Pancreatic neuroendocrine (islet cell) tumor imaging is a type of imaging used to diagnose and monitor pancreatic neuroendocrine tumors. It involves the use of imaging techniques such as computed tomography (CT) scans, magnetic resonance imaging (MRI), and positron emission tomography (PET) scans to create detailed images of the pancreas and surrounding structures. These images can help doctors diagnose and monitor the growth of pancreatic neuroendocrine tumors.

1. Abdominal pain
2. Weight loss
3. Jaundice
4. Nausea and vomiting
5. Abdominal mass
6. Diabetes
7. Abnormal liver function tests
8. Abnormal blood glucose levels
9. Abnormal pancreatic enzymes
10. Abnormal imaging findings on CT scan or MRI, such as a mass or cyst in the pancreas

1. Genetic mutations: Certain genetic mutations, such as those in the MEN1 gene, can increase the risk of developing pancreatic neuroendocrine tumors.

2. Environmental factors: Exposure to certain environmental toxins, such as pesticides, may increase the risk of developing pancreatic neuroendocrine tumors.

3. Family history: Having a family history of pancreatic neuroendocrine tumors may increase the risk of developing the condition.

4. Other medical conditions: Having certain medical conditions, such as type 1 diabetes, can increase the risk of developing pancreatic neuroendocrine tumors.

1. Surgery: Surgery is the primary treatment for pancreatic neuroendocrine tumors. Depending on the size and location of the tumor, the surgeon may remove the entire tumor or just a portion of it.

2. Radiation Therapy: Radiation therapy may be used to shrink the tumor before or after surgery.

3. Chemotherapy: Chemotherapy may be used to shrink the tumor before or after surgery.

4. Targeted Therapy: Targeted therapy is a type of treatment that uses drugs to target specific molecules in the tumor cells. This type of therapy may be used to shrink the tumor before or after surgery.

5. Immunotherapy: Immunotherapy is a type of treatment that uses the body’s own immune system to fight the tumor. This type of therapy may be used to shrink the tumor before or after surgery.

1. Family history of pancreatic cancer
2. Personal history of pancreatic cancer
3. Personal history of other cancers
4. Genetic syndromes associated with pancreatic cancer
5. Smoking
6. Obesity
7. Diabetes
8. Chronic pancreatitis
9. Age (over 50)
10. Gender (male)
11. Exposure to certain chemicals or radiation

There is no cure for pancreatic neuroendocrine (islet cell) tumors. Treatment options depend on the type and stage of the tumor. Treatment may include surgery, chemotherapy, radiation therapy, targeted therapy, and/or hormone therapy. Imaging tests such as CT scans, MRI scans, and PET scans are used to help diagnose and monitor the tumor.