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Posterior Segment

Choroidal Melanoma

Also known as: choroidal melanoma, ocular melanoma, uveal melanoma, pigmented choroidal mass, suspicious choroidal lesion, orange pigment, subretinal fluid

Filed as: Soon

Source-cited from the record's own evidence list. Clinical content programme led by Dr Ankit Mathur, PhD, Grad Cert Ocu Thera, B.S. Optom. How the clinical content is governed

Overview

Choroidal melanoma is a potentially life-threatening intraocular malignancy. Optometry role is detection of suspicious choroidal mass features, careful documentation, and urgent referral to ocular oncology or retinal specialist pathways. Do not reassure a suspicious lesion as a naevus without risk assessment.

Recognition

Symptoms: what patients report

  • May be asymptomatic and found incidentally.
  • Blur, visual field defect, flashes, floaters, or distortion may occur depending on location and associated fluid.
  • Symptoms do not reliably indicate malignancy risk.

Signs: what the examination shows

  • Elevated pigmented choroidal mass.
  • Orange pigment, subretinal fluid, or associated retinal detachment may be present.
  • Document lesion size, thickness if available, margins, symptoms, and proximity to optic disc or fovea.

What OptoGuide™ covers for choroidal melanoma

  • Pattern reasoning: what this combination of findings points to, and its differentiators
  • Don't-miss risks and escalation triggers
  • Management tiers with linked Australian therapeutics
  • Referral urgency, specialty, and letter drafting

Sources

Standard texts: Kanski's Clinical Ophthalmology: A Systematic Approach, The Wills Eye Manual, Oxford Handbook of Ophthalmology, Oxford American Handbook of Ophthalmology, Signs in Ophthalmology: Causes & Differential Diagnosis.

Full bibliography

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