Back to Intro
Click 'Back to Intro' to return to the beginning of this section.

Pancreatic Neuroendocrine Tumor

What is a pancreatic neuroendocrine tumor?

Cancer starts when cells change and grow out of control. The changed (abnormal) cells often grow to form a lump or mass called a tumor. Cancer cells can also grow into (invade) nearby areas. And they can spread to other parts of the body. This is called metastasis.

A pancreatic neuroendocrine tumor is a rare type of cancer that starts in the pancreas. It's often called a pancreatic NET, or a PNET.

The pancreas is an organ that’s behind the stomach and in front of the spine. It’s a gland that has 2 main parts:

  • The exocrine pancreas. This part makes enzymes that go into the intestines and help break down food.

  • The endocrine pancreas. This part makes hormones, like insulin, that are released into the blood.

Most cancers that start in the pancreas are exocrine cancers. Endocrine tumors are much less common and tend to be easier to treat. Endocrine tumors of the pancreas are covered here.

Types of pancreatic neuroendocrine tumors

The hormone-making cells of the pancreas bunch together in small clusters all over the pancreas. These clusters are called islets of Langerhans. When a tumor forms in 1 of these islets, it’s called a pancreatic NET. These tumors can be either cancer (malignant) or not cancer (benign). But both types can cause serious health problems.

Pancreatic NETs are grouped based on the hormones they make. The 5 types are:

  • Gastrinoma. Gastrin is a hormone that causes the stomach to make acid to help digest food. A tumor in gastrin-making cells is called a gastrinoma. Most of these tumors are cancer.

  • Insulinoma. This tumor starts in the cells that make insulin. Insulin helps control the amount of sugar (glucose) in the blood. Most of these tumors grow slowly and are not cancer.

  • Glucagonoma. Glucagon increases the amount of glucose in the blood. A glucagonoma starts in a group of glucagon-making cells. Most of them are cancer.

  • VIPoma. These tumors start in cells that make vasoactive intestinal peptide (VIP). VIP controls the balance of water in your body. Most VIPomas are cancer.

  • Somatostatinoma. Somatostatin is a hormone that stops the body from making other hormones, like insulin, gastrin, and growth hormone. Most of these tumors are cancer.

These tumors may be called functional NETs because they make hormones. They cause symptoms based on the type of hormone they make. The most common types are gastrinomas and insulinomas.

Nonfunctional pancreatic NETs don’t make hormones. They’re often quite large when they’re found because they don’t cause symptoms. They’re more likely to be cancer than functional tumors. They're also more common than functional tumors.

What causes a pancreatic neuroendocrine tumor?

These tumors are fairly rare. Healthcare providers don't know why people develop them.

Who is at risk for a pancreatic neuroendocrine tumor?

A risk factor is anything that may increase your chance of having a disease. The exact cause of someone’s cancer may not be known. But risk factors can make it more likely for a person to have cancer. 

You are at higher risk for pancreatic NETs if you:

  • Have certain inherited genetic syndromes (those passed in families), such as:

    • MEN1 (multiple endocrine neoplasia type 1) syndrome

    • Neurofibromatosis type 1

    • Von Hippel-Lindau syndrome

  • Drink a lot of alcohol

  • Smoke

  • Have type 2 diabetes

  • Have chronic pancreatitis (inflammation of the pancreas)

Talk with your healthcare provider about your risk factors for pancreatic NETs and what you can do about them.

What are the symptoms of a pancreatic neuroendocrine tumor?

Nonfunctioning pancreatic NETs don’t cause symptoms until they’re big enough to put pressure on other organs, such as the bile ducts.

The symptoms of functional pancreatic NETs depend on what type you have because the symptoms are caused by the overproduction of hormones.

Here’s the breakdown of symptoms that you may have based on tumor type.

Nonfunctioning NET

  • Yellowing on the skin or whites of the eyes (jaundice)

  • Diarrhea

  • Indigestion

  • Pain in the belly or back

  • A lump in the belly

  • Weight loss

Gastrinoma

Symptoms are caused by too much stomach acid and include:

  • Acid reflux

  • Stomach ulcers that keep coming back

  • Pain in the belly or back

  • Diarrhea

Insulinoma

Symptoms are caused by low blood sugar levels and include:

  • Blurred vision

  • Weakness

  • Extreme tiredness (fatigue)

  • Headache

  • Feeling lightheaded or dizzy

  • Shakiness

  • Irritability

  • Hunger

  • Fast heartbeat

Glucagonoma

Symptoms are caused by high blood sugars and include:

  • Diarrhea

  • Weight loss

  • Mouth dryness

  • Sores at the corner of the mouth or on the tongue

  • Skin rash or dry skin

  • Headaches

  • Feeling very thirsty and hungry

  • Frequent urination

  • Feeling tired, weak, or dizzy

  • Blood clots

VIPoma

Symptoms include:

  • Weight loss

  • Stomach cramps or pain

  • Large amounts of watery diarrhea

  • Flushing (redness) of the face, chest, and neck

  • Dehydration, which can cause dizziness, low urine output, dry skin and mouth, and tiredness

  • Symptoms linked to low potassium levels, such as muscle weakness, aches, cramps, numbness, tingling, frequent urination, thirst, and irregular heartbeat (palpitations)

Somatostatinoma

Symptoms include:

  • Diarrhea

  • Gallstones

  • Fatty, bad-smelling stools that float

  • Yellowing of the skin or eyes (jaundice)

  • Unexplained weight loss

  • High blood sugar symptoms, such as weakness, hunger, confusion, headaches, frequent urination, and dry skin and mouth

Many of these symptoms may be caused by other health problems. Still, it’s important to see your healthcare provider if you have these symptoms. Only a healthcare provider can tell if you have a tumor or cancer.

