Ito Ken, Suzuki Sayaka, Murofushi Toshihisa, Ishimoto Shin-ichi, Iwasaki Shinichi, Karino Shotaro
Department of Otolaryngology, Faculty of Medicine, University of Tokyo, Tokyo, Japan.
Otol Neurotol. 2005 Jul;26(4):767-72. doi: 10.1097/01.mao.0000178140.27472.b6.
To report neuro-otologic findings concerning the four nerves in the internal auditory meatus (IAM) in patients with isolated congenitally narrow IAM and explore the implications regarding ontogeny of the nerves in the IAM.
Retrospective case series study.
University hospital.
Five consecutive patients between 1997 and 2002 with unilateral isolated narrow IAM demonstrated by high-resolution computed tomography whose chief complaint was hearing loss (1 male and 4 females, 4 right sides and 1 left; age range 5-37 years, mean 20 years; IAM diameter at the porus: 26-33% of that on the normal side).
Functional studies concerning the VIIth cranial nerve and the three branches of the VIIIth cranial nerve.
In all ears, auditory brain stem responses were absent, the speech discrimination score was 0%, and otoacoustic emissions were absent or markedly reduced compared with those on the normal side. Caloric responses were absent in two ears, reduced in two ears, and normal in one ear. Galvanic body sway tests showed no responses in the two ears in which caloric responses were absent. Inferior vestibular nerve function was estimated as normal in all ears on the basis of vestibular evoked myogenic potential recordings. Facial nerve functions were normal in all patients.
In isolated congenital stenosis of IAM, dysfunction of each nerve in the IAM can occur independently. In the ontogeny of the VIIIth cranial nerve, the cochlear and superior vestibular nerves tended to be involved together, whereas the cochlear and inferior vestibular nerves appeared independent of each other.
报告孤立性先天性内耳道狭窄患者内耳道(IAM)中四条神经的神经耳科学检查结果,并探讨其对IAM中神经个体发生的意义。
回顾性病例系列研究。
大学医院。
1997年至2002年间连续5例经高分辨率计算机断层扫描证实为单侧孤立性狭窄IAM的患者,主要症状为听力损失(1例男性,4例女性,4例右侧,1例左侧;年龄范围5 - 37岁,平均20岁;内耳道开口处直径为正常侧的26% - 33%)。
关于第VII对脑神经和第VIII对脑神经三个分支的功能研究。
所有患耳的听觉脑干反应均消失,言语辨别得分均为0%,与正常侧相比,耳声发射消失或明显减弱。两耳冷热试验反应消失,两耳减弱,一例正常。在冷热试验反应消失的两耳中,直流电身体摆动试验无反应。根据前庭诱发肌源性电位记录,所有患耳的下前庭神经功能估计正常。所有患者的面神经功能均正常。
在孤立性先天性内耳道狭窄中,内耳道中各神经的功能障碍可独立发生。在第VIII对脑神经的个体发生过程中,耳蜗神经和上前庭神经倾向于一起受累,而耳蜗神经和下前庭神经似乎相互独立。