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儿童腕管综合征:6例研究

Carpal tunnel syndrome in childhood: study of 6 cases.

作者信息

Cruz Martínez A, Arpa J

机构信息

Electromyography Unit, Hospital La Luz, Madrid, Spain.

出版信息

Electroencephalogr Clin Neurophysiol. 1998 Aug;109(4):304-8. doi: 10.1016/s0924-980x(98)00026-5.

Abstract

Six children, 4 girls and two boys, aged 5-14 years, with carpal tunnel syndrome (CTS) are reported. Median nerve entrapment had different aetiologies in each case. One patient developed unilateral CTS symptoms after intensive basketball training. He improved upon terminating this sporting activity. In 3 patients bilateral CTS was associated with Schwartz-Jampel syndrome, trigger finger and mucopolysaccharidosis I (MPS IS = Scheie syndrome), respectively. The latter subject, a boy aged 11 years who had severe bilateral muscle thenar weakness and atrophy, made a good recovery after surgery. Two cases with bilateral CTS had autosomal dominant disease. One of them showed familial CTS with thickening of the transverse carpal ligament. The other child (5 years old) presented early bilateral CTS as first manifestation of hereditary neuropathy with liability to pressure palsies (HNPP). His relatives were asymptomatic, but they showed electrophysiological and nerve biopsy changes consistent with HNPP. Nerve conduction studies (NCS) are diagnostic in paediatric CTS. Moreover, NCS is an objective method to evaluate the evolution of the nerve lesions after surgery. NCS must be performed in nerves of the propositus other than the median, as well as in first degree symptomatic and asymptomatic relatives in order to identify possible familial neuropathies.

摘要

本文报告了6例年龄在5至14岁的腕管综合征(CTS)患儿,其中4例为女孩,2例为男孩。每例正中神经卡压的病因各不相同。1例患者在高强度篮球训练后出现单侧CTS症状,停止该项体育活动后症状改善。3例患者中,双侧CTS分别与施瓦茨 - 扬佩尔综合征、扳机指和黏多糖贮积症I型(MPS IS = 谢伊综合征)相关。后者是一名11岁男孩,双侧大鱼际肌严重无力和萎缩,术后恢复良好。2例双侧CTS患者患有常染色体显性疾病。其中1例表现为家族性CTS,伴有腕横韧带增厚。另一名儿童(5岁)早期出现双侧CTS,这是遗传性压力易感性神经病(HNPP)的首发表现。其亲属无症状,但电生理和神经活检结果显示与HNPP一致的变化。神经传导研究(NCS)对小儿CTS具有诊断价值。此外,NCS是评估术后神经病变进展的客观方法。NCS必须在患者除正中神经外的其他神经上进行,同时也应对一级有症状和无症状的亲属进行检测,以识别可能的家族性神经病变。

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