Minatogawa T, Nishimura Y, Inamori T, Kumoi T
Department of Otolaryngology, Hyogo College of Medicine, Japan.
Laryngoscope. 1989 Jun;99(6 Pt 1):632-8. doi: 10.1288/00005537-198906000-00011.
The surgical management of congenital aural atresia is a challenging, complex procedure, and the risks are great. The otologic surgeon is responsible for keeping a patent external auditory canal and for achieving satisfactory hearing. The present report studied hearing changes that occurred after tympanoplasty and the long-term results of tympanoplasty in 12 cases of congenital aural atresia or stenosis. Patients were followed for more than 2 years after surgery. In four ears, an allograft of the tympanic membrane with an attached malleus was used, with a good graft take and hearing results. An autograft of temporal fascia was used in eight ears. Hearing acuity decreased in six of the eight ears and was maintained in two ears. Three primary surgery patients required revision surgery for postoperative restenosis of the external auditory canal. Some comments have been made with regard to this problem. Emphasis is also placed on the selection of patients for surgery using a thorough audiologic and roentgenologic evaluation.
先天性外耳道闭锁的外科治疗是一项具有挑战性的复杂手术,风险很大。耳科外科医生负责保持外耳道通畅并实现满意的听力。本报告研究了12例先天性外耳道闭锁或狭窄患者鼓室成形术后的听力变化及鼓室成形术的长期结果。患者术后随访超过2年。4只耳朵使用了带锤骨的鼓膜同种异体移植物,移植物存活良好且听力结果良好。8只耳朵使用了颞筋膜自体移植物。8只耳朵中有6只听力下降,2只听力维持。3例初次手术患者因术后外耳道再狭窄需要进行翻修手术。针对这个问题已发表了一些评论。还强调了通过全面的听力学和放射学评估来选择手术患者。