Bilateral choroidal osteoma with choroidal neovascular membrane treated with bevacizumab in a child
MEAJO-Middle East African Journal of Ophthalmology. 2014; 21 (3): 265-267
in English
| IMEMR
| ID: emr-152714
ABSTRACT
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
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Index:
IMEMR (Eastern Mediterranean)
Type of study:
Case report
Language:
English
Journal:
Middle East Afr. J. Ophthalmol.
Year:
2014
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