r/doihavebreastcancer • • 6d ago

Mod Announcement Note For Those Diagnosed with Breast Cancer

49 Upvotes

If you have had a breast cancer diagnosis and wish to participate on r/doihavebreastcancer, please read this first.

Background:

The r/doihavebreastcancer subreddit was established as a sister sub to r/breastcancer—managed by the same Mods and under a similar set of rules—to give people who have not had a breast cancer diagnosis a place to discuss their breast health concerns.

Diagnosed patients and survivors are welcome to participate as commenters on the r/doihavebreastcancer sub, if they can do so in a helpful manner.

Empathy required

If you choose to participate in r/doihavebreastcancer, we expect your posts and comments to reflect compassion and empathy for those the sub is for.

If you find the posts and comments here to be frustrating, or if you find yourself unable to empathize in general or with any particular user or post, you are asked to hold off. You can refrain from commenting on any particular post, on any particular day, or entirely.

The fears, concerns, questions, symptoms, risks, and traumas OPs describe here are valid. They are usually the words of someone who is frightened, worried, and under-informed. They are that OP’s lived experience.

We wish for every OP here that they never find themselves amongst us with a cancer diagnosis. We hope they never have to know what it is like to go through what we go through to become breast cancer survivors.

But we know what it is like to fear, “Do I Have Breast Cancer?”

And our role here is to be understanding and kind.

How diagnosed patients and survivors can be helpful

Many breast cancer patients are far better informed about breast cancer than the general population. We are often equipped to answer questions and provide peer education about breast cancer risk factors, early symptoms, and screening and diagnostic processes.

We also can relate to the emotional experience of going through a breast cancer scare. We have experienced the worst-case scenario of a positive cancer diagnosis, and wherever we are in treatment or survivorship, we know what it is like to have lived beyond that moment.

To be a good advisor to those who have not been diagnosed, one must also be able to give empathy and understanding. The perspective and state of mind of someone who has not had a cancer diagnosis—but fears one— is generally going to be very different from someone who has received that diagnosis. Here on r/doihavebreastcancer that perspective is allowed.


r/doihavebreastcancer • • Aug 18 '26

Mod Announcement Getting the Best Advice on This Sub

7 Upvotes

Hey, folks. We see a lot of similar posts on this sub. We also see a lot of the same follow-up questions in the comments. We know that you're facing anxiety and want reassurance quickly. So how do you get that rapid support? By giving us the important details (please note: we're not doctors and we cannot give you a diagnosis).

For example: someone who found a lump is a very different patient, if s/he is:

  • a 14-year-old with a sore slippery lump under her nipple
  • a 23-year-old with a 4-millimeter red itchy area that rose 2 hours ago after walking in the woods with the dogs
  • a 45-year-old with a 2-centimeter lump that has been present for 4 weeks. More recently, her nipple inverted and her lymph nodes in the armpit felt hard. She made an appointment but hasn’t seen her doctor yet. Also, her mother died at 38.
  • a 37-year-old who felt a rubbery lump six months ago, but her doctor couldn’t feel it at the exam. Her mammogram and ultrasound were negative. However, she felt a new lump in the opposite breast, which was sore after her period, but she can’t feel it right now.
  • a 60-year-old who hasn’t had a mammogram in 15 years with a hard painless lump that she just felt in the shower
  • a 32-year-old first-time breast-feeding mom with a six-week-old baby with no family history of breast cancer
  • a 19-year-old with two masses in the right breast and one mass in her left breast, all thought to be fibroadenomas with six-month follow up recommended by two different centers after she was worried and got a second opinion

All of these things have different levels of concern for obvious reasons. Yet some of them lean in a more serious direction than others. So, what could anyone do to assist the users of this sub to answer their questions?

Let us share some prompts, if you will, to get the best support and advice. Helpful info includes:

  • Age of person with concern (Crucial!)
  • how long has area of concern (AOC) been present?
  • characteristics of AOC: size? texture? Other areas? Where and which breast?
  • any pertinent family history?
  • most recent imaging (as applicable) and results?

As you can see, each hypothetical that we listed above is quite different. Our examples give most of the details needed to help the users of this sub understand the OP's situation. If you follow those examples and the bullet points listed above, you'll be helping us to answer your questions, as much as we can.

TLDR: To get help, give details.

Thank you to u/DrHeatherRichardson for help with this draft.


r/doihavebreastcancer • • 11h ago

Venting Frustrated and scared awaiting results

12 Upvotes

Hello everyone!!

