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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.
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页码:NP34 / NP39
页数:6
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