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听力丧失作为系统性血管炎的首发特征。

Hearing loss as the presenting feature of systemic vasculitis.

作者信息

Lidar Merav, Carmel Eldar, Kronenberg Yona, Langevitz Pnina

机构信息

Department of Internal Medicine F and Rheumatic Disease Unit, Sheba Medical Center, Tel Hashomer, Israel.

出版信息

Ann N Y Acad Sci. 2007 Jun;1107:136-41. doi: 10.1196/annals.1381.015.

Abstract

Hearing loss, both sensorineural and conductive, is a well-recognized manifestation of systemic vasculitis, yet has only infrequently been described as its initial presentation. We describe three cases in which hearing loss preceded the diagnosis of systemic vasculitis by a period of a few weeks to more than 6 months. While steroid therapy was initiated immediately in one of the cases, comprehensive immunosuppressive therapy was given only after additional manifestations compatible with vasculitis appeared, allowing for a diagnosis of Wegener's granulomatosis in two of the cases and undifferentiated vasculitis, in the third. Hearing improved in all patients, albeit, residual dysfunction remained. Prompt referral for a complete rheumatologic workup in cases of unexplained hearing loss would allow for a timely diagnosis of a collagen vascular disease and facilitate early initiation of systemic therapy, possibly yielding better audiological results.

摘要

感音神经性和传导性听力损失是系统性血管炎一种公认的表现,但很少被描述为其首发症状。我们描述了三例听力损失先于系统性血管炎诊断数周至6个月以上的病例。其中一例立即开始使用类固醇治疗,而仅在出现与血管炎相符的其他表现后才给予全面免疫抑制治疗,最终两例诊断为韦格纳肉芽肿,第三例诊断为未分化血管炎。所有患者听力均有改善,尽管仍有残余功能障碍。对于不明原因听力损失的病例,及时转诊进行全面的风湿病检查将有助于及时诊断胶原血管病并促进全身治疗的早期开始,可能会取得更好的听力结果。

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