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帕里-龙贝格综合征中神经视网膜炎的临床演变

Clinical evolution of neuroretinitis in Parry-Romberg syndrome.

作者信息

de Crecchio Giuseppe, Forte Raimondo, Strianese Diego, Rinaldi Michele, D'Aponte Antonella

机构信息

Department of Ophthalmology, University Federico II, Via Pansini 5, 80131, Naples, Italy.

出版信息

J Pediatr Ophthalmol Strabismus. 2008 Mar-Apr;45(2):125-6. doi: 10.3928/01913913-20080301-04.

Abstract

A 16-year-old girl with Parry-Romberg syndrome presented with monolateral exudative neuroretinitis and retinal telangiectasis that had been observed for 42 months. She was treated with immunosuppressive therapy with A-cyclosporine for 1 year, followed by laser treatment of telangiectasis. Her visual acuity improved from 20/200 to 20/70 in 1 year with a reduction of neuroretinal exudation. Laser treatment resulted in a further improvement of visual acuity to 20/40. Clinical findings remained unchanged during 2 years of follow-up. The association of immunosuppressive treatment and laser therapy may improve neuroretinal disease in the presence of Parry-Romberg syndrome.

摘要

一名患有帕里-龙贝格综合征的16岁女孩出现单侧渗出性神经视网膜炎和视网膜毛细血管扩张,病程已达42个月。她接受了为期1年的环孢素A免疫抑制治疗,随后进行了毛细血管扩张的激光治疗。1年内,她的视力从20/200提高到20/70,神经视网膜渗出减少。激光治疗使视力进一步提高到20/40。在2年的随访中临床症状保持不变。免疫抑制治疗与激光治疗相结合可能会改善帕里-龙贝格综合征患者的神经视网膜疾病。

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