Hi guys,
I know I’ve been posting pretty frequently but I was wondering if anyone has any insights on potentially being misdiagnosed with sjogrens.
Ive had dry eye for a few years and I eventually got a lip biopsy which was lightly positive (1.17 foci score. 1 is considered positive).
Since then I have assumed I have sjogrens. I have been to two rheumatologists to attempt to confirm the diagnosis. The first one is convinced I don’t have it and ignored the dry eye complaint. The second one I went to was impressively thorough. All of my blood work was negative( All of it. Not just SSA and SSB but ANA and sed rates etc). There is no indication of any heightened immune activity of any sort in my blood. So she ordered an MRI to see if there was any parotid gland swelling or lymphocytic infiltration. There was none. My lacrimal glands also apparently looked normal.
To confuse things further, I went to a different ophthalmologist who did a Schirmers test ( my primary doctor only uses tear osmolarity ). My Schirmers was 30 mm in both eyes. However I have 4 punctual plugs which I thought would confuse the results. She said that it can somewhat but that even with plugs sjogrens patients usually have much lower scores.
My aqueous tear production is definitely less than it used to be, I’'m always uncomfortable and my biopsy was positive. I have always had mild dry mouth even before the eye issues, but I’'ve asked dentists who have told me my salivary production is normal, and I haven't had any dental issues. Do I have Sjogrens? My rheumatologist suggested I go to the SS center at Johns Hopkins to get a definitive diagnosis.
Today I am going to get the Sjo test even though my rheum recommended against it because it hasn’t really been accepted by the scientific community. I’m worried because it’s specificity is only around 80%. Which means 20% of people without sjogrens test positive with their panel but more data points will be helpful.
Is anyone else in a similar situation?
I know I’ve been posting pretty frequently but I was wondering if anyone has any insights on potentially being misdiagnosed with sjogrens.
Ive had dry eye for a few years and I eventually got a lip biopsy which was lightly positive (1.17 foci score. 1 is considered positive).
Since then I have assumed I have sjogrens. I have been to two rheumatologists to attempt to confirm the diagnosis. The first one is convinced I don’t have it and ignored the dry eye complaint. The second one I went to was impressively thorough. All of my blood work was negative( All of it. Not just SSA and SSB but ANA and sed rates etc). There is no indication of any heightened immune activity of any sort in my blood. So she ordered an MRI to see if there was any parotid gland swelling or lymphocytic infiltration. There was none. My lacrimal glands also apparently looked normal.
To confuse things further, I went to a different ophthalmologist who did a Schirmers test ( my primary doctor only uses tear osmolarity ). My Schirmers was 30 mm in both eyes. However I have 4 punctual plugs which I thought would confuse the results. She said that it can somewhat but that even with plugs sjogrens patients usually have much lower scores.
My aqueous tear production is definitely less than it used to be, I’'m always uncomfortable and my biopsy was positive. I have always had mild dry mouth even before the eye issues, but I’'ve asked dentists who have told me my salivary production is normal, and I haven't had any dental issues. Do I have Sjogrens? My rheumatologist suggested I go to the SS center at Johns Hopkins to get a definitive diagnosis.
Today I am going to get the Sjo test even though my rheum recommended against it because it hasn’t really been accepted by the scientific community. I’m worried because it’s specificity is only around 80%. Which means 20% of people without sjogrens test positive with their panel but more data points will be helpful.
Is anyone else in a similar situation?
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