Median Arcuate Ligament Syndrome (MALS)
I am looking for other patients that have been diagnosed with Median Arcuate Ligament Syndrome. Although it is caused by compression of the celiac artery many people experience abdominal pain after eating, diarrhea, food avoidance. Usually the first doctors they see are GI doctors. It is a diagnosis that is made after everything else is ruled out. I am curious if anyone else has had surgery?
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@mommyofaudrey15 - Welcome to Mayo Clinic Connect! I had MALS surgically treated and I’m fine now. It is very rare and I didn’t know of anyone with it until I found this wonderful group! It is so hard watching your child in constant pain. She may very well have MALS. Pressure on celiac artery by a ligament from the diaphragm. She has been tested thoroughly, but to discover the abnormal intestinal blood flow secondary the compression of the celiac artery she would need a Doppler ultrasound to detect change in blood flow. To confirm an abnormal test a CT angiogram is used. A regular abdominal ultrasound and CT would not detect it. The pain is caused by decreased blood flow to intestines when they are digesting food. Same principle as angina of the heart with physical activity.
She is currently in the hosptial and they are going back thru all her past CTs MRIs etc...she has had it all but this Dopple ultrasound. I am so I found y
This group. Unfortunately I have heard that our area doesn't have anyone that qualified to do the surgery.
We are thank you so so so much!!!
I don’t know where you live, but we traveled from Arizona to Connecticut to have surgery with Dr. Hsu bc no other surgeon has the knowledge and experience that he has. Check his education, it’s impressive! I got so tired of going to different doctors and they all told me it’s IBS or abdominal migrane. I’m almost 4 months out and feeling better every day and no horrible mals pain.
Our acupuncturist brought up MALS to us 2 weeks ago when I took her there. We are desperate. And ever since we are on that track. His daughter had MALS and went to Dr. Hsu. She is 100% better. We are in Portland Or and there is nobody here that can do this vascular surgery. We are in the hospital right now under PEDS surgery because of other things she had going on but her bowels seem fine its got to be MALS. She has every symptom. It's freaking awful.
I’m sorry to hear she is struggling. I had MALS with surgery at Mayo Rochester. 20+ symptoms disappeared. A year later had some return of symptoms at the same rate and time that my excess low back curved worsened because of hip dysplasia/arthritis. Found Dr Scholbach’s article about excess low back curve causing compression syndromes like MALS. My PT and I developed conservative management strategies and published them last week in a journal. Maybe something in this article may help your daughter. Not all MALS cases are caused by excess spine curve, but it’s worth a try before trying surgery. Hope you find some good help.
https://www.ejcrim.com/index.php/EJCRIM/article/view/1605/2056
Thank you! She does have that low back pain. She already has so many congential anomalies and they think that part of her bowel is not working from previous surgeries and that is what is causinf the pain right now. But who knows. You feel like you are in a hamster wheel just spinning around hoping someone will help. We have never seen her in so much pain. It's debilitating. She is on toradol and tylenol and something for SIBo and she is still at a 6 or 7 for pain. Since Covid is going on no elective surgies. As far as I am concerned this is not elective.
We think its MALS but nobody seems to want to order the testing for it.
Have you been to a Vascular Surgeon? He’s the one who ordered my CT and Doppler Ultrasound of Abdomen and pelvic.
While MALS is listed as a rare disease, Dr. Scholbach and I do not believe MALS is rare; it is uncommonly diagnosed because it is unknown.
Hello! I am so sorry that you are going through such a rough time!
if you are looking for a pediatric MALS surgeon, there is an amazing amazing one at Cincinnati Children's Hospital, Dr. Nathan. (https://www.cincinnatichildrens.org/bio/n/jaimie-nathan). He has a very unique surgery method, and has a very high sucess rate. He is very deliberate and thorough, so rules out everything before surgery, to make sure that the surgery is necessary and will really help treat the symptoms. I can personally vouch for him, he saved my life.