Coats Disease With Macular Nodule.

Q3 Medicine
International Ophthalmology Clinics Pub Date : 2025-10-01 Epub Date: 2025-09-25 DOI:10.1097/IIO.0000000000000592
Anasua Ganguly Kapoor, Sameera Nayak, Simranjeet Aulakh, Vijitha S Vempuluru, Swathi Kaliki
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引用次数: 0

Abstract

Purpose: To describe a case series of Coats disease with macular nodule mimicking retinoblastoma.

Methods: Retrospective case series.

Results: Of 339 patients with Coats disease, 7 (2%) with macular nodules were included. All had a referral diagnosis of retinoblastoma. All were males (mean age-6 y). The most common presenting complaint was decreased vision (n=4, 57%). Median best corrected visual acuity at presentation was counting fingers close to face, which was maintained at last follow-up (mean, 8 months). The nodule had a mean diameter of 5x4x3 mm, was grayish white, and bilobed (n=3, 43%), or dome shaped (n=4, 57%) with surface pigmentation (n=4, 57%), involving fovea (n=5, 71%), with surrounding exudates and second- or third-order retinal vessels. OCT (n=4) showed a well-defined hyperreflective subretinal nodule with posterior shadowing, cysts, and exudates. USG (n=6) showed an echodense intraocular nodule with moderate internal reflectivity with hyperechoic foci in 2 (33%) cases. FFA showed early- and mid-phase hypo-fluorescence with focal leakage with late-phase hyperfluorescence. Focal green laser photocoagulation of the telangiectatic vessels was performed in 5, one underwent subretinal fluid drainage and scleral buckling, and one was observed.

Conclusion: Macular nodule in Coats disease represents a preferential accumulation of lipid in the macula. This rare variant of Coats disease can mimic retinoblastoma process. Be aware of this entity to ensure appropriate diagnosis and treatment.

Coats病伴黄斑结节。
目的:报告一例Coats病合并黄斑结节性视网膜母细胞瘤。方法:回顾性病例系列。结果:339例Coats病患者中,7例(2%)伴有黄斑结节。所有患者转诊诊断为视网膜母细胞瘤。所有患者均为男性(平均年龄6岁)。最常见的主诉是视力下降(n= 4.57%)。就诊时最佳矫正视力中位数为数靠近面部的手指,在最后一次随访中保持(平均8个月)。结节平均直径为5x4x3 mm,呈灰白色,呈双叶状(n=3, 43%)或圆顶状(n=4, 57%),表面有色素沉着(n=4, 57%),累及中央凹(n=5, 71%),周围有渗出物和二级或三级视网膜血管。OCT (n=4)显示清晰的高反射性视网膜下结节,伴后影、囊肿和渗出物。USG (n=6)显示2例(33%)眼内结节回声密集,内反射率中等,伴有高回声灶。FFA表现为早中期低荧光,局灶性渗漏,晚期高荧光。5例行局灶性绿色激光光凝治疗毛细血管扩张血管,1例行视网膜下液引流和巩膜屈曲,1例观察。结论:Coats病黄斑结节表现为脂质在黄斑的优先积累。这种罕见的科茨病可以模拟视网膜母细胞瘤的过程。要了解这个实体,以确保适当的诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Ophthalmology Clinics
International Ophthalmology Clinics Medicine-Ophthalmology
CiteScore
1.40
自引率
0.00%
发文量
94
期刊介绍: International Ophthalmology Clinics is a valuable resource for any medical professional seeking to stay informed and up-to-date regarding developments in this dynamic specialty. Each issue of this quarterly publication presents a comprehensive review of a single topic in a new or changing area of ophthalmology. The timely, tightly focused review articles found in this publication give ophthalmologists the opportunity to benefit from the knowledge of leading experts in this rapidly changing field.
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