Hi,despite my user name,I'm a female,I'm really worried,always at colposcopy clinic,as cells never right,I mentioned yesterday I had lupus,she said that interesting as it can destroy the cells,has anyone had this,iv hardly slept all night ,should I mention this to reumy.
Problems with smear results: Hi,despite my user... - LUPUS UK
Problems with smear results
Hi Jeff! I've also had to repeat my colposcopy some times because the results were never right. But after a full observation, i was ok.
I think you should mention that to your rheumy just in case.
Stay positive!
c
Hi
I too have had a few positive smears and colonscopy clinic biopsies for them to be negative. Prof Cruz at the Lupus Unit wrote a paper a few years ago about it apparently . My gynae at the time researched it and I now have been discharged from colonoscopy and just have the usual smear tests. Good Luck
Mollie
Hi all, just thought you might be interested in a study conducted by Dr Michelle McHenry into cervical smear tests results and lupus sufferers. A link to it can be found on 'Lupussupportgroupni.co.uk ' Under scientific research. I believe you would all find it very interesting and beneficial.
Great link, Bronagh...I followed your instructions and got taken to the Wiley online Library synopsis of: P-14 CERVICAL DYSPLASIA AND RISK FACTORS IN NORTHERN IRELAND SLE PATIENTS
ESPECIALLY interesting to me because I have annual colposcopy at my local NHS gyn clinic due to the combination of 2 factors: my DES daughter birth defects including a history of pre menopausal suspect smears (vaginal adnenosis) + my infant onset SLE. Am now 61
THANKS
Hi, I've had 4 colonoscopies over the past 6 years as I was found to have developed Ulcerative Colitis 4 years ago. It seems connected with the SLE I was diagnosed with last year. There is definitely a correlation in both conditions as they are both auto-immune problems and the mechanisms that cause them are similar!
Well I am stunned !!!! I have had 2 colposcopies and biopsies in the last 6 months. My second one the doctor told me the cells were showing up much worse and to expect treatment this time, but my results letter told me to go back in year. I had no idea at all it could be lupus related!