How does this seem to you?
Comments
-
Hello! I finally got my pathology report yesterday. Here's what it says:
Lobular Carcinoma in situ with stromal microinvasion
Lobular Hyperplasia (LN1-2)
Moderate stromal fibrosis
Microcalcifications identified
My tumor is 0.4 cm and it's not even there anymore since apparently the stereotactic biopsy scooped it up. I have ER + PR pos and Her-2 neu/neg
I spoke to the breat cancer surgeon and she told me the plan was to first have an MRI of my breasts to make sure there are no other small tumors anywhere. Apparently lobular cancer does not show up on a mammogram so for the rest of my life I would have to have mammograms and MRIs.
If there is nothing else on the MRI, then I would have a biopsy of the area (it's at 11:00 on left breast) to make sure there are clear margins and then radiation followed by Tamaxafen. If there are more tumors then possibly double MX.
What I want to know is: Does this sound good? Has anyone else had this? Anything I should know. Thank you, dear ones.
-
I was diagnosed with ILC 2.5 years ago. The lobular cancer mimics natural breast tissue and is usually very difficult to find until it has grown well beyond the size of yours--and mine. Mammograms don't detect it--generally--that's a given, and MRIs are a good way to go. Sounds to me like your bcs is right on target with her plan. My ILC was found quite by accident--I was being prepped for a biopsy of an area of interest that turned out to be non-cancerous, and the ultrasound tech found another area that hadn't shown up on the 2 mammos. That was the ILC. I am convinced there were angels with me, and her, that day. Because I have an implanted defibrillator, MRIs are out of the question, as was radiation. I chose the bilateral mx and I have never regretted my decision. I think your prognosis is great, and you are in good hands with your doctor. Good luck to you, and do keep me posted on your progress:).
-
I was diagnosed with ILC 2.5 years ago. The lobular cancer mimics natural breast tissue and is usually very difficult to find until it has grown well beyond the size of yours--and mine. Mammograms don't detect it--generally--that's a given, and MRIs are a good way to go. Sounds to me like your bcs is right on target with her plan. My ILC was found quite by accident--I was being prepped for a biopsy of an area of interest that turned out to be non-cancerous, and the ultrasound tech found another area that hadn't shown up on the 2 mammos. That was the ILC. I am convinced there were angels with me, and her, that day. Because I have an implanted defibrillator, MRIs are out of the question, as was radiation. I chose the bilateral mx and I have never regretted my decision. I think your prognosis is great, and you are in good hands with your doctor. Good luck to you, and do keep me posted on your progress:).
-
Thank you Gayle for sharing. I think we are lucky in many ways but I am still weighing out the lumpectomy vs. bi-lateral mx. I don't think I want to be worrying about this for the rest of my life, but the mx really does terrorize me I must admit. I was reading today about a procedure call the diep reconstruction and the results look amazing but I am doubting if my insurance would pay. I am really walking around in an unreal world with so much stress - and exhausted at the same time.
My MRI is scheduled for Monday afternoon and soon after I will know if there is more than the one tumor. One step at a time....
Thanks again - no one was responding to my post and I was thinking oh this must be really bad and no one wants to tell me!
-
AnkleEye,
Private insurance should pay for your choice of reconstruction, even if it is DIEP that you are choosing. There are very few who don't.
Gail
-
I had a 2.1 cm tumor at 11 o'clock on the left breast - ER/PR positive, Her2neu negative. Nothing else seen on an MRI, so I had lumpectomy, radiation, and have been taking Tamoxifen. So far, so good. I do have digital mammograms as follow-up - the images are amazing, the technicians are amazing, and I'm good with it. My oncologist believes that MRI's tend to result in lots of benign things "lighting up," leading to unnecessary biopsies. I have no clue if my tumor would have been visible with mammography because the non-digital equipment at the facility I was going to could not capture my tumor in its field. The current digital images I'm having include portions of chest muscle. Painfully thorough, but that's a good thing.
Even with the singular known tumor, it appeared to many (but not all) of the medical people I spoke with to be reasonable to choose anything from a lumpectomy to a bilateral. Pay attention to what YOU want. I would have had radiation even with a mastectomy or two due to the location of my tumor (great margins not possible because it was so high up). It was nice to just get through the smaller surgery and then radiation and the fun side effects of Tamoxifen without worrying about reconstruction. You can always take off more - you can't put anything back.
How did you find this area of concern that was then biopsied? I found mine myself - gynecologist thought it was a rib but suggested diagnostic mammogram. As I said, they couldn't image the area due to the limitations of the machine, so I had a sonogram, where it showed up as a suspicous Birads4 which required a biopsy...
Apparently, 11 o'clock on the left breast (on the inner, upper portion) is sort of unusual, but not in any bad way, from what I've learned. It's just that tumors most often form in other areas of the breast.
Good luck to you! May your MRI reveal nothing of interest!
