• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

咀嚼肌无力:神经肌肉无力的鉴别指标——初步观察。

Jaw muscle weakness: a differential indicator of neuromuscular weakness--preliminary observations.

机构信息

Department of Neurology, Bangur Institute of Neurosciences, Kolkata, West Bengal, India.

出版信息

Muscle Nerve. 2011 Jun;43(6):807-11. doi: 10.1002/mus.21990.

DOI:10.1002/mus.21990
PMID:21607965
Abstract

INTRODUCTION

Flaccid quadriparesis is a common neurological problem. Guillain-Barré syndrome Guillain-Barre syndrome (GBS), polymyositis/dermatomyositis (PM/DM), generalized myasthenia gravis (MG), and hypokalemic periodic paralysis (HPP) constitute the majority of cases of flaccid quadriparesis. Few patients from any of these disease groups lack the cardinal clinical features. We established clinical marker(s) that might have significant discriminating power for diagnosis.

METHODS

Forty-six patients satisfied all of our criteria. Cases were evaluated clinically followed by laboratory and electrophysiological study, and, in selected cases, muscle histopathology.

RESULTS

Twenty-four patients had GBS, 9 had MG, 7 had PM/DM, and 6 had HPP. Jaw-opening weakness was found in 71.4% of PM/DM, 83.3% of HPP, and 4.1% of GBS cases. Jaw-closing weakness was found in 88.8% of MG cases.

CONCLUSIONS

Presence of jaw-closing weakness pointed toward MG, whereas presence of jaw-opening weakness suggested muscle disease (PM/DM and HPP). GBS patients very rarely had jaw muscle weakness.

摘要

介绍

弛缓性四肢瘫痪是一种常见的神经系统问题。格林-巴利综合征(GBS)、多发性肌炎/皮肌炎(PM/DM)、全身性重症肌无力(MG)和低钾性周期性瘫痪(HPP)构成了弛缓性四肢瘫痪的大多数病例。这些疾病组中的极少数患者缺乏主要的临床特征。我们确定了一些临床标志物,这些标志物可能具有重要的诊断鉴别能力。

方法

46 名患者符合我们的所有标准。对病例进行临床评估,然后进行实验室和电生理研究,并在选定的病例中进行肌肉组织病理学检查。

结果

24 名患者患有 GBS,9 名患者患有 MG,7 名患者患有 PM/DM,6 名患者患有 HPP。71.4%的 PM/DM 患者、83.3%的 HPP 患者和 4.1%的 GBS 患者存在张口无力。88.8%的 MG 患者存在闭口无力。

