Epiretinal Membrane
An epiretinal membrane (ERM) is a fibrocellular proliferation occurring on the retinal surface, most commonly in the macular region. ERMs typically occur following a spontaneous partial or complete posterior vitreous detachment, but secondary causes include intraocular surgery, inflammation, ischemic vascular disease, trauma, retinal tear, rhegmatogenous retinal detachment, and intraocular tumors. Cells thought to contribute to ERMs include retinal pigment epithelium (RPE), fibrocytes, myofibrocytes, and intraretinal glial elements.
Spontaneous Release of Epiretinal Membrane
Cases of spontaneous release of ERMs have been reported. Although uncommon, occurring in approximately 1-3% of cases, it is more frequently observed in young, female, myopic patients.
Surgical Treatment
Vitreomacular Traction (VMT)
Vitreomacular traction (VMT) is defined as persistent vitreous attachment to the central macula due to an incomplete posterior vitreous detachment. Histologically, VMT specimens obtained from surgery show a variety of cell types including fibrous astrocytes, myofibroblasts, and fibrocytes, similar to those found in ERMs. In fact, many eyes with VMT have a concurrent ERM and there is considerable overlap between the two entities. With the advent of spectral-domain OCT and vitreolytic agents, an International Vitreomacular Traction Study Classification System for VMA and VMT has been proposed.
Vitreomacular Adhesion (VMA)
VMA is defined as elevation of the cortical vitreous above the retina surface with the vitreous remaining attached within a 3 mm radius of the fovea. There is no change to the inner retina contour on OCT. VMA can be further subclassified by the size of adhesion into focal or broad.
Vitreomacular Traction (VMT)
In VMT, all of the following criteria must exist:
- (1)
Perifoveal vitreous cortex detachment from the retinal surface
- (2)
Macular attachment of the vitreous cortex within a 3 mm radius of the fovea
- (3)
Distortion of the foveal surface, intraretinal structural changes, elevation of the fovea above the RPE or a combination thereof, without full-thickness interruption of retinal layers at sites of vitreous adhesion.