The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology, Chongqing Eye Institute, Chongqing, China.
Cornea. 2011 Dec;30(12):1336-40. doi: 10.1097/ICO.0b013e31820f774c.
To determine the incidence and characterize the clinical features of band-shaped keratopathy in Chinese patients with Vogt-Koyanagi-Harada (VKH) syndrome.
The data of 360 consecutive VKH patients examined from November 2000 to December 2008 were reviewed. The patients were diagnosed with VKH syndrome according to international criteria. The data of VKH patients with band-shaped keratopathy, including age at disease onset, gender, intervals between disease onset and emergence of this complication, other complications, and therapy were collected and analyzed.
Of the 360 VKH patients, 66 patients (132 eyes) visited us at the stage of posterior uveitis or anterior uveal involvement. None of these 132 eyes had band-shaped keratopathy develop. The other 294 VKH patients (587 eyes) visited us at the stage of recurrent, granulomatous, anterior uveitis, and band-shaped keratopathy was observed in 21 eyes of 13 patients (3.6%). Of these 13 patients, there were 6 men and 7 women. Band-shaped keratopathy in 21 eyes was observed from 9 months to 32 years, with a mean of 12.7 years after the first uveitis attack. These patients had been intermittently treated with systemic corticosteroids and occasionally in combination with a transient use of either chlorambucil or azathioprine. All the eyes with band-shaped keratopathy showed recurrent and chronic intraocular inflammation. Complicated cataract, increased intraocular pressure and decreased intraocular pressure were observed in 18, 12, and 5 eyes, respectively. Ocular phthisis was observed in 1 eye. The best-corrected vision of 0.3 or less was observed in 85.1% of the affected eyes.
Band-shaped keratopathy is a relatively uncommon complication in VKH syndrome and mostly occurs in relatively younger patients with a long course of chronic intraocular inflammation. It was frequently associated with complicated cataract and secondary glaucoma and was a marker for poor visual outcome.
确定带状角膜病变在中国人 Vogt-小柳原田(VKH)综合征患者中的发病率并对其临床特征进行描述。
回顾分析 2000 年 11 月至 2008 年 12 月期间就诊的 360 例连续 VKH 患者的数据。患者根据国际标准诊断为 VKH 综合征。收集并分析了患有带状角膜病变的 VKH 患者的数据,包括发病年龄、性别、发病与并发症出现之间的间隔、其他并发症和治疗情况。
360 例 VKH 患者中,有 66 例(132 只眼)就诊时处于后葡萄膜炎或前部葡萄膜受累阶段,这 132 只眼中均未出现带状角膜病变。另外 294 例 VKH 患者(587 只眼)就诊时处于复发性、肉芽肿性前部葡萄膜炎阶段,在 13 例(3.6%)患者的 21 只眼中观察到带状角膜病变。这 13 例患者中,男性 6 例,女性 7 例。21 只眼的带状角膜病变从发病后 9 个月到 32 年不等,平均在首次葡萄膜炎发作后 12.7 年出现。这些患者间歇性接受全身皮质类固醇治疗,偶尔会短暂使用氯苯丁酸或硫唑嘌呤。所有患有带状角膜病变的眼均出现复发性和慢性眼内炎症。18 只眼出现并发性白内障,12 只眼眼压升高,5 只眼眼压降低。1 只眼出现眼球萎缩。85.1%受累眼的最佳矫正视力为 0.3 或更低。
带状角膜病变是 VKH 综合征的一种相对少见的并发症,主要发生在慢性眼内炎症病程较长的较年轻患者中。它常与并发性白内障和继发性青光眼相关,是视力预后不良的标志。