Type 1 Neuroendocrine Tumor with no risk: What should I ask doctor?
Hello,
Yesterday my EGD biopsies revealed the Atrophic Gastritis diagnosis that I already knew about. The polyp that the doctor biopsied in my stomach was benign. According to the doctor, based on guidelines, having one of these benign polyps (called a Type 1 Neuroendocrine Tumor) has no risk. However, in order to be super certain, the doctor recommends repeating my endoscopy at this time to make sure we resect everying and repeating an EGD in 1 year. Is anything that I should be asking the doctor? With all your experiences, what are the steps/things can be recommended for me? I appreciate all your support!
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Thank you for the information Teresa!
Thank you Steve!
Hi Michelle! We did not have any resolution at Mayo last month and are very discouraged. Every time I read more of your experiences and story it sounds so much like my husband’s. They were trying to tell him his could be a splenule as well. Can you give the name of the doctor who finally found you answers we will fly anywhere to get the help he needs. He feels sick everyday and no one seems to want to believe his symptoms and help him! If you would rather just email me my email is tinerobison@comcast.net.
Sometimes MRI doesnt catch it but PET Scan will definitely find em. Hope that help.
Lina
Good point but for sure Type 1 doesn't mean it's not spreading.
That's right. It can be benign, encapsulated and non functioning like my hubby but we don't want to wait until it become malignant, functional and metastasis. So he's had lap panc/spleen removed 6/9 so he is doing well came home D8 post with a drain.
I am so frustrated to hear so many of you have had the option to have the tumors removed and we have been to 2 major hospitals and they won’t give that as an option for us, this is so frustrating! Has anyone experienced the waiting game and continue to not feel well during that time? My husband can’t even enjoy life and is in pain every time he eats!
Why do you want surgery so much?
I don't know your story... sorry. I got progressively sicker for over 3 years before finally being diagnosed. I had a pnet that spread to my liver. Surgery wasn't an option for me. I have had enough surgeries so I was happy to avoid it. I have been on CAPTEM chemo for over a year. Every thing is shrinking. I am very fortunate.
What were your symptoms over the 3 years?