Open AccessBilateral choroidal osteoma with choroidal neovascular membrane treated with bevacizumab in a child
Author(s) -
Manisha Agarwal,
Meha Kantha,
Rahul Mayor,
Ramesh Venkatesh,
Cyrus Shroff
Publication year - 2014
Publication title -
middle east african journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.357
H-Index - 25
eISSN - 0975-1599
pISSN - 0974-9233
DOI - 10.4103/0974-9233.134692
Subject(s) - medicine , osteoma , choroidal neovascularization , choroid , ophthalmology , fundus fluorescein angiography , fundus (uterus) , osteoid osteoma , fluorescein angiography , bevacizumab , radiology , surgery , visual acuity , retina , optics , chemotherapy , physics
Choroidal osteoma is a rare benign tumor. We report a male child diagnosed with bilateral choroidal osteoma, high myopia and secondary choroidal neovascularization (CNV) membrane in one eye. Co-existence of posterior staphyloma made the clinical diagnosis of choroidal osteoma difficult due to the osteoma filling the depression of the posterior staphyloma. Typical findings on fundus fluorescein angiography, optical coherence tomography, B-scan and indocyanine green angiography confirmed the diagnosis. A review of literature was performed. CNV secondary to choroidal osteoma was treated with intravitreal bevacizumab and it responded well. Regular follow-up is essential for recurrence of CNV and decalcification of the osteoma.