跗管综合征。两例罕见病因的报告。
The tarsal tunnel syndrome. Report of two cases of unusual cause.
作者信息
Taguchi Y, Nosaka K, Yasuda K, Teramoto K, Mano M, Yamamoto S
出版信息
Clin Orthop Relat Res. 1987 Apr(217):247-52.
PMID:3829506
Abstract
Since Keck described the tarsal tunnel syndrome (TTS) in 1962, it has been one of the most frequently diagnosed of the entrapment neuropathies. TTS is usually of unknown origin. This is a report of two unusual cases: TTS caused by neurilemmoma in a 33-year-old woman, and TTS caused by subperiosteal ganglion in a 14-year-old girl. The symptoms were relieved, in both instances, with surgical excision.
摘要
自1962年凯克描述跗管综合征（TTS）以来，它一直是最常被诊断出的卡压性神经病之一。TTS通常病因不明。本文报告两例罕见病例：一例为一名33岁女性因神经鞘瘤导致的TTS，另一例为一名14岁女孩因骨膜下神经节导致的TTS。两例均通过手术切除使症状得到缓解。
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