Department of Ophthalmology, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
Department of Ophthalmology, Clinical Emergency Eye Hospital Bucharest, Romania.
Rom J Ophthalmol. 2022 Jan-Mar;66(1):101-108. doi: 10.22336/rjo.2022.20.
The aim of this report was to present a rare case of apparently unilateral Peters anomaly and describe the clinical characteristics, surgical approach, and visual prognosis. We presented the case of a 7-year-old female patient with posterior corneal defect due to kerato-lenticular adhesions along with anterior dislocation and opacification of the lens in the left eye and a history of post-traumatic evisceration of the right eye. Systemic associations included mental underdevelopment, left torticollis and scoliosis. No family history of acquired or inherited diseases were determined. We performed cataract extraction in the left eye and opted for aphakia. Based on clinical findings, we considered unilateral Peters anomaly type II. Cataract surgery slightly improved the visual acuity from hand moving to 20/ 400 UCVA (uncorrected visual acuity) and 20/ 100 with +10.0 diopters at 1 month postoperative. No enlargement of the corneal opacity was observed. In this case, we were able to diagnose Peters anomaly only in one eye. The diagnosis required long follow-up with periodic measurement of intraocular pressure (IOP) to early detect glaucoma. The complexity and uniqueness of the case relied on the difficult approach made by the cloudy cornea and anterior lens dislocation. We applied a combination of techniques including adhesiolysis, cataract extraction and anterior vitrectomy. Further interventions such as secondary IOL (intraocular lens) implantation or PKP (penetrating keratoplasty) will be taken into consideration after six-month and one-year postoperative follow-up. PA = Peters anomaly, DM = Descemet's membrane, IOL = intraocular lens, VA = visual acuity, OVDs = ophthalmic viscosurgical devices, IOP = intraocular pression, PKP = penetrating keratoplasty, BCVA = best corrected visual acuity, UCVA = uncorrected visual acuity.
本报告的目的是介绍一例单侧 Peters 异常的罕见病例,并描述其临床特征、手术方法和视力预后。我们报告了一例 7 岁女性患者,左眼因角膜 - 晶状体粘连导致后角膜缺损,晶状体向前脱位和混浊,并伴有右眼外伤性眼内容物脱出史。全身合并症包括智力发育迟缓、左斜颈和脊柱侧凸。未确定家族遗传性或获得性疾病史。我们对左眼行白内障摘除术,并选择无晶状体眼。根据临床发现,我们考虑为单侧 Peters 异常 II 型。白内障手术后,视力从手动提高到术后 1 个月时的 20/400UCVA(未矫正视力)和 20/100 加+10.0 屈光度。未观察到角膜混浊扩大。在本例中,我们仅在一只眼诊断出 Peters 异常。诊断需要长期随访,定期测量眼压(IOP),以早期发现青光眼。该病例的复杂性和独特性在于混浊的角膜和晶状体前脱位导致手术入路困难。我们应用了多种技术的联合治疗,包括粘连松解、白内障摘除和前段玻璃体切除术。在术后 6 个月和 1 年的随访中,将进一步考虑进行二次人工晶状体(IOL)植入或穿透性角膜移植术(PKP)等干预措施。PA = Peters 异常,DM = Descemet 膜,IOL = 人工晶状体,VA = 视力,OVDs = 眼科粘弹剂,IOP = 眼压,PKP = 穿透性角膜移植术,BCVA = 最佳矫正视力,UCVA = 未矫正视力。