I really need to stop updating you so late at night as I am too tired and make no sense.
The doctors will continue treating me as an IPMN patient as they can’t be 100% certain what my cysts are. By treating me as an IPMN patient we are playing the safe game. I am having an MRCP because thats the general recommendation to my size cyst (scans every 6 months) alternating between MRCP and EUS/FNA.
In regards the CEA , mine was not collected through blood but it was collected through pancreatic fluid. After my badly written msg last night , I searched the Internet and it seems that they are two types of CEA which have led to the confusion.
In a nutshell I was hoping others had their CEA measured using FNA and not through bloods so we can compare values 🙂
I will , like always, keep you updated and please do tag me if I can help others with IPMN but there is a good chance I will be quiet for a while, until the next scan, nothing personal 😉