LCIS/ALH
I was diagnosed with LCIS last December. Hade two biospies, one sterotactic and the one large core from breast surgeon.. Just recently had breast MRI's which showed residual LCIS from same site,, Guess the other surgeon did not get it all as this last time was an excision biospy.. Pathology also show ALH in this most recent one.. I am an anxious person and I know the LCIS is controversial to say the least. I am thinking about a bi-lateral masectomy just for the fact that I don't think can emotionally handle this every time it comes up, This was my 5th biospy in 3 years on the same breast.. Do you wait around and wait till you get it? Worry about it or just get the masectomy and get it off you plate forever. I know many people think it is overly agressive but different people can handle different things. I have been reading stories from alot of you ladies and would appreciate your imput, thoughts on this.. I know insurance will not pay for it and fortunately I can.. Help me with this.. My significant other (female) really wants me to have the bi lateral,, she is a retired nurse and she asked me what I would tell here if the situation was switched,, I would tell her to do it.. Any comments are welcome..
Comments
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Are you sure insurance won't pay for it? I had two biopsies in two years for discharge, the first missed the problem, so two years down the road I had another. It showed ALH and ADH. I figured they could take my breast a piece at a time or I could have them removed. There was no doubt I wanted them off. I never looked back. Insurance paid for it and recon.
I don't think it is overly agressive. One of the main reasons I wanted the BMX besides cancer prevention, was to stop the high risk screening.
Also, what do you know about your breast density?
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Very dense
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I am taking tamoxifin now and really don't want to so that!!
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Hi Shelton,
I didn't do prophylactic mx or any mx, so I don't speak from that angle. I did also have multiple surgical biopsies over the years (including ADH and ALH--prior to recent DCIS--all in same breast). Anyway, since your diagnosis is abnormalities in lobular tissue (ALH and LCIS), it makes sense to do bilateral pmx, because those diagnoses put both breasts at risk. So, either don't do it or do both breasts. My suggestion, anyway. I have resigned myself to more years of surveillance. We'll see how that goes. I'm used to it, but with the DCIS diagnosis it's going to be a bit more anxiety provoking, at least initially--and I won't be getting MRI's, only mammo and ultrasound (my breast surgeon's choice). Next week is first full follow-up post treatment (although I did have an all clear MRI in March). Best of luck!
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I knew I had dense breasts, but was not aware of the degree of density. Apparently they were extremely dense, thus one of the reason the MRI did not pick up the IDC on the screening three months earlier, or two years earlier.
I admit it, I am completely biased. The PBM was tough. The breast cancer DX was tougher.
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I had same as you.
My insurance paid for bilateral mx, I did it and never looked back. Very happy this way. My mom died from it and I didn't want to wait around for it to come.
Good luck with your choice, I know it's hard. You will be ok.
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Shelton,
I was diagnosed a year ago with LCIS.....I started a thread under the LCIS topic called "Surveillance for me? Yeah, Right, Sure......"
I chose the PBMX.....nipple sparing, though I lost my right one - areolas are intact. I also chose to have profile shaped silicone implants placed after tissue expansion (TEs). Sientra and Allergan have profile implants on the market. At the time of my exchange, Sientra was it.
LCIS has a classification in NCCN guidelines. If you desire risk reduction strategies, a preventative (prophylactic) mastectomy is one recommendation, and insurance does pay for it, and the reconstruction to achieve anatomical "normalcy" if you want it.
The nice thing is you don't have to rush and can research your surgeons and choose your hospital, etc. depending on your insurance.
I work in health care and chose to have my procedure here where I know the players. The only thing I paid for was my reconstructive surgeon's time. The docs on my plan offered smooth round saline implants only and wouldn't even discuss fat grafting (I was jumping the gun they said - but I ended up needing it!) I had a greater trust level with the one doc who didn't take my insurance......but he did work with me regarding his fees.
If you have any questions, message me!
Best of luck to you!
Audrey
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Thanks for the comments!! I believe in my heart that the bi lateral is best for me but I want to wait until October,, I am a high level amateur competitive golfer and have a big summer ahead, with several big events. So, waiting till October would be ok, right??
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I had LCIS and chose a PBMX immediately. No reconstruction. I have an anxiety disorder and couldn't see dealing with the constant worry, and regular MRIs. I am very glad I did this. The mastectomy wasn't really that bad at all . No regrets. My insurance did pay. Best of luck in your decision! And yes, waiting would be ok, as long as it's only LCIS and nothing more. Nan
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Sheltion -
I found out about my LCIS in early June. October 1 was my surgery date. In between I did have an MRI and a core biopsy of a suspicious area - if it had been cancer I would have delayed my reconstruction until after treatment.
With LCIS there's no great rush. Have a fabulous summer and do your surgeon research between tournaments!
Audrey
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I am in a similar situation except I had ILC. My 2 biopsies showed LIN, ALH and more calcifications. One thing I learned from a nurse that because I have a job where I use my arms daily lifting 50#, they did not recommend the saline implants because it would be hard to work during the months of stretching the skin. Am waiting to see the surgeon... My oncologist said there wasn't a rush to have the surgery, so am waiting until after my last big job. Perhaps November for me. The stress is something I don't want to deal with.
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