Squamous Cell Vulvar Cancer: Who out there has this cancer?

@bijou68 - I have 2 lesions again after laser ablation in Feb. and excision of a different spot, slightly deeper, in Apr.

2 Qs for now:
1 - I'm using Imiquimod on the 2 spots, but it sure seems it's not (& can't be, by nature) a very targeted application. PLUS, I'm to use the Clobetasol for the rest of this small "inner vulva" (my words) area. How does this all stay targeted when, basically, it is nor more than a 1-inch area? This discovery was just 10+ days ago, so I've just used the Imiquimod 4x (spsd to use it 3x/week for 2 months). Isn't it supposed to burn? I've not felt any burning yet; of course, that is 'nice', but does it mean it's not doing the job?
If this doesn't work, I have to have these 2 areas excised, and it will compromise my urethra opening, which will affect urine flow/direction. And, it will also be very painful until it heals, but I've endured that before: as long as it removes these things, it must be done.
2 - How do you work on 'lessening the intense scratching and burning'?

Thank you so much for any insights, experience, advice you can provide. I can ask (& have asked) my Dr and her nurse, but after a few Qs, I don't want to 'wear out my welcome' if you know what I mean.

Best...

@vickiehane - Oh, my thoughts are with you!

May I ask how it was discovered you have squamous cell vulvar cancer? (i.e., What were the signs, was there a precancerous condition first? Lichen sclerosus, or another pre-existing condition you/your Drs were watching/tracking?)

It sounds like you (& your Drs) are doing all that is needed to keep on top of this.

Appreciate any experience you can share. Hugs.

Hi Brandy: First: ask questions until you are satisfied. It is your right as a patient, and it is your body and you have medical assurance. Is the Dr. you are talking about an oncologist?
I think the Imiquimod will kick in. You only had a few doses so far and i think the effects are cumulative. I think 3 times a week is a good regimen for 2 months. It is what i did at the last manifestation a year ago. The first manifestations 3 years ago was really challenging because i was stold to take it every day and i was a mess with itching endlessly and burning endlessly which made my oncologist changed the protocol to 3 times a week but longer. Last year she gave me a medication to lessen the effects of Imiquimod. I can look at the name of it on my kaiser site. I don't know anything about Clobetasol. What is it for? I have a visual appointment with my gynecologist august 1. Of course, I am not looking forward to it. All i know is that my oncologist 3 years ago proposed an excision of my clitoris but found out Imiquimod was another option. After that with so far a total of 10 different spots in all areas of the vulva, she said that it would be too many spots to excise. So honestly i try to forget i have this strange condition but keep on top of the treatments, the check up appointments etc... If on August the gynecologist who caught all 10 spots, spots again some more manifestation then i will be at a loss. I am keeping you in my prayers and please stay in touch. Brigitte

I thought I had a yeast infection because I was experiencing itching. My doctor prescribed an anti fungal medicine and it didn't work. Went in for an appt 2 weeks later and my primary doctor examined me and told me he thought I had Lichen sclerosis, and that I had squamous cell cancer. He prescribed Clobestal a steroid cream and told me if it hadn't healed in 3 weeks go see my dermatologist. Saw my dermatologist and he did 2 needle biopsies and 2 skin scraping biopsies. The pathologist report came back with squamous cell cancer and he referred me to an Oncologist Gynecologist for a pap smear and to check for cancer inside the vigina. The pap smear came back clear.
I had no signs of anything on January 19th at my yearly physical. It happened very quickly and mine was very aggressive.
If you have surgery ask for a Sentinel Biopsy if you happen to have any tumors.
Best of luck to you!

My doctor would like to remove all of the lymph nodes in my groin area. My concern is if all lymphnodes have been removed there is a chance of Lymphedema. None were removed at the time of surgery because he didn't know I had a cancerous tumor until the pathologist report came back. The tumor was right in the middle 1 mm from my rectum so he is proposing both sides of lymph nodes be removed. There is a 33% Chance of Lympodema if he removes all the groin Lympnodes. The risks seems to high to me because Lymphedema can be very debilitating. Extreme pain, swelling of legs, not being able to walk, painful hot spots on skin. Not to mention you need to wear custom made heavy material compression socks 365 days a year that go from your ankles to the top of your legs. Oh forgot to mention not being able to feel the top of your thighs.
He has proposed removal of all Lympnodes and 2 rounds of radiation. Or radiation, 2 rounds and one round targeting the site of where the tumor was. Or 3rd option do nothing. What do you think?

So glad you had a pet scan BEFORE surgery! I had squamous cell cancer removed and multiple tumors removed. One tumor came back as cancerous and now we are trying to figure out what to do next. 1. Remove all lympnodes in groin area because the tumor was exactly in the middle, followed by 2 rounds of radiation. Risk factor here Lymphedema, which is painful and debilitating. 2. 2 rounds of radiation in the pelvic area and 1 round of radiation targeting the spot where the tumor was. 3. Do nothing now with a yearly follow up.
Sounds to me like you are on the right path and everything is being accessed before surgery! Good Luck!

Wow! That is amazing! So glad you were educated in what you were looking at. I was shocked the first time I looked after surgery. Was told that it would look very different, but it was very shocking!

Hi, Thanks for sharing your story. I have a question about Lymph nodes, did you have any removed?

@vickiehane, I hope @ljchicago will see your question about whether or not she had lymph nodes removed as well.

Vickie, have you decided which course of treatment to get?

Not yet. I have some testing coming up and hopefully I'll know more when I get the results.