肉芽肿病合并多血管炎是突发性双侧感音神经性听力损失的原因:病例报告和初步评估的建议。

IF 0.4 Q4 OTORHINOLARYNGOLOGY Case Reports in Otolaryngology Pub Date : 2021-04-20 eCollection Date: 2021-01-01 DOI:10.1155/2021/6632344
Paul R Ratmeyer, Benjamin R Johnson, Luis P Roldan, Tania L Kraai
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引用次数: 0

摘要

肉芽肿病伴多血管炎(GPA)是一种严重的全身性血管炎,通常影响副鼻窦、上、下呼吸道和肾脏。GPA也与耳蜗炎症引起的感音神经性听力损失(SNHL)有关。早期识别、诊断性实验室评估和适当的治疗对于改善GPA患者的预后和实现缓解至关重要。在此,我们报告一例双侧突发性感音神经性听力损失(SSNHL)和远端对称性多神经病变作为GPA的首发症状。美国耳鼻喉头颈外科学会的临床实践指南中没有明确规定排除双侧SSNHL患者自身免疫性内耳疾病的具体诊断检查。本文的目的是为双侧SSNHL患者描述一个适当的诊断检查,当有自身免疫性疾病的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Granulomatosis with Polyangiitis as a Cause of Sudden-Onset Bilateral Sensorineural Hearing Loss: Case Report and Recommendations for Initial Assessment.

Granulomatosis with polyangiitis (GPA) is a severe systemic vasculitis that commonly affects the paranasal sinuses, upper and lower respiratory tracts, and kidneys. GPA has also been associated with sensorineural hearing loss (SNHL), through inflammation of the cochlear apparatus. Early recognition, diagnostic laboratory evaluation, and appropriate treatment are essential to improve outcomes and achieve remission for patients with GPA. Here, we present a case of bilateral sudden sensorineural hearing loss (SSNHL) and distal symmetric polyneuropathy as the first presenting signs of GPA. A specific diagnostic work-up to rule out autoimmune inner-ear disease in patients with bilateral SSNHL is not clearly stated in the clinical practice guidelines from the American Academy of Otolaryngology-Head and Neck Surgery. The aim of this paper is to delineate an appropriate diagnostic work-up for patients with bilateral SSNHL when there is concern for autoimmune disease.

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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
自引率
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发文量
20
审稿时长
13 weeks
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