Djerić Dragoslava, Perić Aleksandar, Pavlović Bojan, Folić Miljan, Bontić Ana, Baralić Marko, Pavlović Jelena, Radović Milan
School of Medicine, University in Belgrade, Belgrade, Serbia.
Clinic for Otorhinolaryngology and Maxillofacial Surgery, Clinical Center of Serbia, Belgrade, Serbia.
SAGE Open Med Case Rep. 2021 Jul 29;9:2050313X211036006. doi: 10.1177/2050313X211036006. eCollection 2021.
Granulomatosis with polyangiitis is a systemic vasculitis of unknown etiology, characterized by necrotizing granulomas. It is an autoimmune disease affecting small- and medium-sized vessels of upper and lower respiratory tract, kidneys, and other organs. We described a case of a patient with otitis media with effusion as the first manifestations of granulomatosis with polyangiitis. A 54-year-old female presented as an urgent case with history of a severe otalgia, hearing loss, vertigo, and fever. The patient was treated with diagnosis of otitis media with effusion and acute rhinosinusitis, but without significant success. She developed an acute kidney dysfunction as a sign of glomerulonephritis with rapidly progressive renal failure. Diagnosis of granulomatosis with polyangiitis was confirmed after the histopathological analysis of kidney tissue, not by analysis of middle ear and paranasal sinus mucosa specimens. The patient was treated according to generally accepted protocol, and over time, there was an almost complete recovery.
肉芽肿性多血管炎是一种病因不明的系统性血管炎,其特征为坏死性肉芽肿。它是一种自身免疫性疾病,可影响上、下呼吸道、肾脏和其他器官的中小血管。我们描述了一例以分泌性中耳炎为肉芽肿性多血管炎首发表现的患者。一名54岁女性因严重耳痛、听力丧失、眩晕和发热病史作为急诊病例就诊。该患者被诊断为分泌性中耳炎和急性鼻-鼻窦炎并接受治疗,但效果不佳。她出现了急性肾功能不全,表现为肾小球肾炎伴快速进行性肾衰竭。经肾脏组织病理分析而非中耳和鼻窦黏膜标本分析,确诊为肉芽肿性多血管炎。该患者按照公认方案接受治疗,一段时间后几乎完全康复。