I thought I would share my little experience about this.
I had a lump removed in July, a lump that I'd had for many years on my upper thigh and had been told was a benign cyst by my GP. I was told that it would need to be removed but there was no hurry as it was just a cyst. Because I'm scared of needles and hospitals I left it where it was. This was a big mistake!
At the beginning of this year, I kept experiencing pains in my leg around the lump, so I decided I needed to face my fear of needles and get it removed.
So I had it removed and I thought that was that. I saw the consultant and he said he'd only call me back if there was an issue, 7 weeks after the op in July I had a letter to go and see him again. Oh boy! I was told that the lump had been diagnosed as Dermatofibrosarcoma Protuberans, which is a low to intermediate malignant tumour, which is locall aggressive but very unlikely to spread beyond its current area.
I was advised that the suggested way of dealing with this type of tumour is to remove some more tissue from around the area to stop it from reoccurring. A week later I had a second op where the consultant removed a couple of centimeters from around the area down to the muscle layer. Ouch!
Three weeks after the 2nd op, I saw the consultant again. The tissue they removed indicated that there were some cancer cells in that tissue, so here I am facing a 3rd Operation. They are planning to take another couple of centimeters from the area and I will this time need a skin graft as the area removed will be too big to stitch together. My op is this coming week (wish me luck!).
I am scared as I really hate needles and hospitals but the thought of this tumour growing back because there's cancer cells sitting there waiting to grow fills me with more dread.
If anyone else has this type of tumour, I would dearly love to hear from you to share from your experience.
I am also here for anyone who is told they have this. Its supposed to be a rare cancer hence, I am here and will provide whatever support for those who have this. I will continue to post regarding my recovery so anyone who is goes through similar will have some form of reference as I have only found medical reference myself and would have appreciated a personal perspective.
Love and Light.
Rachel
x
Hi Sam,
Thank you for your message. I've been clear nearly 8 years now, it seems so long ago but not so long ago at the same time. There have been no signs of the cancer returning which I am very grateful for. I will look up the group you mention as I'd like to be able to offer hope to others with this rare cancer.
I'm truly glad you are fully recovered, long may it continue..
Rachel
Hi Steve,
Thank you for your comments, my original account has been deactivated and this recent account needed to be reactivated in order for me to reply. I still get the email notifications which are always a timely reminder of how long ago this was. I hope that those who do find and read my posts / blogs on this cancer find comfort in my words.
Blessings
Rachel
Hi Rachel,
I’ve just joined Macmillan after being diagnosed with dermatofibrosarcoma of the vulva, which they tell me is very rare. They’ve assured me after 3 operations and a skin graft that they have got rid of the cancer but I feel a total mess ‘down below’ and still feel sore as it’s such a delicate area. I thought I’d dealt with it all as it’s 11 months since my diagnosis but I think I’ve kept it all bottled up and it’s all coming out now. I keep crying at the slightest thing and I don’t think it’s helped as the other day my husband told me I hadn’t got proper cancer. He said he’s trying to help me as I’m very anxious but it’s left me feeling like I’ve made a big fuss over nothing.
Whatever cancer throws your way, we’re right there with you.
We’re here to provide physical, financial and emotional support.
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