Intravitreal bevacizumab in cystoid macular edema associated to maternally inherited diabetes and deafness's macular dystrophy

被引:2
|
作者
Marco-Campmany, Amelia [1 ]
Pacheco-Cervera, Jana [1 ]
Navarrete-Sanchis, Javier [1 ]
Tomas-Torrent, Juan Miguel [1 ]
Garcia-Canet, Sara [1 ]
Cuadrado-Gomez, Teresa [1 ]
机构
[1] Hosp Univ La Ribera, Dept Ophthalmol, Crtra Corbera,Km 1, Alzira 46600, Spain
关键词
CME; retina; diabetic retinopathy; macular and RPE dystrophies; retinal degenerations associated with systemic disease; medical therapies; MITOCHONDRIAL-DNA; POINT MUTATION; MELLITUS;
D O I
10.1177/1120672120969034
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Introduction: Maternally inherited diabetes and deafness (MIDD) is a rare and infradiagnosed cause of diabetes which can, in a high number of cases, associate a macular dystrophy. Case presentation: We report the case of a 49-year-old man affected of this syndrome, with proven m3243G>A mitochondrial mutation, who developed macular cysts 20 years after the initial presentation of his macular dystrophy. The fluorescein angiography showed no leakage, ruling out a diabetic macular edema. A treatment with intravitreal bevacizumab led to cystic changes resolution and visual acuity recovery. Conclusion: Intravitreal bevacizumab can be successfully employed for this complication of MIDD's macular dystrophy.
引用
收藏
页码:NP34 / NP39
页数:6
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