穿孔硬软化引起的高度散光

T. Rotsos, Konstantinos Andreanos, A. Sideri, I. Georgalas, K. Droutsas, D. Brouzas, D. Papaconstantinou
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引用次数: 0

摘要

我们提出一个病例硬软化穿孔在一个80岁的妇女。她的视力在过去两年中因角膜硬化变薄导致的进行性散光而恶化。穿孔硬化是一种罕见的疾病(占巩膜炎的4%),常见于关节外表现的类风湿性关节炎患者,尤其是女性患者。它的特征是非炎症性的,通常是双侧进行性巩膜变薄,这可能导致巩膜组织缺乏,露出裸露的葡萄膜。它也被描述为许多胶原蛋白和血管疾病,如Wegener肉芽肿病[1],Bechet病[2]和强直性脊柱炎[3]。病例报告我们报告了一位80岁的女性,以前没有全身性病理,在过去的两年里表现为双侧进行性视力丧失。她最后一次眼科检查是在两年前进行了双眼白内障手术后。无严重病理记录,双眼未矫正视力为20/25。在我们的检查中,双眼的视力为数指,右眼-5.00圈x 100°,左眼-5.00圈x 110°,视力将提高到20/40。裂隙灯检查显示鼻和颞巩膜变薄,薄结膜下有葡萄膜影(图1A)。此外,在颞缘和鼻缘均观察到角膜变薄(图1B),同时存在贯穿整个角膜的水平角膜纹(图1C)。前段光学相干断层扫描证实了巩膜组织缺失和穿孔硬化的诊断(图1D)。患者被转诊进行系统性评估,其中类风湿关节炎被诊断出来。结论穿孔硬软化是一种起病隐匿、进展缓慢的严重眼疾[1,2]。进行性高度散光、白内障、青光眼或眼球破裂(通常在外伤后)可导致视力丧失[1,2]。没有任何疗法被证明是有效的,患者*通信:Tryfon Rotsos, 15 Alkmanos街,雅典,希腊,11528;电话:+ 306974727279;电子邮件:tryfonrotsos@hotmail.com
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High astigmatism induced by scleromalacia perforans
We present a case of scleromalacia perforans in an 80-year-old woman. Her vision has deteriorated over the last two years due to progressive astigmatism induced by sclerocorneal thinning. Introduction Scleromalacia perforans is a rare entity (4% of scleritis) that is commonly seen in patients with rheumatoid arthritis with extraarticular presentation, especially women [1]. It is characterized by a non-inflammatory, often bilateral progressive scleral thinning which can lead to a lack of scleral tissue revealing bare uvea. It has also been described in a number of collagen and vasculitic disorders such as Wegener’s granulomatosis [1], Bechet disease [2] and ankylosing spondylitis [3]. Case report We present an 80-year-old woman with no previous systemic pathology, presented with bilateral progressive visual loss over the last two years. Her last ophthalmological examination was after uneventful cataract surgery in both eyes, two years ago. No serious pathology was recorded, and her uncorrected visual acuity was 20/25 in both eyes. During our examination, visual acuity was count fingers in both eyes which would improve to 20/40 with -5.00cyl x 100° in the right eye and -5.00cyl x 110° in the left eye. Slit lamp examination revealed nasal and temporal scleral thinning with uveal show under a thin conjunctival layer (Figure 1A). Moreover, corneal thinning was observed in both the temporal and nasal limbus (Figure 1B) along with the presence of horizontal corneal striae extending throughout the cornea (Figure 1C). Anterior Segment Optical Coherence Tomography confirmed the absence of scleral tissue and the diagnosis of scleromalacia perforans (Figure 1D). The patient was referred for systemic evaluation in which rheumatoid arthritis was diagnosed. Conclusion Scleromalacia perforans is a severe eye disorder with insidious onset, slow progression [1,2]. Visual loss can occur due to progressive high astigmatism, cataract, glaucoma or globe rupture (usually following trauma) [1,2]. No therapy has yet proven efficient and patients *Correspondence to: Tryfon Rotsos, 15 Alkmanos street, Athens, Greece, 11528; Tel: +306974727279; E-mail: tryfonrotsos@hotmail.com
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