Middle East African Journal of Ophthalmology

REVIEW ARTICLE
Year
: 2014  |  Volume : 21  |  Issue : 3  |  Page : 244--250

Review of choroidal osteomas


Ramzi M. Alameddine1, Ahmad M. Mansour1, Eman Kahtani2 
1 Department of Ophthalmology, American University of Beirut, Beirut, Lebanon
2 King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia

Correspondence Address:
Dr Ahmad M. Mansour
Department of Ophthalmology, American University of Beirut, Beirut
Lebanon

Choroidal osteomas are rare benign ossifying tumors that appear as irregular slightly elevated, yellow-white, juxtapapillary, choroidal mass with well-defined geographic borders, depigmentation of the overlying pigment epithelium; and with multiple small vascular networks on the tumor surface. Visual loss results from three mechanisms: Atrophy of the retinal pigment epithelium overlying a decalcified osteoma; serous retinal detachment over the osteoma from decompensated retinal pigment epithelium, and most commonly from choroidal neovascularization. Recent evidence points to the beneficial effects of intravitreal vascular endothelial growth factor antagonists in improving visual acuity in serous retinal detachment with or without choroidal neovascularization.


How to cite this article:
Alameddine RM, Mansour AM, Kahtani E. Review of choroidal osteomas.Middle East Afr J Ophthalmol 2014;21:244-250


How to cite this URL:
Alameddine RM, Mansour AM, Kahtani E. Review of choroidal osteomas. Middle East Afr J Ophthalmol [serial online] 2014 [cited 2019 Aug 19 ];21:244-250
Available from: http://www.meajo.org/article.asp?issn=0974-9233;year=2014;volume=21;issue=3;spage=244;epage=250;aulast=Alameddine;type=0