Anatomical and clinical aspects and outcomes of bilateral cochlear implantation in cochlear hypoplasia type IV - a case report

Agata Szleper, Magdalena Lachowska, A. Pastuszka, Zuzanna Łukaszewicz-Moszyńska, T. Wojciechowski, K. Niemczyk
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Abstract

Cochlear hypoplasia is a congenital inner ear malformation (IEM) characterized by a reduced external cochlear dimension, usually accompanied by an abnormal internal architecture. Type IV cochlear hypoplasia is a cochlea with hypoplastic middle and apical turns. It may occur along with dislocation of the facial nerve, associated with semicircular abnormalities, less clearly marked promontory, or stapedial fixation. Such patients can present a broad spectrum of audiological test results, from sensorineural or mixed mild or profound hearing loss. The above anatomical changes may be responsible for intraoperative difficulties during cochlear implantation. In the studied case, a 6-month-old patient was diagnosed with an inner ear malformation - cochlear hypoplasia type IV on both sides. Computed tomography with multiplanar and 3D reconstruction was performed to analyze the middle and inner ear anatomy in detail. Both types of imaging reconstruction helped decide which cochlear implant electrode to choose. Perimodiolar-positioned cochlear implant electrode was found to be the most suitable choice. The patient underwent sequential bilateral cochlear implantation with expected incomplete electrode array insertion on both sides. First repeatable auditory responses were observed two months after the second implant activation. Good parental cooperation with therapists and adequately defined developmental goals in the presented patient allowed the multidisciplinary team to take advantage of the child's intellectual abilities and choose the suitable communication method; however, the patient's auditory responses were obtained slowly. The final auditory results cannot be predicted in inner ear malformations due to abnormal anatomical structure and, thus, heterogeneous innervation within the deformed cochlea. The programming of the sound processor must be individual in each case, based on the child's behavior observation and, if possible, objective test results. Patients with cochlear malformations usually require higher stimulation intensities to obtain sound sensations than patients with a typical cochlear structure.
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IV型耳蜗发育不全患者双侧人工耳蜗植入术的解剖、临床及疗效1例
耳蜗发育不全是一种先天性内耳畸形(IEM),其特征是外耳蜗尺寸缩小,通常伴有内部结构异常。IV型耳蜗发育不全是指耳蜗中、尖转发育不全。它可伴面神经脱位,伴有半圆形畸形、不明显的岬或镫骨固定。此类患者可表现出广泛的听力学检查结果,从感音神经性或混合性轻度或重度听力损失。上述解剖改变可能是造成人工耳蜗植入术中困难的原因。在本病例中,一名6个月大的患儿被诊断为双侧内耳畸形- IV型耳蜗发育不全。采用计算机断层多平面三维重建对中耳和内耳解剖结构进行详细分析。两种类型的成像重建有助于决定选择哪种人工耳蜗电极。耳蜗周定位电极是最合适的选择。患者接受序贯双侧人工耳蜗植入,预计两侧电极阵列置入不完整。第一次可重复的听觉反应在第二次植入激活两个月后被观察到。家长与治疗师的良好合作以及患者明确的发展目标使多学科团队能够利用儿童的智力能力并选择合适的沟通方法;然而,患者的听觉反应获得缓慢。内耳畸形由于解剖结构异常,最终听觉结果无法预测,因此,畸形耳蜗内神经分布不均。声音处理器的编程必须在每种情况下都是单独的,基于儿童的行为观察,如果可能的话,还有客观的测试结果。与耳蜗结构正常的患者相比,耳蜗畸形患者通常需要更高的刺激强度来获得声音感觉。
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来源期刊
Polish Otorhinolaryngology Review
Polish Otorhinolaryngology Review Medicine-Otorhinolaryngology
CiteScore
0.20
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0.00%
发文量
23
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