Kimura Yusuke, Masuda Takeshi, Tomizawa Akifumi, Sakata Hideaki, Kaga Kimitaka
National Institute of Sensory Organs, National Tokyo Medical Center, Tokyo, Japan.
Department of Otolaryngology-Head and Neck Surgery, Nihon University School of Medicine, Tokyo, Japan.
J Otol. 2017 Mar;12(1):41-46. doi: 10.1016/j.joto.2017.03.002. Epub 2017 Mar 21.
Infants with congenital deafness caused by severe bilateral inner ear malformations frequently suffer from severe hearing loss and poor balance. Unfortunately, the use of hearing aids is usually ineffective in recovering hearing, necessitating cochlear implants. We report a case of a 6-year-old boy with congenital deafness and bilateral inner ear malformations (right side, incomplete partition type I [IP-I]; left side, common cavity deformity). Hearing aids had a remarkable effect in this patient, enabling sufficient and favorable hearing recovery such as to allow the patient to engage in daily conversations. Per-rotatory nystagmus was recorded on an electronystagmogram for both right and left rotations in a damped rotational chair test. It is rare for deaf children with severe bilateral inner ear malformation to demonstrate favorable development in hearing and good equilibrium function. Our findings suggest that auditory-vestibular hair cells in this patient may have been partially preserved despite IP-I in the right ear and common cavity deformity of the left ear.
由严重双侧内耳畸形导致先天性耳聋的婴儿经常遭受严重听力损失和平衡能力差的问题。不幸的是,使用助听器通常在恢复听力方面无效,因此需要进行人工耳蜗植入。我们报告一例6岁先天性耳聋并伴有双侧内耳畸形(右侧,不完全分隔I型[IP-I];左侧,共同腔畸形)的男孩病例。助听器对该患者产生了显著效果,实现了充分且良好的听力恢复,使患者能够进行日常对话。在阻尼旋转椅试验中,通过眼震电图记录了左右旋转时的旋转性眼球震颤。双侧严重内耳畸形的失聪儿童出现听力良好发育和良好平衡功能的情况很少见。我们的研究结果表明,尽管该患者右耳为IP-I且左耳为共同腔畸形,但听觉-前庭毛细胞可能部分得以保留。