DCIS and Mastectomy?
Comments
-
You will worry, and it's totally normal. But give yourself breaks from it to be with friends, get sweaty, enjoy medicinal doses of art, have a wonderful meal. In other words, live! When you are recovering from your surgery, you will be glad you enjoyed your summer and got lots done. I'm glad I had been working out & doing lots of core exercises before I was diagnosed -it has really helped with getting out of bed lately!
-
LAstar excellent advice! I had just started doing Jenny Craig when all of this came about, so having a good meal has not really been on the radar, but I have been giving myself a break here and there. Thanks so much, you are an inspiration.
-
I was very stressed this past couple of weeks as I was waiting for biopsy report, it finally came in on Friday and all was good.
so I celebrated with a dinner of shrimp and scallops..and a glass of wine.
yumm and along with a bunch of phone calls to pals, felt better fast! I think we have to find ways to treat ourselfs well and agree and applaud all ideas, medicinal doses of art sound good to me....maybe this weekend
-
Positiveenergy - Thanks for asking how I'm doing. I went to my PS today for a follow-up and he was very pleased with the FG results. He wasn't even pushing for a second surgery (at least not yet). I could use a tiny bit more FG on my right (cancer) side, but push up bras do hide the small step-off for the most part. The step-off was much more noticeable and embarassing before the FG. So, I am now going to force myself to forget about my BC and surgeries for just a moment.

In regards to your 6 weeks of waiting, I agree with LAstar that it will be tough, but it's not life-threatening. If it makes you feel better, my DCIS has hiding for at least 6 months before I had my BMX! My history went like this:
January '11 - discovered lump and had inconclusive mammogram and ultrasound
February '11 - had inconclusive MRI
March '11 - had one benign biopsy and one ADH biopsy
April 18 '11 - had an excisional biopsy that showed DCIS - a full 2cm of it hiding under the ADH tissue.
May '11 - spent all month in excruciating deliberations about what course of action I'd take - either lump/rads/tamox, UMX or BMX.
June 14 '11 - BMX Day
During those 6 months, I was stressing, losing hair from stress, and generally freaking out. But, if it helps you at all, that time period now seems like it was so long ago, and I've made so much peace with my decision since then. It is NOT easy, it is damn hard, but once you make your decision I'm sure you'll feel good about it!
I also hear you when it comes to worrrying about dying on the operating table. But if you have experienced surgeons at a great surgery center, you have to remind yourself that they do this all the time and they know what they're doing. I needed to remind myself of this same thing.

Meditation and psychotherapy are wonderful and help so much during this stressful time. And just being on here and knowing that others have "been there" helped me a great deal.
Good luck with your waiting period.
-
Great news proudtospin! Congrats on the all clear!
-
Thanks Shayne, I still worry and wonder if this is just a delay and that next mamo will show same junk and I end up in a round about thing of another biopsy. I have come to believe that that is why some of us do the mastectomies
guess I need to take time to understand and will be talking to my onco on my upcoming visit
-
Hopefulfuture: This is all very helpful, sometimes I feel like I'm overreacting. Every time I contact my Oncology Nurse, I say it's me the pain and she says you're not a pain and for some reason I just don't believe her. But, now, with some back up from you, I do believe her. This is terrible and stressful. I have an appointment with a psychotherapist tomorrow, so I am feeling more peaceful about the wait RIGHT NOW, until someone asks me again or it pops into my head.
But for RIGHT NOW, having a good day, at work and grateful they are so supportive. I love that you are going to forget about BS for a bit and let yourself live FREE for a while. I was just talking to my sister about how I can't wait and hope that this experience encourages me to LIVE a happy, full, healthy life when I get on the other side. Love To You, Take Care of You and talk soon. Brenda -
Good luck positivenergy -- and don't forget to pop back in and let us know how you are doing. Good news? There is a great forum for women waiting for surgery, right here on BCO ;-).
-
After everything I have read on these boards and going through 2 excisions before the UMX, if there were any chance of anything in the native breast, I wouldn't hesitate to have a MX on that side. I cannot believe how much is missed in mammos, ultra sounds and MRIs. It is kind of scary.
-
Thank you, I will. Is the forum called Women Waiting for Surgery?
