Yoon T H, Paparella M M, Schachern P A
Department of Otolaryngology, University of Minnesota Medical School, Minneapolis 55455.
Laryngoscope. 1989 Jun;99(6 Pt 1):600-9. doi: 10.1288/00005537-198906000-00007.
Systemic vasculitis includes a broad spectrum of disorders that may involve blood vessels of any size in any organ system. Systemic vasculitis is associated with immunopathogenic mechanisms. Sixteen temporal bones from eight persons were studied to determine histopathologic changes that occur in systemic vasculitis. Three persons had Wegener's granulomatosis, two had polyarteritis nodosa, and three had systemic lupus erythematosus. Otitis media was seen in 15 ears, with ten ears showing chronic middle ear changes and two showing fibrotic inner ear changes. In Wegener's granulomatosis, granulation tissue was observed around the eustachian tube and protympanum, and in polyarteritis nodosa, inflammatory cell infiltrate and thickened blood vessels were observed around the facial nerve. Although sensorineural hearing loss has been described clinically in systemic lupus erythematosus, the present report describes findings in temporal bones, including severe fibrosis and new bone formation throughout the inner ear.
系统性血管炎包括一系列广泛的疾病,这些疾病可能累及任何器官系统中任何大小的血管。系统性血管炎与免疫致病机制相关。对来自8人的16块颞骨进行了研究,以确定系统性血管炎中发生的组织病理学变化。3人患有韦格纳肉芽肿,2人患有结节性多动脉炎,3人患有系统性红斑狼疮。15只耳朵出现中耳炎,其中10只耳朵表现为慢性中耳变化,2只表现为内耳纤维化变化。在韦格纳肉芽肿中,在咽鼓管和鼓室前部观察到肉芽组织,在结节性多动脉炎中,在面神经周围观察到炎性细胞浸润和血管增厚。虽然临床上已描述系统性红斑狼疮存在感音神经性听力损失,但本报告描述了颞骨的研究结果,包括内耳广泛的严重纤维化和新骨形成。