How is a pancreatic neuroendocrine tumor diagnosed?

If you have any of these symptoms and your healthcare provider thinks you may have a pancreatic NET, you'll be asked about your health history, symptoms, and family history. A physical exam will be done. 

You may also need 1 or more of these tests:

  • Blood tests and other lab tests. These can show high hormone levels in your blood.

  • Imaging tests. These are used to look for a tumor inside the pancreas. They include CT scan, PET scan, MRI, ultrasound, and somatostatin receptor scintigraphy.

A biopsy is the only way to know if the tumor is cancer. Small pieces of the tumor are taken out and tested for cancer cells. 

After a diagnosis of pancreatic NET, you’ll need more tests. These help your healthcare providers learn more about the exact type of cancer. They can help figure out how fast the cancer is likely to grow and the stage and grade of cancer.

The stage is how much and how far the cancer has spread (metastasized) in your body. The stage grouping used is a scale of 1 to 4. Roman numerals I (1), II (2), III (3), and IV (4) are used. Stage I tumors are small and only in the pancreas. A stage IV pancreatic NET has spread to other parts of the body. The stage is 1 of the most important things to know when deciding how to treat the cancer.  

The grade is how fast the cancer cells are growing and dividing. It's a scale of 1 to 3 and is based on 2 things:

  • Mitotic index. This is measured by using a microscope to count the number of cells that are dividing.

  • Ki-67 index. This is the percentage of cells that are ready to start splitting or dividing.

Once your cancer is staged, your healthcare provider will talk with you about what these details mean for your treatment. Ask your healthcare provider to explain the details of your cancer to you in a way you can understand.

How is a pancreatic neuroendocrine tumor treated? 

Your treatment choices depend on the type of pancreatic NET you have, test results, if the tumor is cancer, and the stage of the cancer. The goal of treatment may be to cure you, control the tumor or cancer, or to help ease problems caused by the tumor or cancer. Talk with your healthcare team about your treatment choices, the goals of treatment, and what the risks and side effects may be.

Types of treatment for cancer are either local or systemic. Local treatments remove, destroy, or control cancer cells in 1 area. Surgery and radiation are local treatments. Systemic treatment is used to destroy or control cancer cells that may have traveled around your body. When taken by pill or injection, chemotherapy and targeted therapy are systemic treatments. You may have just 1 treatment or a combination of treatments.

Surgery is the most common treatment, if the tumor can be removed. The type of surgery depends on how big the tumor is and where it is in the pancreas. Nearby tissues, such as parts of the pancreas, stomach, small intestine, or liver may also need to be removed.

For tumors that can’t be removed by surgery, or that have spread to other parts of the body, other treatments may be used to shrink the tumor, destroy it, or control the symptoms it’s causing. These include:

  • Active surveillance if the tumor is slow-growing and not cancer

  • Chemotherapy

  • Hormone therapy

  • Targeted therapy

  • Radiofrequency ablation, or using heat to destroy the tumor

  • Cryosurgical ablation, or freezing the cancer cells

How do I manage a pancreatic neuroendocrine tumor?

Your healthcare provider uses medicines to help manage your symptoms from the pancreatic NET. These may include:

  • Medicines for stomach ulcers

  • Therapy or over-the-counter remedies to deal with diarrhea

  • IV fluids to help prevent dehydration

  • Medicines or other strategies to keep your blood sugar in a healthy range

Talk with your healthcare providers about your treatment options. Make a list of questions. Think about the benefits and possible side effects of each option. Talk about your concerns with your healthcare provider before making a decision.

When should I call my healthcare provider?

Call your healthcare provider if you have: 

  • New symptoms or symptoms that get worse

  • Signs of an infection, such as a fever

Key points about a pancreatic neuroendocrine tumor

  • A pancreatic NET is a tumor that forms in the pancreas.

  • These tumors are rare. Experts don’t know what causes them.

  • Not all pancreatic NETs are cancer.

  • Some of these tumors don’t cause any symptoms. Others do because of the overproduction of hormones.

  • Blood tests and imaging scans can help diagnose these tumors.

  • Surgery is the main treatment.

Next steps

Tips to help you get the most from a visit to your healthcare provider:

  • Know the reason for your visit and what you want to happen.

  • Before your visit, write down questions you want answered.

  • Bring someone with you to help you ask questions and remember what your provider tells you.

  • At the visit, write down the name of a new diagnosis and any new medicines, treatments, or tests. Also write down any new directions your provider gives you.

  • Know why a new medicine or treatment is prescribed and how it will help you. Also know what the side effects are.

  • Ask if your condition can be treated in other ways.

  • Know why a test or procedure is recommended and what the results could mean.

  • Know what to expect if you do not take the medicine or have the test or procedure.

  • If you have a follow-up appointment, write down the date, time, and purpose for that visit.

  • Know how you can contact your healthcare provider if you have questions, especially after office hours and on weekends and holidays.

Online Medical Reviewer: Jessica Gotwals RN BSN MPH
Online Medical Reviewer: Sabrina Felson MD
Online Medical Reviewer: Todd Gersten MD
Date Last Reviewed: 8/1/2023
© 2000-2024 The StayWell Company, LLC. All rights reserved. This information is not intended as a substitute for professional medical care. Always follow your healthcare professional's instructions.