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Myopic neovascularization

Description

It is defined as a neovascularization of choroidal origin (neovascular membrane) in the context of pathological myopia. Typically, they tend to be subretinal neovascular membranes (type 2 or classic) and are generally located in the foveal or juxtafoveal area, although they can also appear extrafoveal or peripapillary. In the fundus, they appear as a grayish lesion with pigmented edges, and may or may not be associated with retinal hemorrhage or exudation. Typically, these membranes can be active, giving rise to symptoms in the patient, without the presence of fluid, hemorrhage or exudation, so when deciding whether to treat the patient, the presence of symptoms is essential. In its evolution, three phases can be distinguished:

  • Active phase: The membrane presents activity that is generally reflected in the appearance of symptoms by the patient and that may or may not be associated with the presence of retinal hemorrhage, fluid in the OCT or exudation.
  • Scarring phase (Fuchs’ spot): Over time, a scarring process usually occurs, leading to pigmentation of the membrane and reduction of exudation.
  • Atrophic phase: Occasionally, the membranes may develop chorioretinal atrophy around the neovascular lesion, leading to severe visual loss.

Comments

Indication

61-year-old woman with severe myopic syndrome. She reports metamorphopsia and visual loss of 1 month's duration in the right eye (OD). History of refractive surgery using PRK (2006). Pre-surgical spherical equivalent -5.50 D OD and –5.75 D left eye (LE). Corrected visions of 0.2 OD and 1.00 OI. The examination revealed the presence of a myopic neovascular membrane in the OD. Treatment was performed with 4 injections of anti-VEGF in the OD, achieving a visual acuity of 0.8 OD.