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肌萎缩侧索硬化症并发脊髓空洞症的临床病例

Clinical cases of amyotrophic lateral sclerosis concurrent with hydromyelia.

作者信息

Bogdanov Enver I, Mendelevich Elena G, Khabibrakhmanov Aydar N, Bogdanov Shamil E, Mukhamedzhanova Gyulnara R, Mukhamedyarov Marat M

机构信息

Neurology and Rehabilitation Department Kazan State Medical University Kazan Russia.

Normal Physiology Department Kazan State Medical University Kazan Russia.

出版信息

Clin Case Rep. 2021 Feb 2;9(3):1571-1576. doi: 10.1002/ccr3.3832. eCollection 2021 Mar.

DOI:10.1002/ccr3.3832
PMID:33768891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7981723/
Abstract

A comprehensive work-up, clinical correlation, and differential diagnosis are needed to determine if abnormal findings such us hydromyelia in ALS patients are causative or incidental in order to rule out other, more curable conditions that resemble ALS.

摘要

需要进行全面的检查、临床关联分析和鉴别诊断，以确定肌萎缩侧索硬化症（ALS）患者出现的诸如脊髓空洞症等异常发现是病因性的还是偶然的，从而排除其他类似ALS但更可治愈的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/ead91635bd2e/CCR3-9-1571-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/400fc69df497/CCR3-9-1571-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/e5a662eea8bb/CCR3-9-1571-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/14a03e7ee235/CCR3-9-1571-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/7791fc3fbbfe/CCR3-9-1571-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/ead91635bd2e/CCR3-9-1571-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/400fc69df497/CCR3-9-1571-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/e5a662eea8bb/CCR3-9-1571-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/14a03e7ee235/CCR3-9-1571-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/7791fc3fbbfe/CCR3-9-1571-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19d8/7981723/ead91635bd2e/CCR3-9-1571-g002.jpg

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本文引用的文献

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Biochem Biophys Res Commun. 2017 Feb 19;483(4):1187-1193. doi: 10.1016/j.bbrc.2016.07.055. Epub 2016 Jul 11.
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Hereditary Spastic Paraplegia: Clinical and Genetic Hallmarks.遗传性痉挛性截瘫：临床与遗传特征
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Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56.遗传性痉挛性截瘫：SPG56中的新突变及表型变异性的扩展
Eur J Paediatr Neurol. 2016 May;20(3):444-8. doi: 10.1016/j.ejpn.2016.02.001. Epub 2016 Feb 18.
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A comprehensive review of amyotrophic lateral sclerosis.肌萎缩侧索硬化症的全面综述。
Surg Neurol Int. 2015 Nov 16;6:171. doi: 10.4103/2152-7806.169561. eCollection 2015.
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Primary Lateral Sclerosis.原发性侧索硬化症
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A revision of the El Escorial criteria - 2015.《埃尔埃斯科里亚尔标准（2015年修订版）》
Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(5-6):291-2. doi: 10.3109/21678421.2015.1049183. Epub 2015 Jun 29.
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A case report of amyotrophic lateral sclerosis in a patient with Klippel-Feil syndrome—a familial occurrence: a potential role of TGF-β signaling pathway.
Medicine (Baltimore). 2015 Jan;94(4):e441. doi: 10.1097/MD.0000000000000441.
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Charcot-Marie-Tooth disease type 2A: from typical to rare phenotypic and genotypic features.腓骨肌萎缩症 2A 型：从典型到罕见的表型和基因型特征。
JAMA Neurol. 2014 Aug;71(8):1036-42. doi: 10.1001/jamaneurol.2014.629.
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Chapter 11 Monomelic amyotrophy of upper or lower limbs.第11章 上肢或下肢单肢肌萎缩
Handb Clin Neurol. 2007;82:207-27. doi: 10.1016/S0072-9752(07)80014-5.
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European Federation of Neurological Societies/Peripheral Nerve Society guideline on management of multifocal motor neuropathy.欧洲神经病学学会联合会/周围神经学会多灶性运动神经病管理指南
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