HYBRID EVENT: You can participate in person at Tokyo, Japan from your home or work.
Retinal tumors are abnormal growths that develop in the retina, the light-sensitive tissue at the back of the eye. These tumors can be classified as either benign or malignant, with each type presenting its own set of challenges and potential complications. Benign retinal tumors, such as retinoblastomas, are non-cancerous growths that often affect young children. These tumors originate from immature cells in the retina and, if detected early, can be effectively treated. However, if left untreated, they may lead to vision loss or even spread to other parts of the eye. Malignant retinal tumors, on the other hand, are cancerous and can be primary (originating in the eye) or secondary (spreading from other parts of the body). These tumors are relatively rare but can have serious implications for vision and overall health. Common symptoms of retinal tumors include vision changes, such as blurry or distorted vision, and in some cases, the appearance of flashes of light or shadows. Regular eye exams are crucial for early detection and prompt intervention. Treatment options for retinal tumors vary depending on the type, size, and location of the tumor. Approaches may include laser therapy, cryotherapy, radiation, or, in more severe cases, surgical removal of the affected part of the retina or the entire eye. Early diagnosis and appropriate treatment play a crucial role in managing retinal tumors and preserving vision. Regular eye check-ups, especially for those with a family history of eye conditions, are essential for detecting any abnormalities in the early stages and ensuring timely intervention. If any unusual symptoms are experienced, seeking prompt medical attention from an eye care professional is crucial for a comprehensive evaluation and appropriate management.