-
Mooleen...ditto....I had a mammo 6 months prior that showed nothing, not even the original lump. And even the multiple MRI's still missed some areas that the MD found when he operated. By having both done, if all is clear and nodes are clear, I am done...no chemo, rads or hormones...or further mammograms! And a lot less worry. I know it is huge surgery and hoping on the other side I will be able to say I made the right choice!
Kathy....7 days and counting
-
I am about to have my double mastectomy (one breast as preventative) on September 6th. I still have to do tamoxifen tho and IM not happy about it. But I have DCIS and dont want to chance getting back and needing chemo! How are you feeling since your surgery?
-
I got diagnosed in June and I have my surgery at PRMA coming up on 8/1/12. I am having a double mastectomy, but that said, even with DCIS, there is no guarantee with cancer...some who have this surgery will find cancer in the future. It just raises our odds not to get cancer again. After my experience with the so called benign biopsy and clear MRI, I say get a LUMPECTOMY NOW. They just cannot see stuff until they have a bigger piece of you. If I had said no, I would be facing a much worse trip than I am now...as it is, I had ITC in my lymph nodes and no one knows why YET. I can't wait to get these boobs off and remade...
Lisa
-
ditto Mooleen! After two biopsy's, 4 mammo's, and one MRI, my final pathology report showed the others missed LCIS, DCIS and some pre LCIS and pre DCIS. and the "highly suspicious mass" behind my DCIS that showed up in the MRI was not there in the final path report.
-
Just goes to show you this is not a perfect science. I had a lumpectomy 5 years ago in the side and area I know have DCIS, did they miss it? Perhaps...
-
Lisa, what is ITC?
-
They might have missed it but I doubt it. It could have been just a few cells then and undetectable.
But you still had the same tissue that necessitated the first lumpectomy. I think you have done the right thing . It is what I would do with a recurrence.
-
ITC = isolated tumor cells
-
Lannie, who told you that you will need to take Tamoxifen after a bilateral mastectomy for DCIS? Was it your surgeon or have you spoken to an oncologist?
Tamoxifen usually is not recommended after a BMX for DCIS (or any other pre-invasive condition or pre-cancerous condition). This is because the risk of a recurrence or new BC after a bilateral MX for DCIS usually is only about 1% - 2% (assuming adequate surgical margins). It's true that Tamoxifen can cut this risk by about 45% - but with such a low risk to being with, the benefit from Tamoxifen is at most 1% (a 50% reduction of a 2% risk). Overall Tamoxifen is a very safe drug but like all drugs it comes with the risk of side effects. Most of the side effects from Tamoxifen affect quality of life and do not present serious health risks however there are a number of small but very serious possible health-related side effects. Depending on one's age and overall health, the risk of serious side effects from Tamoxifen can range from about 1% to about 3%.
What this means is that the risk of serious side effects from Tamoxifen, even though very low, can range fom 1% - 3%, whereas the benefit from Tamoxifen in terms of the reduction in BC risk is only about 1%. So by taking Tamoxifen you may be putting yourself at a greater overall health risk. This is why standard of care guidelines do not recommend Tamox. for those who've had a BMX for DCIS. So please discuss this with an oncologist before you make the decision to start Tamoxifen.
Obviously for those who have a lumpectomy and have a greater recurrence and/or new BC risk, or for those who have invasive cancer and have a risk of mets, the benefit from Tamoxifen in terms of risk reduction is much greater. For example, if your recurrence risk after a lumpectomy is 10%, Tamox. can cut this risk to 5.5%. This benefit from Tamoxifen is greater than the risks you'd expose yourself to by taking Tamoxifen. This is why Tamoxifen is recommended to women with these different diagnoses. The benefit vs. risk equation is completely different than it is for someone who's had a BMX for DCIS.
Greenmonkey, "Isolated tumor cells (ITC) are defined as single tumor cells or small cell clusters not greater than 0.2 mm, usually detected only by immunohistochemical (IHC) or molecular methods, but which may be verified on H&E stains. ITCs do not usually show evidence of malignant activity (eg, proliferation or stromal reaction)." ITC are classifed as pN0, i.e. those who have ITC are considered to be node negative. Usually if someone with DCIS is found to have ITC, it is assumed that the cancer cells were moved into the nodes by a surgical instrument. http://www.adjuvantonline.com/breasthelp0306/AjccVersion6Staging.html
-
This looks good. I don't understand it though. I have ITC with two of three nodes so where does that put me? This baffles me...and if ITC gets to nodes does it make cancer someplace else in your body? I am so confused.
