Nager G T, Proctor B
Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine and Hospital, Baltimore, Maryland.
Otolaryngol Clin North Am. 1991 Jun;24(3):531-53.
Congenital bony dehiscences in the facial canal result from incomplete closure during development and are observed in approximately 55% of temporal bones. Anomalies involving the facial canal frequently are encountered in malformations of the temporal bone. These anomalies include aberrations of the course of one or all of the segments of the canal; abnormal relation to the oval and round window; bifurcations and trifurcations of the nerve; and associations with dysplasia of the stapes, oval window, external ear canal, and auricle. Rarely, the facial nerve may be hypoplastic or totally absent. Two abnormal vessels occasionally may accompany the facial nerve in the Fallopian canal: a persistent stapedial artery and a persistent lateral capital vein.
面神经管先天性骨质缺损是由于发育过程中闭合不全所致,约55%的颞骨中可观察到这种情况。颞骨畸形中经常会遇到涉及面神经管的异常。这些异常包括面神经管一个或所有节段走行异常;与卵圆窗和圆窗的关系异常;神经分叉和三叉;以及与镫骨、卵圆窗、外耳道和耳廓发育异常相关。面神经很少会发育不全或完全缺失。在面神经管中,偶尔会有两条异常血管伴随面神经:永存镫骨动脉和永存外侧颈静脉。