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2
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本文引用的文献

1
Neuromyotonia.神经性肌强直
Clin Neurophysiol. 2006 Oct;117(10):2118-27. doi: 10.1016/j.clinph.2006.03.008. Epub 2006 Jul 14.
2
Guidelines for the treatment of autoimmune neuromuscular transmission disorders.自身免疫性神经肌肉传递障碍的治疗指南。
Eur J Neurol. 2006 Jul;13(7):691-9. doi: 10.1111/j.1468-1331.2006.01476.x.
3
Neuromyotonia with neuropathy and muscle hypertrophy: association or cause?伴有神经病变和肌肉肥大的神经性肌强直:关联还是病因?
Electromyogr Clin Neurophysiol. 2006 Jan-Feb;46(1):17-20.
4
Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis.钾通道抗体相关脑病:一种可能对免疫治疗有反应的边缘叶脑炎形式。
Brain. 2004 Mar;127(Pt 3):701-12. doi: 10.1093/brain/awh077. Epub 2004 Feb 11.
5
Chronic postoperative epidural abscess with ascending neuromyotonia.慢性术后硬膜外脓肿伴上行性神经肌强直。
Anesth Analg. 2002 Dec;95(6):1770-1, table of contents. doi: 10.1097/00000539-200212000-00056.
6
Phenotypic variants of autoimmune peripheral nerve hyperexcitability.自身免疫性周围神经兴奋性过高的表型变异
Brain. 2002 Aug;125(Pt 8):1887-95. doi: 10.1093/brain/awf178.
7
Acquired neuromyotonia in a patient with spinal epidural abscess.一名患有脊髓硬膜外脓肿患者的获得性神经性肌强直。
Muscle Nerve. 1998 May;21(5):672-4. doi: 10.1002/(sici)1097-4598(199805)21:5<672::aid-mus21>3.0.co;2-w.
8
Ocular neuromyotonia in a patient with cavernous sinus thrombosis secondary to mucormycosis.一名因毛霉菌病继发海绵窦血栓形成的患者出现眼部神经肌强直。
Am J Ophthalmol. 1997 Jul;124(1):122-3. doi: 10.1016/s0002-9394(14)71663-0.
9
Immunological associations of acquired neuromyotonia (Isaacs' syndrome). Report of five cases and literature review.
Brain. 1993 Apr;116 ( Pt 2):453-69. doi: 10.1093/brain/116.2.453.
10
Neuromyotonia in hereditary motor neuropathy.遗传性运动神经病中的神经性肌强直
J Neurol Neurosurg Psychiatry. 1991 Mar;54(3):230-5. doi: 10.1136/jnnp.54.3.230.

上呼吸道感染后获得性神经性肌强直:一例报告

Acquired neuromyotonia following upper respiratory tract infection: a case report.

作者信息

Imam Ibrahim, Edwards Simon, Hanemann C Oliver

机构信息

Neurology Department, Torbay Hospital, Torquay TQ2 7AA, UK.

出版信息

Cases J. 2009 Sep 8;2:7952. doi: 10.4076/1757-1626-2-7952.

DOI:10.4076/1757-1626-2-7952
PMID:19918441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2769391/
Abstract

We present a 37-year-old male subject who presented with burning sensations in his hands and feet with generalised twitching of his limbs, trunk and face. His symptoms developed 2 weeks after an upper respiratory tract infection. There was associated facial flushing and disturbed night sleep but no memory impairment or generalised sweating. Examination showed generalised myokymia and fasciculations and electromyography revealed widespread continuous semi-rhythmic doublets and triplets of low frequency with interspersed silent periods. Anti voltage gated potassium channel antibodies, antinuclear antibodies, anti-acetylcholine receptor antibodies and the anti-neuronal antibodies anti Hu, anti Yo and anti Ri were all negative. His symptoms improved slightly on lamotrigine and amitriptyline.

摘要

我们报告一名37岁男性患者,其双手和双脚有烧灼感,伴有四肢、躯干和面部的全身性抽搐。他的症状在上呼吸道感染后2周出现。伴有面部潮红和睡眠障碍,但无记忆障碍或全身性出汗。检查发现全身性肌束震颤和肌束颤动,肌电图显示广泛的连续低频半节律性双峰和三峰,其间有间歇期。抗电压门控钾通道抗体、抗核抗体、抗乙酰胆碱受体抗体以及抗神经元抗体抗Hu、抗Yo和抗Ri均为阴性。他的症状在服用拉莫三嗪和阿米替林后略有改善。