Neuroendocrine tumours (NETs) can cause a wide range of symptoms, often depending on their location and whether they produce excess hormones.
While most people associate NETs with digestive issues, flushing, or hormonal imbalances, they can also affect vision in several ways. Vision changes in NET patients may result from hormonal fluctuations, metabolic imbalances, nerve involvement, or treatment-related side effects.
Understanding the link between NETs and vision is essential for early detection and management.
This article explores how NETs impact vision, the mechanisms behind these changes, how they are diagnosed, and potential treatment options for preserving eye health.
Neuroendocrine Cancer Australia (NECA), is dedicated to assisting patients diagnosed with NETs and their loved ones. NECA offers a wealth of resources, educational programs, and advocacy efforts aimed at deepening the understanding of NETs, improving patient care, and encouraging research advancements. Patients can engage with NECA’s comprehensive support and information by calling the NET nurse line.
The symptoms of NETs aren’t usually limited to the neuroendocrine system. Vision changes in NET patients can arise from a variety of causes, including:
Because NETs can be slow-growing or asymptomatic for years, vision-related symptoms may go unnoticed or be misattributed to aging or unrelated conditions.
It’s important to understand the distinction between direct and indirect causes of vision changes, particularly in the diagnosis and treatment phases.
Early identification of vision problems in NET patients is crucial, as they may signal tumour progression, treatment side effects, or secondary complications requiring intervention.
Functional NETs that produce excess hormones can affect multiple systems, including vision. Common hormone-related vision problems include:
Patients with carcinoid syndrome, caused by serotonin-secreting NETs, may experience flushing, watery eyes, light sensitivity, or even blurred vision. In some cases, prolonged exposure to high serotonin levels may contribute to retinal damage.
Insulinomas, a rare type of pancreatic NET, produce excess insulin, leading to recurrent low blood glucose levels (hypoglycaemia). When blood glucose levels drop too low, patients may experience:
Since these symptoms can resemble neurological conditions, insulinomas are sometimes misdiagnosed initially.
Von Hippel-Lindau (VHL) syndrome is a genetic condition linked to NETs and other tumours. VHL patients often develop retinal hemangioblastomas (benign tumours in the retina), which can cause vision loss or blindness if untreated. Regular ophthalmologic exams are essential for early detection.
While most NETs originate in the digestive tract or lungs, in rare cases, they can spread to the brain or optic nerve, causing:
These symptoms may indicate tumour progression or metastatic disease affecting the nervous system.
Several vision changes are possible during the course of treatment for NETs. While these are rare, it’s important to note that every patient’s reaction to treatment will be different.
Somatostatin analogues (SSAs) like octreotide and lanreotide are commonly used to manage hormone-producing NETs. Although generally well-tolerated, rare ocular side effects include:
Patients using SSAs should have regular eye exams to monitor for any subtle changes.
For patients receiving radiation therapy near the head or neck, possible vision-related side effects include:
Close monitoring and early intervention can help manage these risks effectively.
NET patients should immediately seek medical attention if they experience:
Early diagnosis can prevent complications and help adjust treatment plans if necessary.
Common diagnostic tools for vision issues can include:
Decisions around tests and courses of treatment should be made in conference with the patient, their family, and their primary care team.
Fortunately, vision changes associated with NETs can be managed and treated. If a NET treatment is causing significant vision problems, oncologists may consider:
Depending on the cause, treatments may include:
NET patients can help protect their vision by:
Researchers are exploring the molecular pathways linking NET-related hormones to vision problems, as well as potential treatments to prevent ocular damage.
With advances in targeted therapies and precision medicine, future NET treatments may reduce vision-related side effects while maintaining efficacy.
Vision changes in NET patients can stem from hormonal imbalances, tumour location, metabolic disturbances, or treatment effects.
While many cases are mild and manageable, some may indicate serious complications requiring immediate medical attention.
Regular eye exams, early symptom recognition, and coordinated care between oncologists and ophthalmologists are crucial for maintaining long-term vision health in NET patients.
For additional support, patients can reach out to Neuroendocrine Cancer Australia for guidance and resources on managing NET-related vision concerns.