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2.
Case Rep Ophthalmol ; 10(2): 200-204, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31692601

RESUMO

INTRODUCTION: To demonstrate, with the aid of retinal imaging, an abnormal post-operative macular appearance caused by the presence of a "fragmented" pre-retinal bubble of octafluoropropane (C3F8) masquerading as retained subretinal perfluorocarbon liquid (PFCL). METHODS: This is an interventional case presentation. RESULTS: Colour fundus photography high-resolution spectral domain-optical coherence tomography (SD-OCT) and clinical progress demonstrate that the abnormal reflex was caused by the presence of a small fragment of C3F8 becoming lodged at the pre-foveal area. CONCLUSION: Submacular entrapment of various substances used during vitrectomy has been described in a number of case reports and case series. To our knowledge, this is the first described case of a retained fragment of fluorocarbon gas trapped at the macula following successful retinal detachment repair and highlights a previously unreported cause of an abnormal foveal appearance. However, clinical examination together with the use of SD-OCT is helpful in differentiating the appearance from that seen in other retained vitrectomy adjuncts.

3.
Graefes Arch Clin Exp Ophthalmol ; 248(12): 1719-28, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20640437

RESUMO

PURPOSE: The aim of this study is to image and describe the in vivo choroidal changes in various retinal dystrophies using the technique of enhanced depth imaging (EDI) optical coherence tomography (OCT) and to correlate these findings with the clinical appearance. Associations between choroidal change and genotype, visual acuity and results of retinal electrophysiology are also explored. DESIGN: Retrospective observational case series. METHODS: Twenty patients attending the medical retina clinics at Moorfields Eye Hospital underwent EDI OCT choroidal scans as part of the scanning protocol when they underwent OCT imaging with the Spectralis HRA and OCT. The choroidal images were obtained by moving the Spectralis camera close enough to obtain an inverted image of the retina. The scans were read by two experienced OCT readers assessing the choroidal thickness as well as the choroidal contour for focal areas of choroidal thinning corresponding to the areas of RPE/outer retinal atrophy. The spectrum of patients included those with Stargardt macular dystrophy, macular dystrophies secondary to known mutations such as peripherin/RDS, uncharacterised macular dystrophies, Best disease, bifocal chorioretinal atrophy, Bietti crystalline retinal dystrophy and choroideraemia. RESULTS: The choroidal appearance was symmetrical in all patients who had both eyes scanned. Ten patients showed no choroidal thinning, five had focal mild to moderate choroidal thinning, three had focal severe choroidal thinning, and two patients had diffuse severe choroidal thinning. There was no association between choroidal thinning and visual acuity [Fisher's exact test, p = 0.350 (right eye), p = 1.000 (left eye)], or extent of retinal dysfunction on electrophysiology (Fisher's exact test, p = 1.000). CONCLUSION: Enhanced depth imaging using spectral domain OCT can be used to identify choroidal changes in inherited retinal disease. The pattern of choroidal change correlates well with the clinical appearance. It appears that the extent and pattern of choroidal thinning is dependent on the stage of the disease in some cases, and in others the causative gene defect.


Assuntos
Doenças da Coroide/diagnóstico , Corioide/patologia , Distrofias Retinianas/genética , Tomografia de Coerência Óptica , Transportadores de Cassetes de Ligação de ATP/genética , Adolescente , Adulto , Criança , Eletrofisiologia , Genótipo , Humanos , Proteínas de Filamentos Intermediários/genética , Glicoproteínas de Membrana/genética , Pessoa de Meia-Idade , Proteínas do Tecido Nervoso/genética , Periferinas , Proteínas Proto-Oncogênicas/genética , Receptores Proteína Tirosina Quinases/genética , Distrofias Retinianas/fisiopatologia , Estudos Retrospectivos , Acuidade Visual/fisiologia , Adulto Jovem , c-Mer Tirosina Quinase
4.
Artigo em Inglês | MEDLINE | ID: mdl-19963839

RESUMO

The Argus II 60 channel epiretinal prosthesis has been developed in order to provide partial restoration of vision to subjects blinded from outer retinal degenerative disease. To date the device has been implanted in 21 subjects as part of a feasibility study. In 6 month post-implantation door finding and line tracking orientation and mobility testing, subjects have shown improvements of 86% and 73%, respectively, for system on vs. system off. In high-contrast Square Localization tests using a touch screen monitor 87% of tested subjects performed significantly better with the system on compared with off. These preliminary results show that the Argus II system provides some functional vision to blind subjects.


Assuntos
Cegueira/cirurgia , Próteses e Implantes , Retina/cirurgia , Adulto , Idoso , Estudos de Viabilidade , Feminino , Humanos , Locomoção/fisiologia , Masculino , Pessoa de Meia-Idade , Orientação/fisiologia , Retinose Pigmentar/cirurgia
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