For those with similar issues searching for an answer: I did an EUS which was also clear. The doctors cannot really explain my symptoms and say it's a functional disorder coupled with a milder pancreatic insufficiency. The doctor however told me that an early chronic pancreatitis might not be visible. Good luck to you too!
My bad, I meant PET scan but I have a very "helpful" spell/word choice program that I get out of sync with. What you have is odd so my thought was to get a different imaging mode involved, just to see if there is new information and if there is a very different blood perfusion going on. It's just a thought.
Your GI maybe thinking of at least trying to resolve the issue. Hope that it works.
What is a PETA test? Do you think I still have reasons for concern as far as Pan Can, and should I push for an endoscopic ultrasound? My GI thinks I might have some form of functional pancreatic insuficiency, so she will put me on digestive enzymes. However, my mind is still not at ease...they do not have an explanation for the pain I am having :-(
Sounds like there might be a blood supply issue. Surprising that the CT didn't identify at least portion of the issue. CT are "slice" based imaging so getting just the right slice position can be a bit of dumb luck. Maybe a PETA test might point to the cause of the duodenal atrophy. At least you have some progress.
Ok, so here is an update. I went to the hospital for investigation, and I know nothing more than before :-( all my blood test are normal, CT - normal, gastroscopy and colonoscopy mostly normal, except that they found some "duodenal atrophy". What could be causing all of my symptoms then?! Does anyone know the significance of duodenal atfophy?
I was a smoker until a year ago. I drink rarely and in small quantities (not since the pain started) and I try to eat healthy: home cooked with a lot of veggies, organic eggs, etc. It is worth maybe mentioning that before the pain started, I had a really stressful period: lost my job, found out I had infertility issues and starting the whole IVF process with my husband. I was also taking a LOT of supplements, including DHEA hormone to prepare myself for the IVF and have better chances. It might have triggered something.
I forgot to mention that those days when my pain is worse, I also feel very thirsty and have dry mouth...another indication of a pancreatic problem.
Hi, thanks for answering! No, all my other parameters (except ferritin) were normal all the time. They checked liver and pancreatic enzymes and everything else. Everything seems normal, but I feel like crap, losing weight and having pains. On top of that, I am hypochondriac and when I google my symptoms, it seems to match pancreatic cancer. Also, I read that this type of cancer can be very difficult to diagnose, and there were people with normal CT scans who still had tumors. I know I shouldn't be thinking that way, but it's been lasting for months now, and I still have no answer and it is very frustrating. I tried taking Nexium for 2 weeks, based on a suggestion from my doctor that it might be gastritis, but it didn't help.
Given your normal imaging along with clean blood work, I wouldn't worry too much. The doctors have done a pretty through job and even included the CA19-9 tumor marker. Did they also test you for CEA and AFP?
When you were having your GI issues, were your doctor's able to do some blood work during this flare period? That might be a bit more informative of you're dealing with a transient issue like chronic biliary sludge or very small gallstones, etc. And have you ever seen an elevated Bilirubin level or Alp level in any of your blood work?
I also have IBS from years of opiate analgesic abuse. You know. Sometimes, it's just the food moving through that cause the most uncomfortable, nauseous, painful, severe signs and symptoms. It's simply your bowels working. Unfortunately, those of us with IBS, know EXACTLY when our pyloric valve opens and when we dump something into out small intestine. It's sensation of peristalsis that causes our enteric nervous system to interpret that as pain. Have you been checked for any nerve disorders? How is your diet? Sleeping habits? Tabacco use?
One thing I know that works for me... This is going to be painful the first time... Peppers. Hot as hell peppers. Cayenne chili powder added to a salad with chopped apple, walnuts and seseme seeds. Use only olive oil and balsamic vinegar for dressing and EAT SLOW.
That'll get stuff moving.
I forgot to mention that I had pale stools on a couple of occasions during these 2 months. They seem to appear after I have stronger pain under ribs. Then, the day after they are back zo normal. I am really puzzled.