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Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature

OBJECTIVE: Cervical spondylotic amyotrophy (CSA) is a relatively rare entity caused by cervical degenerative spinal diseases and characterized by motor weakness accompanied by remarkable muscle atrophy in the upper extremities without significant sensory deficits or spastic paraparesis in the lower...

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Autores principales: Takahashi, Toshiyuki, Hanakita, Junya, Minami, Manabu, Tomita, Yosuke, Sasagasako, Tomoki, Kanematsu, Ryo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Spinal Neurosurgery Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790744/
https://www.ncbi.nlm.nih.gov/pubmed/31607092
http://dx.doi.org/10.14245/ns.1938210.105
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author Takahashi, Toshiyuki
Hanakita, Junya
Minami, Manabu
Tomita, Yosuke
Sasagasako, Tomoki
Kanematsu, Ryo
author_facet Takahashi, Toshiyuki
Hanakita, Junya
Minami, Manabu
Tomita, Yosuke
Sasagasako, Tomoki
Kanematsu, Ryo
author_sort Takahashi, Toshiyuki
collection PubMed
description OBJECTIVE: Cervical spondylotic amyotrophy (CSA) is a relatively rare entity caused by cervical degenerative spinal diseases and characterized by motor weakness accompanied by remarkable muscle atrophy in the upper extremities without significant sensory deficits or spastic paraparesis in the lower extremities. Postoperative outcomes and predictive prognostic factors vary among previous reports. In the present report, we describe the surgical results in patients who were surgically treated for CSA and present a literature review. METHODS: In total, 33 patients with CSA were retrospectively analyzed. Correlations between the surgical outcome and the following factors were statistically analyzed: age, sex, type of impaired muscle, preoperative severity of motor weakness, number of levels of cord or root compression, presence of a T2 high-intensity area in the spinal cord, cervical kyphosis, and methods of surgical procedure. RESULTS: On postoperative neurological evaluation, 25 patients (75.8%) had favorable outcomes and 8 had unfavorable outcomes (proximal type, 72.2%; distal type, 78.6%). Patients with favorable outcomes were significantly younger than those with unfavorable outcomes (p=0.013). Patient’s characteristics except for age and radiological factors were not correlated to surgical outcome. CONCLUSION: The present study focused on the surgical results in patients who were surgically treated for CSA along with updated information from a literature review. Improvement of motor weakness is expected with acceptable prevalence although higher age can be a negative factor. Surgical outcomes and predictive factors related to a poor prognosis were determined and compared with those of previous articles.
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spelling pubmed-67907442019-11-12 Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature Takahashi, Toshiyuki Hanakita, Junya Minami, Manabu Tomita, Yosuke Sasagasako, Tomoki Kanematsu, Ryo Neurospine Original Article OBJECTIVE: Cervical spondylotic amyotrophy (CSA) is a relatively rare entity caused by cervical degenerative spinal diseases and characterized by motor weakness accompanied by remarkable muscle atrophy in the upper extremities without significant sensory deficits or spastic paraparesis in the lower extremities. Postoperative outcomes and predictive prognostic factors vary among previous reports. In the present report, we describe the surgical results in patients who were surgically treated for CSA and present a literature review. METHODS: In total, 33 patients with CSA were retrospectively analyzed. Correlations between the surgical outcome and the following factors were statistically analyzed: age, sex, type of impaired muscle, preoperative severity of motor weakness, number of levels of cord or root compression, presence of a T2 high-intensity area in the spinal cord, cervical kyphosis, and methods of surgical procedure. RESULTS: On postoperative neurological evaluation, 25 patients (75.8%) had favorable outcomes and 8 had unfavorable outcomes (proximal type, 72.2%; distal type, 78.6%). Patients with favorable outcomes were significantly younger than those with unfavorable outcomes (p=0.013). Patient’s characteristics except for age and radiological factors were not correlated to surgical outcome. CONCLUSION: The present study focused on the surgical results in patients who were surgically treated for CSA along with updated information from a literature review. Improvement of motor weakness is expected with acceptable prevalence although higher age can be a negative factor. Surgical outcomes and predictive factors related to a poor prognosis were determined and compared with those of previous articles. Korean Spinal Neurosurgery Society 2019-09 2019-09-30 /pmc/articles/PMC6790744/ /pubmed/31607092 http://dx.doi.org/10.14245/ns.1938210.105 Text en Copyright © 2019 by the Korean Spinal Neurosurgery Society This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Takahashi, Toshiyuki
Hanakita, Junya
Minami, Manabu
Tomita, Yosuke
Sasagasako, Tomoki
Kanematsu, Ryo
Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature
title Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature
title_full Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature
title_fullStr Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature
title_full_unstemmed Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature
title_short Cervical Spondylotic Amyotrophy: Case Series and Review of the Literature
title_sort cervical spondylotic amyotrophy: case series and review of the literature
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790744/
https://www.ncbi.nlm.nih.gov/pubmed/31607092
http://dx.doi.org/10.14245/ns.1938210.105
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