伊凡综合征病例报告

Houda Bezza, Asma El Adrari, Oumayma El Mansouri, Kawtar Zaoui, L. A. Lhaj, Mohamed Kriet, Fouad Elasri
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引用次数: 0

摘要

特发性视网膜血管炎、动脉大动脉瘤和神经视网膜炎(IRVAN)是一种罕见疾病,主要影响无全身性疾病的年轻健康女性。我们介绍了一例 35 岁女性的病例,她出现视力下降 3 个月,但无相关症状。眼科检查发现双眼视力下降、乳头状水肿、星状黄斑水肿和双侧出血。视网膜成像证实了 IRVAN 综合征。治疗包括全视网膜光凝(PRP)和玻璃体内贝伐单抗注射,结果黄斑水肿消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case Report on IRVAN Syndrome
Idiopathic retinal vasculitis, arteriolar macroaneurysms, and neuroretinitis (IRVAN) is a rare condition predominantly affecting young, healthy females without systemic disease. We present the case of a 35-year-old female who presented with a 3-month history of decreased visual acuity without associated symptoms. Ophthalmological examination revealed reduced visual acuity in both eyes, papillary oedema, stellate macular oedema, and haemorrhages bilaterally. Retinal imaging confirmed IRVAN syndrome. Treatment included pan-retinal photocoagulation (PRP) and intravitreal bevacizumab injections, resulting in macular oedema regression.
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