Clinical Presentation and Treatment Outcomes of Adult-Onset Coats Disease.

IF 0.8 Q4 OPHTHALMOLOGY Journal of VitreoRetinal Diseases Pub Date : 2024-09-30 eCollection Date: 2025-01-01 DOI:10.1177/24741264241286580
Saarang Hansraj, Vishal Raval, Subhadra Jalali, Niroj Sahoo, Anthony Vipin Das
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Abstract

Purpose: To study the clinical profile, treatment, and outcomes of patients 35 years or older diagnosed with Coats disease. Methods: A cross-sectional observational hospital-based study was performed. Results: The study included 74 eyes diagnosed with adult-onset Coats disease. The mean age at presentation was 50 years (range, 35-75). Most patients were men (72.5%) and had a unilateral presentation (92.8%). The most common stage at presentation was 2A (extrafoveal exudation [39.2%]) followed by 2B (foveal exudation [33.7%]). Optical coherence tomography was performed in 40 eyes; 32 eyes (80.0%) had intraretinal fluid (IRF), 31 eyes (77.5%) had hard exudates, and 22 eyes (55.0%) had a disorganized retinal inner layer. Fluorescein angiography was performed in 35 eyes and showed an irregular foveal avascular zone in 28 eyes (80.0%). Multiple leaking microaneurysms were seen in 32 eyes (91.4%), with extensive vascular abnormalities involving the macula (86%) and extramacular zones (91%). Treatment modalities comprised laser photoablation (43.4%), cryotherapy with or without laser application (5.7%), and intravitreal injections (49%), alone or in combination. At a mean follow-up of 28 months (range, 3-293), 23 eyes (39.6%) had anatomic resolution of subretinal fluid and/or IRF. No statistically significant improvement was found in the mean best-corrected visual acuity (VA) between preoperatively and postoperatively (P > .05). Conclusions: Patients with adult-onset Coats disease have a unilateral presentation with a less severe stage than patients with childhood-onset disease. Despite the good anatomic response after treatment, the final VA remained unchanged.

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成人高兹病的临床表现和治疗效果
目的:研究 35 岁或以上确诊为高兹病患者的临床概况、治疗方法和效果。研究方法以医院为基础进行横断面观察研究。研究结果研究共纳入 74 例确诊为成人柯茨病的患者。平均发病年龄为 50 岁(35-75 岁)。大多数患者为男性(72.5%),单侧发病(92.8%)。发病时最常见的阶段是 2A(眼窝外渗出)(39.2%),其次是 2B(眼窝渗出,33.7%)。对 40 只眼睛进行了光学相干断层扫描,其中 32 只眼睛(80.0%)有视网膜内积液(IRF),31 只眼睛(77.5%)有硬性渗出物,22 只眼睛(55.0%)有紊乱的视网膜内层。对 35 只眼睛进行了荧光素血管造影,结果显示 28 只眼睛(80.0%)出现了不规则的眼窝血管缺失区。32只眼睛(91.4%)出现多个渗漏性微动脉瘤,黄斑区(86%)和黄斑外区(91%)出现广泛的血管异常。治疗方法包括激光光消融(43.4%)、冷冻疗法(含或不含激光)(5.7%)和单独或联合玻璃体内注射(49%)。在平均 28 个月(3-293 个月)的随访中,有 23 只眼睛(39.6%)的视网膜下积液和/或 IRF 在解剖学上得到了缓解。术前和术后的平均最佳矫正视力(VA)没有统计学上的改善(P > .05)。结论与儿童期发病的患者相比,成人期发病的科茨病患者多为单侧发病,病情较轻。尽管治疗后患者的解剖反应良好,但最终的视力仍保持不变。
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