Median Arcuate Ligament Syndrome (MALS)

Sure. His name is dr Gary Kimble Jett. He is at Baylor heart hospital in Plano. I consulted with a general surgeon who was my second choice. I also sent my test to Dr. west in Fort Worth. I found his name on the MALS pals page on Facebook. He used to be in Houston and several on Facebook recommended him, however, when I sent him my test results, I received a call from his office saying that he would not take my case. Dr. Dennis gable was the surgeon assisting on my surgery. He Actually saw me in the hospital when I was first diagnosed. When i started getting worse again and was considering the surgery, he will referred me to Dr. Jett for the surgery. I decided to go with dr Jett because Of his credentials and at my first appointment he knew exactly what I was talking about and had no hesitation telling me what procedure he would do. Dr gable and Jett are both vascular surgeons. I am from Houston originally and a friend there recommended Dr. Charlton-Ouw. You might consider a second opinion with him. I’ll keep you posted.

Congratulations on a successful surgery and thank you so much for replying. Do you mind sharing what doctor you have seen in Dallas? I hope all goes well and look forward to hearing back from you on your progress.

Also wanted to post this article if possible. The Cleveland Clinic has reached out to other hospitals to share their knowledge on vascular issues for people that cannot travel to the clinic. https://consultqd.clevelandclinic.org/cleveland-clinic-teams-with-three-baylor-hospitals-to-provide-heart-care/. I consulted with three docs before deciding. Two vascular and one general surgeon.

Hi Shawnee, I live in Dallas. I just had robotic lapriscopic surgery on Wednesday. I am just starting third day post op so I can’t say yet how I feel cause I have all the pain from the surgery. My surgeon is older so he has done this before. He was very confident in what needed to be done. He told my family when came out that it was very successful. Another vascular surgeon was ready to assist but was not needed. They were ready to convert to open if needed but didn’t him after al. I will update as I progress. I believe I can tell that I am able to eat more and don’t have that after eating pain but as I said, I’m holding cmmenting too much till I am out of this surgical pain.

Hi Mark,
Mine is a weird story. Nothing about my medical conditions is 'normal' or fit the profile. I just went to the er one night for pain meds cause it was really bad. They did ct scan and told me my arteries are narrowed and to see a vascular surgeon. I saw the chief of vascular surgery at a university hospital. I was lucky. I had no idea what to expect, didn't think a big deal. I was a special ed teacher and thought I would be back in a month. That was almost 5 years ago. It was about an 8 hour open surgery. ICU for 3 days then reg room. I was totally drugged up, don't remember much. The surgeon wrote and published a journal article on me since I was so rare. The diaphragm was not only crushing the celiac but also the SMA, which is extremely. It was a lot of work in there. My pain was gone but a very long difficult recovery. Then major stresses. My dad suddenly passed away and I was POA. I had 2 sisters who were extremely pissed and started 3 years of pure hell for me. My mom had beginning Alzheimer's and I was the one that would care for her when my dad passed, of course thinking that would be way down the road. She was all upset with my sisters, it was just terrible.
So the reason I say this is the stress during this basically killed my body. During this time, not even a year after first surgery my arteries narrowed again. I should have had a by pass but way to weak. Surgeon said I would never make it. So I got stents put in each artery. That held for awhile then, balloon. My original surgeon moved to another state. My second surgeon was good. I didn't know about the nerves and all that because I never researched or anything because I was taking care of my mother and dealing with them. I learned things on these sites. My mom passed and my sisters were taking me to court, basically my lawyer said to go because I had all evidence and I would win, but my body just couldn't take it so we settled in mediation and signed contract to communication. So sad. My dad said they would give me trouble, he was right. Anyway, The reason I tell you this is because I just got diagnosed with dysautonomia, POTS and MCAS. This is all from what my sisters did to me. I would have been able to go back to work and probably had the bypass so my condition is not from the MALS.
My surgeon now is from Mayo and he is awesome, but not to familiar with MALS. I may need to get back in contact with my original surgeon. He is chief of staff at Baylor College of medicine, but I know he will remember me.....haha
Well that is sort of my story summed up. Sorry this is so long. I never thought about the flying. I do have reports with dilation, and we were going to do celiac block, but all the dysautonomia stuff took over.
Well good luck to you,
Jill

