Organ pain from auto immune?

Posted by nanke99 @nanke99, Oct 9, 2016

Ok so I've been having upper right quadrant abdomen pain for 1 1/2 years now! I've had a sonogram, an upper GI series and a HIDA scan with contrast- showed nothing. It is definitely in the liver/kidney area, and clearly feels like kidney pain (back) often. My blood work is otherwise normal, excepting the SED and CRP's which have gone down slightly since i have been medicated.
So can Fibro cause organ pain???? Inflammation? My Rheum doesn't seem to think so but I have seen that online. My Gastro doc isn't sure either.
Anyone heard of such a thing?

Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.

I have Sjogrens Syndrom and i never heard of this causing organ pain. I also have upper right quadrant pain. My gastro dr told me its due to my cryptogenic cirrhosis and my GERD. If you find out anything new, please keep us informed.

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What does cryptogenic mean? Also, do you have elevated ammonia levels. Mine are only slightly elevated but I am concerned. Thank you for your help.

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Hey mollyb 1968
Cryptogenic means they are unsure what exactly caused my cirrhosis. I have never been told about my ammonia levels being elevated but my LFTs are always elevated and my platelettes(spelling) have been running low. I hope this explained better.

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how does a sjogren's flare manifest other than tiredness and slight fever?

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@jeanniene

how does a sjogren's flare manifest other than tiredness and slight fever?

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Good morning @jeanniene and welcome to Mayo Connect. We’re a group of patients, patient’s families and caregivers. We try to help each other with information, resources, and tips from our own experiences. I found this discussion that has already been started. You should be able to connect with other members through the discussion.
https://connect.mayoclinic.org/discussion/sjogrens/

Is this your first flare of sjogrens? What has your doctor suggested for treatment?

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@becsbuddy

Good morning @jeanniene and welcome to Mayo Connect. We’re a group of patients, patient’s families and caregivers. We try to help each other with information, resources, and tips from our own experiences. I found this discussion that has already been started. You should be able to connect with other members through the discussion.
https://connect.mayoclinic.org/discussion/sjogrens/

Is this your first flare of sjogrens? What has your doctor suggested for treatment?

Jump to this post

Thank you, Becky, for your reply to my question. I have had Sjogren's diagnosis since the 1980's. Plaquenil and Tylenol are all that I use. It is nice to connect with someone who knows that Sjogren's involves more than just dry eyes. Thanks for caring. Jeanniene

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@jeanniene

how does a sjogren's flare manifest other than tiredness and slight fever?

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Hello @jeanniene. I have “extraglandular” Sjogren’s which erupted dramatically a few months after my liver transplant (which resulted from another autoimmune disease), a year ago. I have peripheral neuropathy in all extremities (numbness, tingling, and pain), tremors, and muscle and joint pain. Plus, oral thrush, sore throat, eye issues.

Sjogren’s Advocate is a good website to learn more about the systemic nature of Sjogren’s that often medical providers know little about.

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