Evereklioglu C, Cokkeser Y, Doganay S, Er H, Kizilay A
Department of Ophthalmology, Inönü University Medical Faculty, Turgut Ozal Medical Center, Research Hospital, Malatya, Turkey.
J Laryngol Otol. 2001 Sep;115(9):704-8. doi: 10.1258/0022215011908946.
A prospective controlled clinical study was carried out at the Department of Ophthalmology and ENT, Inönü University Medical Faculty, Turgut Ozal Medical Center, Research Hospital, to evaluate the audio-vestibular involvement in patients with Behçet's syndrome compared with controls. Twenty-five consecutive patients with Behçet's syndrome (mean age +/- SD, 34.96 +/- 8.50) and 20 age- and sex-matched healthy volunteers (hospital staff) as control subjects (mean age +/- SD, 34.45 +/- 9.16) were included in this study. Behçet's patients were divided into two groups according to the number of criteria, complete (all four major criteria) and incomplete (three major criteria without ocular involvement). The groups were compared with each other or controls regarding inner ear involvement. Audiometric pure-tone thresholds at 125 to 8000 Hz were obtained in all subjects in both groups, and pure tone average (PTA) hearing thresholds were calculated for the middle, high and low frequencies. In addition, short increment sensitivity index (SISI), tone decay and BERA examinations were performed in all Behçet's patients. Sensorineural hearing loss (SNHL) was present in six of 25 patients with Behçet's syndrome. Two Behçet's patients had unilateral total SNHL, two had bilateral moderate level SNHL, one had bilateral low-frequency SNHL and one bilateral high frequency SNHL. In two, BERA, and in five SISI, examination disclosed inner ear involvement. In control subjects, the past medical history was normal and there was no consistent audio-vestibular complaint. Their PTA thresholds were all in the normal range. Otoscopic examination findings were normal, with intact, mobile tympanic membranes in both groups. The present study showed that audio-vestibular involvement is not infrequent in Behçet's syndrome compared with age- and sex-matched healthy controls, and it is under-estimated. All Behçet's patients should regularly be followed by an otolaryngologists and be given information about the possibility of inner ear involvement. According to our results, hearing loss occurs more often in older patients and also in the complete form of Behçet's syndrome.
在图尔古特·奥扎尔医疗中心伊诺努大学医学院眼科与耳鼻喉科研究医院进行了一项前瞻性对照临床研究,以评估白塞病患者与对照组相比的听前庭受累情况。本研究纳入了25例连续的白塞病患者(平均年龄±标准差,34.96±8.50)和20名年龄及性别匹配的健康志愿者(医院工作人员)作为对照(平均年龄±标准差,34.45±9.16)。白塞病患者根据标准数量分为两组,即完全型(所有四项主要标准)和不完全型(三项主要标准且无眼部受累)。比较两组患者之间以及与对照组在内耳受累方面的情况。两组所有受试者均获得了125至8000Hz的纯音听力阈值,并计算了中、高、低频的纯音平均(PTA)听力阈值。此外,对所有白塞病患者进行了短增量敏感指数(SISI)、音衰和脑干听觉诱发电位(BERA)检查。25例白塞病患者中有6例存在感音神经性听力损失(SNHL)。2例白塞病患者为单侧全聋,2例为双侧中度SNHL,1例为双侧低频SNHL,1例为双侧高频SNHL。2例患者的BERA检查以及5例患者的SISI检查显示存在内耳受累。对照组既往病史正常,无一致的听前庭主诉。他们的PTA阈值均在正常范围内。两组的耳镜检查结果均正常,鼓膜完整、活动。本研究表明,与年龄及性别匹配的健康对照组相比,白塞病患者的听前庭受累并不罕见,且常被低估。所有白塞病患者都应由耳鼻喉科医生定期随访,并告知他们内耳受累的可能性。根据我们的结果,听力损失在老年患者以及完全型白塞病患者中更常见。