Celiac Artery Aneurysm: Anyone else with same illness?
Hello! I was recently diagnosis with a celiac artery aneurysm in June 2016. I underwent a embolization w/ coils procedure since the aneurysm had grown while in the hospital. I was trying to reach out to someone who suffered the same illness but have not been lucky. I would like to locate someone with my same illness. I would appreciate any help. Thank you
Interested in more discussions like this? Go to the Aortic Aneurysms group.
Excellent to hear, all is well. Based on research I’ve done there has been no one who had the surgery that had bad results. Mine is only 1.8 CM so they want to wait and see but I’m heavily leaning towards getting it done after next follow up in 3 months.
Mine was 5.5 so had grown quite a bit so it had to be operated on. I am glad it is over.
Where did you have your surgery? Dr.’s name?
I had my surgery at Abbott the Doctors name is Timothy M. Sullivan. Very good Dr explains everything. Takes time not just in and out. Would highly recommend him.
Dr.Sullivan is a wonderful physician, I agree with your recommendation!
I was diagnosed with celiac artery aneurysm June 3, 2017. I was diagnosed with Crohn’s Disease in 2005, underwent a resection in my ilium 2009 and have been on Humira since. I have just joined this forum because I understand how rare CAA is and wonder if it has to do with the Crohn’s as well as the Humira. Any insight would be appreciated.
Doug,
I was diagnosed with celiac artery aneurysm two weeks ago when I presented with severe abdominal pain in ER and CT scans revealed aneurysm. I cannot believe how rare the disorder is. Was admitted and told by vascular surgeon, that if caused by inflammation, they would do steroid treatment, if caused by infection, I would be life-flighted to Philadelphia since the vascular surgeon was not experienced. That was Friday, 6/3/17. They kept me in to do another CT that following Monday. Evidently they didn’t see a remarkable increase so was discharged with orders for follow up CT Scan (this week) and follow up with a different surgeon. Back story here….I’m following up with the colon/rectal surgeon who did my bowel resection after my Crohn’s Disease flared and fistulated into my bladder in 2009. Diagnosed with Crohn’s 2005. I have been on Humira ever since.
I feel like a walking time bomb, not knowing what’s going on in my gut.
Not that I’d wish this on anybody, but finally glad to know I’m not alone.
Karen
Jefferson Hospital and University of Penn are good. Are you near Philadelphia Pa?
I’m in the Wilkes-Barre/Scranton area, northeast Pa. How was the decision made for you to have surgery? Size of aneurysm? Surgery recommended for something like this? I have so little information about the condition, except that it’s rare.
I go back this week for my follow up CT 3 months after original diagnosis. In the meantime I talked with the vascular surgeon who told me my chances of having it burst are infinitesimal. So I’m glad mine is small and as long as it doesn’t grow I should be good to go. We will see after this weeks CT.
Am looking forward to the conversation with my surgeon – hope he says some similar like infinitesimal. Have you ever experienced any gut issues before? Hope all goes well for your prognosis.
Karen
I have GERD (acid re-flux) that I take a daily pill for, but nothing like the pain I experienced with this. They said the same thing with me that the pain was most likely from the inflammation around the aneurysm. Since it’s gone down no more pain. That doesn’t mean it wont flare up again at some point. I think they are most reluctant to do anything because I have no present symptoms. If I had constant pain I’m sure they would consider surgery to eliminate the problem. I also had some colon polyps removed but nothing serious. They found some diverticulitis but again nothing to worry about. I was concerned because my Father died of esophageal cancer and my Mom had to have a colostomy because of bowel blockage. So I have tried to address any gastrointestinal issues early.