Hi! Curious what you have found out since. I had a double biopsy (two lumps found originally) - both came back negative for BC; but before those results came back, I had an MRI, which should nothing but inflammation (which is what the mammogram and biopsy indicated). The pathologist in my hometown did NOT see the granulomatous cells; it wasn't until I went to a specialist in a larger city were the cells seen and I was properly diagnosed. I understand the stressful month...We were going thru this at the same time, apparently...Found lumps Dec 24, 2014; diagnosed end of February. January totally and completely sucked.
Go see a specialist. Get a referral to someone who knows about this. BC doesn't typically come on that fast (i know IBC does, but it has certain characteristics that GM doesn't. I was convinced I had IBC too, but I don't), and most cancers do not hurt like GM does.
My biopsy sites became the first extraction points for the puss GM exudes. Just fyi. Since then one site has been created and opened all on its own, and i have another one on the way...How are you?? :)
Hi - I am JoJo45. I am in Toronto. Doctors at Sunnybrook and Women's College Breast Centre (where I was treated) do know about IGM. Try there if you are still suffering. All the best.