Moschos Marilita M, Nitoda Eirini, Fenzel Isabelle, Song Xuefei, Langenbucher Achim, Kaesmann Barbara, Seitz Berthold, Gatzioufas Zisis
First Department of Ophthalmology, General Hospital of Athens G. Gennimatas, Medical School, National and Kapodistrian University of Athens, 6, Ikaria Street, Ekali, 14578, Athens, Greece.
Department of Ophthalmology, Saarland University Medical Center, Homburg/Saar, Germany.
Int Ophthalmol. 2019 Feb;39(2):359-373. doi: 10.1007/s10792-018-0819-0. Epub 2018 Jan 18.
To correlate the features of certain types of infantile glaucoma with the progression and the prognosis of the disease, highlighting probable risk factors.
Seventy-six patients with pediatric glaucoma were recruited in this retrospective study. All patients underwent ophthalmological examination in the Department of Ophthalmology of the Saarland University Medical Center from January 2001 to December 2012. Our pediatric patients were classified into four different categories of glaucoma: (1) primary congenital glaucoma (presenting buphthalmus), (2) aniridia-related glaucoma, (3) Peters/Rieger's anomaly-related glaucoma and (4) congenital cataract-related glaucoma. Personal data comprised age, sex, nationality, systemic diseases and gestational age. The best-corrected visual acuity (BCVA), the cup-disk ratio (CDR), the intraocular pressure (IOP), the corneal diameter and thickness, along with the Haab striae and corneal haze, were recorded.
The majority of the children were male (58%) and suffered from aniridia-related glaucoma (38%). Children with aniridia exhibited the worst BCVA. The CDR and IOP were significantly higher in children with primary congenital glaucoma, compared to the other groups, at the first visit. Those children also were with the largest corneal diameter and prevalence of Haab striae compared to the rest groups, whereas corneal haze was found more often and was more pronounced in children with Peters/Rieger's syndrome.
We concluded that glaucoma was earlier detected in children with primary congenital glaucoma, who exhibited increased corneal diameter and high percentage of Haab striae comparing to the other groups. However, these children responded successfully to any therapeutic intervention, exhibiting better BCVA and IOP values than the rest groups at the second visit.
将某些类型的婴幼儿青光眼的特征与疾病的进展及预后相关联,突出可能的风险因素。
本回顾性研究招募了76例小儿青光眼患者。2001年1月至2012年12月期间,所有患者均在萨尔州大学医学中心眼科接受眼科检查。我们将小儿患者分为四种不同类型的青光眼:(1)原发性先天性青光眼(表现为牛眼),(2)无虹膜相关性青光眼,(3)彼得斯/里格尔异常相关性青光眼,以及(4)先天性白内障相关性青光眼。个人数据包括年龄、性别、国籍、全身性疾病和孕周。记录最佳矫正视力(BCVA)、杯盘比(CDR)、眼压(IOP)、角膜直径和厚度,以及哈布条纹和角膜混浊情况。
大多数儿童为男性(58%),患有无虹膜相关性青光眼(38%)。无虹膜患儿的BCVA最差。初次就诊时,原发性先天性青光眼患儿的CDR和IOP显著高于其他组。与其他组相比,这些患儿的角膜直径最大,哈布条纹的发生率也最高,而彼得斯/里格尔综合征患儿的角膜混浊更常见且更明显。
我们得出结论,原发性先天性青光眼患儿的青光眼更早被发现,与其他组相比,其角膜直径增大,哈布条纹比例较高。然而,这些患儿对任何治疗干预反应良好,在第二次就诊时,其BCVA和IOP值均优于其他组。