When there are cancer cells in the pancreas, it is called pancreatic cancer. The pancreas is a pear-shaped gland that sits between the stomach and spine. There are three parts to the pancreas: the head, the body, and the tail. The pancreas makes digestive enzymes and hormones that help control blood sugar.
The most common type of pancreatic cancer is adenocarcinoma of the pancreas, which targets the exocrine cells. Pancreatic neuroendocrine tumors (NETs) are a less common type of pancreatic cancer. About 2 out of 100 cases of pancreatic cancer are NETs. Staging and treatment may be similar for both adenocarcinoma and pancreatic NETs but talk with your care team about your type of cancer and treatment options.
Staging is a way to find out if and how far the cancer may have spread in your body (metastasized). Your provider will have you get a few tests to figure out the stage of your cancer. For pancreatic cancer, these tests may be:
Physical Exam: This is a general exam to look at your body and to talk about past health issues.
Imaging: Radiology tests can look inside your body at the cancer and see if it has spread. These tests are:
Blood Tests: Labs may be drawn to look for any changes in your blood. You may also be checked for tumor markers, such as CA 19-9 and carcinoembryonic antigen (CEA).
Pancreatic cancer can metastasize (spread) to other parts of the body through the tissue, lymphatic, and blood systems. Your healthcare team will use the American Joint Committee on Cancer TNM staging system to figure out:
The TNM is then used to assign a stage from 0 to IV (4).
Many types of procedures can be used to help diagnose and treat pancreatic cancer. These are:
The method used for these surgeries (open vs laparoscopic) is based on many factors. Your provider will talk to you about what surgery is best for you.
Sometimes, more surgery is needed later for neuroendocrine tumors to remove liver and/or lung metastasis. Your healthcare provider will talk with you about these procedures.
As with any surgery, there are risks and likely side effects. These can be:
A stay in the hospital may be needed for one to three weeks, based on the type of surgery done. While in the hospital you may have:
Depending on your situation, you may also have:
You may leave the hospital with some of these drains, tubes, or intravenous lines. You will be taught how to care for these.
Before leaving the hospital, your medical team will talk with you about the medications you will be taking for blood clot/infection prevention and pain management.
Your healthcare team will give you information on your diet after surgery. Digestive enzyme supplements may be needed to prevent diarrhea, aid in food digestion, and help control blood sugar levels. This may be brief or lifelong, based on your situation.
Your team will also talk with you about any activity changes you need to make while you are at home. These changes may be to:
You will be told how to care for your incision before leaving the hospital.
To care for your incision you should:
You may need a family member or friend to help you with your daily tasks until you are feeling better. It may take some time before your team tells you that it is ok to go back to your normal activity.
Be sure to take your prescribed medications as directed to prevent pain, infection and/or constipation. Call your team with any new or worsening symptoms.
There are ways to manage constipation after your surgery. You can change your diet, drink more fluids, and take over-the-counter medications. Talk with your care team before taking any medications for constipation.
Taking deep breaths and resting can help manage pain, keep your lungs healthy after anesthesia, and promote good drainage of lymphatic fluid. Try to do deep breathing and relaxation exercises a few times a day in the first week, or when you notice you are extra tense.
This article contains general information. Please be sure to talk to your care team about your specific plan and recovery.
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