Quirk Bernadine, Youssef Adam, Ganau Mario, D'Arco Felice
Great Ormond Street Hospital for Children NHS Foundation Trust.
Department of Neurosurgery, Oxford University Hospitals NHS Foundation Trust.
BJR Open. 2019 Jun 14;1(1):20180050. doi: 10.1259/bjro.20180050. eCollection 2019.
Malformations in either the inner ear, vestibulocochlear nerve (VIIIth) or auditory cortex of the brain can lead to congenital sensorineural hearing loss (SNHL). In most cases the underlying disorders involve the membranous labyrinth at a microscopic level and therefore radiological examinations are entirely normal. In a significant proportion however (up to 20%), there are abnormalities visualized in the inner ear and/or the VIIIth nerve; the type of abnormality is relevant for the surgical planning of a cochlear implant. Imaging and the accurate radiological identification of the affected inner ear structures therefore plays an integral role in the clinical evaluation of sensorineural hearing loss. In this pictorial review, we describe the main malformations of the inner ear in view of recent classifications and briefly explore the surgical implications.
内耳、前庭蜗神经(第八对脑神经)或大脑听觉皮层的畸形可导致先天性感音神经性听力损失(SNHL)。在大多数情况下,潜在疾病在微观层面累及膜迷路,因此放射学检查完全正常。然而,在相当大比例(高达20%)的病例中,内耳和/或第八对脑神经存在可见的异常;异常类型与人工耳蜗植入的手术规划相关。因此,成像以及对受影响内耳结构的准确放射学识别在感音神经性听力损失的临床评估中起着不可或缺的作用。在本图片综述中,我们根据最近的分类描述内耳的主要畸形,并简要探讨其手术意义。