If you or someone you know has been diagnosed with a neuroendocrine tumor, you should be aware of some of the symptoms that you should look out for. If you have a family history of the disease, you're more likely to develop the condition. If you have MEN 1 syndrome, your risk increases even more. Your doctor should perform an exam and rule out any other medical conditions before recommending a specific course of treatment.
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Some symptoms of pancreatic neuroendocrine tumors are very similar to those of other diseases. You may not notice any specific symptoms, or you may be suffering from some other problem. Your healthcare provider will be able to tell you whether you're suffering from a neuroendocrine tumor based on your symptoms and medical history. Blood tests can also show high levels of hormones in your blood.
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Usually, pancreatic neuroendocrine tumors can be diagnosed with a clinical exam, detailed history, and specialized tests. However, the diagnosis of pancreatic NETs can vary widely from one patient to the next. A diagnosis of pancreatic neuroendocrine tumors is essential for your overall health and well-being. You should schedule an appointment with a healthcare provider as soon as you notice any symptoms.
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In some cases, patients may not show symptoms at all. These symptoms indicate that your pancreatic neuroendocrine tumor is nonfunctional, but has spread to nearby organs or blood vessels. The disease may have metastasized to other parts of the body, such as the spleen or large intestine. Symptoms of pancreatic neuroendocrine tumors may include shortness of breath, weakness, or heart murmur.
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Treatment for pancreatic neuroendocrine tumors depends on the location of the tumor, and the stage of the disease. Some treatments are local while others may be systemic. Radiation, chemotherapy, and targeted therapy are common forms of treatment. Surgery is often the preferred treatment option for pancreatic neuroendocrine tumors. The type of surgery depends on the location of the tumor, whether it's nearby or distant.
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NETs are rare but can be life-threatening. Fortunately, they rarely cause pancreatic cancer. Only one in every thousand cases of pancreatic cancer is pancreatic neuroendocrine tumors. The symptoms of pancreatic neuroendocrine tumors depend on the location of the tumor and its production of hormones. Some people experience severe intermittent diarrhea, which can lead to dramatic potassium loss.
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In some cases, patients may not show symptoms at all. These symptoms indicate that your pancreatic neuroendocrine tumor is nonfunctional, but has spread to nearby organs or blood vessels. The disease may have metastasized to other parts of the body, such as the spleen or large intestine. Symptoms of pancreatic neuroendocrine tumors may include shortness of breath, weakness, or heart murmur.
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Treatment for pancreatic neuroendocrine tumors depends on the location of the tumor, and the stage of the disease. Some treatments are local while others may be systemic. Radiation, chemotherapy, and targeted therapy are common forms of treatment. Surgery is often the preferred treatment option for pancreatic neuroendocrine tumors. The type of surgery depends on the location of the tumor, whether it's nearby or distant.
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NETs are rare but can be life-threatening. Fortunately, they rarely cause pancreatic cancer. Only one in every thousand cases of pancreatic cancer is pancreatic neuroendocrine tumors. The symptoms of pancreatic neuroendocrine tumors depend on the location of the tumor and its production of hormones. Some people experience severe intermittent diarrhea, which can lead to dramatic potassium loss.
