视神经脊髓炎的阵发性疼痛性强直性痉挛

Q3 Neuroscience
Shoena Lucas , Patrice H. Lalive , Agustina M. Lascano
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引用次数: 1

摘要

最近,疼痛性强直性痉挛(PTS)与视神经脊髓炎光谱障碍(NMOSD)之间的关联被确立。目的通过录像资料描述NMOSD患者PTS的临床特点,并对相关文献进行综述。方法我们报告了一例38岁的女性,诊断为NMOSD和水通道蛋白-4 IgG抗体阳性,在纵向广泛横行性脊髓炎(LETM)发作后5周发生PTS。结果患者左手出现反复、短暂、疼痛的肌肉收缩发作,并向左臂扩散,然后延伸至四肢。虽然普瑞巴林和托吡酯对这些发作没有影响,但患者对卡马西平(CBZ)有反应,一年后无症状复发。结论spts合并LETM可视为NMOSD的典型症状。虽然确切的机制尚不清楚,但脊髓损伤后的触觉传递和急性炎症反应中释放的兴奋性可溶性因子被认为参与其中。在我们的病例中,用CBZ对症治疗达到了垃圾邮件的缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Paroxysmal painful tonic spasms in neuromyelitis optica spectrum disorder

Paroxysmal painful tonic spasms in neuromyelitis optica spectrum disorder

Background

Recently, an association between painful tonic spasms (PTS) and Neuromyelitis Optica Spectrum Disorder (NMOSD) was established.

Objective

To describe the clinical characteristics of PTS in NMOSD based on a video recording and to provide a literature review on the topic.

Methods

We report a case of a 38 years-old woman with a diagnosis of NMOSD and positive aquaporin-4 IgG antibody status who developed PTS five weeks after an episode of longitudinal extensive transverse myelitis (LETM).

Results

Repetitive, brief, and painful episodes of muscle contraction were observed on the patient's left hand, spreading to the left arm, and then extending to the four limbs. While pregabalin and topiramate had no influence on these episodes, the patient responded to carbamazepine (CBZ), without symptom recurrence after one year.

Conclusions

PTS in association with LETM can be considered typical for NMOSD. Although the exact mechanism is unknown, ephaptic transmission after spinal cord damage and excitatory soluble factors released during acute inflammation responses are sought to be involved. Symptomatic treatment with CBZ achieved remission of spams in our case.

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来源期刊
eNeurologicalSci
eNeurologicalSci Neuroscience-Neurology
CiteScore
3.50
自引率
0.00%
发文量
45
审稿时长
62 days
期刊介绍: eNeurologicalSci provides a medium for the prompt publication of original articles in neurology and neuroscience from around the world. eNS places special emphasis on articles that: 1) provide guidance to clinicians around the world (Best Practices, Global Neurology); 2) report cutting-edge science related to neurology (Basic and Translational Sciences); 3) educate readers about relevant and practical clinical outcomes in neurology (Outcomes Research); and 4) summarize or editorialize the current state of the literature (Reviews, Commentaries, and Editorials). eNS accepts most types of manuscripts for consideration including original research papers, short communications, reviews, book reviews, letters to the Editor, opinions and editorials. Topics considered will be from neurology-related fields that are of interest to practicing physicians around the world. Examples include neuromuscular diseases, demyelination, atrophies, dementia, neoplasms, infections, epilepsies, disturbances of consciousness, stroke and cerebral circulation, growth and development, plasticity and intermediary metabolism. The fields covered may include neuroanatomy, neurochemistry, neuroendocrinology, neuroepidemiology, neurogenetics, neuroimmunology, neuroophthalmology, neuropathology, neuropharmacology, neurophysiology, neuropsychology, neuroradiology, neurosurgery, neurooncology, neurotoxicology, restorative neurology, and tropical neurology.
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