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儿童运动障碍急症。

Movement disorder emergencies in childhood.

机构信息

Southampton University Hospitals NHS Trust, UK.

出版信息

Eur J Paediatr Neurol. 2011 Sep;15(5):390-404. doi: 10.1016/j.ejpn.2011.04.005. Epub 2011 Aug 10.

Abstract

The literature on paediatric acute-onset movement disorders is scattered. In a prospective cohort of 52 children (21 male; age range 2mo-15y), the commonest were chorea, dystonia, tremor, myoclonus, and Parkinsonism in descending order of frequency. In this series of mainly previously well children with cryptogenic acute movement disorders, three groups were recognised: (1) Psychogenic disorders (n = 12), typically >10 years of age, more likely to be female and to have tremor and myoclonus (2) Inflammatory or autoimmune disorders (n = 22), including N-methyl-d-aspartate receptor encephalitis, opsoclonus-myoclonus, Sydenham chorea, systemic lupus erythematosus, acute necrotizing encephalopathy (which may be autosomal dominant), and other encephalitides and (3) Non-inflammatory disorders (n = 18), including drug-induced movement disorder, post-pump chorea, metabolic, e.g. glutaric aciduria, and vascular disease, e.g. moyamoya. Other important non-inflammatory movement disorders, typically seen in symptomatic children with underlying aetiologies such as trauma, severe cerebral palsy, epileptic encephalopathy, Down syndrome and Rett syndrome, include dystonic posturing secondary to gastro-oesophageal reflux (Sandifer syndrome) and Paroxysmal Autonomic Instability with Dystonia (PAID) or autonomic 'storming'. Status dystonicus may present in children with known extrapyramidal disorders, such as cerebral palsy or during changes in management e.g. introduction or withdrawal of neuroleptic drugs or failure of intrathecal baclofen infusion; the main risk in terms of mortality is renal failure from rhabdomyolysis. Although the evidence base is weak, as many of the inflammatory/autoimmune conditions are treatable with steroids, immunoglobulin, plasmapheresis, or cyclophosphamide, it is important to make an early diagnosis where possible. Outcome in survivors is variable. Using illustrative case histories, this review draws attention to the practical difficulties in diagnosis and management of this important group of patients.

摘要

儿科急性运动障碍的文献较为分散。在一项前瞻性队列研究中,52 名儿童(21 名男性;年龄 2 个月至 15 岁)中,最常见的运动障碍依次为舞蹈症、肌张力障碍、震颤、肌阵挛和帕金森病。在这一系列主要由隐源性急性运动障碍的既往健康儿童组成的病例中,识别出以下三组:(1)精神障碍(n=12),通常年龄大于 10 岁,更可能为女性,表现为震颤和肌阵挛;(2)炎症或自身免疫性疾病(n=22),包括 N-甲基-D-天冬氨酸受体脑炎、眼阵挛-肌阵挛、风湿热舞蹈病、系统性红斑狼疮、急性坏死性脑病(可能为常染色体显性遗传)和其他脑炎;(3)非炎症性疾病(n=18),包括药物诱导的运动障碍、泵后舞蹈病、代谢紊乱,如戊二酸血症、血管疾病,如烟雾病。其他重要的非炎症性运动障碍,通常见于有潜在病因的有症状儿童,如创伤、严重脑瘫、癫痫性脑病、唐氏综合征和雷特综合征,包括胃食管反流引起的张力障碍性姿势(桑德弗综合征)和伴有张力障碍的阵发性自主神经不稳定(PAID)或自主神经“风暴”。已知有锥体外系疾病的儿童(如脑瘫),或在治疗管理改变时(如神经安定药或鞘内巴氯芬输注的引入或停用),可能会出现肌张力障碍性危象;从横纹肌溶解引起的肾功能衰竭的角度来看,死亡率的主要风险。尽管证据基础薄弱,因为许多炎症/自身免疫性疾病可以用类固醇、免疫球蛋白、血浆置换或环磷酰胺治疗,但尽早诊断是很重要的。幸存者的预后各不相同。本文通过列举病例,提请注意诊断和治疗这一重要患者群体的实际困难。

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