Hi, my name is Michelle. I was first diagnosed with melanoma in January 1999, center of my back, 1.28 Breslow, Clark III: treated with WLE, lymphoscintigraphy and SNB to both axilla – no regional/distant mets found, NED since then (other than about a dozen severely atypical moles that have been removed and treated with WLEs). So almost 20 years without a serious issue, an excellent result!
Yesterday I saw the derm and had a super fast-growing & changing mole (totally unlike anything I’d had before) removed from the back side of my left shoulder as suspicious for amelanotic nodular melanoma (eeeeeek!!!), plus a smaller satellite bump removed as suspicious for superficial spreading melanoma (which is what I had previously). Not a great morning, and I am now in the ‘biting my nails waiting for the pathology report’ phase. 😯
I’m also trying to come up to speed a little on the world of melanoma treatment in case the either biopsy actually does come back melanoma — boy have things changed alot since 1999!
Questions:
1. I asked my derm about genetic testing of the biopsies (if melanoma). I was told that his pathology lab does not do genetic testing because it generates too many false positives/negatives. I just don’t know enough about this issue — is this something I should only worry about if I get staged with more advanced disease later, or do I need to be aggressive about that sort of information right out of the gate with these biopsies?
2. Since I’ve already had SNB to both axilla, can I actually have another SNB to the left armpit should that be necessary?
3. Anything else I need to do/ask about right up front?
Thank you for any information you care to share!
Best to all,
Michelle