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自身免疫性感音神经性听力损失

Autoimmune sensorineural hearing loss.

作者信息

McCabe B F

出版信息

Ann Otol Rhinol Laryngol. 1979 Sep-Oct;88(5 Pt 1):585-9. doi: 10.1177/000348947908800501.

Abstract

The author proposes the existence of a new entity, autoimmune sensorineural hearing loss, on the basis of diagnostic study and treatment experience with a series of 18 patients. In each case the clinical pattern did not fit with known entities and thus seemed to merit distinctive categorization. In the one patient in whom tissue was available, a vasculitis was evident, a feature of autoimmune disease. All patients responded to treatment for an autoimmune disease, namely, chronic cortisone and cyclophosphamide therapy. The author suggests that all otolaryngologists should be aware of the possibility of this condition, because it is one of the few forms of sensorineural deafness for which we have a treatment.

摘要

作者基于对18例患者的诊断研究和治疗经验,提出存在一种新的疾病实体——自身免疫性感音神经性听力损失。在每一个病例中,临床症状均不符合已知的疾病实体,因此似乎值得进行独特的分类。在有组织样本的1例患者中,明显存在血管炎,这是自身免疫性疾病的一个特征。所有患者对自身免疫性疾病的治疗,即长期使用可的松和环磷酰胺治疗均有反应。作者建议所有耳鼻喉科医生都应意识到这种疾病的可能性,因为它是我们有治疗方法的少数几种感音神经性耳聋之一。

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