Eye Cancer, Retinoblastoma

Familial Retinoblastoma

Familial Retinoblastomas

Glioblastoma, Retinal

Glioblastomas, Retinal

Glioma, Retinal

Gliomas, Retinal

Hereditary Retinoblastoma

Hereditary Retinoblastomas

Neuroblastoma, Retinal

Neuroblastomas, Retinal

Retinal Glioblastoma

Retinal Glioblastomas

Retinal Glioma

Retinal Gliomas

Retinal Neuroblastoma

Retinal Neuroblastomas

Retinoblastoma, Familial

Retinoblastoma, Hereditary

Retinoblastoma, Sporadic


Retinoblastomas, Familial

Retinoblastomas, Hereditary

Retinoblastomas, Sporadic

Sporadic Retinoblastoma

Sporadic Retinoblastomas

A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104)