Most are asymptomatic; can have decreased or distorted vision or both. Incidence increases with age. Twenty percent bilateral, though often asymmetric.
(See Figure 11.26.1.)
Spectrum ranges from a fine, glistening membrane (cellophane maculopathy) to a thick, gray-white membrane (macular pucker) present on the surface of the retina in the macular area.
Retinal folds radiating out from the membrane; displacement, straightening, or tortuosity of the macular retinal vessels; ME or macular detachment. A ring-shaped condensation of the ERM around the fovea may simulate a macular hole (pseudohole).
PVD. See 11.1, Posterior Vitreous Detachment.
Retinal break, RRD. A higher risk of ERM for PVD patients who also have a tear or RRD versus PVD alone. See 11.2, Retinal break and 11.3, Retinal Detachment.
Idiopathic. ERM can occur without obvious cause and has been seen in very young children.
Uveitis. See Chapter 12, Uveitis.
Retinal dystrophies. See 11.28, Retinitis Pigmentosa and Inherited Chorioretinal Dystrophies.
Other retinal vascular disease (diabetic retinopathy, vein occlusion, etc.).
Complete ocular examination, particularly a thorough dilated fundus evaluation and careful macula evaluation with a slit lamp and a handheld lens. A careful peripheral examination should be performed to rule out a retinal break.
OCT can show a hyperreflective layer over the surface of the retina, loss of foveal depression, and intraretinal cysts (See Figure 11.26.2).