“…Nowadays, LMH are defined by qualitative aspects found on OCT, according to the International Vitreomacular Traction Study (IVTS), such as (1) irregularity of the foveal contour, (2) internal break in the fovea, (3) dehiscence of the internal fovea from the external retina, or (4) lack of a full-thickness defect with preservation of the photoreceptor layer [2, 3]. LMH management is still a matter of debate, but in asymptomatic LMH patients, observation complemented with serial OCT follow-up is usually the preferred approach, while in patients complaining of metamorphopsia or visual acuity changes, a surgical approach is to be considered in order to restore both foveal anatomy and visual performance [4, 5]. However, studies have demonstrated varying anatomical and visual outcomes after surgery [6-9] that may in part be explained by lamellar hole-associated epiretinal proliferations (LHEP) [10], which are related with a minimal traction component compared to typical hyperreflective epiretinal membranes (ERM).…”