There are several common symptoms of pancreatic neuroendocrine tumors. The tumors produce hormones that control blood pressure and sugar levels. You may experience a high fever, weakness, diarrhea, or an increased thirst. You may also experience an unintended weight loss or develop a pronounced heart murmur. In some cases, you may also experience a loss of appetite or fatigue.
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While symptoms of pancreatic neuroendocrine tumors are often similar to those of other conditions, they are more specific to this type of cancer. In addition, some of them may be mistaken for symptoms of irritable bowel syndrome. While abdominal discomfort is usually relieved by visiting the bathroom, these symptoms may signal other health conditions. If the symptoms persist or worsen, you should consult a healthcare provider for an accurate diagnosis.
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Treatment for pancreatic neuroendocrine tumors depends on the stage of the tumor. Treatment options may include surgery, hormonal therapy, or chemotherapy. Surgery is the most common treatment, but the type of surgery you receive depends on the size of the tumor. Surgery may also include removing nearby tissues. If the tumor has metastasized to distant organs, you may need to undergo surgery to remove it.
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Diagnosis of pancreatic neuroendocrine tumors depends on the characteristics of the tumor. Your doctor will need to review your medical history and perform several specialized tests to determine the specific type of tumor you have. Pancreatic neuroendocrine tumors are difficult to diagnose because they may be metastatic. Because of this, diagnosis and treatment are crucially important. While the symptoms of pancreatic neuroendocrine tumors may not be obvious, they may help you make the right choice.
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A biopsy can be performed to confirm a diagnosis. It is often a combination of procedures, and the results of the biopsy may help determine treatment options. Treatment for pancreatic neuroendocrine tumors is based on location, stage, and MEN1 syndrome. Treatment for pancreatic neuroendocrine tumors may vary, and some patients may experience a range of symptoms.
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Most pancreatic neuroendocrine tumors are nonfunctional and are not associated with symptoms of hypersecretion. They are discovered incidentally during imaging procedures for other conditions, or at an advanced stage when the tumor has bulked up. Patients with hypersecretory pancreatic neuroendocrine tumors experience a variety of symptoms, which can be confusing and disabling. Because of these symptoms, specific treatments for pancreatic neuroendocrine tumors are recommended.
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Patients with pancreatic neuroendocrine tumors may have some of the most common symptoms. Symptoms are often similar to those of pancreatic duct adenocarcinoma, but may not be as obvious. However, some patients may experience bleeding in their stool, abdominal pain, or diarrhea. In rare cases, patients may even experience jaundice. However, it is important to note that the symptoms of pancreatic NETs should not be misinterpreted as signs of other illnesses.
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Almost everyone has the potential to develop pancreatic neuroendocrine tumors. However, the cause of these tumors is unknown. Most cases occur randomly without apparent reason. Genetic predispositions may occur but not manifest in early childhood. In rare cases, the tumor may be associated with other diseases, including multiple endocrine neoplasia type 1 syndrome (MEN1).
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NETs are classified according to the type and spread of the tumors. A doctor will grade the tumors based on the type of cells that are present. A grade one pNEN looks more like normal cells than cancerous ones. A grade two pNET exhibits features of both low-grade and high-grade tumors. The higher the grade, the worse the symptoms will be.
