Rathi Varsha M, Murthy Somasheila I, Bagga Bhupesh, Taneja Mukesh, Chaurasia Sunita, Sangwan Virender S
Cornea Services, L V Prasad Eye Institute, Kallam Anji Reddy Camus, Hyderabad, Telangana, India.
Indian J Ophthalmol. 2015 Mar;63(3):233-8. doi: 10.4103/0301-4738.156927.
This study was carried out as a part of an internal audit and is the largest series of patients having keratoglobus, published in the literature. Poor visual acuity of the patients indicates the blinding nature of the disease.
We report our experience with patients having keratoglobus at a tertiary eye care center in India.
Retrospective study.
We analyzed adults and pediatric patients (<16 years) with keratoglobus, seen during 2008-2012. The age, gender, consanguinity, presenting ocular signs, ocular and systemic associations, visual acuity, corneal topography, and surgeries were documented.
Forty-eight patients (mean age 22 ± 15 years, 31 males) having keratoglobus were analyzed. 21 patients (42 eyes) were <16 years. Twelve eyes (16 events) had positive history of trauma. The presenting clinical signs were corneal scars/scars of tear repair (15 eyes), hydrops, healed and acute (14 eyes) and corneal or globe rupture (9 eyes). Best-corrected visual acuity was >20/40 in 6/42 (14.3%) pediatric eyes and 15/53 (28.30%) adults. Visual acuity ranging from counting of fingers to no light perception was noted in 20/53 (37.74%) adults and 21/42 (50%) pediatric patients; 13/20 (65%) with blue sclera and 8/22 eyes (36.37%) without blue sclera. Vernal keratoconjunctivitis was present in one pediatric patient. Choroidal osteoma, retinitis pigmentosa, and retinal detachment were present in adults. Surgeries performed were corneal tear repair (5 eyes), tissue adhesive application (2 eyes), descematopexy (4 eyes) and penetrating keratoplasty (PK - 8 eyes: Three had post-PK glaucoma, graft failure-one eye, 4 patients wore scleral lens - prosthetic replacement of the ocular surface ecosystem).
About 50% of pediatric eyes (65% having blue sclera) had no functional vision. Trivial trauma was responsible for corneal rupture indicating need for protective glasses. About 50% patients had post-PK glaucoma though grafts were clear.
本研究作为内部审计的一部分开展,是文献中报道的最大规模圆锥角膜患者系列研究。患者视力差表明该疾病具有致盲性。
我们报告在印度一家三级眼科护理中心治疗圆锥角膜患者的经验。
回顾性研究。
我们分析了2008年至2012年期间诊治的圆锥角膜成年及儿童(<16岁)患者。记录了患者的年龄、性别、近亲结婚情况、眼部体征、眼部及全身相关疾病、视力、角膜地形图及手术情况。
分析了48例圆锥角膜患者(平均年龄22±15岁,男性31例)。21例患者(42只眼)年龄<16岁。12只眼(16次事件)有外伤史。主要临床体征为角膜瘢痕/泪液修复瘢痕(15只眼)、水肿,愈合期及急性期(14只眼)以及角膜或眼球破裂(9只眼)。在42只儿童眼中,6只(14.3%)最佳矫正视力>20/40,53只成人眼中15只(28.30%)最佳矫正视力>20/40。20/53(37.74%)成人和21/42(50%)儿童患者的视力从指数到无光感。13/20(65%)有蓝色巩膜,8/22只眼(36.37%)无蓝色巩膜。1例儿童患者患有春季角结膜炎。成人患者存在脉络膜骨瘤、视网膜色素变性和视网膜脱离。所进行的手术包括角膜泪液修复(5只眼)、应用组织粘合剂(2只眼)、后弹力层固定术(4只眼)和穿透性角膜移植术(PK - 8只眼:3例发生PK术后青光眼,1只眼移植失败,4例患者佩戴巩膜镜 - 眼表生态系统假体置换)。
约50%的儿童眼(65%有蓝色巩膜)无功能性视力。轻微外伤导致角膜破裂,提示需要佩戴防护眼镜。尽管移植片透明,但约50%的患者发生了PK术后青光眼。