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。
MACULAR HOLE ASSOCIATED RETINAL DETACHMENT IN PRESUMED AUTOSOMAL RECESSIVE BESTROPHINOPATHY: A RETROSPECTIVE OBSERVATIONAL SERIES OF TWO CASES.
Purpose: The objective of this study was to evaluate surgical outcome of presumed autosomal recessive bestrophinopathy with full-thickness macular hole and retinal detachment managed by pars plana vitrectomy.
Methods: This was 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 VA, 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.