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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
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HugInterested in more discussions like this? Go to the Digestive Health Support Group.
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You are doing all the right things.
Hi all,
I’m new to this group as I recently learned via a CT (Sept 9th) that I may have MP. I’ve not yet had a biopsy so confirmation is still pending. We were going to perform a biopsy but the surgeon determined the location was too risky. He referred me for a second opinion but I have yet to schedule that appointment. Additionally, after consultation with my GP, we thought a watch and wait approach might be the best choice to see if my symptoms subside.
A little bio on me - I’m 56, Male with a history of Follicular Non-Hodgkin’s Lymphoma- Diagnosed in 2006 and in remission since 2007. I recently had my Gallbladder removed Sept -2018. Both may have played a role in the development and triggering of MP, purely a guess based on research.
My question for the group is, should I continue to watch and wait or is early diagnosis critical? I realize the MayoClinic is leading the charge with this disease and therefore pending symptoms and feedback I plan to schedule an appointment.
As for my status, I’ve noticed I’m very sensitive to stress i.e. stomach tightens when I feel a stress load, sensitive to certain foods red meat, chz, etc. so I've altered my diet, but other than that, my lower backache is the only consistent symptom I have and there I have arthritis so its somewhat expected.
I appreciate your thoughts and I pray for a cure to MP.
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1 ReactionHi David,
Welcome to the group! I'm not sure that you need to rush for the biopsy to be done. In your situation, considering your past health history, I would want a clear diagnosis. Are they treating you with medication? I am currently on Prednisone (5 mg), tamoxifen (20 mg) and azathioprine 200 mg. I hope this helps!
Hi Kim,
Thank you for the quick reply. No medication yet and again, thank you for the feedback.
No problem! I was diagnosed at 49 and after going through Prednisone treatment, I was in remission for two years! I almost forgot that I had MP. Anyway, after a very stressful time in my life, the disease reared it's ugly head and I have been battling to get back in remission for over two years now. I have good days and bad days. Acceptance was hard for me, but once I accepted that this is something I will probably always have, my mental state improved.
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1 ReactionHeading to my first appointment at Mayo GI tomorrow. Any words of advice? I'm nervous that this is going to be a wasted trip, that I will be told it's all in my head.
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1 ReactionA CT scan will alleviate that fear! Very good luck to you and please keep us updated!
I would like to join the support group please. I was recently diagnosed.
Welcome!
Welcome jr8865! It’s always good to have one more of us communicating! I am in Canada and diagnosed many years ago by CT. How are you managing?