Angiographically silent macular retinoschisis and vitreomacular traction in a patient with same - side Duane retraction syndrome.

IF 0.8 Q4 OPHTHALMOLOGY Strabismus Pub Date : 2025-03-01 Epub Date: 2024-09-03 DOI:10.1080/09273972.2024.2399351
Işıl Kefeli, Aylin Yaman, Ali Osman Saatci
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Abstract

Introduction: To report the unusual fundus features of a case with unilateral Duane retraction syndrome (DRS) with same-side extensive macular retinoschisis. Methods: A 75-year-old woman was diagnosed to have DRS type 3 and several multimodal fundus imaging modalities were performed. Results: There was limited abduction and adduction, globe retraction, and narrowing of the palpebral fissure on the adduction of the left eye without a compensatory face turn. Concurrently, spectral domain optical coherence tomography revealed marked macular retinoschisis and severe vitreoretinal traction without any evidence of dye leakage or pooling on fluorescein angiography in the left eye. Discussion: Various ocular abnormalities may rarely accompany DRS and the present case is the first reported case of most likely coincidental macular retinoschisis in association with DRS.

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一名同侧杜安回缩综合征患者的血管造影无黄斑视网膜裂孔和玻璃体黄斑牵引。
导言:报告一例单侧杜安回缩综合征(DRS)伴同侧广泛黄斑视网膜裂孔的异常眼底特征。方法:对一名 75 岁的女性患者诊断为 DRS 3 型,并进行了多种多模态眼底成像检查。结果:左眼外展和内收受限,眼球后缩,内收时睑裂变窄,无代偿性转脸。同时,光谱域光学相干断层扫描显示左眼有明显的黄斑视网膜裂孔和严重的玻璃体视网膜牵引,但荧光素血管造影没有任何染料渗漏或汇集的迹象。讨论:各种眼部异常很少会伴随 DRS,本病例是第一例报告的很可能与 DRS 同时发生的黄斑视网膜裂孔。
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来源期刊
Strabismus
Strabismus OPHTHALMOLOGY-
CiteScore
1.60
自引率
11.10%
发文量
30
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