Mesenteric Panniculitis or Sclerosing Mesenteritis
I thought I would start a discussion for patients with Mesenteric Panniculitis. From what I know, this auto-immune disorder has three stages to it, each with differing names (Mesenteric Panniculitis, Schlerosing Mesenteritis, Retractile Mesenteritis). Typically, this appears to be in older individuals with some other under-lying problem (Lymphoma, tumor, diverticulitis).
I have an atypical presentation because I do not have an underlying cause. The doctors seem to be hoping for Lymphoma to appear so they can treat it and have the auto-immune go away. I am interested in hearing from others with this. I had this diagnosed in 2011, so I am interested in hearing more about what this is like to live with. I want to hear from others who also have an atypical presentation. Did is come back? Also interested in hearing from those with Lymphoma. How was the treatment? Did it address the auto-immune?
Pretty much, I am interested in hearing from anyone who has had this, so i can better understand it, and not feel so alone with this!!
Bill
Interested in more discussions like this? Go to the Digestive Health Support Group.
I am a 40 yr old woman, with no symptoms. I went in for roux Y gastric bypass surgery and the surgeon discovered the mass before performing the surgery. I have been diagnosed with M/P and since I have no symptoms (pain, discomfort) I have been given no treatment. I go back in 2 months for a follow up CT Scan. I'm wondering does this disease go away on its own? Is there anything I can do to help get rid of this mass? TIA
There is always a reason to be optimistic. If you are not in much pain that is a good start. I am wondering how many people have this and don't know it and it never progresses. If your pain and other symptoms are manageable, continue with a normal life until something changes.<br />
Keep a folder with all of your medical test. Ask for copies of everything even CT's and MRI's, get a paper report and disc CD copy put it all in one file folder you can take with you if you have any issues.<br />
Keep your chin up and remember, this body we have is pretty tough and it wants to survive at all cost. Live your life as normal as possible. Best wishes for normalcy<br />
<br />
VonD<br />
Hi there my name is Mary. I think it's interesting that people are talking about paleo because I have just been thinking about it since grains, beans, nuts and dairy all seem to irritate. (If I ate nothing but chicken and lettuce I would probably be fine.)
I'm 51. I was so scared when I was diagnosed with SM. And that was weeks ago, I only just found this group. My gastroent. doctor told me not to worry, not that big a deal, but that's easy for him to say....Try to ease your mind a little. At least you have no symptoms and it is possible it will go into remission. Your doctor might recommend a colonoscopy just to be on the safe side. I have relatively mild symptoms and I'm hoping I don't have to start medication. You are in the best possible position and it's been found very early. Good luck.
That is freaky....I was just thinking yesterday about trying this.
Just so people can see this when coming here - but as of 8/12/15 - we now have 124 in our support group all with SM and/or MP. Contact me for info if you're interested and I can get your info and get you added in! We're about to be listed with NORD shortly as well. Thx. Lisa (mom of kiddo with SM diag. age 14 and now age 22)
Hey Lisa, you mean the group is? How soon do you think that will happen? My ssa hearing is on sept 18th and it couldn't hurt to show the alj that!! Hope you and ms Mac are doing okay! Wish me luck on my hearing! I'm just on pain meds now, fentanyl 25 and hi singla 30.(straight time release hydrocodone. <br />
Mark<br />
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Mark - yes, our group over there with be listed with NORD shortly. Finishing up with what i need to do for them! 🙂 Lisa
The information you've received is a little different from what I have learned. My understanding is that the medical community does not know what causes SM. Some think it may be an autoimmune disorder, some think it may be caused by a virus or bacterium, and there used to be a theory that it co existed with cancer but that is no longer a dominant theory. But the consensus of medical sites I've seen and my own doctor is that the cause is unknown (hence one of the names, idiopathic sclerosing mesenteritis). So I am not sure you're atypical.
Recently I have noticed a vibrating sensation in my chest sometimes it feels like a swooshing sound or a vibrating cell phone this started this month August. I had four stents replaced due to 99% blockage, could one of the tents have moved or erupted? the sensation doesn't go away, I am in a very stressful situation, I am raising my 10yr old grandson whom has a strong character and very defiant. He
has his grandfathers character, could it just be stress? I personally don't think so what kind of tests should I have done to find the problem?