Kulahli Ismail, Balci Kadir, Koseoglu Emel, Yuce Imdat, Cagli Sedat, Senturk Mehmet
Ear Nose Throat KBB, Erciyes University, Talas Yolu Erciyes Universitesi Kulak Burun Bogaz, Kayseri 38015, Turkey.
Hear Res. 2005 May;203(1-2):28-31. doi: 10.1016/j.heares.2004.11.020.
This study was carried out to determine the characteristics and incidence of hearing loss and vestibular disturbance in Behcet's syndrome with a large number of patients. Sixty-two patients with Behcet's syndrome were included in this study, 34 men and 28 women whose mean age was 33.7 (15-60). Sixty-two healthy normal control subjects (38 male and 24 female) were included. Patient and control groups were questioned about any history of audio-vestibular disturbance and underwent physical and ENT examination and the following audiologic tests: pure tone audiometric test (0.25, 0.5, 1, 2, 4, and 6 kHz), tympanogram, speech discrimination, short increment sensitivity index, tone-decay test, auditory brainstem response. Vestibular system was evaluated by videonistagmogram and caloric test. Cranial and brainstem magnetic resonance imagine (MRI) of patients who have vestibular disturbances were practiced to examine the central nervous system. Both the patient and the control groups were tested with the HLA-B51 antigen. Pure tone audiogram showed sensory-neural hearing loss (25 dB hearing level in at least two frequencies) in 20 of the 62 (32%) Behcet's patients while the control group were normal. There was a hearing loss involving high frequencies in the audiograms of Behcet's patients with hearing disturbances. The recruitment investigation tests and auditory brain stem response confirmed cochlear involvement in all 20 patients. Caloric stimulation tests revealed a normal vestibular function in all patient and control group. In electronystagmography, 21 (34%) patients had hypometric or hypermetric saccades and smooth pursuit tests showing that 4 (6%) patients had pathological changes while the control group was normal. HLA-B51 antigen was found positive in 15 of 20 Behcet's patient with hearing loss.
(1) The hearing and vestibular disturbances in Behcet's syndrome is more prevalent than previously recognized; (2) Hearing loss in high frequencies in Behcet's patients is an indicator of cochlear involvement in this disease; (3) There is a higher prevalence of central vestibular syndrome in Behcet's patients than it was thought before; (4) HLA-B51 antigen may be able to be a prognostic factor for sensorineural hearing loss in Behcet's patients.
本研究旨在通过大量患者确定白塞病中听力损失和前庭功能障碍的特征及发生率。本研究纳入了62例白塞病患者,其中34例男性,28例女性,平均年龄为33.7岁(15 - 60岁)。还纳入了62名健康正常对照者(38名男性和24名女性)。对患者组和对照组询问了任何听觉 - 前庭功能障碍病史,并进行了体格检查和耳鼻喉检查以及以下听力学测试:纯音听力测试(0.25、0.5、1、2、4和6kHz)、鼓室图、言语辨别、短增量敏感指数、音衰测试、听觉脑干反应。通过视频眼震图和冷热试验评估前庭系统。对有前庭功能障碍的患者进行头颅和脑干磁共振成像(MRI)以检查中枢神经系统。对患者组和对照组都进行了HLA - B51抗原检测。纯音听力图显示62例白塞病患者中有20例(32%)存在感音神经性听力损失(至少两个频率的听力水平为25dB),而对照组正常。有听力障碍的白塞病患者的听力图显示高频听力损失。重振试验和听觉脑干反应证实所有20例患者均有耳蜗受累。冷热刺激试验显示所有患者组和对照组的前庭功能正常。在眼震电图检查中,21例(34%)患者有眼跳幅度减小或增大,平稳跟踪试验显示4例(6%)患者有病理改变,而对照组正常。20例有听力损失的白塞病患者中有15例HLA - B51抗原呈阳性。
(1)白塞病中的听力和前庭功能障碍比之前认识到的更为普遍;(2)白塞病患者的高频听力损失是该病耳蜗受累的一个指标;(3)白塞病患者中枢前庭综合征的患病率比之前认为的更高;(4)HLA - B51抗原可能是白塞病患者感音神经性听力损失的一个预后因素。