Erosive oral lichen planus
Hello
I'm new to the group. I was diagnosed with erosive lichen planus 4 years ago and it has been a nightmare since. Mine has progressed from my mouth to my esophagus, nose and eyes. I've seen so many doctors @ Vanderbilt and St Thomas Hospital who have no idea how to treat my illness. I've. Even advised to go to the Mayo Clinic in Rochester but I'm really not sure what doctor or doctors have experience with treating this disease. Any help would be appreciated
Thanks
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@bebold Thanks for the info, I did not get thre trochee because it was made with citric acid I stuck with the lower dose capsules that have the naltrexone and the microcrystalene cellulose and that is from a plant source. But I get your point and since this started I dbl check everything I eat. Happily my tummy issues are resolving on the lower dose so I am pretty happy with that! I really hope you find some comfort after your extractions. I had read that metal fillings can cause issues. I appreciate all your insight. it has been helpful. Thanks!
@kmm29 Good Morning! I have been treated for about 8 years I think. At the time I was diagnosed I had erosive lichen planus. My gums were so very red-I was under a great deal of stress at work and I think that was the reason my immune system went wonky!! Anyway, my dentist was on top of things-sent me to a specialist who is a dermatologist as well as a dentist and also to an another oral specialist. The only way to diagnosis lichen planus is with biopsy. I use Clobetasol gel on my gums 3x week, a tacrolimus solution swish also 3x week. For the most part my symptoms have been kept under control but stress and alcohol seem to get symptoms beginning again. It’s hard to restrict things I enjoy so I really try moderation. I have to say that I am “lucky” that my symptoms are generally pain free even though there are blisters etc.
I wish you the best and hope that your dr is helpful! What frightens me is that lichen planus can lead to oral cancer.