Best disease

最佳疾病
  • 文章类型: Journal Article
    遗传性视网膜疾病(IRD)是一组临床和遗传异质性疾病,可能因需要手术方法的几种玻璃体视网膜疾病而复杂化。在这些情况下,平坦部玻璃体切除术(PPV)是一种有价值的治疗选择,但是它在脉络膜视网膜结构严重受损的眼睛中的应用仍然存在争议。此外,基因治疗的推广和视网膜假体的日益使用将导致IRD患者对PPV手术的需求显著增加.通常影响遗传性视网膜疾病患者的视网膜变性可能会影响手术的执行和预期的结果。考虑到PPV在IRD相关并发症中应用的重要性,尝试从文献中了解在后眼节手术中什么是足够和安全的是至关重要的。使用染料,光毒性,伤疤发展的风险一直是阻碍在已经受损的眼睛中执行玻璃体视网膜手术的主题。因此,这篇综述旨在全面总结所有PPV在不同IRD中的应用,强调在这些眼睛中进行玻璃体视网膜手术时的有利结果以及需要考虑的潜在预防措施。
    Inherited retinal diseases (IRDs) are a group of clinically and genetically heterogeneous disorders that may be complicated by several vitreoretinal conditions requiring a surgical approach. Pars plana vitrectomy (PPV) stands as a valuable treatment option in these cases, but its application in eyes with such severely impaired chorioretinal architectures remains controversial. Furthermore, the spreading of gene therapy and the increasing use of retinal prostheses will end up in a marked increase in demand for PPV surgery for IRD patients. The retinal degeneration that typically affects patients with hereditary retinal disorders may influence the execution of the surgery and the expected results. Considering the importance of PPV application in IRD-related complications, it is fundamental to try to understand from the literature what is adequate and safe in posterior eye segment surgery. Use of dyes, light toxicity, and risk of wounding scar development have always been themes that discourage the execution of vitreoretinal surgery in already impaired eyes. Therefore, this review aims to comprehensively summarize all PPV applications in different IRDs, highlighting the favorable results as well as the potential precautions to consider when performing vitreoretinal surgery in these eyes.
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  • 文章类型: Journal Article
    光学相干断层扫描血管造影(OCT-A)是一种有价值的成像技术,允许非侵入性,深度解决,运动对比,视网膜和脉络膜血管网络的高分辨率图像。OCT-A的成像功能增强了我们对遗传性视网膜疾病(IRD)中发生的视网膜和脉络膜改变的理解,一组临床和遗传异质性疾病,可能因几种需要及时诊断的血管疾病而复杂化。在这次审查中,我们旨在全面总结OCT-A在IRD诊断和管理中的所有临床应用,突出视网膜色素变性的重要血管发现,Stargardt病,脉络膜炎,最佳疾病和其他不太常见的视网膜营养不良形式。还将讨论这种新颖成像模式的所有优点和局限性。
    Optical coherence tomography angiography (OCT-A) is a valuable imaging technique, allowing non-invasive, depth-resolved, motion-contrast, high-resolution images of both retinal and choroidal vascular networks. The imaging capabilities of OCT-A have enhanced our understanding of the retinal and choroidal alterations that occur in inherited retinal diseases (IRDs), a group of clinically and genetically heterogeneous disorders that may be complicated by several vascular conditions requiring a prompt diagnosis. In this review, we aimed to comprehensively summarize all clinical applications of OCT-A in the diagnosis and management of IRDs, highlighting significant vascular findings on retinitis pigmentosa, Stargardt disease, choroideremia, Best disease and other less common forms of retinal dystrophies. All advantages and limitations of this novel imaging modality will be also discussed.
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