结论

存在闭口无力提示为 MG,而存在张口无力提示为肌肉疾病(PM/DM 和 HPP)。GBS 患者很少出现咀嚼肌无力。

相似文献

1
Jaw muscle weakness: a differential indicator of neuromuscular weakness--preliminary observations.咀嚼肌无力:神经肌肉无力的鉴别指标——初步观察。
Muscle Nerve. 2011 Jun;43(6):807-11. doi: 10.1002/mus.21990.
2
Combined Guillain-Barré syndrome and myasthenia gravis.吉兰-巴雷综合征合并重症肌无力。
Brain Dev. 2013 Oct;35(9):865-9. doi: 10.1016/j.braindev.2012.10.016. Epub 2012 Nov 22.
3
Myasthenia gravis and Guillain-Barré cooccurrence syndrome.重症肌无力与吉兰-巴雷综合征共存。
Am J Emerg Med. 2013 Aug;31(8):1264-7. doi: 10.1016/j.ajem.2013.05.029. Epub 2013 Jul 1.
4
Clinical approach to the weak patient in the intensive care unit.重症监护病房中虚弱患者的临床处理方法
Respir Care. 2006 Sep;51(9):1024-40; discussion 1040-1.
5
[Catastrophic neuromuscular diseases].[灾难性神经肌肉疾病]
Neurologia. 2010 Oct;25 Suppl 1:37-45. doi: 10.1016/S0213-4853(10)70049-9.
6
[Cause and diagnosis of a dropped head].
Ned Tijdschr Geneeskd. 2009 Apr 11;153(15):716-20.
7
[Hypokalemic thyrotoxic periodic paralysis (HTPP). Rare differential diagnosis in case of acute tetraparesis in Europe].[低钾性甲状腺毒症性周期性麻痹(HTPP)。欧洲急性四肢轻瘫病例中的罕见鉴别诊断]
Med Klin (Munich). 2005 Sep 15;100(9):583-6. doi: 10.1007/s00063-005-1080-7.
8
Distinguishing acute-onset CIDP from Guillain-Barré syndrome with treatment related fluctuations.鉴别急性起病的慢性炎症性脱髓鞘性多发性神经病与伴有治疗相关波动的吉兰-巴雷综合征。
Neurology. 2005 Jul 12;65(1):138-40. doi: 10.1212/01.wnl.0000167549.09664.b8.
9
Tongue weakness is associated with respiratory failure in patients with severe Guillain-Barré syndrome.在严重吉兰-巴雷综合征患者中,舌肌无力与呼吸衰竭相关。
Acta Neurol Scand. 2009 Jun;119(6):364-70. doi: 10.1111/j.1600-0404.2008.01107.x. Epub 2008 Oct 22.
10
[Hypokalemic thyrotoxic periodic paralysis--a rare differential diagnosis in patients presenting acute tetraparesis].[低钾性甲状腺毒症性周期性麻痹——急性四肢瘫患者罕见的鉴别诊断]
Ugeskr Laeger. 2008 Sep 22;170(39):3070.

引用本文的文献

1
Guillain-Barré Syndrome Presenting With Masticatory Disturbance and Reduction in Bite Force.以咀嚼障碍和咬合力降低为表现的吉兰-巴雷综合征。
Cureus. 2023 Oct 17;15(10):e47174. doi: 10.7759/cureus.47174. eCollection 2023 Oct.
2
Exploring the Gut Microbiome in Myasthenia Gravis.探讨重症肌无力中的肠道微生物组。
Nutrients. 2022 Apr 14;14(8):1647. doi: 10.3390/nu14081647.
3
The mouth-opening muscular performance in adults with and without temporomandibular disorders: A systematic review.张口肌能表现:颞下颌关节紊乱症患者与非患者的系统评价。
J Oral Rehabil. 2022 Apr;49(4):476-494. doi: 10.1111/joor.13303. Epub 2022 Jan 31.
4
Oral function in patients with myasthenia gravis.重症肌无力患者的口腔功能
PeerJ. 2021 Jun 29;9:e11680. doi: 10.7717/peerj.11680. eCollection 2021.
5
Phenotypical Variation with Same Genetic Mutation in Familial Hypokalemic Periodic Paralysis.家族性低钾性周期性麻痹中相同基因突变的表型变异
J Pediatr Neurosci. 2018 Apr-Jun;13(2):218-220. doi: 10.4103/jpn.JPN_44_17.
6
Inflammatory myopathies: One-center experience.炎性肌病:单中心经验
Eur J Rheumatol. 2014 Sep;1(3):96-100. doi: 10.5152/eurjrheumatol.2014.033. Epub 2014 Sep 1.
7
Idiopathic inflammatory myopathies.特发性炎性肌病。
Neurol Clin. 2014 Aug;32(3):595-628, vii. doi: 10.1016/j.ncl.2014.04.007.
8
Myasthenia gravis: a review.重症肌无力:综述
Autoimmune Dis. 2012;2012:874680. doi: 10.1155/2012/874680. Epub 2012 Oct 31.
9
Idiopathic inflammatory myopathies.特发性炎性肌病。
Semin Neurol. 2012 Jul;32(3):227-36. doi: 10.1055/s-0032-1329201. Epub 2012 Nov 1.