1.
J AAPOS
; 21(1): 73-75, 2017 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27866070
RESUMO
We report the rare case of an 8-year-old boy with spontaneous scleral perforation secondary to an isolated congenital chorioretinal coloboma. Visual acuity was 20/200 and examination revealed severe hypotony with subcapsular cataract, complete exudative retinal detachment, hypotonous optic nerve swelling, and hypotony retinal fold. In the temporal periphery, there was a chorioretinal coloboma with a central full-thickness defect. The scleral defect was successfully treated with an autologous temporalis fascia graft. One year later, and after cataract surgery, visual acuity had improved to 20/20, with normal intraocular pressure.
Assuntos
Corioide/anormalidades , Coloboma/diagnóstico , Retina/anormalidades , Doenças da Esclera/diagnóstico , Criança , Coloboma/cirurgia , Fáscia/transplante , Humanos , Pressão Intraocular/fisiologia , Imageamento por Ressonância Magnética , Masculino , Ruptura Espontânea , Doenças da Esclera/cirurgia , Acuidade Visual/fisiologia
2.
J Fr Ophtalmol
; 42(7): e333-e334, 2019 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31133397