Plontke S K, Kösling S, Pazaitis N, Rahne T
Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital and Medical School, Martin Luther University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120, Halle (Saale), Germany.
Department of Radiology, University Hospital and Medical School, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
HNO. 2017 Aug;65(Suppl 2):158-162. doi: 10.1007/s00106-017-0348-6.
We report about a patient, who in 2005, as a 37-year-old, experienced a sudden, mild to moderate, mid-frequency sensorineural hearing loss in the right ear, along with tinnitus and mild dizziness. MRI of the temporal bone revealed a very small (1 mm) enhancing lesion in the second turn of the right cochlea after injection of contrast medium. Hearing gradually deteriorated, with complete hearing loss in 2015. At this time, an MRI scan showed a lesion completely filling the cochlea.The tumor was removed through a subtotal cochleoectomy. The cochlea was partially reconstructed with cartilage and fascia. A cochlea implant dummy electrode was inserted as a placeholder in order to try to preserve a channel within the most likely fibrosing "neocochlea" during follow-up MRI examinations.Vestibular function tests 2 months postoperatively showed preserved caloric excitability and a normal vestibulo-ocular reflex (video head impulse test, vHIT) in all three planes. The patient is free of vertigo.Intralabyrinthine schwannomas (ILS) are a rare differential diagnosis of sudden hearing loss. Surgical removal of an intracochlear ILS through partial or subtotal cochleoectomy with preservation of vestibular function is possible.
我们报告了一名患者,该患者在2005年37岁时,右耳突然出现轻度至中度的中频感音神经性听力损失,伴有耳鸣和轻度头晕。颞骨MRI显示,注射造影剂后,右耳蜗第二圈有一个非常小的(1毫米)强化病变。听力逐渐恶化,2015年完全失聪。此时,MRI扫描显示病变完全充满耳蜗。通过部分耳蜗切除术切除肿瘤。用软骨和筋膜对耳蜗进行了部分重建。插入了一个耳蜗植入假电极作为占位符,以便在后续的MRI检查中试图在最可能发生纤维化的“新耳蜗”内保留一个通道。术后2个月的前庭功能测试显示,所有三个平面的冷热刺激兴奋性均保留,前庭眼反射(视频头脉冲试验,vHIT)正常。患者无眩晕症状。迷路内神经鞘瘤(ILS)是突发性听力损失的一种罕见鉴别诊断。通过部分或全耳蜗切除术切除耳蜗内ILS并保留前庭功能是可行的。