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苍白球内侧部脑深部电刺激治疗成人起病性肌张力障碍所致角弓反张:一种个性化方法

Globus Pallidus Internus Deep Brain Stimulation for Dystonic Opisthotonus in Adult-Onset Dystonia: A Personalized Approach.

作者信息

Tambirajoo Kantharuby, Furlanetti Luciano, Samuel Michael, Ashkan Keyoumars

机构信息

Department of Neurosurgery, King's College Hospital, London, United Kingdom.

Department of Basic and Clinical Neuroscience, IoPPN, King's College London, London, United Kingdom.

出版信息

Front Hum Neurosci. 2021 Jun 10;15:683545. doi: 10.3389/fnhum.2021.683545. eCollection 2021.

Abstract

INTRODUCTION

Dystonic opisthotonus is defined as a backward arching of the neck and trunk, which ranges in severity from mild backward jerks to life-threatening prolonged severe muscular spasms. It can be associated with generalized dystonic syndromes or, rarely, present as a form of axial truncal dystonia. The etiologies vary from idiopathic, genetic, tardive, hereditary-degenerative, or associated with parkinsonism. We report clinical cases of dystonic opisthotonus associated with adult-onset dystonic syndromes, that benefitted from globus pallidus internus (GPi) deep brain stimulation (DBS).

METHODS

Clinical data from patients with dystonic syndromes who underwent comprehensive medical review, multidisciplinary assessment, and tailored medical and neurosurgical managements were prospectively analyzed. Quantification of dystonia severity pre- and postoperatively was performed using the Burke-Fahn-Marsden Dystonia Rating Scale and quantification of overall pain severity was performed using the Visual Analog Scale.

RESULTS

Three male patients, with age of onset of the dystonic symptoms ranging from 32 to 51 years old, were included. Tardive dystonia, adult-onset dystonia-parkinsonism and adult-onset idiopathic axial dystonia were the etiologies identified. Clinical investigation and management were tailored according to the complexity of the individual presentations. Although they shared common clinical features of adult-onset dystonia, disabling dystonic opisthotonus, refractory to medical management, was the main indication for GPi-DBS in all patients presented. The severity of axial dystonia ranged from disturbance of daily function to life-threatening truncal distortion. All three patients underwent bilateral GPi DBS at a mean age of 52 years (range 48-55 years), after mean duration of symptoms prior to DBS of 10.7 years (range 4-16 years). All patients showed a rapid and sustained clinical improvement of their symptoms, notably of the dystonic opisthotonos, at postoperative follow-up ranging from 20 to 175 months. In some, the ability to resume activities of daily living and reintegration into the society was remarkable.

CONCLUSION

Adult-onset dystonic syndromes predominantly presenting with dystonic opisthotonus are relatively rare. The specific nature of dystonic opisthotonus remains a treatment challenge, and thorough investigation of this highly disabling condition with varying etiologies is often necessary. Although patients may be refractory to medical management and botulinum toxin injection, Globus pallidus stimulation timed and tailored provided symptomatic control in this cohort and may be considered in other carefully selected cases.

摘要

引言

张力障碍性角弓反张被定义为颈部和躯干向后弓起,严重程度从轻微的向后抽搐到危及生命的持续性严重肌肉痉挛不等。它可与全身性张力障碍综合征相关,或很少表现为轴性躯干张力障碍的一种形式。病因包括特发性、遗传性、迟发性、遗传性退行性或与帕金森病相关。我们报告了与成人起病的张力障碍综合征相关的张力障碍性角弓反张的临床病例,这些病例受益于内侧苍白球(GPi)深部脑刺激(DBS)。

方法

对接受全面医学评估、多学科评估以及量身定制的医学和神经外科治疗的张力障碍综合征患者的临床数据进行前瞻性分析。术前和术后使用伯克-法恩-马斯登肌张力障碍评定量表对肌张力障碍严重程度进行量化,并使用视觉模拟量表对总体疼痛严重程度进行量化。

结果

纳入了3名男性患者,其肌张力障碍症状的发病年龄在32至51岁之间。确定的病因包括迟发性肌张力障碍、成人起病的肌张力障碍-帕金森综合征和成人起病的特发性轴性肌张力障碍。根据个体表现的复杂性进行临床调查和治疗。尽管他们具有成人起病的肌张力障碍的共同临床特征,但导致功能障碍的张力障碍性角弓反张对药物治疗无效,是所有患者接受GPi-DBS的主要指征。轴性肌张力障碍的严重程度从日常功能障碍到危及生命的躯干畸形不等。所有3例患者均在平均年龄52岁(范围48 - 55岁)时接受了双侧GPi DBS,DBS术前症状的平均持续时间为10.7年(范围4 - 16年)。在术后20至175个月的随访中,所有患者的症状均迅速且持续改善,尤其是张力障碍性角弓反张。在一些患者中,恢复日常生活活动和重新融入社会的能力显著。

结论

以张力障碍性角弓反张为主的成人起病的张力障碍综合征相对罕见。张力障碍性角弓反张的特殊性质仍然是治疗挑战,对于这种病因各异的严重致残性疾病,通常需要进行全面调查。尽管患者可能对药物治疗和肉毒杆菌毒素注射无效,但适时且量身定制的苍白球刺激在该队列中提供了症状控制,在其他经过精心挑选的病例中也可考虑使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0771/8222606/c8743e5a65f8/fnhum-15-683545-g001.jpg

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