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Bilateral sudden sensorineural hearing loss as a presenting feature of systemic lupus erythematosus: Case report and brief review of other published cases

机译:双边突然的感音神经性听力丧失是系统性红斑狼疮的表现特征:病例报告及其他已发表病例的简要回顾

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Introduction:Sudden sensorineural hearing loss is an unusual presenting clinical feature of systemic lupus erythematosus.Case report:We report the case of a young woman who was admitted to hospital for sudden sensorineural hearing loss and hemophagocytic syndrome which was attributed to systemic lupus erythematosus on the basis of specific renal involvement, thrombocytopenia, and consistent autoantibodies. Favorable outcome was obtained on high-dose corticosteroids, and the hearing fully recovered.Discussion:Sudden sensorineural hearing loss in systemic lupus erythematosus is seemingly more frequently associated with severe systemic involvement and antiphospholipid antibodies may be present. Although management remains empirical, the high risk of permanent hearing impairment seems to justify emergency treatment with high-dose corticosteroids. When the clinical and laboratory criteria of antiphospholipid syndrome are met, antiplatelets agents or anticoagulation therapy shall be considered.
机译:简介:突发性感音神经性听力丧失是系统性红斑狼疮的临床表现的异常表现。病例报告:我们报告了一名因突然性感音神经性听力丧失和吞噬细胞综合征而入院的年轻患者,该病例归因于系统性红斑狼疮特定肾脏受累,血小板减少和一致的自身抗体的基础。大剂量皮质类固醇激素治疗效果良好,听力完全恢复。讨论:系统性红斑狼疮突然感觉神经性听力减退似乎与严重的全身性累及有关,并且可能存在抗磷脂抗体。尽管管理仍是经验性的,但是永久性听力障碍的高风险似乎证明了大剂量皮质类固醇紧急治疗的合理性。当达到抗磷脂综合征的临床和实验室标准时,应考虑使用抗血小板药物或抗凝治疗。

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