In the event you suspect that you have pancreatic neuroendocrine tumors, you should know what to look for in the symptoms of the disease. These tumors can cause diarrhea, which often worsens over time. Other symptoms of this condition include muscle cramps, bloating, flushing, and nausea. Patients with these tumors often have low stomach acid, resulting in a difficult time digesting food.
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People with a family history of pancreatic neuroendocrine tumors are at a higher risk. People with multiple endocrine neoplasia type 1 (MEN1) syndrome are also more likely to develop pancreatic neuroendocrine tumors. A physician will perform surgery at the Pancreas Institute if it's suspected. If you have symptoms and think that you might have pancreatic neuroendocrine tumors, consider seeking a second opinion.
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Among other symptoms of pancreatic neuroendocrine tumors, you should be aware of any sudden changes in your blood sugar levels or other signs of diabetes. Diarrhea and constipation are common symptoms of pancreatic cancer. Some people will experience a rash on the skin and yellowing of the eyes. If you feel faint or weak, see a doctor right away for a diagnosis.
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During treatment, you can choose from surgery or radiation. Surgery is the most common form of treatment for pancreatic neuroendocrine tumors. Surgery may involve the removal of the entire tumor or nearby tissues. Surgery is the most common treatment, although you should also consider the side effects of undergoing it. In the long run, though, you'll have a much better chance of survival than with other pancreatic cancers.
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A pancreatic neuroendocrine tumor begins in cells called endocrine, which produce hormones for digestion and blood sugar regulation. The pancreas is a small, 6 inch-long organ. It resembles a thin pear on its side. The islet cells, which are responsible for producing insulin, play a key role in controlling blood sugar levels. When a pancreatic neuroendocrine tumor starts, they produce too much insulin, which leads to symptoms such as fatigue, blurred vision, and rapid heartbeat.
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Pancreatic neuroendocrine tumors are either functional or nonfunctional. While the former does not produce hormones, functional PNETs produce them and cause symptoms. Insulinomas are the most common types of functional PNET. Insulinomas are benign, but they are not always easy to detect with the naked eye. If you suspect that you have one of these tumors, make sure to see a doctor right away. If you have any symptoms, the best course of action is to undergo surgery.
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In addition to symptoms associated with pancreatic neuroendocrine tumors, patients may also experience a variety of other medical conditions. A physical exam, health history, and blood tests can help your doctor diagnose the condition. For instance, a blood test can detect high levels of certain hormones, which may indicate the presence of a pancreatic neuroendocrine tumor. This can help you manage diabetes and avoid life-threatening complications.
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Because these tumors produce hormones, they produce symptoms in their patients. These symptoms can be mistaken for other health conditions, including irritable bowel syndrome, asthma, and menopause. Unfortunately, these symptoms can last for up to five years before you have a diagnosis. And if you do not get treated, it can spread to other parts of the body. This is the biggest risk factor of all, as more than half of all NETs spread to other organs.
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The Pancreatic Neuroendocrine Tumor market is expected to increase in the future, driven by increasing awareness of the disease and a growing number of approved therapies. While the current pipeline for new PNET therapies is weak, new research and clinical trials will change the landscape and the treatment options for patients suffering from this disease. This will allow drug manufacturers to penetrate the market more easily. In the meantime, companies and academics are continuing to analyze the challenges and opportunities in the Pancreatic Neuroendocrine Tumors market and continue to develop novel treatments.
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The clinical presentations of pancreatic neuroendocrine tumors are often variable, and the symptoms of the disease may depend on the type. If the tumor is located in the pancreas, it may be occult and require specialized imaging to confirm the diagnosis. In some cases, patients may have symptoms related to tumor bulk, which may require surgical resection.
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Patients who are diagnosed with advanced pancreatic neuroendocrine tumors may benefit from hepatic-directed therapies, such as hepatectomy or hepatic artery embolization. These treatments may require a different approach, such as chemotherapy.
