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先天性腕管综合征:常染色体显性遗传病例报告及文献复习

Congenital carpal tunnel syndrome: case report of autosomal dominant inheritance and review of the literature.

作者信息

Michaud L J, Hays R M, Dudgeon B J, Kropp R J

机构信息

Department of Rehabilitation Medicine, Children's Hospital and Medical Center, Seattle, WA 98105.

出版信息

Arch Phys Med Rehabil. 1990 May;71(6):430-2.

PMID:2185719
Abstract

Carpal tunnel syndrome (CTS) is unusual in childhood, and familial occurrence has been reported infrequently. A case of CTS in a seven-year-old boy, associated with abnormal thickening of the transverse carpal ligament and aplasia of the median nerve distal to this ligament, is described. Clinical, electrodiagnostic, and surgical findings are presented: all were consistent with absence of the median nerve distal to the transverse carpal ligament. Family history of CTS was positive in a pattern consistent with autosomal dominant transmission in three generations. Thickening of the transverse carpal ligament has been described, although infrequently, in childhood and familial CTS. Aplasia of the median nerve distally has not been reported in association with this anatomic abnormality. Case reports of familial CTS are reviewed, and other congenital anomalies which should be considered in the differential diagnosis of CTS in children and adults are discussed.

摘要

腕管综合征(CTS)在儿童中并不常见,家族性发病的报道也很少。本文描述了一例七岁男孩的CTS病例,该病例伴有腕横韧带异常增厚以及该韧带远端正中神经发育不全。文中呈现了临床、电诊断及手术结果:所有结果均与腕横韧带远端正中神经缺失相符。CTS家族史呈阳性,其模式符合三代常染色体显性遗传。腕横韧带增厚在儿童和家族性CTS中虽有报道,但并不常见。此前未见有远端正中神经发育不全与这种解剖学异常相关的报道。本文回顾了家族性CTS的病例报告,并讨论了在儿童和成人CTS鉴别诊断中应考虑的其他先天性异常。

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