Hypoglossal-facial nerve “side”-to-side neurorrhaphy for persistent incomplete facial palsy

医学 神经再支配 面神经 联会 舌下神经 麻痹 面瘫 面部肌肉 解剖 外科 搅打动物 舌头 病理 精神科 体感系统 替代医学
作者
Hong Wan,Liwei Zhang,Dezhi Li,Shuyu Hao,Jie Feng,Jean Paul Oudinet,Michaël Schumacher,Song Liu
出处
期刊:Journal of Neurosurgery [Journal of Neurosurgery Publishing Group]
卷期号:120 (1): 263-272 被引量:17
标识
DOI:10.3171/2013.9.jns13664
摘要

Object Hypoglossal-facial nerve neurorrhaphy is a widely used method for treating complete facial palsy. However, the classic surgical procedure using a “side”-to-end neurorrhaphy is not suitable for incomplete facial palsy (IFP), because sectioning of the facial nerve for neurorrhaphy compromises remnant axons and potential spontaneous reinnervation. For the treatment of persistent IFP, the authors investigated in rats a modified method using hypoglossal-facial nerve “side”-to-side neurorrhaphy. Methods An IFP model was created by crushing the facial nerve and then ligating the injury site to limit axonal regeneration. After 9 weeks, rats with IFP were submitted to hypoglossal-facial nerve “side”-to-side neurorrhaphy: The gap between the 2 nerves was bridged with a predegenerated peroneal nerve graft, which was sutured to only one-half of the hypoglossal nerve and to the remnant facial nerve through a small window created by removing the epineurium, thus preserving regenerating facial axons. Results Four months after repair surgery, double innervation of the target whisker pad by hypoglossal and facial motor neurons was supported by the recording of muscle action potentials and their retrograde labeling. Regenerated hypoglossal and facial motor neurons effectively participated in the reinnervation of the whisker pad, significantly improving facial symmetry without evident synkinesis, compared with rats that underwent IFP without hypoglossal-facial nerve neurorrhaphy. Conclusions This study demonstrates that hypoglossal-facial nerve “side”-to-side neurorrhaphy with a predegenerated nerve graft can lead to rapid functional benefits for persistent IFP without compromising the remnants of facial axons, thus providing a proof-of-feasibility for further studies in humans.
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