Tissue Expanders After Radiation
Age: 35
Stage 3/IDC
I just under went a bilateral mastectomy 1.5 weeks ago. I requested delayed immediate reconstruction with TE since I was undergoing radiation after surgery. I could tell PS was not pleased with my choice and said he would "try" to accommodate my decision. He did not want to take the chance of delaying my radiation due to a failed reconstruction attempt. He advised that if he felt the tissue was not healthy enough for a TE after removal of my breast he would not proceed with the reconstruction. I felt right then and there that my decision would not be carried out. I woke up after surgery to find out that TE were not installed b/c the PS felt that the skin would not survive due to the unexpected excess amount of tissue the surgeon had to remove during the MX (I don't get that because I thought they removed all of the tissue anyway). So I am left with excess skin and no expanders going into radiation. I am truly devastated because I know the unlikelihood of my skin expanding after radiation, and I do not want to under go a FLAP procedure whatsoever.
Has anyone had TE after radiation? What was your outcome?
Comments
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Dear Yvettelk,
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I had a bmx in July, 2014, as my initial lumpectomy in January, 2014, did not have clear margins & they wanted me to have chemo before another surgery...so that leads me to radiation.
At the time of my bmx, I did not have TEs placed for 2 reasons. 1: my PS said he did not want to place them prior to my radiation because of concerns with skin and tissue breakdown. 2: I had not completely decided what I wanted to do...recon, no recon, lat-flap, etc.
Prior to starting radiation a month later, I met with my PS again. I told him I wanted to try recon with no flaps or other moving of muscles to support the implant. He told he would see me 6 to 9 months after radiation, and we could talk again. I finished radiation October 1. I went and saw him in March, 2015. He agreed my tissue and skin had recovered enough to try placing the expander. I had my surgery April 7. We agreed my fills would be low and slow. Started with 30 ml per week. It worked for a bit, but then was too painful on my radiated side, so we reduced to 15 ml per week. I was able to get to 450 ml each side. Now I am waiting until December, and I will have my exchange.
It wasn't easy, but I am happy with my choices and my surgeon. He was clear with me at the outset it may fail, but we agreed to work together to try to make it work.
Good luck.
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That gives me encouragement! Thank you for your post.
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