Granulomatosis with polyangiitis presenting as isolated ear involvement: a case series and literature review.

Silvia Zorzi, Gabriele Testa, Michele Tomasoni, Stefano Taboni, Nader Nassif, Gina Alessandra Gregorini, Tommaso Sorrentino, Cesare Piazza, Luca Oscar Redaelli de Zinis
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Abstract

Objective: To describe the clinical characteristics and outcomes of patients affected by granulomatosis with polyangiitis (GPA) presenting with isolated ear involvement.

Methods: A retrospective review of patients affected by GPA and treated at the University of Brescia, Italy, from 2002 to 2023 was conducted. Only patients with exclusive otologic manifestation as first presentation were included.

Results: Among 610 patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAV) diagnosed and followed at our Institution, 6 (0.8%) presented with exclusive ear involvement as first presentation, all affected by GPA. Most frequently patients presented with otitis media with effusion, sensorineural or mixed hearing loss, and dizziness. Two patients developed systemic symptoms. All patients experienced at least a partial recovery of middle ear function after starting immunosuppressive therapy.

Conclusions: AAVs rarely show initial presentation as isolated ear involvement, and more commonly present as otitis media with hearing loss that is unresponsive to conventional therapy. Once an AAV is suspected, surgery should be avoided since further damage can be caused by local iatrogenic inflammation sustained by the underlying condition. Local improvement is generally seen after the start of immunosuppressive therapy.

肉芽肿病合并多血管炎表现为孤立性耳部受累:一个病例系列和文献回顾。
目的:探讨以孤立性耳部受累为表现的肉芽肿病合并多血管炎(GPA)患者的临床特点及预后。方法:回顾性分析2002年至2023年在意大利布雷西亚大学接受治疗的GPA患者。仅包括首次出现独家耳科表现的患者。结果:在本研究所诊断并随访的610例抗中性粒细胞细胞质抗体相关血管炎(AAV)患者中,6例(0.8%)首次表现为独家耳部受累,均受GPA影响。最常见的患者表现为中耳炎伴积液、感音神经性或混合性听力丧失和头晕。两名患者出现全身症状。所有患者在开始免疫抑制治疗后至少部分恢复了中耳功能。结论:aav的初始表现很少表现为孤立的耳部受累,而更常见的表现是中耳炎伴听力损失,对常规治疗无反应。一旦怀疑AAV,应避免手术,因为潜在疾病持续的局部医源性炎症可引起进一步的损害。局部改善通常在免疫抑制治疗开始后出现。
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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