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Carcinoid tumors are a type of neuroendocrine tumor that can develop in various parts of the body, including the lungs, gastrointestinal tract, and other organs. They are typically slow-growing and may not cause symptoms for many years. However, as the tumors grow, they can produce hormones and other substances that can cause a range of symptoms, such as flushing, diarrhea, wheezing, and abdominal pain. Treatment options for carcinoid tumors depend on the location and size of the tumor, as well as the extent of the disease. Surgery may be recommended to remove the tumor, and other treatments such as chemotherapy, radiation therapy, or targeted therapy may be used to help control the growth and spread of the tumor. It is important for individuals with carcinoid tumors to work closely with a healthcare provider to develop a personalized treatment plan and monitor their condition over time.
It's not clear what causes carcinoid tumors. In general, cancer occurs when a cell develops mutations in its DNA. The mutations allow the cell to continue growing and dividing when healthy cells would normally die.
The accumulating cells form a tumor. Cancer cells can invade nearby healthy tissue and spread to other parts of the body.
Doctors don't know what causes the mutations that can lead to carcinoid tumors. But they know that carcinoid tumors develop in neuroendocrine cells.
Neuroendocrine cells are found in various organs throughout the body. They perform some nerve cell functions and some hormone-producing endocrine cell functions. Some hormones that are produced by neuroendocrine cells are histamine, insulin and serotonin.
Treatment for a carcinoid tumor depends on the tumor's location, whether cancer has spread to other areas of the body, the types of hormones the tumor secretes, your overall health and your own preferences.
Carcinoid tumor treatment options may include: