Neuroendocrine tumors (NETs) are rare types of tumors that arise from neuroendocrine cells—specialized cells that have characteristics of both nerve cells and hormone-producing cells. These tumors can develop in various organs throughout the body, but they most commonly occur in the gastrointestinal (GI) tract, pancreas, and lungs. Some NETs are functional, meaning they produce excess hormones that can cause a range of symptoms, while others are non-functional and may remain silent until they grow large or spread.

NETs are categorized based on their location in the body and whether they produce hormones. Common types include:
The symptoms of NETs vary depending on their location and whether they secrete hormones. They are generally categorized into functional and non-functional types.
Regular follow-up care is essential for managing neuroendocrine tumors after treatment. Your doctor may schedule imaging scans and blood tests every 3–6 months to monitor for recurrence or progression.
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