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与HLA A1-B8-DR3单倍型相关的突发性双侧感音神经性听力损失

Sudden Bilateral Sensorineural Hearing Loss Associated with HLA A1-B8-DR3 Haplotype.

作者信息

Psillas G, Daniilidis M, Gerofotis A, Veros K, Vasilaki A, Vital I, Markou K

机构信息

1st Academic ENT Department, Ahepa University Hospital, Aristotle University, 54006 Thessaloniki, Greece.

出版信息

Case Rep Otolaryngol. 2013;2013:590157. doi: 10.1155/2013/590157. Epub 2013 Sep 9.

Abstract

Sudden sensorineural hearing loss may be present as a symptom in systemic autoimmune diseases or may occur as a primary disorder without another organ involvement (autoimmune inner ear disease). The diagnosis of autoimmune inner ear disease is still predicated on clinical features, and to date specific diagnostic tests are not available. We report a case of bilateral sudden hearing loss, tinnitus, intense rotatory vertigo, and nausea in a female patient in which the clinical manifestations, in addition to raised levels of circulating immune complexes, antithyroglobulin antibodies, and the presence of the HLA A1-B8-DR3 haplotype, allowed us to hypothesize an autoimmune inner ear disease. Cyclosporine-A immunosuppressive treatment in addition to steroids helped in hearing recovery that occurred progressively with normalization of the hearing function after a five-month treatment. Cyclosporine-A could be proposed as a therapeutic option in case of autoimmune inner ear disease allowing the suspension of corticosteroids that, at high dose, expose patients to potentially serious adverse events.

摘要

突发性感音神经性听力损失可能作为全身自身免疫性疾病的一种症状出现,也可能作为一种无其他器官受累的原发性疾病发生(自身免疫性内耳疾病)。自身免疫性内耳疾病的诊断仍基于临床特征,迄今为止尚无特异性诊断测试。我们报告一例女性患者,出现双侧突发听力损失、耳鸣、强烈旋转性眩晕和恶心,其临床表现除循环免疫复合物水平升高、抗甲状腺球蛋白抗体以及存在HLA A1 - B8 - DR3单倍型外,使我们推测为自身免疫性内耳疾病。除类固醇外,环孢素A免疫抑制治疗有助于听力恢复,经过五个月治疗后,听力功能逐渐恢复正常。对于自身免疫性内耳疾病,环孢素A可作为一种治疗选择,从而能够停用高剂量时会使患者面临潜在严重不良事件的皮质类固醇。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b237/3782810/6c622cb4ce08/CRIM.OTOLARYNGOLOGY2013-590157.001.jpg

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