Islet cell cancer, also known as pancreatic neuroendocrine tumor or PNET, is a rare type of pancreatic cancer that originates in the islet cells, which are responsible for producing hormones that regulate blood sugar levels. Islet cell tumors can be non-cancerous (benign) or cancerous (malignant).
Symptoms of islet cell cancer may include abdominal pain, nausea, vomiting, diarrhea, weight loss, and low blood sugar levels. Treatment options for islet cell cancer depend on the size and location of the tumor, as well as whether it has spread to other parts of the body. Surgery to remove the tumor is often the primary treatment, along with chemotherapy and radiation therapy.
Some people with islet cell cancer may also have a genetic condition called multiple endocrine neoplasia type 1 (MEN1), which increases the risk of developing tumors in the endocrine system, including the pancreas. In these cases, regular monitoring and screening for tumors may be recommended.
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