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Amyotrophic lateral sclerosis mimicking radiculopathy: a case series
The clinical findings of early stage amyotrophic lateral sclerosis (ALS) are similar to those of cervical or lumbar radiculopathy. In the current study, we describe 3 cases of ALS that were misdiagnosed as cervical or lumbar radiculopathy. Three patients (a 48-, a 52-, and an 80-year-old) visited ou...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nagoya University
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648534/ https://www.ncbi.nlm.nih.gov/pubmed/34916730 http://dx.doi.org/10.18999/nagjms.83.4.877 |
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author | Kwak, Soyoung Kim, Du Hwan Boudier-Revéret, Mathieu Chang, Min Cheol |
author_facet | Kwak, Soyoung Kim, Du Hwan Boudier-Revéret, Mathieu Chang, Min Cheol |
author_sort | Kwak, Soyoung |
collection | PubMed |
description | The clinical findings of early stage amyotrophic lateral sclerosis (ALS) are similar to those of cervical or lumbar radiculopathy. In the current study, we describe 3 cases of ALS that were misdiagnosed as cervical or lumbar radiculopathy. Three patients (a 48-, a 52-, and an 80-year-old) visited our clinic due to motor weakness on either the upper or lower extremities. At other clinics or hospitals, they were diagnosed with radiculopathy due to herniated lumbar disc or cervical foraminal stenosis. The motor weakness in these patients was ipsilateral or bilateral but dominant on one side. Sensory deficits or bulbar symptoms were not observed. Of the 3 patients, 2 had neuropathic pain, but it was not dermatome related. We conducted an electrodiagnostic test and observed a low amplitude of compound motor action potential on the affected nerve and positive sharp waves on muscles of involved segments, including thoracic paraspinalis. All the patients were diagnosed with probable laboratory-supported ALS or possible ALS based on the established diagnostic criteria (El Escorial Criteria). In the present study, we showed three cases of ALS that were misdiagnosed as radiculopathy. Our study would be helpful for early and accurate diagnosis of patients with ALS. |
format | Online Article Text |
id | pubmed-8648534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nagoya University |
record_format | MEDLINE/PubMed |
spelling | pubmed-86485342021-12-15 Amyotrophic lateral sclerosis mimicking radiculopathy: a case series Kwak, Soyoung Kim, Du Hwan Boudier-Revéret, Mathieu Chang, Min Cheol Nagoya J Med Sci Case Report The clinical findings of early stage amyotrophic lateral sclerosis (ALS) are similar to those of cervical or lumbar radiculopathy. In the current study, we describe 3 cases of ALS that were misdiagnosed as cervical or lumbar radiculopathy. Three patients (a 48-, a 52-, and an 80-year-old) visited our clinic due to motor weakness on either the upper or lower extremities. At other clinics or hospitals, they were diagnosed with radiculopathy due to herniated lumbar disc or cervical foraminal stenosis. The motor weakness in these patients was ipsilateral or bilateral but dominant on one side. Sensory deficits or bulbar symptoms were not observed. Of the 3 patients, 2 had neuropathic pain, but it was not dermatome related. We conducted an electrodiagnostic test and observed a low amplitude of compound motor action potential on the affected nerve and positive sharp waves on muscles of involved segments, including thoracic paraspinalis. All the patients were diagnosed with probable laboratory-supported ALS or possible ALS based on the established diagnostic criteria (El Escorial Criteria). In the present study, we showed three cases of ALS that were misdiagnosed as radiculopathy. Our study would be helpful for early and accurate diagnosis of patients with ALS. Nagoya University 2021-11 /pmc/articles/PMC8648534/ /pubmed/34916730 http://dx.doi.org/10.18999/nagjms.83.4.877 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Case Report Kwak, Soyoung Kim, Du Hwan Boudier-Revéret, Mathieu Chang, Min Cheol Amyotrophic lateral sclerosis mimicking radiculopathy: a case series |
title | Amyotrophic lateral sclerosis mimicking radiculopathy: a case series |
title_full | Amyotrophic lateral sclerosis mimicking radiculopathy: a case series |
title_fullStr | Amyotrophic lateral sclerosis mimicking radiculopathy: a case series |
title_full_unstemmed | Amyotrophic lateral sclerosis mimicking radiculopathy: a case series |
title_short | Amyotrophic lateral sclerosis mimicking radiculopathy: a case series |
title_sort | amyotrophic lateral sclerosis mimicking radiculopathy: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8648534/ https://www.ncbi.nlm.nih.gov/pubmed/34916730 http://dx.doi.org/10.18999/nagjms.83.4.877 |
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