Neusy C, Choufani G, Dolhen P, Louryan S
Service d'ORL, Hôpital Erasme, La Louvière.
Rev Med Brux. 2004 Oct;25(5):462-5.
Congenital anomalies of the middle ear associated to anomalies of the inner ear are rarely described. Our case displays a malformation due to an association of congenital absence of the round window and aplasia of the semi-circular canals, causing conductive hearing loss. First diagnosis was a congenital atresia isolated of the round window, related to a previous surgical exploration. We tried a novel technique designed to restore the function of the round window. Labyrinthine anomalies prevented a good outcome. This kind of malformative association could be due to the complexity of early genetic control of ear development. Attentive analysis of imaging should be performed before middle ear surgery to determine the presence of inner ear anomalies which are quite frequent and which would limit its usefulness.
与内耳异常相关的中耳先天性异常鲜有报道。我们的病例显示了一种畸形,其原因是圆窗先天性缺失与半规管发育不全相关联,导致传导性听力损失。最初的诊断是孤立的圆窗先天性闭锁,这与之前的手术探查有关。我们尝试了一种旨在恢复圆窗功能的新技术。内耳迷路异常导致效果不佳。这种畸形关联可能归因于耳部发育早期基因控制的复杂性。在中耳手术前应仔细分析影像学检查结果,以确定内耳异常的存在,内耳异常相当常见,会限制手术的效用。