Over recent years I have had numerous BCC's which have been treated in a variety of ways. I had my first melanoma in 2010 - excised successfully, with no further treatment or complications and no more melanomas - until 15th June, 2021. Which is when I saw a plastic surgeon in preparation for some more surgery of BCC's on my face. Whilst examining me, he noticed a spot which was suspicious - a possible Melanoma on my back - which was removed on 25th June and sent for a biopsy. At the same time the other Bcc's (in 4 different places) were excised. Hats off to the NHS for getting this done so quickly. Now the long wait to discover if the suspicions are born out by the testing. I'm down for a possible follow-up consultation in 4 weeks' time. Does it take that long to confirm a diagnosis? I think my nymph nodes are slightly swollen - but I could be wrong - and I've lost about 2Kgs in weight since. Any advice?
Hi Brian and a very warm welcome to the melanoma group
In my experience my biopsy results have always taken between 4-6 weeks to come back so having an appointment for 4 weeks time sounds about right.
Lymph nodes can swell for a number of reason including when they're fighting off infection but if you're worried you could always give your SCNS a call to talk it through with her. If you haven't been assigned one yet you could call the consultant's secretary and ask to be put through to whoever is the SCNS.
Let us know how you get on
x
Hello, Latchbrook. I had my results today from the consultant plastic surgeon. I don't have melanoma, but I have been diagnosed with Merkel-cell carcinoma - a rare and aggressive form of skin cancer - on my face. I can find little information about it, except that it seems to be more aggressive than the surgeon knew. So I am seeking reassurance and help from anyone who knows more about this and can advise me -please.
Hi Brian
That's great news that the lesion on your back didn't turn out to be melanoma but I'm sorry to read that what was thought to be a BCC on your face has turned out to be Merkel cell carcinoma (MCC). I don't have any personal experience with this type of cancer but I've found this information for you from Cancer Research UK.
I've also had a look in the skin cancer group and found a few people there who were diagnosed with MCC, so that would probably be a good group to join and post in. I also keep an eye on that group so will keep an eye out for you and tag people who might be able to help you if they don't see your post. Clicking on the link I've created will take you straight there where you can join and post in the same way as you did here.
Do you know what treatment you'll be having and when it will start?
x
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
© Macmillan Cancer Support 2024 © Macmillan Cancer Support, registered charity in England and Wales (261017), Scotland (SC039907) and the Isle of Man (604). Also operating in Northern Ireland. A company limited by guarantee, registered in England and Wales company number 2400969. Isle of Man company number 4694F. Registered office: 3rd Floor, Bronze Building, The Forge, 105 Sumner Street, London, SE1 9HZ. VAT no: 668265007