Kempf H G
ENT-Clinic, University of Tübingen, FR Germany.
Clin Otolaryngol Allied Sci. 1989 Oct;14(5):451-6. doi: 10.1111/j.1365-2273.1989.tb00403.x.
In 16 of 19 patients with biopsy-proved Wegener's granulomatosis the early manifestations were limited to the ear and nose. The audiological data of 13 patients revealed middle ear involvement in 16 of 26 ears. Twenty-one of 26 ears presented with a low to moderate sensorineural hearing loss. One ear remained deaf after a sudden hearing loss in the early stage of the disease. Serologically, 4 of 6 tested patients with sensorineural hearing loss demonstrated antibodies against sarcolemma. One patient showed antinuclear antibodies. It is remarkable that these antibodies can often be detected in classic inner ear disorders. The course of inner ear function, serum findings and the success of immunosuppressive therapy in Wegener's granulomatosis are comparable with immunologically mediated vasculitis in the inner ear.
在19例经活检证实为韦格纳肉芽肿病的患者中,有16例早期表现局限于耳和鼻。13例患者的听力学数据显示,26只耳中有16只中耳受累。26只耳中有21只表现为轻度至中度感音神经性听力损失。1只耳在疾病早期突然听力丧失后仍失聪。血清学检查显示,6例感音神经性听力损失患者中有4例检测出抗肌膜抗体。1例患者显示抗核抗体。值得注意的是,这些抗体在典型的内耳疾病中也常常可以检测到。韦格纳肉芽肿病内耳功能的病程、血清学检查结果以及免疫抑制治疗的效果与内耳免疫介导的血管炎相当。