-
damn... thanks Beesie. You are a wealth of information. I can read info elsewhere but it doesn't always make sense or stick. You make it clear.
-
Congratulations, proudtospin!
-
...hi ladies, been a while since I posted, but this thread seemed like a good place to pop back in... my surgery is booked for Aug 1st, and it's decision time as I need to let the docs know tomorrow AM which surgery I'm choosing. 3 consults later, and I've been told either lx + rads or mx will result in same survivabilty, with a *slightly* higher risk of recurrence in choosing lx + rads. I've decided to opt for a mx. The lx is very alluring (even with the possible 5-8 weeks of rads) and I sure was tempted to go that route, but with a 3 cm tumour, a palpable lump (not always the case with DCIS), high nuclear grade showing on biopsy, dense breasts and a nagging sense of dread with the idea of lumpectomy - I've made the choice... so now the only thing remains what kind of reconstruction. I'm leaning toward TRAM flap, but the idea of such a long recovery is so, so scary. All will be decided tomorrow, not anticipating a lot of sleep tonight!
-
I'm 5 weeks out of a hip flap reconstruction after BMX. It's been no picnic, but nothing has been unmanageable either. After hearing how uncomfortable TE's can be, I feel that this is still a good option for me in the long run. Good luck with your decision! I hope you are feeling some relief from choosing between LX and MX -- it's so hard to make these decisions!!!
-
Ottawamom12, I wish you peace and luck with your decision. I know it's not easy. Keep us posted on what you decide!
-
... just got off phone with surgeon's office... They wouldn't be able to do the flap until end of Sept, so I've decided that the skin sparing / alloderm / hopefully even straight to implant is the way I'm going (I told myself last night that the clincher would be the date - if they could accommodate Aug 1 for the flap, I'd go for it, but I think my heart of hearts knew they wouldn't be able to, so it was a bit of a red herring to my psyche!) with a reduction on the other side for symmetry. Although just had a funny "karma" moment as I spoke to the receptionist at the BS's office and she told me as she hadn't heard from me yet, she assumed I was going with lumpectomy and had just shredded my mastectomy consent, so have to swing in and sign a new one... aack! Is it a sign! lol - kidding, my mind is made up, I feel intense relief and am ready to get this show on the road.
Question - anyone had any experience with the Alloderm straight to implant route? I'll start searching the breast recon boards...
-
I did the UMX with TEs and have no regrets. I am now waiting for my exchange. I did not have to do tx and rads and I am glad about that. If I had anything suspicious show up in the other breast, I wouldn't hesitate for the MX.
-
OttowaMom: I had one-step recon with Alloderm last year. Everything went beautifully for me and I am happy with the results and am doing really well. You can PM me if you want more details, or have more questions. - Jen
-
i'm 4 yrs out from bilat mx and immediate DIEP reconstruction. Had DCIS in one breast, but opted for bilateral. Mine was high grade, comedo necrosis. Everyone tried to change my mind about the bilat but I was sure this was the right option for me. After mx, pathology came back with 2 more spots of DCIS in that breast. I knew I was doing the right thing.... The oncologist that tried to talk me out of a bilat agreed also, After The Fact.
Good luck in whatever you ladies choose to do.. Know that YOUR decision is the RIGHT decision.
-
Hey Ladies - my first time back in a week or so. Things have been a little overwhelming here. We lost our 9 year old golden retriever, Abigail, very unexpectedly on Saturday, and she was supposed to be my recovery buddy! It has been a heartbreaking few days.
Since I last posted, my BMX has been set for 8/16, with DIEP scheduled for 8/30 provided the pathology does not require further treatment. My DCIS area is so large (8cm) on the MRI and ultrasound that I am fearful the surgical pathology will show more. There were no calcifications in September 2011 mammogram, and now there are "extensive" and "significant" calcifications. I was worried about the seven week delay between diagnosis and surgery, but my BS says not to worry . . . Easier said than done.
I have a question about the "black grains" of sand and comedeo necrosis. Is that the same as central necrosis? My biopsy showed some central necrosis, but they gave it a grade 2. I am being treated at Vanderbilt, which I know is supposed to be one of the best breast pathology places in the country so I trust the grade 2. I just wondered if there is necrosis how do they decide between 2 and 3?
Heather
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team