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Pancreatic Neuroendocrine Tumors Symptoms - Oren Zarif - Pancreatic Neuroendocrine Tumors


If you have been diagnosed with pancreatic neuroendocrine tumors, you might be wondering what the symptoms of these tumours are. In some cases, neuroendocrine pancreatic tumors don't have any symptoms. However, some symptoms may indicate the presence of a tumor. Some symptoms of pancreatic neuroendocrine tumors include stomach ulcers, diabetes, anemia, and abdominal pain. Other symptoms may include jaundice, muscle weakness, or even a skin rash.

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The symptoms of pancreatic neuroendocrine tumors are different in each type. Some produce hormones while others don't. The most common ones are insulinomas and gastrinomas. Some people may experience pain or abdominal discomfort, but these symptoms are usually relieved by going to the bathroom. In some cases, the symptoms of pancreatic neuroendocrine tumors are similar to other conditions. In some cases, symptoms may be mistaken for those of irritable bowel syndrome.

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If symptoms are present, consult a doctor for further tests and diagnostic evaluation. Treatments for pancreatic neuroendocrine tumors can vary depending on the location of the tumor. Local treatments may include surgery, chemotherapy, and targeted therapy. Surgery is the most common form of treatment for pancreatic neuroendocrine tumors. Depending on the size of the tumor, nearby tissues may also need to be removed.

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The presence of symptoms of pancreatic neuroendocrine tumors may be difficult to detect because the disease is sporadic. Although 90% of pNETs are sporadic, they are linked to several hereditary syndromes. Therefore, your healthcare provider may suggest genetic testing and screening for pNETs even if there are no symptoms. However, the prognosis of pNET is dependent on its stage of development and the type of tumor.

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Patients with a family history of pancreatic neuroendocrine tumors have a higher risk of developing this type of cancer. Individuals with a MEN1 syndrome are also at increased risk for developing pancreatic neuroendocrine tumors. If you are a woman diagnosed with pancreatic neuroendocrine tumor, you will want to consult your doctor as soon as possible. You might want to seek a second opinion as early diagnosis can help you manage the condition.

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The main symptoms of pancreatic neuroendocrine tumors are often similar to those of other types of cancer. They are both cancers of the pancreas and begin in cells called neuroendocrine. Some of these tumors secrete excess hormones, while others don't. However, if they produce hormones, they will produce them in a high enough concentration to cause symptoms.

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Insulinomas are small neoplasms of the pancreas. Ninety percent of these tumors will behave benignly. However, the appearance of bone metastases can negatively impact the prognosis of midgut neuroendocrine tumors. Patients who develop bone metastases are at risk for increased pain, diminished quality of life, and reduced functional status.

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Symptoms of pancreatic neuroendocrine tumors vary from one patient to another. Patients with symptoms related to hormone secretion may need to undergo medical interventions geared to correct hormone secretion. Sometimes, patients may have advanced disease and require surgical resection. If they develop tumors in the liver, they may undergo hepatic directed therapies such as partial hepatectomy or hepatic artery embolization. Alternatively, a chemotherapy regimen may be used.

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A gastrinoma is a type of neuroendocrine tumor that forms in cells that produce gastrin, a hormone responsible for regulating the secretion of stomach acid. It may cause symptoms such as high blood sugar, facial flushing, or unintended weight loss. In some cases, the symptoms of pancreatic neuroendocrine tumors can be difficult to detect.

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When diagnosed, VIPomas, which produce the hormone vasoactive intestinal polypeptide (WDHA), may be malignant. Patients with VIPomas may develop diarrhea, hypokalemia, and dehydration. Some may also experience excessive stomach acid or steatorrhoea. Symptoms may be vague, and treatment is often determined by imaging studies and blood tests.

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