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

God bless you! I was diagnosed with vulva cancer about 2-3 years ago. Thankfully it was caught in time. I went through the surgery with flying colors by a gynecological oncologist in my state. The surgery was radical, I had seven lymph nodes removed, all of which were negative for malignancy. I did not require any chemo or radiation. I have been cancer free since that time and am eternally grateful to my fantastic surgeon!!!!

Just got the pathology report (at my urging after 11 days): it is invasive squamous cell carcinoma, CD31 revealed no lymphovascular invasion. I think this was a surprise to everyone but me. As I always said, something that hurt that much HAD to be something, especially since the pain ended the day it was removed. Not clear from the report whether the margins are clear. Meet with surgeon in about a week. Well at least I know. I'm 73 and this happened fast. Was symptomatic from beginning of March on.

God bless you! I was diagnosed with vulva cancer about 2-3 years ago. Thankfully it was caught in time. I went through the surgery with flying colors by a gynecological oncologist in my state. The surgery was radical, I had seven lymph nodes removed, all of which were negative for malignancy. I did not require any chemo or radiation. I have been cancer free since that time and am eternally grateful to my fantastic surgeon!!!!

I completed 6 weeks of chemo and radiation in March for Vulvar cancer. I seem to have 2 new "lumps" down there where my lymph nodes are. Is this normal?

@bobette1 Oh, that’s over a month away. I wouldn’t want to wait that long to ask about something that worries me. Did you send a message yet via your patient portal? Perhaps you can make an appointment before 6/27?

Next appointment until 6/27/23. Thank you for your response.

They are free to reach out to me. Sadly, not new to it, but the first one was literally "scarring" both physically and mentally, and as problems persist, it would be nice to "speak" to people. I can't find a local "in person" group. Even mastectomies have become openly spoken about, but I feel like women's genital areas are off-limits for any kind of talk. We even talked testicular cancer when it was Lance Armstrong! Why did I not even know I HAD a vulva, considering I had dealt with endometriosis, nerve pain in utero, 2 vulvectomies, 3 laps for cervix, partial ovarian removal, etc.??? You'd think I'd be an expert. I had to read up on the topic! But nothing prepared me for being told it was no big deal, when they can only see the surface. They basically fully diagnose/remove any cancer at the moment of surgery, so they can only guess how "bad" until they actually get you under...then you have no say. I felt mutilated after my first. They said it was necessary. The second was much less traumatic and hopeful for me in the future. I was already told at my follow up today that there is new growth, but mild, so it's already coming back! But they don't touch at VIN 1, so Im basically waiting for it to grow until they have to remove again. At my rate, probably early 2023. On top of that, I hit menopause pre-50 and have some spotted bleeding 1+ after, so multiple biopsies on the uterus today. One week to worry about that one. Prayers it's no big deal. Bobette, boxermomma and wheaton, reach out if you want. - Undesirable nearly 50 singleton mom of 3 female teens here in flyover country feeling all alone in this. Seriously could use some sisterhood here.