← Return to Anyone have/had BD-IPMN?

Discussion

Anyone have/had BD-IPMN?

Pancreatic Cancer | Last Active: Mar 21 5:31pm | Replies (39)

Comment receiving replies
@colleenyoung

I’m tagging @pattyclaire to make sure she saw your question. @cjmchicago. Good question. Patty how are you doing now?

Cjmchicago, have you recently been diagnosed with an intraductal papillary mucinous neoplasm (IPMN)? How are you doing?

Jump to this post


Replies to "I’m tagging @pattyclaire to make sure she saw your question. @cjmchicago. Good question. Patty how are..."

Hello,
Yes, I was diagnosed with an 8mm possible IPMN in the uncinate process a couple of months ago without ductal dilation or concerning features from the CT scan. I am having an MRCP in July to see where things are at.
I am concerned because I have so many GI issues, but everything I read, and the GI doc thinks my GI symptoms and IPMN are not related. I guess I'm also worried because I had 2 abdominal CT scans about 16 months ago and they didn't see an IPMN. It said my pancreas was normal. This makes me think it is growing quickly. I also read so much conflicting information online about IPMN's. Some say it's a 30% chance a side branch will turn into cancer in my life and other studies say my risk is 1-2%. It's hard to know what to believe or how to prepare for this. At 54, I wonder if I should stop putting money into my retirement.