Mesenteric Panniculitis or Sclerosing Mesenteritis

Posted by BillyMac65 @billymac65, Dec 6, 2012

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.

@gmeg

<br />
Hi The lumps and bumps were described by an MD long ago as fatty tissue under the skin. GMeg<br />
<br />
<br />

Jump to this post

What did your Dr. say what to do to dissolve them? TY in advance.

REPLY
@nedradenise

Does anyone have this rare inflammatory disease? If so how do you deal with the pain and still function every day? I would love some advice.

Thank you

Jump to this post

Hello I have this condition the way I deal with the pain is raking Turmeric
I also changed my diet to only eating anti inflammotory foods. No Caffeine
Beef in moderation
Pork in moderation
I mainly eat chicken and turkey.
No sugar.

A gluten free diet can help also.

Starches I only eat brown rice and if potatoes a small portion.

Whole grain cereals
Beans are great to I have done alot of research. Changing my diet and taking Turmeric has helped alot

Anti inflammatory is the key to keeping this rare disease at bay.
eating junk food and stress Causes flares as well as eating sugar and drinking sodas.

The antinflammatory diet also helps to stay regular.

Im all about natural I only take medicine when needed.

Hope this helps

REPLY
@mom2three

Hello I have this condition the way I deal with the pain is raking Turmeric
I also changed my diet to only eating anti inflammotory foods. No Caffeine
Beef in moderation
Pork in moderation
I mainly eat chicken and turkey.
No sugar.

A gluten free diet can help also.

Starches I only eat brown rice and if potatoes a small portion.

Whole grain cereals
Beans are great to I have done alot of research. Changing my diet and taking Turmeric has helped alot

Anti inflammatory is the key to keeping this rare disease at bay.
eating junk food and stress Causes flares as well as eating sugar and drinking sodas.

The antinflammatory diet also helps to stay regular.

Im all about natural I only take medicine when needed.

Hope this helps

Jump to this post

What kind of medication you take when need , my family only offer me Ibuprofen, I start drinking Tumeric tea with little black paper or do You think Tumeric pills better, It’s rate disease am not getting any help from doctors , am still looking for the right doctor heard about it or know how to deal with it. Thanks

REPLY
@lobell2

The GI doctor listened and took notes. He doesn't want to say MP as the CT showed. Wants to rule out other things..so have to have colonoscopy and another test - but can't get in until June 22.
Just dealing and trying to push through. He said if the pain gets worse go to ER.. I laughed and said I am here trying to get help- what could an ER doctor do? Well if you need pain meds..I told him I wasn't seeking pain medication.. I want answers.
I know my comments are one sided -how I feel and understood the appointment.
I guess I have to deal with it and wait. The pain is now a dull ache in the side and I have been eating more.

Jump to this post

Just had my follow up appointment with the GI doctor. Well the CT is correct it is MP. Again- he hasn't dealt with anyone with this. He could put me on tamoxifen and prednisone- from what he's read. My choice... He said I am welcome to come back any time. I left in tears.
I don't know where to turn. I haven't found what triggers mine and don't want to be on medication.
Feeling lost in the wilderness.

REPLY
@amandaa

Hi @nnewins, welcome to Mayo Clinic Connect. If you scroll to the top of this page and click digestive health in the headline at that says:

Groups / Digestive Health / Mesenteric Panniculitis or Sclerosing Mesenteritis

You will see in the first blue box that it has a plus sign and the word follow. Once you start following, you will get email updates whenever someone posts to the group.

Have you been diagnosed with Mesenteric Panniculitis or Sclerosing Mesenteritis?

Jump to this post

Yes I have

REPLY

Is there a diet for Sclerosing mesenteritis?

REPLY
@informe

Is there a diet for Sclerosing mesenteritis?

Jump to this post

There is diet when I search on the internet, so fare avoid diary’s except yogurt it help build probiotics , no wheats , no sugar, no Caffeine

REPLY
@smezaael

There is diet when I search on the internet, so fare avoid diary’s except yogurt it help build probiotics , no wheats , no sugar, no Caffeine

Jump to this post

Thank you.

Sharon Barker

REPLY

Try Removing sugar and dairy. When having a flare up stay on soft food diet. Small portions. I’m recently diagnosed and it’s trial and error as I think we all have different triggers. I stopped gluten and meat as well. Sticking to anti inflammatory foods. Mostly shakes with a little chia seed and I take a probiotic. It’s been quite a process. I just finished a three day water fast. Best of luck to all

REPLY

Hi, so grateful to have found this group. I’m a44 year old Irish female diagnosed with MP two years ago with no other underlying conditions. Like many others on here my doctor had never treated anyone with this before. My gastric consultant said it’s an autoimmune disease so passed me off to a rheumatologist who said as I had no obvious joint problems that it wasn’t her area so I get fobbed off again and left to fend for myself. My GP suggested I take prednisone for flare ups and that usually helps for a while. Currently going through a flare up right now with abdominal pain, back pain under my rib cage, bloating, constipation and pain in my right eye.

REPLY
Please sign in or register to post a reply.