Hi Kanaaz

Thank you for the welcome and thank you for the links to studies, I look forward to reading them. I agree with what you say, but hope that consultants don't leave looking for MALs until the very last moment. It is the very fact that MALs is considered to be a diagnosis of exclusion and every other possibility that might be causing the pain must be ruled out that worries me. 10 years ago my symptoms became chronic, for the first 3 years I could barely leave the house and I looked like a skeleton. They went by that very premise and started ruling out other things. Over the 10 years I had numerous operations i.e they took out a perfectly healthy appendix hoping it would solve the problem; it didn't. In fact I got peritonitis which nearly ended my life. Then they took out my gall bladder hoping it would solve the problem. They also performed exploratory laparotomy and found nothing. After so many operations I ended up with Adhesions which they had to open me up for twice. Even up to a few months ago they were ready to discharge me to the pain specialist for a spinal cord stimulator, but I refused to give up. It was after talking to an consultant immunologist about my symptoms he recommended the angiogram which showed the compression. The CT report stated that i was not eligible for stenting or angioplasty. I can't help wondering if like @shawbing they had seen it at the early stage 10 years ago a minor operation to release the artery from the ligament would have provided long lasting or total pain relief. My concern is if consultants continue with that line of thinking they will keep catching patient at an advanced stage where major damage has been done by the ligament and possibly the lack of blood supply. Making any surgery useless further validifying their notion that MALs is a diagnosis of exclusion; a cycle that must be stopped. They should be looking at what symptoms should be present for them to immediately do an angiogram to look at the celiac trunk. In my view ruling out everything else first is being reactive rather than proactive. Just because they don't know the cause doesn't mean it is not a real illness.

Mark

Welcome, @ukmalsman. Mayo Clinic Connect is all about meeting other members who experience things similar to yourself, share information, and encourage one another – I'm so glad you've joined this group and shared some incredible insights.

It's interesting that you note, "Currently there is very little research into MALs with consultants looking at the condition with blinkers on unable to even agree on how the pain is caused." I agree – the diagnosis of MALS has been the subject of much debate.There are several factors (about the lack of clarity) that I thought I'd mention.

Because the cause of MALS is not clear and symptoms may persist even after surgical treatment, its diagnosis is considered controversial. The challenge lies in the fact that it mimics other GI symptoms. Therefore, MALS is considered to be a diagnosis of exclusion – every other possibility that might be causing pain must be ruled out before making a clinical diagnosis.

In MALS, the medial arcuate ligament compresses the celiac artery, reducing blood flow to the stomach/intestines; surgery, where the ligament is cut away from the artery, doesn’t always get rid of the pain and symptoms. Many surgeons reason that if compression of this artery was causing the pain and other symptoms, then eliminating the compression should get rid of it – which may not be the case.
Although, I've learned that it's become less challenging to treat, since surgical intervention now includes removing the celiac ganglion, which is the mass of nerves in that area (some call it the “solar plexus”) because pressure on the nerves may be causing the abdominal pain. https://pdfs.semanticscholar.org/d6b6/4ec69d1cd3ef5f02036362f960d3b0be0181.pdf

That being said, I'd also like to mention these very encouraging published studies that show the tremendous advancements taking place (imaging techniques, laparoscopic surgery), which would help in establishing diagnoses of this condition:
- Contemporary management of median arcuate ligament syndrome provides early symptom improvement https://bit.ly/2Rrfop4
- A predictive model for patients with median arcuate ligament syndrome https://bit.ly/2pDJQzN

@ukmalsman, if there is one thing I've learned from the members of Connect, including you, is that you should never give up until you find the right physician or the right treatment that can help you in the best possible way. I'm certain @kariulrich will join in soon, and I look forward to seeing more posts from you.

Hi Shawnee
Welcome to Mayo. From my research the procedure your Dr recommended has worked for many in the past. Is the doctor doing the surgery a vascular surgeon? May I ask if you have got to the stage of not eating yet. If you are lucky and they caught the compression early having the surgery may be beneficial. I feel the longer the condition goes un-diagnosed the worse the symptoms get. in many of the posts you will find they can not eat as the pain gets worse leading to them losing weight rapidly. I have my surgery consultation in 2 weeks, here are the questions I will be asking that may be relevant for you too:
1) What part of the celiac trunk has been compressed?
2) What is the mean systolic velocity of the celiac artery?
3) Have you as a surgeon dealt with celiac compression before.
4) If so what is your success rate? (how many patients are pain free?)
5) Will it be necessary to have an angioplasty or stent in the artery?

I am hoping your compression is minor and you don't need the angioplasty or stenting. If the answers to the questions are satisfactory then I wouldn't leave it too long to make your decision. The longer you leave it the worse you will get. I wish you all the best, please keep us informed.

Mark

Hello, my name is Shawnee. I live in Houston, TX and was recently diagnosed with Celiac Artery Compression Syndrome after 2 CT scans, 2 Ultrasounds, and a lot of abdominal pain/nausea. Of course, I’m one of the “out of the norm” patients whose compression occurs when I inhale (not exhale). I’m 44 years old and I’ve been dealing with this for over a year which all started with GERD. The pain and nausea didn’t occur until just 4 months ago. I see Dr. Galvani here in Houston at the Baylor College of Medicine. He suggests robotic surgery to cut the ligament and remove some of the nerves. Has anyone else had this done? I was hoping to get a second opinion but having a hard time finding a doctor who is familiar with this particular medical condition. All information, suggestions, advice would be greatly appreciated. I requested to join the MALS PALS FB group today. Thank you all in advance for your help and support.

Thanks for the reply, for me it was fast food. No matter how much I ate I remained skinny.