LCIS: What treatment(s) did you choose?
Hello, I have been given the diagnosis of LCIS a few months ago, not invasive yet. After reading posts about invasive lobular carcinoma and that it is more difficult to treat than invasive duct carcinoma, I am now seriously considering pushing for a double mastectomy rather than taking tamoxifen, which will just lower the risk by 50%. Is there any LCIS patient whose doctor advise against this aggressive route? My doc isn’t totally against it given my age of 52. Any thoughts?
Interested in more discussions like this? Go to the Breast Cancer Support Group.
Lobular Carcinoma in Situ
Would anyone discuss this diagnosis and the options you chose based on post menopausal woman?
@southgawalker, to help you connect with fellow members who have face LCIS treatment choices like @lisakinpa @michelleah @delormv @mayo101 @bfly1 @kel6022 @bgs1961 @slmremy, I moved your message to this existing discussion:
- LCIS: What treatment(s) did you choose? https://connect.mayoclinic.org/discussion/lcis-and-double-mastectomy/
You may also be interested in this related discussion:
- LCIS: should I take Tamoxifen? https://connect.mayoclinic.org/discussion/lcis-should-i-take-tamoxifen/
What treatment are you considering?
Thanks. Just processing now.
Do you mind sharing where you found your dr that deals only with breasts?
In 2013 I had bil Mx based in large part on decisions I made after MRI showed many more tumors. My bx showed ILC
I did not take tamoxifen because of the side effects and the stats did not show >17%
Hello, May I ask what follow up screenings do you do after bilateral mastectomy. Since mammograms won’t be possible, how do you screen for breast cancer going forward because mastectomy doesn’t completely remove all the breast tissue.
My initial pathology report indicated that I had LCIS (which unlike DCIS, is not cancer). I’m told LCIS cannot be see on any imaging but rather usually found by chance through a biopsy or surgery and subsequently through a pathology report.
I was diagnosed with stage 1 invasive lobular cancer along with LCIS. My breast surgeon wasn’t concerned with the LCIS.
I had a lumpectomy and almost four years later, doing very well. I’m now 64.
Hope this might help. ♥️
I was diagnosed with LCIS and hyperplasia 4 years ago. It was found incidentally with a pet scan and missed by mammogram and u/s. I know it's harmless although I did have a lumpectomy and I go for annual mammogram and ultrasound. There is a lump that they biopsied 2 years ago and it's harmless scar tissue. I couldn't feel the lump personally.
My question is if LCIS doesn't show up why do we do follow ups? Also I have lost Approximately 7 kg in last 6 months for no reason. With that I can now see the lump that was biopsied and can also feel a hard lump under the nipple.
Am I right to assume it's more scar tissue as you wouldn't feel LCIS?
Also did anyone grow a hard lump after lumpectomy?
My understanding is that LCIS is only diagnosed through a biopsy. You can’t detect it on your own.
That's what I thought. It must be scar tissue from the lumpectomy. Thank you