Retinoblastoma

A rare eye tumor disease representing the most common intraocular malignancy in children. It is a life threatening neoplasia but is potentially curable and it can be hereditary or non hereditary, unilateral or bilateral.

Scarring



Total: 3

                       


(per page)
PMID (PMCID)
16543200
 MALE Infant, Newborn
Atrophic chorioretinal scar and focal scleral bowing following thermochemotherapy with a diode laser for retinoblastoma.
de Graaf P, Castelijns JA, Moll AC, Imhof SM, Schouten-van Meeteren AY.
Ophthalmic Genet. 2006;27(1):33-5.
Very little is known about the evolution of laser scars resulting from diode laser treatment for retinoblastoma.
10927003
 MIXED_SAMPLE Infant
Rhegmatogenous retinal detachment in retinoblastoma patients undergoing chemoreduction and cryotherapy.
Anagnoste SR, Scott IU, Murray TG, Kramer D, Toledano S.
Am J Ophthalmol. 2000;129(6):817-9.
Three patients with intraocular retinoblastoma were referred after poor response to systemic chemotherapy and local cryotherapy; three eyes of these three patients were noted to have rhegmatogenous retinal detachment and active retinoblastoma, with retinal breaks adjacent to cryotherapy scars.
10927003
 MIXED_SAMPLE Infant
Rhegmatogenous retinal detachment in retinoblastoma patients undergoing chemoreduction and cryotherapy.
Anagnoste SR, Scott IU, Murray TG, Kramer D, Toledano S.
Am J Ophthalmol. 2000;129(6):817-9.
Three patients with intraocular retinoblastoma were referred after poor response to systemic chemotherapy and local cryotherapy; three eyes of these three patients were noted to have rhegmatogenous retinal detachment and active retinoblastoma, with retinal breaks adjacent to cryotherapy scars.