儿童腕管综合征6例分析

A.Cruz Martı́nez , J Arpa
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引用次数: 35

摘要

本文报告了6例儿童,4女2男,年龄5-14岁,患有腕管综合征(CTS)。每个病例的正中神经卡压有不同的病因。1例患者在高强度篮球训练后出现单侧CTS症状。他改进了终止这项体育活动。3例患者双侧CTS分别伴有Schwartz-Jampel综合征、触发指和粘多糖病I (MPS IS=Scheie综合征)。后者是一名11岁的男孩,他患有严重的双侧肌肉大鱼际无力和萎缩,手术后恢复良好。2例双侧CTS伴常染色体显性遗传病。其中1例表现为家族性CTS伴腕横韧带增厚。另一名儿童(5岁)表现为早期双侧CTS,首次表现为遗传性神经病变伴压迫性麻痹(HNPP)。他的亲属无症状,但他们表现出与HNPP相符的电生理和神经活检改变。神经传导研究(NCS)是诊断小儿CTS。此外,NCS是评估术后神经病变演变的客观方法。为了鉴别可能的家族性神经病变,NCS必须在除正中神经外的枕骨神经以及有一级症状和无症状的亲属中进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Carpal tunnel syndrome in childhood: study of 6 cases

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.

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