investigations to rule out other etiologies affecting the spinal cord. CASE PRESENTATION: We described a...

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Autores principales: Alroughani, Raed Abdullah, Ahmed, Samar Farouk, Khan, Riyadh Ahmed, Al-Hashel, Jasem Yousef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347575/
https://www.ncbi.nlm.nih.gov/pubmed/25879483
http://dx.doi.org/10.1186/s12883-015-0271-y
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author Alroughani, Raed Abdullah
Ahmed, Samar Farouk
Khan, Riyadh Ahmed
Al-Hashel, Jasem Yousef
author_facet Alroughani, Raed Abdullah
Ahmed, Samar Farouk
Khan, Riyadh Ahmed
Al-Hashel, Jasem Yousef
author_sort Alroughani, Raed Abdullah
collection PubMed
description BACKGROUND: Unusual presentations of multiple sclerosis (MS) at onset may post a diagnostic dilemma to the treating neurologists. Spinal myoclonus is rare in MS and may lead to perform extensive investigations to rule out other etiologies affecting the spinal cord. CASE PRESENTATION: We described a 31-year-old male who presented with involuntary brief jerky movements of the left shoulder and arm with significant wasting of shoulder muscles. In retrospect, the patient had a progressive right leg weakness one year prior to his presentation. Needle electromyography confirmed the presence of rhythmic irregular burst discharges in motor units of muscles expanding from the third to the sixth cervical region with normal nerve conduction parameters. There was no evidence of cortically generated myoclonic jerks using time-locked electroencephalogram. Magnetic Resonance Imaging of the brain and cervical cord along with the presence of oligoclonal bands in cerebral spinal fluid confirmed the diagnosis of MS. Based on the history and progressive clinical features, a diagnosis of primary progressive MS was established. CONCLUSION: Spinal myoclonus can be the presenting manifestation of MS in association with demyelinating plaques in the root exit zones of the spinal cord. Spinal myoclonus may pose a diagnostic challenge when it presented at the disease onset and especially in patients with progressive course at onset. Our patient represents the first reported primary progressive MS case in the literature with spinal myoclonus presentation.
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spelling pubmed-43475752015-03-04 Spinal segmental myoclonus as an unusual presentation of multiple sclerosis Alroughani, Raed Abdullah Ahmed, Samar Farouk Khan, Riyadh Ahmed Al-Hashel, Jasem Yousef BMC Neurol Case Report BACKGROUND: Unusual presentations of multiple sclerosis (MS) at onset may post a diagnostic dilemma to the treating neurologists. Spinal myoclonus is rare in MS and may lead to perform extensive investigations to rule out other etiologies affecting the spinal cord. CASE PRESENTATION: We described a 31-year-old male who presented with involuntary brief jerky movements of the left shoulder and arm with significant wasting of shoulder muscles. In retrospect, the patient had a progressive right leg weakness one year prior to his presentation. Needle electromyography confirmed the presence of rhythmic irregular burst discharges in motor units of muscles expanding from the third to the sixth cervical region with normal nerve conduction parameters. There was no evidence of cortically generated myoclonic jerks using time-locked electroencephalogram. Magnetic Resonance Imaging of the brain and cervical cord along with the presence of oligoclonal bands in cerebral spinal fluid confirmed the diagnosis of MS. Based on the history and progressive clinical features, a diagnosis of primary progressive MS was established. CONCLUSION: Spinal myoclonus can be the presenting manifestation of MS in association with demyelinating plaques in the root exit zones of the spinal cord. Spinal myoclonus may pose a diagnostic challenge when it presented at the disease onset and especially in patients with progressive course at onset. Our patient represents the first reported primary progressive MS case in the literature with spinal myoclonus presentation. BioMed Central 2015-02-27 /pmc/articles/PMC4347575/ /pubmed/25879483 http://dx.doi.org/10.1186/s12883-015-0271-y Text en © Alroughani et al.; licensee BioMed Central . 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Alroughani, Raed Abdullah
Ahmed, Samar Farouk
Khan, Riyadh Ahmed
Al-Hashel, Jasem Yousef
Spinal segmental myoclonus as an unusual presentation of multiple sclerosis
title Spinal segmental myoclonus as an unusual presentation of multiple sclerosis
title_full Spinal segmental myoclonus as an unusual presentation of multiple sclerosis
title_fullStr Spinal segmental myoclonus as an unusual presentation of multiple sclerosis
title_full_unstemmed Spinal segmental myoclonus as an unusual presentation of multiple sclerosis
title_short Spinal segmental myoclonus as an unusual presentation of multiple sclerosis
title_sort spinal segmental myoclonus as an unusual presentation of multiple sclerosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347575/
https://www.ncbi.nlm.nih.gov/pubmed/25879483
http://dx.doi.org/10.1186/s12883-015-0271-y
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