Liu Yi, Wang Chih-Wei, Sung Yueh-Feng, Yang Fu-Chi
Department of Neurology, Tri-Service General Hospital, National Defense Medical Center, No. 325, Section 2, Cheng-Kung Road, Neihu District, Taipei City, 114, Taiwan.
Department of Radiology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Neurol Sci. 2022 Jan;43(1):683-686. doi: 10.1007/s10072-021-05581-9. Epub 2021 Sep 4.
Susac syndrome is a rare disease presenting with a classic triad of symptoms. These are sensorineural hearing loss, encephalopathy, and branch retinal artery occlusions. Initial presentation is usually headache and symptoms of encephalopathy. Hearing loss is unusual in the early stages but, when it does present, can often lead to a misdiagnosis of sudden sensorineural hearing loss. Hence, neurological and retinal examinations are essential to an accurate diagnosis. In this study, we aimed to raise awareness of Susac syndrome among physicians and facilitate recognition of its manifestation, especially in those patients presenting with hearing loss alone. Identifying Susac syndrome that presents as sudden sensorineural hearing loss can be challenging but a number of case reviews have been reported in recent years and treatment guidelines are available.
Susac综合征是一种罕见疾病,具有典型的三联征症状。这些症状包括感音神经性听力损失、脑病和视网膜分支动脉阻塞。最初的表现通常是头痛和脑病症状。听力损失在早期并不常见,但一旦出现,往往会导致对突发性感音神经性听力损失的误诊。因此,神经学和视网膜检查对于准确诊断至关重要。在本研究中,我们旨在提高医生对Susac综合征的认识,并促进对其表现的识别,特别是在那些仅表现为听力损失的患者中。识别表现为突发性感音神经性听力损失的Susac综合征可能具有挑战性,但近年来已有多篇病例报告,并且有治疗指南可供参考。