School of Medicine, Vita-Salute San Raffaele University, Milan, Italy; and.
Division of Head and Neck, Ophthalmology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Retin Cases Brief Rep. 2024 Jul 1;18(4):517-520. doi: 10.1097/ICB.0000000000001426.
To describe a unique case of X-linked Coats'-like retinitis pigmentosa, a form of exudative retinitis pigmentosa, in association with an RPGR variant, and its management with intravitreal anti-vascular endothelium growth factor drugs, along with a peculiar optical coherence tomography finding observed in a late stage of disease.
Case report.
A 33-year-old man previously treated with anti-vascular endothelium growth factors for macular edema came to our clinic for bilateral visual loss. A hemizygous RPGR variant (c.2442_2445del) was found and a diagnosis of Coats'-like Retinitis Pigmentosa was made. He was initially treated with carbonic anhydrase inhibitors; when efficacy wore off, he was switched to anti-vascular endothelium growth factor injections in both eyes with improvement. After a year without treatment, VA drastically worsened in both eyes; optical coherence tomography displayed disruption and increased hyper-reflectivity of the inner retinal layers in the right eye.
The c.2442_2445del variant is added to a number of known ORF 15 RPGR mutations associated with Coats'like Retinitis Pigmentosa. Anti-vascular endothelium growth factor treatment was successful in blocking visual loss in our patient and withholding treatment had a negative impact on his visual outcome.
描述一种独特的 X 连锁 Coats 样视网膜色素变性病例,这是渗出性视网膜色素变性的一种形式,与 RPGR 变异体相关,并描述其使用抗血管内皮生长因子药物进行治疗,以及在疾病晚期观察到的一种特殊的光相干断层扫描发现。
病例报告。
一名 33 岁男性曾因黄斑水肿接受抗血管内皮生长因子治疗,因双眼视力丧失就诊于我院。发现其存在 RPGR 半合子变异体(c.2442_2445del),诊断为 Coats 样视网膜色素变性。他最初接受碳酸酐酶抑制剂治疗;当疗效消退后,他被转用双眼抗血管内皮生长因子注射治疗,视力有所改善。一年未治疗后,他双眼的视力急剧恶化;右眼光相干断层扫描显示内层视网膜中断且反射增加。
c.2442_2445del 变异体是已知的与 Coats 样视网膜色素变性相关的 ORF15 RPGR 突变之一。抗血管内皮生长因子治疗成功阻止了我们患者的视力丧失,而停止治疗对他的视力结果产生了负面影响。