Casos
Solitary congenital hypertrophy of the retinal pigment epithelium (CHPRE)
Solitary HCEPR is a single, highly pigmented, flat lesion with well-defined borders, usually located in the mid-periphery. It may be surrounded by a h
Multifocal congenital hypertrophy of the RPE (CHRPE) in “bear tracks”
Grouped HCEPR are small, multiple, well-demarcated, flat pigmented lesions grouped in a “bear print” pattern with a sectoral distribution. They ar
RPE hamartomas associated with family adenomatous polyposis (FAP)
Pigmented fundus lesions associated with familial adenomatous polyposis (FAP) are multiple bilateral lesions, with poorly defined borders, sometimes d
Congenital simple hamartoma of RPE
Simple hamartoma of the retinal pigment epithelium is a highly pigmented, flat, solitary lesion of a congenital and benign nature, very rare.
OCT sho
Combined hamartoma of the retina and retinal pigment epithelium
Combined hamartoma of the retina and retinal pigment epithelium (HCREPR) is a benign tumor that can cause significant visual loss. HCREPR is usually a
Tuberous sclerosis
Tuberous sclerosis is a rare genetic disease of autosomal dominant inheritance. It causes multiple hamartomas that appear in various organs such as th
Choroidal osteoma
Choroidal osteoma is a rare, benign ocular tumor, primarily composed of mature bone, that forms in the choroid.
It is most often diagnosed in young w
Retinoblastoma
Retinoblastoma is a malignant tumor of the retina that predominantly occurs in childhood, being the most common ocular tumor in children. The most com
Racemose Hemangioma
Racemose hemangioma, also called retinal arteriovenous malformation, is a hemangioma of the retina or optic nerve that may be part of Wyburn-Mason syn