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 Support Group.
Oh Jen, I am really sorry to hear about a new aneurysm. Think positively, if you can. 🙄 At least it's small. How did they discover it? I'm coming up for my first tests for measuring growth since my CA was found last August. Then, it was 1.2 cm. I'm in Florida, so I understand your concern about no hospital beds. Please keep us posted and know that our best thoughts are sent your way. COVID free so far, too! 🤞Mary
Thanks for adding that info Chris. I am 63 yers old and last Wednesday the Docs just found a 1,4cm celiac artery aneurysm on a Cat scan. i only know this because I have access via Mychart to my records and i read the results of the Scans. pretty bummed that after 5 days, i have not received a call. It is almost 2021 now and there still is little about this out there.
Hope you are doing well.
Hi @finled...I'm new here...first post. My husband is 58 and a few weeks ago, they found a 1.3 cm celiac artery aneurysm on a Cat scan, that was for an unrelated gastric issue. The vascular surgeon wants to see him every 6 months, and if it gets to 2 cm. he will do endovascular repair. His advice was to stop smoking, no fattening food (control cholesterol), keep a very close eye on his blood pressure, no heavy lifting, and limit stress! Like you, I cannot believe it's almost 2021 and it is still so rare, that I cannot find anything on google for 'how to live with a celiac artery aneurysm". Take good care of yourself. All the best.
Thanks for the reply. The 2cm level seems to be the magic number for repair. I really appreciate you sharing the advice of his Vascular Surgeon. I will now give up that occasional cigar, start taking the statin that I never can remember to take, talk to my wife about the Keto diet we have been on, and watch my blood pressure more carefully- Great advice that makes sense.
In my case I have gone in for CAT scans on pretty much a yearly basis to monitor the progression of Follicular Lymphoma. I have been on a watch and wait program for this NHL, so I have experience with that. The difference is- with NH Follicular Lymphoma the process of watch and wait can last years, before they reach levels that indicate treatment and the treatment is well understood. I had CHOP Chemotherepy in 2011. Unfortunately it is incureable, but fortunately it is considered more of a chronic low grade cancer condidtion today.
I was shocked to see the scan indicate the 1.4cm Celiac Artery Aneurysm last week. My scan of 1 yr ago did not mention it at all. Also troubling is the fact that this scan was at a different hospital than last years and the difference between the scans at the NHL Lymph Node level are of great concern. Last year they were watching a couple of particular nodes that we identified in 2018. Last year they had not grown-All good. This new hospital did not mention them at all-last week, but they did find a few others that were out of range. The results don't make sense in comparison, which makes me question the CAA finding along with all the other data. Not that I don't believe it as much as I would like to not believe it.
I will ask to have the new hospital do an analyis that compares against my past few years of scans from the old one. I made sure they had all the data, but simply assumed they would actually do all of that.
My best to you and your husband. God bless you and all of you that contribute to this site. It was a fabulous find for me toady as this Aneurysm thing is really scary.
Merry Christmas to you all!
David
Tulsa
I am so sorry to hear about the NH Follicular Lymphoma! Wishing you a healthier 2021...stay safe and it would be great if the CAA finding was in error...Merry Christmas to All who contribute here & I am so grateful this outlet exists!
Michele
Toronto, Canada
@finled, that does sound confusing and worth going back to ask questions about test results. It's so important to be your own advocate. I also wanted to mention that there are members talking about NHL and follicular lymphoma in this group:
- Blood Cancers & Disorders https://connect.mayoclinic.org/group/blood-cancers-disorders/
@imahotmess13, welcome. How is your husband taking the news of the diagnosis and especially the prescribed changes to diet and lifestyle? That can be tough to accept.
@colleenyoung Thank you! My husband never shows worry on the outside, but I'm sure it shook him up - he did quit smoking cold turkey the same day as the diagnosis. Our daughter is very worried, and has been quite vocal about eating a proper diet, and getting more exercise. I think over the last couple of weeks we have all grown to accept it, but it makes us uneasy. This Group certainly helps me to learn, to vent, and to know we are not alone in this. Thanks again,
Michele
Hi I was told yesterday that I have a fusiform aneurysm of the celiac artery. They said it was 1cm, it was found on the CT scan. I went to ER I was having intermittent epigastric area pain that radiates into my upper back, between my shoulder blades. When the pain was intermittent it was after eating and then it was constant for 2days. I was worried something was going on with my heart, I’m 57 and have hypertension. They said my heart enzymes were negative and ekg was good, then they did CT and found the celiac artery aneurysm. I didn’t know how rare it is until I looked it up. I could tell the ER doctor wasn’t familiar with it by the look on her face. What I’m wondering has anyone who has a celiac aneurysm have any similar symptoms as mine? I’m going to make an appointment Monday with my primary doctor, since it’s this weekend this occurred. I would appreciate any information anyone can give me. It’s kinda overwhelming.
@kimberlyh57 We called 911 for my husband (age 58) on a Saturday night , as we thought he was having a heart attack. His pain was middle & upper chest & very intense & into his back & he was sweaty & short of breath. Among other tests, they referred for an ultrasound, where results would be sent to one of their vascular surgeons. Two days later on the Monday, he had a light meal for lunch & immediately after that meal the same intense epigastric pain came back. It was only then that we realized the Saturday attack had also been triggered by a meal.
A few days later he had an ultrasound of his stomach, and from that the vascular surgeon gave us the diagnosis of a 1.3 cm celiac artery aneurysm. I previously posted here - his advice was no smoking, control cholesterol, keep a close eye on blood pressure, no heavy lifting, and limit stress.
Take care and All the best,
Michele
Toronto, Canada
Thank you so much Michele, I really appreciate it! I’m definitely going to follow your husband’s advice. I wish the best for him also!