Burns J, Lister G D
J Hand Surg Am. 1984 Jan;9A(1):99-103. doi: 10.1016/s0363-5023(84)80195-1.
Three patients, one with bilateral disease, experienced spontaneous onset of radial nerve dysfunction. Each demonstrated significant motor paralysis and had surgical exploration 3 weeks to 3 months after symptoms were first noted. All three patients showed well-localized hourglass constrictions of the radial nerve that could not be attributed to extrinsic compression. Each subsequently required tendon transfers for a persistent radial nerve palsy. Each showed electrical evidence of late recovery, although this was incomplete in two out of three.
三名患者（其中一名为双侧病变）出现了桡神经功能障碍的自发发作。每名患者均表现出明显的运动麻痹，并在首次出现症状后3周 至3个月接受了手术探查。所有三名患者的桡神经均出现了定位明确的沙漏样狭窄，这不能归因于外部压迫。随后，每名患者均因持续性桡神经麻痹而需要进行肌腱转移。每名患者均显示出晚期恢复的电生理证据，尽管三名患者中有两名恢复不完全。
