Median Arcuate Ligament Syndrome (MALS)

Posted by Kari Ulrich, Alumna Mentor @kariulrich, Dec 26, 2016

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?

Interested in more discussions like this? Go to the Digestive Health Support Group.

Profile picture for lhorton73 @lhorton73

Hello..I've attached a list if doctors in Canada, hope this helps. I'm in a Facebook group and it has been very helpful navigating through this process.

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Thank you. I started out here and eventually found the online Facebook groups. Thanks for your information.

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Profile picture for lisa01 @lisa01

Are you aware of a FB support group called MALS PALS. It is a support group for people suffering with MALS and their loved ones. It gives a tremendous amount of informstion of individual struggles, and various treatments and specialists that treat MALS. Highly recommended!!

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Thank you for the info about the FB group!

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Profile picture for Kari Ulrich, Alumna Mentor @kariulrich

Thank you, Yes @lisa01 I am part of MALS PALS, but I do like the security of being here on Mayo connect vs Facebook when it comes to health information security. I was hoping that a group would start here for MALS. If we had enough patients here on Mayo Connect maybe they would consider doing a webinar in the future. I really like the format of this site. I have had Open Mals surgery twice, once for a bypass and then a revision several years later. If there is anyone interested in joining me here let me know.

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I would.

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Profile picture for Kanaaz Pereira, Connect Moderator @kanaazpereira

Hi @kariulrich,

We have a fairly recent discussion on Celiac Artery Aneurysm; is there any connection between MALS and celiac artery aneurysms?
You can find the discussion here:
https://connect.mayoclinic.org/discussion/celiac-artery-aneurysm/

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They are different. MALS comes from a blockage from pressure from the mediun arcuate ligamate, but left untreated, it can cause an aneurysm.

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Profile picture for cnash1 @cnash1

My daughter kk er recently had cdif from antibiotics. This triggered a severe lower abdominal pain. In doing a complete work up at the hospital they found a rare condition called Mals. Looking for any journeys regarding this syndrome as well as anyone who experienced severe chronic pain after a cdif infection.

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So sorry to hear this . I had c.diff in 2014 and had to have a fecal transplant. I was diagnosed with mals in 2021 .
I am currently in bedridden nonstop pain living on high dose opiods .
I believe my c.Difficile comes back as repetitive c.diff bc the pain is excruciating.
The mals pain is also excruciating. I keep getting hospitalized for pancreatitis or liver enzymes going very high causing insane pain .
I sm going yo Utah to see Dr. Richards on September 5 th . I’m going to Utah also on September 20 to have my celiac plexus block. I live in Las Vegas and there aren’t any qualified interventional radiologist here. I had a anesthesiologist. Tell me he could do my block last summer and he did it, and did it incorrectly and didn’t know what he was doing. Anyways, I believe due to the mals and the fact that our intestines ,pancreas and liver do not receive the proper blood flow and we experience constipation which is why we get c.difficile sale in SIBO . and other infections.

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Hi -- I had laparoscopic surgery for MALS last November, and the pain is now back. I don't seem to have a path forward here in North Carolina. My GP ordered a CT scan and the results suggested that the flow through the celiac artery has improved, but I have worse nerve pain than before. No next steps here. Any suggestions or thoughts?

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Profile picture for evenc1 @evenc1

Hi -- I had laparoscopic surgery for MALS last November, and the pain is now back. I don't seem to have a path forward here in North Carolina. My GP ordered a CT scan and the results suggested that the flow through the celiac artery has improved, but I have worse nerve pain than before. No next steps here. Any suggestions or thoughts?

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For Neurogenic MALS you need to have a ct scan with pictures taken on inhale and exhale, have a diaphragm that’s low and a CP block which you can eat with no pain. Many doctors treat mals as a blood flow problem only.

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I had all those things before the surgery last year.

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Profile picture for Rachel @racheldmark

Hey everyone,

This is a new topic of conversation for me, has anyone tried Ketamine infusion treatment for chronic nerve pain reduction?

A friend of mine had amazing results with depression treatment so I thought I would look into it. I just contacted this local clinic and will let you know what I find out. Reading through the Infusion Clinic of Albuquerque's website has extensive documentation on recent research that looks very promising: infusionclinicabq.com/providers

Thanks,
--Rachel

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I have chronic abdominal pain caused by nerve damage in my abdomen following a surgery in March. This past week I had my first Ketamine Infusion after reading a lot of information about it. So far I have not seen any great results, but it may take a couple of days I am told. I have also been told that I may need to have one or two more infusions in the next couple weeks to see any reduction in pain.

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