Vasoproliferative tumor of retina

Vasoproliferative tumor of the retina is a rare, benign, retinal vascular disease characterized by solitary or multiple, unilateral or bilateral, intra-retinal tumor(s), usually located in the peripheral infero-temporal quadrant, and often associated with sub- and intraretinal exudates, epiretinal membranes, exudative retinal detachment and cystoid macular edema, as well as, occasionally, retinal and vitreous hemorrhage. Patients may present with visual loss, floaters, and/or photopsia. Association with various conditions, such as retinitis pigmentosa, congenital retinal toxoplasmosis, retinopathy of prematurity, or coloboma, has been reported.

Also known as: VPTR, retinal vasoproliferative tumor, retinal vasoproliferative tumour, vasoproliferative tumor of ocular fundus, vasoproliferative tumor of the ocular fundus, vasoproliferative tumour of ocular fundus, vasoproliferative tumour of the ocular fundus, vasoproliferative tumor of the retina

1465 clinical trials for this condition and its sub-types, 0 tagged with Vasoproliferative tumor of retina itself.