Iridocorneal Endothelial Syndrome Management is tough but Never Impossible. A Case Series Study

S. Noman
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Abstract

Purpose: To document and describe clinical manifestations and management approaches to patients diagnosed with Iridocorneal Endothelial (ICE) syndrome presenting at the Glaucoma Department, Chittagong Eye Infirmary and Training Complex, Chittagong, Bangladesh. Design: A hospital-based prospective observational case series review. Participants: 25 patients who were diagnosed as ICE syndrome from November 2007 to October 2009. Method: Patient particulars, history with main causes of hospital presentations were recorded. Ophthalmic examination details including tonometry, slit lamp examination, gonioscopy, indirect ophthalmoscopy, visual fluid examination and management given were documented. Similar relevant details were recorded for three follow up periods on all patients extending over a total period of 12 months. Main outcome measure: Significant observations, pattern or associations within the cohort. Results: 25 patients were included in the study. There were 15 female and 10 male patients. All 25 cases were unilateral. The mean age of the patients was 41 ± 15.27 years. Among them 15(60%) had pre-treatment visual acuity between 6/9 – 6/18 and 10(40%) had 6/24 – 6/60). Improved visual acuity was observed one year after starting treatment. 21 patients (84%) presented with eccentric pupil (corectopia), 9 patients (36%) with peripheral anterior synechiae, 6 patients (32%) with iris atrophy, 6 patients (24%) with mild corneal oedema, 3 patients (12%) with ectropion uveae, 2 patients (8%) with polyconic and 11 patients (44%) presented with pigmentary changes over iris (like diffuse iris naevus). Mean IOP at presentation was 24.08 ±14.3 mmHg and that of last follow-up was 17.38 ± 7.57 mmHg. IOP was controlled with 2 – 3 topical anti glaucoma medications in 8 patients (32%); with only observation in 5 patients (20%) and with surgical intervention in 12 patients (48%). Conclusion: Although ICE syndrome is a refractory glaucoma, control of Intraocular Pressure (IOP) and preservation of visual acuity were seen in 52% of cases which had conservative management with topical medications and observation. Patients not responding to medical management needed surgery for the control of intraocular pressure.
虹膜内皮综合征的治疗是困难的,但从来都不是不可能的。案例系列研究
目的:记录和描述孟加拉国吉大港眼科医院和培训中心青光眼科诊断为虹膜角膜内皮(ICE)综合征患者的临床表现和治疗方法。设计:以医院为基础的前瞻性观察病例系列综述。研究对象:2007年11月至2009年10月诊断为ICE综合征的25例患者。方法:记录患者资料、病史及主要住院原因。记录眼科检查细节,包括眼压计、裂隙灯检查、角膜镜检查、间接眼镜检查、视液检查和治疗。对所有患者进行为期12个月的三次随访,记录了类似的相关细节。主要结果测量:在队列中有意义的观察、模式或关联。结果:25例患者纳入研究。女性15例,男性10例。25例均为单侧。患者平均年龄41±15.27岁。其中15例(60%)术前视力在6/9 ~ 6/18之间,10例(40%)术前视力在6/24 ~ 6/60之间。开始治疗一年后,视力有所改善。21例(84%)患者表现为瞳孔偏心(纠正斜视),9例(36%)患者表现为周围前粘连,6例(32%)患者表现为虹膜萎缩,6例(24%)患者表现为轻度角膜水肿,3例(12%)患者表现为葡萄膜外翻,2例(8%)患者表现为多圆锥,11例(44%)患者表现为虹膜色素改变(如弥漫性虹膜痣)。患者首发时平均眼压为24.08±14.3 mmHg,末次随访时平均眼压为17.38±7.57 mmHg。8例患者(32%)使用2 - 3种外用抗青光眼药物控制IOP;仅观察5例(20%),手术干预12例(48%)。结论:虽然ICE综合征是一种难治性青光眼,但在局部用药和观察保守治疗的情况下,52%的患者眼压得到了控制,视力得到了保持。治疗无效的患者需要手术控制眼压。
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