Multimodal imaging in early onset non-neovascular pigment epithelial detachments

Author:

Goudot Mathilde M1,Rothschild Pierre-Raphael12,Bauters Gautier1,Vagge Aldo3ORCID,Miere Alexandra4ORCID,Souied Eric H4,Behar-Cohen Francine12,Bernabei Federico1ORCID

Affiliation:

1. Department of Ophthalmology, Cochin Hospital, Paris, France

2. Université Paris-Cité, Centre de Recherches des Cordeliers, Paris, France

3. University Eye Clinic of Genoa, IRCCS Ospedale Policlinico San Martino, Genoa, Italy

4. Department of Ophthalmology, Centre Hospitalier Intercommunal de Creteil University Paris XII, Creteil, France

Abstract

Purpose To describe multimodal imaging of two cases of bilateral non-vascularized pigment epithelial detachments (PED) in young patients with a long-term follow-up. Methods A complete ophthalmological examination was performed at each follow-up visit including best corrected visual acuity (BCVA), intraocular pressure, slit lamp examination, spectral domain optical coherence tomography (SD-OCT), fluorescein and indocyanine green angiography, OCT angiography. Results Multimodal imaging of two women presenting avascular PED, aged 43 and 57, respectively, was described. In both patients, SD-OCT revealed a high central macular hyporeflective elevation corresponding with PED. Both patients showed a choroidal layer thicker than 420 μm. Fluorescein and indocyanine green angiography didn’t show any choroidal neovascularization either at early or late frames. Cross-sectional and en face optical coherence tomography angiography (OCTA) didn’t show any flow beneath the PED. During the follow up period one eye showed a retinal pigment epithelium tear and all eyes showed the presence of apical sub-retinal fluid and hyperreflective material on the top of the PED. None of the two patients showed any sign of atrophy during the follow-up period. Conclusion The peculiar characteristics of the presented cases suggest that specific pathogenetic mechanisms, not necessarily related to age related macular degeneration, may play a key role in the development of these lesions. Whether early onset of such drusenoid PED is a specific entity resulting from a genetic deficit of lipid transporters in the RPE is unknown. Further genetic and metabolic studies should be conducted.

Publisher

SAGE Publications

Subject

Ophthalmology,General Medicine

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