SNB for dcis BMX
Comments
-
Hi, Judeshome!
I'm so sorry to hear about your news. You're at one of the best places to come to talk about what's going on...and naturally you're feeling petrified. Everything is always a little unknown until after surgery...and two or three months to wonder? No wonder you're feeling that way. There are two separate things I'd like to discuss with you:
1. Info on DCIS & its treatment. Since you've recently been diagnosed with DCIS, you might want to read Beesie's posts on "A layperson's guide to DCIS." As you'll note when you read this, there are lots of variations in a DCIS diagnosis and the treatment approaches you may be asked to consider. For example, many women are asked to choose whether they want a LX, or a MX or a BMX. There may well be reasons that one or more of those choices aren't being offered to you.
Beesie's posts on LX vs. MX vs BMX can be very helpful if you're thinking about surgical options. You can take a look at it "here."
Both are very helpful, as Beesie is one of the best researchers and most articulate writers here.
2. Maybe a second opinion? I was wondering what sort of facility you've been seen at? And if your BS primarily limits her practice to breast cancer surgery? Has she had fellowship training in either oncoplastic surgery or breast surgery? Or (if she was trained before such programs were available, does she go to the conferences/participate in research on breast cancer?)
The advice you've received, based on what you've said about your diagnosis seems a bit odd. Increasingly they are minimizing surgical treatments for low-grade DCIS (grade 1 DCIS is low-grade DCIS). So such a strong suggestion for a BMX seems a bit much (instead of breast conserving surgery as an alternative you can choose). I have to wonder if there is more to your diagnosis that you have told us/or have understood during your consultation with your BS?
If you aren't being seen at an NCIC designated breast cancer center, you might want to consider a second opinion at such a facility. Just for some peace of mind.
HTH,
LisaAlissa
-
I was diagnosed with DCIS last fall. Family history, and dense breasts led to my decision for bmx. More DCIS was found, but even more shocking was a 8mm tumor not seen in any imaging. It was a good decision for me, My originial BS recommended lumpectomy, and thought I was over reacting. Glad my second BS agreed with me, as it was HER+. So 12 doses of taxol, and nearing the end of herceptin and grateful it was caught.
-
Judeshome, I agree with LisaAlissa about the second opinion. If you don't get the SNB prior to mx, then you won't be able to get one later. I believe the NCCN protocols include MX for DCIS both with and without SNB, but it would provide that extra level of certainty for you. I also had multi-focal dcis, 3 locations on the right, so had to have mx. There was never any mention of having bilateral disease, and I got a second opinion on my pathology from a DCIS expert. Not sure where your provider is getting those stats about 90% chance it's also on the other side. I had UMX, and have been NED for 14 almost 15 years.
-
Thanks for your reply MTWoman, I intend to talk to my surgeon again about SNB, I want the reassurance that there is nothing unexpected in the pathology after the BMX yet am concerned about lymphedema too.. My BS said my breasts are so dense, they can’t really see clearly what is in there, I have multiple papillomas still in my left breast so it seems likely I have more DCIS too. I am 65 and simply want to get back to my life without worrying about tests every 6 months....this is a steep learning curve, I know from my own past experience that the shock will diminish somewhat in time, but I am over emotional at the moment and bursting into tears at the drop of a hat and am sure this is something most women experience under these circumstances. It seems like with DCIS you roll the dice, no way to know if it is aggressive or not there seems to be such a wide range of types. Jude
-
I didn't have SNB, but I had already had a biopsy and two lumpectomies with only DCIS ...but poor margins, then the MX. There are newer proceedures to mark the sentinal node that allows them to go back for it up to 3-4 days later if pathology warrents. I tend to get all kinds of soft tissue injuries, so thought I was probably a good candidate for LE if I had the SNB and didn't want to do it just because...after a lengthy discussion with my BS he agreed that my LXs made the decision tree different than if I had chosen MX to begin with.
-
There are risks in not taking the nodes, like for my friend whose IDC was only found in her lymph nodes and not found in her breast tissue. This may be less of a risk for Grade 1 DCIS. I had 3 lymph nodes removed and deal with low-level lymphedema regularly. I have to wear a sleeve whenever I exercise, garden, lift things, etc. and have had LE triggered from hangnails, bumps against things, bug bites, and lifting heavy things. I will have to wear my sleeve whenever I fly or do anything strenuous for the rest of my life. My arm gets sore and achy, so it's not the worst thing ever but it's an issue I will always have. If it's true DCIS, there will be no lymph node involvement.
Some surgeons use the dye to locate the sentinel nodes during mastectomy, mark them, and then if anything invasive is found during the mastectomy go back afterward to check them. Then the lymph system is not disrupted unnecessarily. Angelina Jolie's surgeons did this and wrote about it here: https://pinklotus.com/powerup/breastcancer101/prop...
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