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成人脑缺氧损伤后进行性迟发性肌张力障碍

Progressive delayed-onset dystonia after cerebral anoxic insult in adults.

作者信息

Kuoppamäki Mikko, Bhatia Kailash P, Quinn Niall

机构信息

Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, Queen Square, London, United Kingdom.

出版信息

Mov Disord. 2002 Nov;17(6):1345-9. doi: 10.1002/mds.10260.

Abstract

The basal ganglia, especially the globi pallidi (GP), are highly vulnerable to generalized cerebral anoxia/hypoxia. We report on 2 new cases with delayed-onset generalized dystonia due to cerebral anoxia. The onset of dystonia in both of our patients was delayed by about 2 months. In both cases, the unusual feature was the progressive worsening and the spread of dystonia over many years after delayed onset. Dystonia progressed for 16 years in Case 1 and for 4 years in Case 2. Furthermore, initial magnetic resonance imaging (MRI) scan of Case 1 showed mild changes of the internal capsule sparing the basal ganglia. Years later, in line with clinical progression, the follow-up MRI scan showed isolated bilateral lesions involving the entire GP. MRI scans in Case 2 showed bilateral lesions of caudate and lentiform nuclei. There may be several mechanisms underlying delayed and progressive symptoms after time-limited brain anoxia. We hypothesize that anoxia-induced excitotoxicity resulting in mitochondrial dysfunction and subsequent apoptosis may explain, at least partly, the delayed-onset and progressive extrapyramidal syndromes seen in these patients.

摘要

基底神经节,尤其是苍白球(GP),极易受到全身性脑缺氧/缺血的影响。我们报告了2例因脑缺氧导致迟发性全身性肌张力障碍的新病例。我们的两名患者肌张力障碍的发作均延迟了约2个月。在这两个病例中,不寻常的特征是在延迟发作后的许多年里,肌张力障碍逐渐加重并扩散。病例1的肌张力障碍进展了16年,病例2进展了4年。此外,病例1的初始磁共振成像(MRI)扫描显示内囊有轻度改变,基底神经节未受累。数年后,与临床进展一致,随访MRI扫描显示双侧孤立性病变累及整个苍白球。病例2的MRI扫描显示尾状核和豆状核双侧病变。在限时性脑缺氧后出现延迟和进行性症状可能有多种机制。我们推测,缺氧诱导的兴奋性毒性导致线粒体功能障碍和随后的细胞凋亡,可能至少部分解释了这些患者中出现的迟发性和进行性锥体外系综合征。

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