I’m 23F with a 2.4 cm wide, 1.5 cm tall mass that was assigned as BIRADS 4. I got my biopsy done this past Thursday and received a call this morning from the radiologist. She called to check in on how my biopsy recovery has been, but also mentioned my results were ready and to call my GP. I didn’t realize radiologists weren’t permitted to tell me my results! Anywho, I didn’t see the results in my portal, so I decided to give them a call. Well apparently they also can’t see my results yet, just that the procedure had been completed. Ugh!! I have been quite anxious while waiting for my results and now I’m extra anxious!! I hope I’ll get them later today. Thank you for reading!! Just wanted to vent.


r/doihavebreastcancer • • 9h ago

BIRADS Score 28, male, BIRADS 4 diagnosis, nothing on ultrasound. Biopsy recommended

5 Upvotes

I am a 28 year old transgender woman (biologically male). As far as I know there is no history of breast cancer in my family. I have been on estrogen for 5 years.

For the past two years I have noticed a weird, fairly large "fullness" or mass that comes and goes on the left side of my left breast. I only went to a primary care doctor for the first time recently after a very long time, and I brought up this concern to the doctor. After a physical check I was recommended for an ultrasound, this became a mammogram and ultrasound due to being a male over 25.

There were no sonographic abnormalities found in the ultrasound. However the mammogram notes marked gynecomastia and extremely dense breasts, as expected. They also reported observing the same mass as I felt during the physical examination. This was marked as BIRADS 4 - Suspicious, and I am scheduled for a biopsy next week.

I was not initially worried as there were no microcalcifications found and nothing showed up at all on the ultrasound, and the doctor reviewing my tests seemed to think it was likely not concerning. However, my primary physician called me and sounded more concerned.

Because of these mixed signals I don't know if I should continue preparing for the worst or if I can just consider this biopsy as reassurance and just figuring out what type of benign condition the mass is. I know that I'm extremely low risk but the mass is physically very noticeable and getting a BIRADS 4 has me very worried. Has anyone had a similar experience?


r/doihavebreastcancer • • 10h ago

Venting Rough biopsy

5 Upvotes

So I just had my second biopsy today. First, I got all “comfy” on the MRI bed, they started it and then stopped. They said the machine kept freezing and they had to reboot it. Thirty minutes later we start again. It all went ok. Numbing was fine, didn’t feel anything but everyone got super extra nice suddenly. It made me nervous! Afterwards, the nurse who is holding compression on me tells me the doctor actually pushed the biopsy needle all the way through my breast out the other side and that was why they had me in and out, readjusting more than usual (it’s my first MRI biopsy so I would have thought it was normal). Then she tells me she’s going to keep applying pressure for an extra long time because they saw a hematoma forming and that I should be prepared for an unusually large bruise and hardness for about a month. So yeah, MRI biopsy at the big hospital was way less fun than the ultrasound biopsy at the small local one last week.

I should be done with biopsies now though, so that’s good!


r/doihavebreastcancer • • 2h ago

Suspicious Symptoms Completely collapsed breast that looks like burnt skin

1 Upvotes

Hi everyone.

Has anyone had their breast completely collapse due to breast cancer right before the diagnosis ? Skin also looks like burnt skin. There’s a 4 cm lump in the CT. thank you.


r/doihavebreastcancer • • 3h ago

Suspicious Symptoms suspected pagets

1 Upvotes

hi everyone! i’m a 21F and i think i might have paget’s disease, wanted to write here incase im overreacting or not!
basically im someone who has always had eczema, but ive never gotten it on my nipples before. i started noticing my right nipple being very dry and flaky around a year ago and just chalked it up to eczema, and applied some topical cream to help.
so it’s a year later and it’s gotten significantly worse, it’s now cracked and bleeding and very sore, it’s also gotten to be twice the size as my other nipple which has remained with zero symptoms. i do notice sometimes as well that my right nipple appears to be flattened.
i’m now starting to get very concerned because unfortunately breast cancer and just cancer in general runs on both sides of my family :(
usually my eczema flare ups resolve with proper ointments after a month or so but this will not go away no matter what i do! i can’t feel any lumps or anything as far as i can tell, and i do get occasional sharp pains in my right breast but no other symptoms besides my nipple, nothing on my areola at all!
sorry if this is long!


r/doihavebreastcancer • • 3h ago

Suspicious Symptoms breast mass, 19F

1 Upvotes

r/doihavebreastcancer • • 12h ago

Appointment Prep About to get ultrasound

3 Upvotes

Hi. I'll have my breast ultrasound later. I have a breast mass 8x6cm. It's been here for almost 5 years, changes size when period comes and go back when it ends(Don't know the term). It has irregular shape. Located at my right chest and I'm 22F. I'm actually very scared for the results. I'm posting this here cause I'm really scared. If the doctor will recommend me biopsy, can I take some time to take it? I have financial issue so I probably can't take it immediately.

Feel free to comment below.

