İnanç Merve, Şimşek Mert, Çakar Özdal Müge Pınar
Erciş State Hospital, Ophthalmology Clinic, Van, Turkey
Ulucanlar Eye Training and Research Hospital, Ophthalmology Clinic, Ankara, Turkey
Turk J Ophthalmol. 2019 Feb 28;49(1):10-14. doi: 10.4274/tjo.galenos.2018.53896.
To investigate the demographic, etiologic, and clinical features of HLA-B27-associated uveitis.
The clinical records of 91 patients diagnosed with HLA-B27-associated uveitis at the Ulucanlar Eye Training and Research Hospital between the years of 2005 and 2016 were reviewed. Each patient’s presenting complaints, best-corrected visual acuities in first and last visits, biomicroscopic and fundoscopic examination findings, frequency and seasonal distribution of attacks, and demographic data such as age and sex were noted. Therapeutic approaches, duration of follow-up, and complications were analyzed.
A total of 91 patients (179 eyes) aged 19-82 years (mean age 46.52±13.06 years) were included. Forty-three patients (47.3%) were female and 48 (52.7%) were male. Bilateral involvement was observed in 44 (48.4%) and unilateral involvement was observed in 47 (51.6%) patients. The most frequent complaint was redness (67%), followed by decreased and/or blurred vision (50.5%). The mean follow-up time was 38.2 months (range, 1-245 months). Anterior uveitis was most common anatomical subtype, seen in 86 (94.5%) of the patients. Mean number of attacks was 1.93±1.45 per patient-year and a significantly higher number of uveitis attacks (47%) occurred in winter. Twenty-four patients (26.3%) were diagnosed with ankylosing spondylitis. Fibrinous uveitis was detected in 36 patients (39.5%). Posterior synechia developed in 41 (22.9%) and hypopyon developed in 7 (3.9%) eyes. The most common complications were cataract (n=12, 6.7%) and ocular hypertension (n=15, 8.3%).
Ninety-one (6.3%) of the 1422 patients followed in our uvea clinic were diagnosed with HLA-B27-associated uveitis. HLA-B27-associated uveitis is characterized by acute, recurring sudden-onset iridocyclitis with a moderate to severe amount of fibrin and cells in the anterior chamber, and is easily treatable. Visual prognosis is good despite the complications.
研究HLA - B27相关性葡萄膜炎的人口统计学、病因学及临床特征。
回顾了2005年至2016年间在乌鲁坎拉尔眼科培训与研究医院诊断为HLA - B27相关性葡萄膜炎的91例患者的临床记录。记录了每位患者的就诊主诉、首次和末次就诊时的最佳矫正视力、生物显微镜和眼底检查结果、发作频率和季节分布,以及年龄和性别等人口统计学数据。分析了治疗方法、随访时间和并发症情况。
共纳入91例患者(179只眼),年龄19 - 82岁(平均年龄46.52±13.06岁)。43例(47.3%)为女性,48例(52.7%)为男性。44例(48.4%)患者为双侧受累,47例(51.6%)患者为单侧受累。最常见的主诉是眼红(67%),其次是视力下降和/或视物模糊(50.5%)。平均随访时间为38.2个月(范围1 - 245个月)。前葡萄膜炎是最常见的解剖学亚型,86例(94.5%)患者出现该类型。每位患者每年发作的平均次数为1.93±1.45次,且葡萄膜炎发作次数在冬季显著更高(47%)。24例(26.3%)患者被诊断为强直性脊柱炎。36例(39.5%)患者检测到纤维素性葡萄膜炎。41只眼(22.9%)出现后粘连,7只眼(3.9%)出现前房积脓。最常见的并发症是白内障(n = 12,6.7%)和高眼压(n = 15,8.3%)。
在我们葡萄膜炎门诊随访的1422例患者中,91例(6.3%)被诊断为HLA - B27相关性葡萄膜炎。HLA - B27相关性葡萄膜炎的特征为急性、复发性、突然发作的虹膜睫状体炎,前房内有中度至大量的纤维素和细胞,且易于治疗。尽管有并发症,但视力预后良好。