假定为常染色体隐性遗传性富营养化病(ARB)的黄斑孔相关性视网膜脱离--两例病例的回顾性观察系列。

Naresh Babu Kannan, Muthukrishnan Vallinayagam, Ananya Goswami, Reshma Dara
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引用次数: 0

摘要

目的:推测常染色体隐性遗传嗜酸性粒细胞增多症(ARB)伴全厚黄斑裂孔和视网膜脱离的手术治疗效果:回顾性观察病例系列,对两名患者的两只眼睛进行了25 G玻璃体旁切除术,同时剥离内缘膜和SF6填塞,并对最佳矫正视力、眼底照片和光谱域光学相干断层扫描进行了评估:结论:25 G 玻璃体旁切除术联合剥离内缘膜和 SF6 填塞术可为推测为常染色体隐性遗传的 Bestrophinopathy 患者的黄斑孔相关视网膜脱离带来良好的治疗效果。
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Macular hole associated Retinal Detachment in presumed Autosomal Recessive Bestrophinopathy (ARB)- A retrospective observational series of two cases.

Purpose: Surgical outcome of presumed Autosomal Recessive Bestrophinopathy (ARB)with full thickness macular hole and retinal detachment managed by pars plana vitrectomy.

Methods: A retrospective observational case series of two eyes of two patients who underwent 25 G pars plana vitrectomy with peeling of internal limiting membrane and SF6 tamponade and were assessed with respect to best corrected visual acuity, fundus photographs and spectral domain optical coherence tomography.

Results: Type 1 closure of macular hole was achieved along with resolution of retinal detachment in both patients.

Conclusion: 25 G pars plana vitrectomy with peeling of internal limiting membrane and SF6 tamponade can result in favorable outcome in macular hole associated retinal detachment in patients with presumed Autosomal recessive Bestrophinopathy.

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来源期刊
Retinal Cases and Brief Reports
Retinal Cases and Brief Reports Medicine-Ophthalmology
CiteScore
2.10
自引率
0.00%
发文量
342
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