Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis: Cataract Surgery.

IF 0.7 Q4 OPHTHALMOLOGY
Case Reports in Ophthalmological Medicine Pub Date : 2022-09-09 eCollection Date: 2022-01-01 DOI:10.1155/2022/7404138
Sofie Van der Auwera, Oscar Kallay
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引用次数: 1

Abstract

Purpose: We present the first case described in the literature of cataract surgery in a patient with stellate nonhereditary idiopathic foveomacular retinoschisis (SNIF).

Methods: In this case report, we describe the extensive workup we did on our patient, including optical coherence tomography, fundus autofluorescence, fluo-angiography, full field electroretinogram, and genetic testing. We moreover describe the cataract surgery with clear lens extraction and implanting of a multifocal implant.

Results: The refractive and lifestyle profile of our patient made implantation of multifocal intraocular implants the only solution for this case. During preoperative measurements, a SNIF diagnosis was suspected after optic coherence tomography imaging which led to an even more extensive workup of our patient and the diagnosis of stellate nonhereditary idiopathic foveomacular retinoschisis. We then proceeded to cataract surgery, which was performed safely and without any sequellae.

Conclusion: Stellate nonhereditary idiopathic foveomacular retinoschisis (SNIF) is a relatively new disease entity. Only few cases in the literature describe this disease, and none of them describe cataract surgery in a patient with SNIF. We therefore describe the first known cataract surgery in such a case. Long term follow-up results show that the procedure can be performed safely. Summary Statement. We hereby present the first case described in the literature of cataract surgery of a patient diagnosed with stellate nonhereditary idiopathic foveomacular retinoschisis. A clear lens extraction with implantation of a multifocal intraocular implant was conducted with excellent postoperative results and a happy patient.

Abstract Image

Abstract Image

星状非遗传性特发性中央黄斑视网膜裂:白内障手术。
目的:我们报告了文献中第一例星状非遗传性特发性中央黄斑视网膜裂(SNIF)的白内障手术。方法:在本病例报告中,我们描述了我们对患者所做的广泛的检查,包括光学相干断层扫描、眼底自体荧光、荧光血管造影、全视野视网膜电图和基因检测。此外,我们描述了白内障手术与透明晶状体提取和植入多焦人工晶体。结果:本例患者的屈光和生活方式使多焦点眼内植入成为该病例的唯一解决方案。在术前测量中,在光学相干断层扫描成像后,怀疑SNIF诊断,导致对患者进行更广泛的检查,并诊断为星状非遗传性特发性中央黄斑视网膜裂。然后我们进行了白内障手术,手术很安全,没有任何后遗症。结论:星状非遗传性特发性中央黄斑视网膜裂(SNIF)是一种较新的疾病。文献中只有少数病例描述了这种疾病,并且没有一例描述了SNIF患者的白内障手术。因此,我们描述了在这种情况下的第一个已知的白内障手术。长期随访结果表明,该手术可以安全进行。总结陈述。我们在此提出第一例白内障手术的文献描述的病人诊断为星状非遗传性特发性中央黄斑视网膜裂。我们进行了透明晶状体摘除术和多焦人工晶状体植入术,术后效果良好,患者心情愉快。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
14 weeks
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