Overview

Choroidal melanoma is the most common primary intraocular malignant tumor however in practice, it may be difficult to distinguish from a suspicious choroidal naevus. Please refer to the page "Choroidal naevus" in this resource for factors predictive of growth into melanoma (link provided at the bottom of this page).

Funduscopic features include a dome shaped lesion that may be associated with an exudative retinal detachment, orange pigment (lipofuscin), sentinel vessels, choroidal folds, subretinal fluid or haemorrhage. They are usually pigmented but can also mixed or amelanotic.

OCT EDI features include increased tumour thickness, subretinal fluid and overlying retinal disruptions including shaggy photoreceptors (irregular and elongation of the photoreceptors).

Autofluorescence imaging showed confluent areas of hyper-autofluorescence which correlates to the clinically orange pigment. The presence of subretinal fluid may also exhibit hyper-autofluorescence.

B-scan ultrasound shows an acoustically hollow lesion which may be dome or mushroom shaped.

Case Examples

Differential Diagnosis

References

Shields, CL. et al. (2012). Enhanced depth imaging optical coherence tomography of small choroidal melanoma: comparison with choroidal nevus. Archives of Ophthalmology, 130(7), 850-856.

Singh, P. et al. (2012). Choroidal melanoma. Oman journal of ophthalmology, 5(1), 3.