Coleen
-
Hello Coleen - Thank you for sharing your experience. What happened to me is I had a digital mammogram at the end of January and I then received a letter saying they had discovered a "finding" and to call to reschedule another mammo at the end of July. Honestly, I didn't give it a second thought as I was always being called in for ultrasounds for my dense breasts. So, after the end of July mammo the radiologist sat down with me and told me they saw an usual group of calcifications that were in a perfect ring shape in this 11:00 place. By the next week I was having the stereotactic biopsy and then the diagnosis. The tumor was only 0.4 cm and apparently it was sucked up into the biopsy needle!! So, now still waiting for results of yesterday's MRI to see if anything else was revealed. Interesting to hear about things "lighting up". I know I am changing to a better surgeon and hospital now anyway, but I must say the first hospital was incredible to find such a small tumor in such an unusual place. I am still debating what I will do once the MRI results are in.
Nancy
-
Have you looked at Dr. Susan Love's "The Breast Book"? Excellent and detailed descriptions of different surgery and treatment options. I found it to be very helpful in evaluating what to do. That's awesome that they found such a small tumor. I'm a BIG fan of digital mammogram technology!
-
Ok. This is weird. Absolutely nothing showed up on the MRI except the clip the radiologist put in me when I had the stereotactic biopsy. It shows everything is normal.
I see a second opinion tomorrow, but the first surgeon told me she wanted to do a lumpectomy (hmmm, there is no lump) followed by radiation and tamoxifen. Does this seem a little odd to anyone? I mean, I don't like the idea of someone removing a golfball sized piece of my breast unneccesarily!!!??? Good thing I am having a new pathology report done at another hospital. Those results should be interesting.
-
AnkleEye
My MRI showed absolutely nothing, too. It didn't even show my existing 1.5 cm tumor. Even MRI's aren't 100%, I think the studies say they pick up tumors 83% of the time. Not very reassuring. I had a lumpectomy, chemo, radiation and am taking Tamoxifen. I'm a little over 1 year since diagnosis and at my 1st follow-up mammo and ultrasound the radiologist suggested alternating mammo's with MRI's every 6 months. I have very dense breast tissue.
-
Hi AnkleEye,
I was DX'd with ILC after an excisional biopsy that the docs thought for sure was just a skin thing. They wanted to remove it just for peace of mind. Turned out to be a small ILC. Very lucky as the other poster noted, ILC is usually not found until it's much larger.
Following I had an MRI & US and nothing showed. I still had a further excision because the margin was close, but they found no further bc in that sample. I'm sure they want to get the area around your biopsy to make sure the margins are clear of any stray cells that wouldn't show on an MRI.
Did they also suggest a sentinel node biopsy? Usually that is done at the same time to make sure your lymph system is clear as well.
My general surgen offered the choice of either a BMX or a MX of the cancer side only. The breast specialist for my second opinion said the MX or a lumpectomy plus radiation would both give an equal chance of recurrence...less than 5%. I chose the lump and rads which I just finish. All to be followed by 5 years of Tamoxifen.
The thought of a big surgery and long recovery with the DIEP or TRAM personally scared me. I will be vigilent with monitoring, digital mammo's and alternating MRIs, and if anything more pops up I know I still can have the MX.
Good luck with your further opinions and your decision. It's a really difficult one, but you can do it and in the end you'll make the right choice for you.
Keep us posted. Donna.
-
Hi all,
Just thought I'd share some info regarding MRIs. Following mammo and ultrasound, I had MRIs of both breasts with contrast, since biopsies confirmed BC.
I had two areas that on MRI bumped up mass size to 2.3 and noted only the clip left in a smaller suspicious area found when having ultrasound guided needle biopsies.
Unfortunately, the first Path report from biopsies turned out to be incorrect, (Infiltrating Carcinoma Favor Lobular for larger mass and IDC for smaller mass. Subsequently went to Yale which reread the biopsy slides and said both areas were EXACTLY the same and were ILC!
At that point I switched surgeons and hospitals (1st surgeon had recommended lumpectomy with radiation or UMX without rads.....my call she said)
Back to MRI, 2nd surgeon read my MRI written report and viewed actual MRI I brought on disk (Disks have to be Dicom or Dicom compatible). She said the MRI was virtually worthless bc the MRI machine was older (a 3) and didn't have the best resolution (a 5). I asked if we should repeat it but she said insurance would only pay for it 1X annually.
Long story short, I ended up having a UMX with Diep reconstruction the same day, and when she got into OR mass ended up being 6 cm X 2.2 cm!
Knowing what I now know, about MRI equipment and the reality of what they found, I'm second guessing and wondering if higher resolution would have shown more and maybe I should have had a BMX.
Ladies, please make sure your MRI is being done on the latest and the greatest since it might make a difference as to your course of treatment.
I'm getting a 3rd med onco consult (at Memorial Sloan Kettering this week) but will have to undergo chemo, and possibly rads too, or so I've been told be 1st 2 med onco consults.
Geez I thought having a MX meant no rads!
-
AnkleEye, have any of your doctors talked to you about possible lymph node involvement? That will also help guide your course of action and treatment. (I see this has already been mentioned by MagPag. Sorry about that.)
-
MX can mean no rads if the tumor was located toward the center of your breast and away from the chest wall. If even a mastectomy doesn't give good margins, you're still in for radiation. I would've had radiation no matter what, as my tumor was way up high at 11 o'clock on my breast and there were no good margins to be had - there was nothing up there but chest muscle, tumor, and skin...
Never heard that about MRI's - that there's variance in machines. Greeeeeeeeat. Something else to worry about...
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