帕金森病患者深部脑刺激的视觉效果

A. Mitchell
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摘要

背景:帕金森病(PD)是一种由多巴胺缺乏引起的进行性神经退行性疾病,表现为运动症状。视力障碍可能同时发生,但经常被忽视。深部脑刺激(DBS)是一种有效的治疗方法,可以改善震颤、僵硬和整体活动能力,但对其对视觉系统的影响知之甚少。病例报告:一名75岁白人男性PD表现为长期双眼复视。基线检查时,每只眼的最佳矫正视力为20/25。经观察,他有明显的震颤,步态不稳。距离交替覆盖试验显示外斜视伴右斜视。近交变覆盖度显示外视野明显增大,近会聚点减小。额外的24-2 Humphrey视野测试和神经和黄斑的光学相干断层扫描(OCT)无显著性。患者在初次检查后5周植入dbs,并在4周后激活该装置。随访时,患者仍主诉间歇性复视。明显折射和棱镜校正没有明显变化。经观察,患者震颤明显改善,步态稳定。所有测量参数不变。患者在装置激活后7个月再次接受评估。虽然在所有距离的聚光范围得到改善,但患者仍有间歇性复视的症状。视神经OCT扫描显示每只眼睛有边缘性但对称的变薄。所有其他测量参数不变。结论:本例PD患者DBS植入和激活后眼科检查无明显变化。据作者所知,文献中没有其他病例研究DBS植入和激活前后对PD患者视觉系统通路的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visual Effects of Deep Brain Stimulation in a Patient with Parkinson’s Disease
Background: Parkinson’s disease (PD) is a progressive neurodegenerative disorder caused by a dopamine deficiency that presents with motor symptoms. Visual disorders can occur concomitantly but are frequently overlooked. Deep brain stimulation (DBS) has been an effective treatment to improve tremors, stiffness and overall mobility, but little is known about its effects on the visual system. Case Report: A 75-year-old Caucasian male with PD presented with longstanding binocular diplopia. On baseline examination, the best-corrected visual acuity was 20/25 in each eye. On observation, he had noticeable tremors with an unsteady gait. Distance alternating cover test showed exophoria with a right hyperphoria. Near alternating cover test revealed a significantly larger exophoria accompanied by a reduced near point of convergence. Additional testing with a 24-2 Humphrey visual field and optical coherence tomography (OCT) of the nerve and macula were unremarkable. The patient underwent DBS implantation five weeks after initial examination, and the device was activated four weeks thereafter. At follow up, the patient still complained of intermittent diplopia. There was no significant change in the manifest refraction or prism correction. On observation, the patient had remarkably improved tremors with a steady gait. All parameters measured were unchanged. The patient was evaluated again seven months after device activation. Although vergence ranges at all distances were improved, the patient was still symptomatic for intermittent diplopia. OCT scans of the optic nerve showed borderline but symmetric thinning in each eye. All other parameters measured were unchanged. Conclusion: The case found no significant changes on ophthalmic examination after DBS implantation and activation in a patient with PD. To the best of the authors’ knowledge, there are no other cases in the literature that investigated the effects of DBS on the visual system pathway in a patient with PD before and after DBS implantation and activation.
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