Choroidal melanoma is a rare but serious eye cancer that develops in the choroid, the pigmented layer of blood vessels beneath the retina. It is the most common primary intraocular tumor in adults and can cause vision changes, retinal detachment, or remain asymptomatic in early stages. Diagnosis typically involves an eye exam, ultrasound, and imaging tests. Treatment options include radiation therapy, laser therapy, or surgery, depending on tumor size and spread. If left untreated, it can metastasize, most commonly to the liver.
Patients are the experts in their condition and advocacy groups provide a platform for patient voices. Working directly with these communities is the key to pushing research forward in an inclusive way.
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