Lapointe Annie, Viamonte Carlo, Morriss M Craig, Manolidis Spiros
Department of Otolaryngology-Head & Neck Surgery, University of Montreal, 3175 Côte-Sainte-Catherine, Montreal, Que., Canada H3T 1C5.
Int J Pediatr Otorhinolaryngol. 2006 May;70(5):863-8. doi: 10.1016/j.ijporl.2005.09.022. Epub 2005 Nov 8.
High-resolution magnetic resonance studies are an important tool in the investigation of the etiology of childhood sensorineural hearing loss. An added benefit with magnetic resonance is the ability to screen the central nervous system for findings which may adversely affect the neurodevelopmental outcome of these children.
To determine the proportion of cases and significance of associated intracranial abnormalities as detected by central nervous system high-resolution magnetic resonance imaging in children with profound sensorineural hearing loss.
Retrospective chart review of children undergoing evaluation for cochlear implantation in a tertiary care academic children's hospital with high-resolution magnetic resonance of the temporal bone and brain during a 21 month period. Magnetic resonance studies were interpreted by an experienced senior neuroradiologist blinded to the identity and clinical data of the patients.
Forty patients were identified. All had the same magnetic resonance study consisting of a 3D high-resolution sequence through the temporal bone as well as a T1 sagittal and T2 axial screening sequence of the brain. Eight patients (20%) showed significant brain abnormalities by magnetic resonance imaging ranging from myelination delays to migrational anomalies. Temporal bone abnormalities were not seen. Three patients with Connexin-26 mutations had no associated brain abnormalities by magnetic resonance.
A significant proportion of our patients being investigated by magnetic resonance imaging for profound sensorineural hearing loss show migrational abnormalities of the central nervous system, suggesting a central origin to their hearing loss. Some of these findings may result in neurodevelopmental delay and hence, negatively impact the success of cochlear implantation. We propose that magnetic resonance imaging of the temporal bone as part of the evaluation protocol for cochlear implantation in children should include central nervous system screening.
高分辨率磁共振研究是调查儿童感音神经性听力损失病因的重要工具。磁共振的一个额外好处是能够筛查中枢神经系统,以发现可能对这些儿童的神经发育结果产生不利影响的情况。
确定在重度感音神经性听力损失儿童中,通过中枢神经系统高分辨率磁共振成像检测到的相关颅内异常的病例比例及意义。
对一家三级医疗学术儿童医院在21个月期间接受人工耳蜗植入评估的儿童进行回顾性病历审查,这些儿童同时接受了颞骨和脑部的高分辨率磁共振检查。磁共振研究由一位经验丰富的高级神经放射科医生解读,该医生对患者的身份和临床数据不知情。
共确定了40名患者。所有人都进行了相同的磁共振检查,包括通过颞骨的3D高分辨率序列以及脑部的T1矢状位和T2轴位筛查序列。8名患者(20%)通过磁共振成像显示出明显的脑部异常,范围从髓鞘形成延迟到迁移异常。未发现颞骨异常。3名携带连接蛋白26突变的患者通过磁共振检查未发现相关脑部异常。
在因重度感音神经性听力损失接受磁共振成像检查的患者中,很大一部分显示出中枢神经系统的迁移异常,这表明他们的听力损失源于中枢。其中一些发现可能导致神经发育延迟,从而对人工耳蜗植入的成功产生负面影响。我们建议,作为儿童人工耳蜗植入评估方案一部分的颞骨磁共振成像应包括中枢神经系统筛查。