There are some that have bad experiences with ANY procedure, so you will come across those who had one with the lip biopsy. Keep in mind that people don't go out of their way to post on a forum about good experiences, so I bet for every 1 bad experience there are hundreds that went fine...maybe even more.
Ask the doctor how much experience he/she has in doing these. I would stick with a large academic hospital as they would do more...also the pathologist reading it might have more experience, and this is just as important as the doctor doing the procedure. ENT's do them, so do some dermatologist (mine was done by a derm at Hopkins), and some oral surgeons. I don't know of many rheumys that do them, but that's not to say that some don't...I just don't think it's common. As for understanding the disease itself better, the rheumatologist.
And don't forget to request a copy of the pathologist report.
I have not heard of Sarcoidosis and/or amyloid polyneuropathy being diagnosed from a lip biopsy. Must be something new. Medscape is a reliable source, I'd be curious to know
how or whatthey look at in this case that's different from diagnosing Sjogren's...which is looking (and counting) lymphocytic infiltrates.
Quote:
Originally Posted by Idiopathic PN
Hi en bloc,
I will discuss about Sjorgren's with the rheumatologist tomorrow morning...
I have been reading about experiences of those who had lip biopsy and it seems a painful experience, though, you mentioned that your experience was not bad. Who normally perform the lip biopsy, ENT or the rheumatologist? Who has the better understanding of the disease?
I read today on one article that lip biopsy confirms not only Sjorgren's but may also confirm sarcoidosis and amyloid polyneuropathy. How true is this? This has never been mentioned in our forum (or maybe I have not just read it).
http://emedicine.medscape.com/article/1520068-overview
Thank you so much, en bloc.
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