Overview

Choroidal osteomas are rare benign ossifying tumours, often unilateral. They may show slow growth over time and complications include serous retinal detachments, subretinal fluid, haemorrhage and choroidal neovascularisation. Tumour decalcification can also occur and is characterised by overlying RPE and choriocapillaris atrophy.

Funduscopic features include an irregularly, slightly elevated, yellow-orange choroidal mass with sharply defined or scalloped borders. They affect the juxtapapillary and macula region and can have multiple fine vascular networks on its surface.

The colour of the tumour relates to the level of RPE depigmentation. In early stages, it tends to be orange-red in colour but progress to a yellowish colour in latter stages.

OCT shows a latticework pattern with variable choroidal reflectivity. Outer retinal thinning and photoreceptor loss occurs in a decalcified choroidal osteoma.

OCT angiography can be useful in identifying a choroidal neovascular membrane.

FAF features can be variable depending on the degree of decalcification, atrophy and subretinal fluid. Generally, decalcified osteomas exhibit a reduced autofluorescence.

B-scan ultrasound shows high acoustic reflectivity (due to the calcification). A ‘pseudo optic nerve’ appearance can be seen as there is also a characteristic shadowing posterior to the tumour.

Case Examples

Differential Diagnosis

References

Alameddine, R. M., Mansour, A. M., & Kahtani, E. (2014). Review of choroidal osteomas. Middle East African journal of ophthalmology, 21(3), 244.

Olguin-Manríquez, F., Enríquez, A.B., Crim, N. et al. (2018) Multimodal imaging in choroidal osteoma. Int J Retin Vitr 4, 30

Theodoros E. et al. (2014) Diagnosis and Monitoring of Choroidal Osteoma through Multimodal Imaging. Case Reports in Medicine Volume 2014, Article ID 393804, 4 pages