Unidentified abdominal pain
I wasnt sure where to ask this, but I've had severe abdominal pain for 16 years. Pain radiating from my back all the way around and sharp upper right abdomen pain. Lasted a few hours-a day for 16 years a couple times a year. Then recently i had an episode that went off and on for two weeks straight. Now when it happens theres pressure all around my abdomen and back, and sharp pains randomly around my torso, no sharp pain felt when they push on my abdomen, all blood and urine tests good, xray and ultrasound show nothing. Doesnt seem to be linked to eating seems to happen at random. Anyone experienced anything like this?
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My gallbladder was taken out due to it not functioning, it was only functioning at 18%. Up until this point I’ve had no problems except I used to get diarrhea after eating something fatty.
@amm97 - A 30 lbs weight loss is significant, no appetite change- do you eat the same amount of food and type of food?
Do you know if the Duplex ultrasound showed a significant narrowing of a couple of arteries? Do you know which arteries are involved?
Even though the CTA and MRI didn’t show any abnormalities I’m still not convinced that all is well.
Did they explain MALS to you? It’s Median Arcuate Ligament Syndrome. It’s rare, but we are quite a few here on Connect that have been treated for it.
There is a ligament that originates in the diaphragm- median arcuate ligament- that can compress the celiac artery in the intestinal blood supply. This means that the intestines don’t get enough blood flow for digestion- also causing severe pain when this happens.
Maybe you can ask for a review of that testing or even repeat the CTA. A vascular surgeon would know.
I might be eating a smaller amount at meal times but still the same food. The duplex ultrasound sound narrowing of the celiac and sma. I’ve actually researched MALS quite a bit and I think this is still a possibility even though the CTA doesn’t show it. A vascular surgeon told me that the CTA doesn’t show it and that he doesn’t think it’s MALS. The surgeon said that the ultrasound isn’t reliable because it’s “operator dependent”. But the research I’ve done said that the duplex ultrasound may replace the CTA someday.
@amm97 - Your research is correct! The duplex ultrasound has replaced CTA in many places.
At my last follow up at the university medical center where I had my MALS surgery, I was told they are changing to duplex ultrasound for my next follow up. This happened quite a while ago.
Maybe you could look for a university medical center that are skilled in evaluating MALS?
That is probably going to be my next step.
There are some similarities between our stories . Do these areas hurt all of the time for you. Mine is below the xiphoid process, down the middle to lower pelvic. And hurt at a pain level 6 to 8.5 all of the time.
There is nothing worse than chronic pain hurting this bad. Have you worked with a big hospital pain management department. What you probably have is abdominal nerve pain. They can try various injections. It’s tough, my mind can’t handle two years of this pain, it’s hard hard hard to keep pushing on.
Right now the pain is on and off. I have not been worked up for pain management yet at a hospital yet.
I also had my gallbladder taken out this time last year. So two years ago I slowly stopped eating due to a lack of appetite. I am a male 6ft tall 228 lbs to 179lbs in eleven months then had GB out. Slowly started eating to now year later gained it all back by eating late at night. I’m struggling to keep on going with such chronic pain.
Hi! Hopefully your CT scan had pictures taken on inspiration and expiration, otherwise they would not be able to see the “hook” that causes mals. My doctor had me do the ct and duplex ultrasound for comparison. I hope you find answers.
I think it did, they had me hold my breath and let it out. The ultrasound showed the hooked appearance.