If you have pancreatic neuroendocrine tumors, you may experience some of the symptoms below. While these symptoms can also be attributed to other health conditions, your healthcare provider can diagnose them with your health history and physical exam. Blood tests may also be recommended to see if you have high levels of hormones. If you notice any of these symptoms, you should consult your healthcare provider immediately.
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Most patients who have neuroendocrine pancreatic tumors will not exhibit any noticeable symptoms. However, you may experience other symptoms, including abdominal pain, indigestion, and diarrhea. You may also experience weight loss and muscle weakness. You may experience a coma if your blood sugar drops below normal. Listed below are some symptoms of pancreatic neuroendocrine tumors.
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Intestinal symptoms. Your body produces an enzyme called VIP, which is produced by the tumors. The excessive amount of this chemical in your body can cause diarrhea, and the diarrhea will worsen over time. In addition to diarrhea, you may also experience flushing and muscle cramps. In addition, people with these tumors often have lower stomach acid, which makes digestion difficult. Therefore, you should see a doctor for an exam.
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Pancreatic Neuroendocrine Tumor Symptoms may be present or absent. These symptoms may indicate other health issues, or they may be signs of pancreatic cancer. While there are no specific symptoms of pancreatic neuroendocrine tumors, patients may experience some of the following. A doctor may recommend surgery to remove the tumour if the symptoms persist. The symptoms will depend on the type of tumour and its location.
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While there are no known causes of pancreatic NETs, certain risk factors can make you more susceptible to developing the disease. Discuss with your healthcare provider any risk factors that you may have and discuss the best course of treatment with your doctor. A nonfunctioning pancreatic NET may not cause symptoms until it has become large. As it grows, it may cause pressure on other organs and over-produce hormones, leading to symptoms of abdominal pain and vomiting.
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Surgical removal of pancreatic neuroendocrine tumors is a common treatment for these patients. While a high failure-to-rescue rate and complication rate are associated with surgery for pancreatic neuroendocrine tumors, the survival rate for these patients is 93%. In a center of excellence, a distal pancreatectomy (removing the tail and body of the pancreas) is a standard treatment for localized neuroendocrine tumors.
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Early diagnosis is crucial for pancreatic neuroendocrine tumors. A multidisciplinary approach to care for pancreatic neuroendocrine tumors is crucial for a successful treatment. Surgery is the preferred treatment for pancreatic neuroendocrine tumors, but it may not be an option in some cases. The treatment for pancreatic neuroendocrine tumors depends on the type and stage of the disease, and can include surgery, distal pancreatectomy, or splenectomy.
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Surgical treatment involves powerful cancer killing drugs, usually administered intravenously. In some cases, the pancreatic neuroendocrine tumors cannot be surgically removed, but powerful chemotherapy drugs are used to treat these tumors. Treatment of unresectable tumors may include hormones to control symptoms. If the treatment for pancreatic neuroendocrine tumors is unsuccessful, patients may require hormone replacement.
