经颅磁刺激治疗脊髓小脑性共济失调6型复视1例。

Q3 Medicine
Cerebellum and Ataxias Pub Date : 2018-11-20 eCollection Date: 2018-01-01 DOI:10.1186/s40673-018-0094-x
Kentaro Kawamura, Seiji Etoh, Megumi Shimodozono
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引用次数: 7

摘要

背景:脊髓小脑性共济失调6型(SCA6)患者通常采用经颅磁刺激(TMS)对运动皮层和小脑进行治疗。然而,很少有报道研究了SCA6患者复视的有效治疗方式。在本病例中,我们在运动皮层和小脑上应用单脉冲TMS来改善共济失调,并观察到复视的意想不到的改善。病例介绍:一名62岁日本男性脊髓小脑性共济失调6型(SCA6)因共济失调加重而入院。我们使用单脉冲经颅磁刺激(TMS)在手运动区和小脑与圆形线圈减少共济失调。经颅磁刺激开始后,由于复视出乎意料地改善,我们开始通过计算他在视野中观察到的注视点数量来定量评估复视。这一评估表明经颅磁刺激对复视有直接和累积的影响。我们还用图8线圈在运动皮层上施加了更多的局部刺激,复视立即得到改善。此外,在对运动皮层和小脑进行真正的刺激之前,我们进行了一次假刺激。假性刺激改善复视,随后的真实刺激改善更大。我们还使用赫斯图检查和双眼大体外观录像来客观地阐明眼球运动的变化。然而,这些检查未发现任何明显的动眼力变化。结论:我们将单脉冲经颅磁刺激应用于一例SCA6型复视患者,病情得到改善,无任何不良反应。经颅磁刺激可能有治疗SCA6患者复视的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcranial magnetic stimulation for diplopia in a patient with spinocerebellar ataxia type 6: a case report.

Transcranial magnetic stimulation for diplopia in a patient with spinocerebellar ataxia type 6: a case report.

Transcranial magnetic stimulation for diplopia in a patient with spinocerebellar ataxia type 6: a case report.

Transcranial magnetic stimulation for diplopia in a patient with spinocerebellar ataxia type 6: a case report.

Background: In Patients with spinocerebellar ataxia type 6 (SCA6) are often treated by transcranial magnetic stimulation (TMS) over the motor cortex and cerebellum. However, few reports have examined effective therapeutic modalities for diplopia in SCA6 patients. In the current case, we applied single-pulse TMS over the motor cortex and cerebellum to improve ataxia, and observed an unexpected improvement of diplopia.

Case presentation: A 62-year-old Japanese male with spinocerebellar ataxia type 6 (SCA6) was admitted to our hospital for exacerbation of ataxia. We administered single-pulse transcranial magnetic stimulation (TMS) over the hand motor area and the cerebellum with a circular coil to reduce ataxia. After the initiation of TMS, since diplopia unexpectedly improved, we started a quantitative assessment of diplopia by counting the number of fixation spots that he observed in his visual field. This assessment suggested that TMS had an immediate and cumulative effect on diplopia. We also delivered more localized stimulation only over the motor cortex with a Figure-8 coil, and diplopia improved immediately. Additionally, we administered a sham stimulation before the real stimulation over the motor cortex and the cerebellum. The sham stimulation improved diplopia, and greater improvement was observed with subsequent real stimulation. We also used a Hess chart examination and video recordings of binocular gross appearance to elucidate the changes in ocular movement objectively. However, these examinations did not reveal any obvious oculomotor changes.

Conclusions: We applied single-pulse TMS to a SCA6 patient with diplopia, which improved without any adverse effects. TMS may have potential for the treatment of diplopia in SCA6 patients.

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Cerebellum and Ataxias
Cerebellum and Ataxias Medicine-Neurology (clinical)
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