Uveal melanoma is the most common eye tumor in adults. This malignant tumor grows from the pigment cells of the choroid, and its other name is choroidal melanoma. The insidious nature of this disease is that it often goes undetected for a long time, so our specialists detect this tumor in its early stages and select treatment that preserves vision.
The exact cause of the disease is unknown, but certain conditions are known to increase the risk. Choroidal melanoma occurs more often in people with light-colored irises and specific pigment cells; this tumor is sometimes referred to as eye cancer.
The risk of developing the disease increases with age, peaking after age fifty. This tumor is rare in children and young adults.
Hereditary traits and mutations in choroidal cells play a role. Certain syndromes and family history increase susceptibility to the disease.
The influence of fair skin, sun exposure, and chronic changes in the fundus are discussed. A direct link has not been proven for all factors, but their combination merits consideration.
Manifestations depend on the location and size of the lesion, and in the early stages they may not be present at all. The first symptoms of uveal melanoma are often noticed incidentally, during an examination for another reason.
One of the early signs is a gradual decrease in visual acuity or image distortion. The tumor presses on the retina, affecting visual function.
Patients describe a dark spot in their field of vision, flashes of light, and floaters. These can be signs of ocular melanoma, so these sensations are a reason to see a specialist rather than wait.
Pain appears late, when the lesion is large or intraocular pressure increases. Redness and a feeling of fullness in the eye are less common.
Many complaints are nonspecific, but their persistent combination should not be ignored. It's worth making an appointment with a specialist if you experience the following symptoms:
Early diagnosis is crucial, so don't delay a visit to an ophthalmic oncologist.
Vision tumors are managed by a team: an ophthalmic oncologist, a radiation therapist, and an oncologist work together. In our practice, the patient undergoes the entire process in one place:
This format saves time and increases the chances of preserving vision.
Doctor's quote:
"Early diagnosis of uveal melanoma is of great importance in our practice. Modern imaging methods allow us to detect the tumor in its early stages and select an individualized treatment strategy based on the patient's clinical situation and vision preservation goals," — oncologist, ocular tumor specialist.
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What is uveal melanoma?
This is an intraocular tumor that develops from melanocytes—the pigment cells of the uveal tract. This type of ocular oncology is an aggressive oncological disease, and the malignant tumor itself is capable of metastasizing. In ophthalmology, it is considered the most common intraocular tumor in adults.
What structures of the eye are affected by the tumor?
The uveal tract consists of three parts: the iris, the ciliary body, and the choroid—the vascular membrane itself. The lesion most often occurs in the choroid, which is why this form is called choroidal melanoma; less commonly, the iris or ciliary body are affected.
Characteristics of the disease?
The main characteristic is its latent course: the tumor in the eye grows for a long time without pain or noticeable symptoms. Uveal melanoma grows inside the visual organ, rather than on the surface like some forms of ocular melanoma, and requires a separate approach.