Phyllodes Tumor vs. Fibroadenoma
Hi everyone,
I recently had my 6-month breast scan via mammogram (we alternate between MRI and mammo every 6 months) and they found a solid mass. I have a history of breast cancer (invasive ductal carcinoma), but I've been clear for almost 16 years! The initial mammo diagnosis was "probably fibroadenoma" because it was a circumscribed oval mass. However, because it doubled in size in a matter of 6 months (it was on my MRI in May, which they thought was a probable fibroadenoma) the radiologist suggested we do a biopsy just to be sure. We went ahead and did a core needle biopsy and the results were: "Fibroepithelial tumor with cellular stroma and rare stromal mitotic figures. The differential diagnosis could be fibroadenoma and benign phyllodes tumor. Lumpectomy highly recommended and to be scheduled." I meet with the surgeon in January to discuss.
Obviously, I am beyond relieved that it does not appear to be malignant. I've been reading up on Phyllodes tumors and have a fair understanding about them. But I am still worried. I believe the chances between fibroadenoma and phyllodes tumor are almost 50/50. Anyone else have a biopsy diagnosis like mine? And I'm also wondering if a benign appearing phyllodes tumor on core needle biopsy could turn out to be borderline (or even malignat) upon lumpectomy biopsy?
Happy Holidays to all, and for a healthy, peaceful and happy New Year!
Comments
-
I really am unable to answer your questions, Spero... I don't have that knowledge. I want to welcome you. I am glad you posted and am hoping someone will come along who can respond to your questions. I've been diagnosed with two fibroadenomas and they've never recommended any more than biopsy to confirm that is what they were (in the first case - not the 2nd). So it sounds like they really do want to know for sure what they are dealing with. I do not know if phyllodes tumor puts one at greater risk for cancer or not.
-
LivinLife, thank you for your response. I found it very comforting, which is just what we need sometimes. Thanks again.
-
Spero,
In 1996 I had a Phyllodes Tumor which presented as a fibroadenoma and just like yours, it grew significantly in six months (from peanut to lime sized). When MD Anderson did the biopsy, they did it without Ultrasound (not standard at the time), so it was a guess at best. The pathologist called it a giant fibroadenoma. It was removed because it was growing so quickly (would have taken over my breast if left alone) and when the pathologist examined it, there were parts that turned out to be a Phyllodes.
All those years ago, standard of care was wide excision/partial mastectomy. The new standard is lumpectomy with good margins. Twenty-two years later I developed breast cancer in the other breast, but completely unrelated.
There are a few of us on here who've had Phyllodes tumors, but not many. Three docs at MD Anderson have told me that they see only 1 case yearly, which is astounding. Obviously, I'm not an expert on Phyllodes, but it is not anything like you've been through with IDC, based on my experience with both. I can direct you to some threads about Phyllodes tumors if you're interested (I've bookmarked them since they appear rarely) and am happy to answer any questions as I'm able.
Wishing all the best for you, Spero!
-
Welcome to BC.org Spero
To answer your questions, any of the possible outcomes you propose could happen. There's no way to know until the lump is out and pathology done.
I've had a borderline phyloides tumour that kept returning and got more aggressive becoming malignant over time. I had 6 lumpectomies over10 years. Two of those turned out to be abnormal scar tissue. The other 4 were phyloides. It's very hard to tell preop. Both phyloides and fibroids grow very large very quickly.
So sorry you have to deal with this uncertainty at Christmas time. Happy to answer any questions for you.
De
-
Thank you for your responses, it's just comforting to connect with others on this topic, especially who have experienced this uncertainty and possible outcome. Yes, my radiologist said that the only the way to know is via surgery. I meet with the surgeon on 1/7, so we'll see how that goes. Beesy_The_Other_One, yes, I'd love for you to direct me to the other threads.
Hope you're all having a great holiday season, and I'll be back with more questions tomorrow!
-
Hey Spero,
Did you get any answers from the surgeon appointment yet?
De
-
Hi, thank you for checking in. Yes, I saw my surgeon a couple of days ago. She said it could be either - fibroadenoma OR phyllodes. And that it needs to be removed via Lumpectomy, because there's a 10% chance it's malignant. Although she's leaning more on the side of benign, but there's no way to tell. But either way, she said we should remove it. So we scheduled the surgery and at that point we'll confirm the mystery. I hate not knowing. But it won't change anything. She said no matter what it is, there's really nothing more to be done. Maybe a follow up surgery if the margins aren't clear, or if it keeps coming back. But surgery is all there is. No hormonal therapy, etc. I was hoping to discuss the pathology from the biopsy, but she said we need to wait until the surgery to really discuss pathology.
Was your initial diagnosis borderline phyllodes, that came back malignant at some point? she mentioned that they can recur, which is the biggest pain of phyllodes.
-
Spero,
I was so glad to see that ddfair was so thoughtful to ask you how you are doing--what a great community! In my experience, everything your doctor said was correct, and they will be able to do an accurate pathology once it's removed. My initial diagnosis was borderline phyllodes, but they went back in and took half my breast (standard of care then) and it never grew back. Ten years after surgery, MD Anderson declared it would not come back.
If MD Anderson sees only two phyllodes tumors a year, they are rare. A malignant phyllodes is VERY rare.
Spero, looking at my response above, I said I would send you links and I realize that in the hubbub of Christmas, I did not follow through! I apologize! In the two years I've been here, these are the threads that I've seen:
https://community.breastcancer.org/forum/137/topic...
https://community.breastcancer.org/forum/5/topics/...
https://community.breastcancer.org/forum/137/topic...
https://community.breastcancer.org/forum/137/topic...
https://community.breastcancer.org/forum/137/topic. . ..
https://community.breastcancer.org/forum/83/topics...
https://community.breastcancer.org/forum/5/topics/.. . .
Let us know how things go!
-
Spero,
Thanks so much for posting an update. Have they set a surgery date for you? I'm sure you will be glad to have this behind you regardless of the outcome. If the surgeon takes wide margins, that should be the end of it for you. My first lumpectomy the surgeon didn't take wide margins. When the pathology report showed borderline phyllodes they had to do a re-excision surgery to get clear margins.
You might want to educate yourself on what to expect with a lumpectomy surgery. There are many threads here with a wealth of information and helpful hints to prepare for surgery. Sending hugs.
De
-
They scheduled my lumpectomy for January 25. They're going to use the Radioactive Seed Localization (scheduled a couple of days before my surgery). With my first lumpectomy 15 years ago, they did the wire localization. I'm told the seed is less barbaric, but who knows. Anyone have any experience with it? Other than that, just going through the typical pre-surgery protocols (e.g. pre-surgery testing, COVID-19 testing, and the See Localization).
-
I do not have experience with that.... Just want to wish you well!! That is just around the corner... please let us know how things go....
-
I'm really confused on the radioactive seed location you mentioned. What is the purpose of that? Is it radiation therapy or is it to locate the tumour?
-
It’s a radioactivelocator for the surgery instead of having to have a wire placed
-
Thanks for the explanation Melissa.
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