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Amyotrophic lateral sclerosis with a sudden-onset history
OBJECTIVE: We report on two patients with amyotrophic lateral sclerosis (ALS) complaining of sudden-onset difficulty in finger elevation. CASE REPORT: A 65-year-old man (the first patient) and a 66-year-old man (the second patient) suddenly became aware of difficulty in finger elevation of one hand....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123847/ https://www.ncbi.nlm.nih.gov/pubmed/30214980 http://dx.doi.org/10.1016/j.cnp.2017.04.003 |
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author | Kanbayashi, Takamichi Mikata, Takashi Hatanaka, Yuki Sonoo, Masahiro |
author_facet | Kanbayashi, Takamichi Mikata, Takashi Hatanaka, Yuki Sonoo, Masahiro |
author_sort | Kanbayashi, Takamichi |
collection | PubMed |
description | OBJECTIVE: We report on two patients with amyotrophic lateral sclerosis (ALS) complaining of sudden-onset difficulty in finger elevation. CASE REPORT: A 65-year-old man (the first patient) and a 66-year-old man (the second patient) suddenly became aware of difficulty in finger elevation of one hand. They were not aware of any other symptoms prior to the onset. In the first patient, cerebral infarction at the precentral gyrus was initially suspected. In the second patient, cervical spondylosis was initially suspected, and cervical spine surgery was planned. However, needle EMG revealed widespread neurogenic changes and abundant fasciculation potentials for both patients. Widespread weakness emerged in time and relentlessly progressed, and finally the diagnosis of ALS was made. In both cases, notable weakness in the extensor digitorum (ED) muscle with relatively mild weakness in the other muscles in the affected limb was a characteristic finding. Loss of one motor unit in ED that has already enlarged due to reinnervation must have caused sudden awareness of the weakness. SIGNIFICANCE: Clinicians should recognize the presence of ALS patients with a sudden-onset history because the risk of initial misdiagnosis is high for such patients. |
format | Online Article Text |
id | pubmed-6123847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61238472018-09-13 Amyotrophic lateral sclerosis with a sudden-onset history Kanbayashi, Takamichi Mikata, Takashi Hatanaka, Yuki Sonoo, Masahiro Clin Neurophysiol Pract Clinical and Research Article OBJECTIVE: We report on two patients with amyotrophic lateral sclerosis (ALS) complaining of sudden-onset difficulty in finger elevation. CASE REPORT: A 65-year-old man (the first patient) and a 66-year-old man (the second patient) suddenly became aware of difficulty in finger elevation of one hand. They were not aware of any other symptoms prior to the onset. In the first patient, cerebral infarction at the precentral gyrus was initially suspected. In the second patient, cervical spondylosis was initially suspected, and cervical spine surgery was planned. However, needle EMG revealed widespread neurogenic changes and abundant fasciculation potentials for both patients. Widespread weakness emerged in time and relentlessly progressed, and finally the diagnosis of ALS was made. In both cases, notable weakness in the extensor digitorum (ED) muscle with relatively mild weakness in the other muscles in the affected limb was a characteristic finding. Loss of one motor unit in ED that has already enlarged due to reinnervation must have caused sudden awareness of the weakness. SIGNIFICANCE: Clinicians should recognize the presence of ALS patients with a sudden-onset history because the risk of initial misdiagnosis is high for such patients. Elsevier 2017-05-06 /pmc/articles/PMC6123847/ /pubmed/30214980 http://dx.doi.org/10.1016/j.cnp.2017.04.003 Text en © 2017 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. http://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 | Clinical and Research Article Kanbayashi, Takamichi Mikata, Takashi Hatanaka, Yuki Sonoo, Masahiro Amyotrophic lateral sclerosis with a sudden-onset history |
title | Amyotrophic lateral sclerosis with a sudden-onset history |
title_full | Amyotrophic lateral sclerosis with a sudden-onset history |
title_fullStr | Amyotrophic lateral sclerosis with a sudden-onset history |
title_full_unstemmed | Amyotrophic lateral sclerosis with a sudden-onset history |
title_short | Amyotrophic lateral sclerosis with a sudden-onset history |
title_sort | amyotrophic lateral sclerosis with a sudden-onset history |
topic | Clinical and Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123847/ https://www.ncbi.nlm.nih.gov/pubmed/30214980 http://dx.doi.org/10.1016/j.cnp.2017.04.003 |
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