对侧眼星状非遗传性特发性中央黄斑视网膜裂的自发消退和非同步发病。

IF 0.5 Q4 OPHTHALMOLOGY
Mauricio Bayram-Suverza, Abel Ramírez-Estudillo
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引用次数: 0

摘要

目的:介绍一例星状非遗传性特发性中央黄斑视网膜裂的多模态影像学表现。方法:对单个病例进行评价。结果:一位70岁的女性在黄斑光学相干断层扫描上表现为左眼外丛状层裂腔。荧光素血管造影未见渗漏。在排除非血管源性囊样黄斑病变的其他原因后,患者被诊断为星状非遗传性特发性中央黄斑视网膜裂。5年后,最佳矫正视力保持稳定。左眼视网膜裂消失,右眼黄斑下部出现囊状间隙,但未行玻璃体黄斑牵引。在此期间,没有眼部手术或药物使用的历史,可能会影响病理过程。结论:本病例强调了在星状非遗传性特发性中央黄斑视网膜裂的发展过程中进行多模态影像学监测的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spontaneous Resolution and Asynchronous Onset of Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis in the Contralateral Eye.

Purpose: To present a patient with stellate nonhereditary idiopathic foveomacular retinoschisis found with multimodal imaging. Methods: A single case was evaluated. Results: A 70-year-old woman presented with schisis cavities in the outer plexiform layer in the left eye on macular optical coherence tomography. No leakage was detected by fluorescein angiography. After ruling out other causes of nonvasogenic cystoid maculopathy, the patient was diagnosed with stellate nonhereditary idiopathic foveomacular retinoschisis. After 5 years, the best-corrected visual acuity remained stable. The retinoschisis in the left eye had resolved, and cystoid spaces appeared in the lower portion of the macula in the right eye despite the absence of vitreomacular traction. There was no history of ocular procedures or medication use that could have affected the course of the pathology during the intervening period. Conclusions: This case emphasizes the importance of performing multimodal imaging to monitor the characteristics of stellate nonhereditary idiopathic foveomacular retinoschisis as they evolve.

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CiteScore
1.20
自引率
16.70%
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