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Magnetic resonance imaging findings in idiopathic sudden sensorineural hearing loss

机译:特发性突如其来的感官听力损失中的磁共振成像结果

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Background The unpredictability in presenting signs and symptoms of idiopathic sudden sensorineural hearing loss (SSNHL) presents a notable diagnostic challenge for clinicians. Previous studies have confirmed the potentially important role of magnetic resonance imaging (MRI) in the diagnosis and prognostication of idiopathic SSNHL to guide definitive medical therapy, but correlations of these findings with outcomes remain controversial. Purpose To evaluate and identify magnetic resonance imaging (MRI) findings associated with idiopathic sudden sensorineural hearing loss (SSNHL). Material and Methods Sixty-eight patients with a documented diagnosis of idiopathic SSNHL and 20 controls underwent 1.5-T or 3-T MRI of the brain. Age, gender, ethnicity, associated co-morbidities, and audiometry findings were also recorded. Statistical analysis was performed to compare outcome measures between idiopathic SSNHL and control groups. Results The mean age of the cohort was 57 +/- 17 years, with a male-to-female ratio of 1:1.1. MRI findings include 25.0% (P = 1.000) with chronic microangiopathic disease, 14.7% (P = 0.165) with temporal bone aberrations, 13.2% (P = 0.165) with facial and/or vestibulocochlear nerve complex changes, 11.8% (P = 1.000) with venous malformations, 8.8% (P = 0.104) with arterial malformations, and 8.8% (P = 0.184) with cerebral and/or brainstem parenchymal disease. Conclusion Arteriovenous malformations and central neurologic disease are not directly associated with idiopathic SSNHL on MRI. However, visualized signal changes of inner ear structures and facial/vestibulocochlear nerve complex support previously postulated theories, which include viral as well as inflammatory processes in the development of idiopathic SSNHL.
机译:背景技术呈现特发性突然感官听力损失(SSNHL)的迹象和症状的不可预测性对临床医生来说具有显着的诊断挑战。以前的研究已经证实磁共振成像(MRI)在特发性SSNHL的诊断和预测中的潜在重要作用,以指导明确的药物治疗,但这些发现与结果的相关性仍然存在争议。目的评估和识别与特发性突然感觉术后听力损失(SSNHL)相关的磁共振成像(MRI)发现。材料与方法六十八名患有特发性SSNHL的记录诊断和20个对照的脑卒中的脑卒中的1.5-T或3-T MRI。还记录了年龄,性别,种族,相关的共同病态和听力测定结果。进行统计分析以比较特发性SSNHL和对照组之间的结果措施。结果队列的平均年龄为57 +/- 17岁,雄性与女性比例为1:1.1。 MRI发现包括25.0%(p = 1.000),慢性微观疗法疾病,14.7%(P = 0.165),颞骨畸变,13.2%(p = 0.165),面部和/或前颈织物神经复合变化,11.8%(P = 1.000 )具有静脉畸形,8.8%(p = 0.104),动脉畸形,8.8%(p = 0.184),脑和/或脑干实质疾病。结论动脉畸形和中枢神经疾病与MRI的特发性SSNHL没有直接相关。然而,内耳结构和面部/ vertibuloChlear神经复合物的可视化信号变化先前假设的理论,包括病毒和发作性SSNHL的发育中的炎症过程。

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