Sjogren's syndrome and sarcoidosis may co-exist. They may also mimic each other. The basis of this relationship is unclear. Sarcoidosis is not ordinarily characterized as an autoimmune disease. Non-caseating granulomas suggest sarcoidosis, but are not diagnostic. They can also be seen in other diseases, including tuberculosis.
Your history suggests that you may have some type of immunodeficiency problem, such as common variable immunodeficiency. You should have a thorough evaluation of your immune system. Your initial symptoms 2
i don't know what Sjogen's is yet ( going to look it up) but I have Sarcoidosis, so I can only confirm some of your dilemma's the eyesight being one - mine is getting worse since diagnosis. I was diagnosed with pulmonary sarc 3 years ago, after needle biopsy. My X ray's since then and up to six months ago have been clear, my ace levels have been normal. My symptoms however don't resemble the same clarity. I too had problems with my teeth, one root canal that turned into an extraction that wouldn't be removed by a normal dentist ( had to be surgically extracted) and recently a tooth literally crumbling away - there is a connection with too much Vit D and Sarc dont' know if this is related. i have also had recent problems with an irregular heart beat again the docs didn't relate this to sarc but after searching the web I have found this to be related. I feel I am having to tell the docs here about sarcoid rather than them telling me, this is frustrating but the effects of it seem to be different in a lot of cases and it is a systematic disorder so it can affect many organs including the eyes, lungs, heart and in some cases the kidney, I am on a waiting list to see a sarc specialist to confirm whether I have had this condition longer than assumed by my doctors, I have the cough also and get it frequently when the condition seems to flare up. I'm learning to live with it but I hope someday they can find what the hell is causing this and hopefully a cure. I really don't know if Sarcoid is self limiting, I think the jury is still out on that one, it is for some I know, but others do get flare ups of their symptoms at certain points in their life. Some say that if you have the nodes on your legs - which I do also ( just bruise marks now) - it will burn itself out - so heres hoping. I hope you get better and you get some relief from this distressing disorder which I think doctors in the main seem not to take as seriously as they should.
Regards
Jane