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Epithéliopathie rétinienne diffuse
We report the case of a 52-year old man with no previous significant medical history presenting with progressive decrease in visual acuity (VA) of the right eye evolving over 10 years. Corrected visual acuity was 2/10 - P6 in the RE and 10/10 - P2 in the LE. The examination of the anterior segment w...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847254/ https://www.ncbi.nlm.nih.gov/pubmed/29541328 http://dx.doi.org/10.11604/pamj.2017.28.182.11355 |
Sumario: | We report the case of a 52-year old man with no previous significant medical history presenting with progressive decrease in visual acuity (VA) of the right eye evolving over 10 years. Corrected visual acuity was 2/10 - P6 in the RE and 10/10 - P2 in the LE. The examination of the anterior segment was unremarkable. Fundus examination showed alteration of the pigment epithelium (APE) in the RE associated with osteoblast-like pigment migrations involving the macula and a wide area due to gravitational descent of the superior temporal arcade onto the lower temporal quadrant. The left eye had a similar appearance especially in the inter-papillo-macular region (A,B). Fluorescein angiography showed early hyperfluorescence areas in the PE depigmented areas associated with pigment migrations giving a comet tail appearance by gravity casting in both eyes (C,D). Optical coherence tomography (OCT) showed retrofoveolar epithelial detachment (PED) at the level of the RE (E). The patient received Diamox therapy with regular monitoring to manage possible leakage points. Patient ’s evolution was marked by PED regression and VA improvement. |
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