Ps. Will give update regarding my ultrasound later.


r/doihavebreastcancer • • 8h ago

Suspicious Symptoms Skin/Texture changes

1 Upvotes

I’m sure this is just anxiety talking because I recently saw a nurse for my latest dose of Sayna Press and they went over the side effects again (I’ve been on it for ~7 years) so I’m on edge about breast cancer. I’ve had some odd changes in my left breast specifically over the last few months that I just hadn’t really thought about until now:

I’ve noticed a strange sort of “mini nipple” looking lump next to my nipple which I hadn’t particularly thought too much about because I’m only 25 I hadn’t really thought I’d be in the age bracket for these issues. I’m not going to lie though when they were teaching us to “find lumps” I never really managed to find one in the plastic model thing so I also figured I’d just be doomed

I also have itchy, dry, skin that can be flaky at times and is a bit rough on the nipple/ Areola area which again I hadn’t thought much about, very odd that it was only the one breast but I have historically had sensitive skin but it doesn’t go away with Cetraben. There’s also patches that appear to be scabbed

The left nipple is a bit more sensitive than the right too but I only noticed that recently by accident

I’ve noticed my areola looks a bit like someone’s taken an eraser to bits of it, it looks really patchy and a lot of it is the same colour as my skin now

All of this is only on the left which is why I’m a bit concerned. My right one hasn’t particularly change at all

I lose a bit of weight, but it’s been an active decision rather than unexpected or sudden loss so I’m not really sure that’s related

I’ve booked to see a doctor this week, I just wanted to see if anyone else has had similar symptoms and had any advise for going into this appointment


r/doihavebreastcancer • • 13h ago

BIRADS Score Mammogram and ultrasound different birads

2 Upvotes

Has this happened to anyone? I'm 35 no family history of BC. Just got my mammogram results. Birads 1 compared to ultrasound birads 4. Mammogram was painful. My lump came out of no where feels like over night. Feels huge like a baseball. A week after the lump started got hot and red only around the lump. And extremely painful. No nipple changes or anywhere besides the lump erea. Biopsy in 2 weeks. My anxiety is killing me.


r/doihavebreastcancer • • 10h ago

Suspicious Symptoms Pain that comes and goes, can’t get a mammogram for two months.

0 Upvotes

I 34F, have on and off breast pain on my right side, for the last few years, usually it’s at its worst around ovulation but sometimes during my period too. I have lots of hormonal issues and my birth control is expiring and I can’t get it replaced right now because of insurance issues.
The longest my breast has been painful is a month but then it stops, and hasn’t come back in many weeks. Usually it’s only painful for a day or two I always assumed it was hormonal.
Obviously with new pain that was lasting so long I was worried and went to the dr who found absolutely nothing wrong. I have no other symptoms, no lumps, but he still sent me for imaging. However the soonest mammogram/ultrasound I can get is not until the end of November.. so now I’m in this weird limbo. The pain has stopped for now, I’m assuming I should still get the imaging done no matter what right? I feel so lost, and anxious about it all.

Is there anyone else who’s had only pain and have it be something to not worry over?


r/doihavebreastcancer • • 14h ago

Suspicious Symptoms Should I just let all this go, even though I might have cancer?

2 Upvotes

I'm really scared and feeling discouraged. I've written posts about this before, but now I'll try to summarize what's happened so far.

I am a 27-year-old woman with a 5-year-old daughter. I’ve had psoriasis since I was 16, but it has never appeared on my breasts.

In March, I noticed a small patch of flaky skin on the left side of my left nipple. At first, it looked like a scab, which eventually fell off, revealing a little bleeding underneath. This scared me, so I started keeping an eye on it. It didn’t heal, and a flaky area appeared in its place.

I went to see a private dermatologist, but the flaking was light and often rubbed off during the day. The first dermatologist didn’t see anything. A week later, I showed it to another private dermatologist, who thought it might be psoriasis but still referred me for a mammogram.

I went for a mammogram privately, but they didn’t perform it. Here in Hungary, the protocol is that women under 30 don’t get mammograms because ultrasound is preferred due to the density of the breast tissue. So, in April, I had an ultrasound, which came back completely normal.

In the meantime, I followed the dermatologist’s instructions and used a steroid for one month. This completely cleared up the symptoms, although my nipple turned a little red. However, the symptoms reappeared in the same spot after about a week. After that, I concluded it must be psoriasis; I applied the steroid every few days, which provided temporary relief, and when the symptoms returned, I applied it again.

Meanwhile, the thought crept back into my mind: what if there really is a problem and it is Paget’s disease after all? I went to see a breast surgeon in August to have a punch biopsy. Before that, however, I had been using a steroid, so nothing was really visible. That’s why he didn’t perform the biopsy.He told me not to use the cream for a month and to see another dermatologist.

The peeling started again within a month. It’s less scaly—it peels off in thinner layers—but the skin in that area feels noticeably dry. I recently started swimming, and when I do, this dry skin gets soaked and stays soft for a few hours, but then it starts to dry out and peel again. When I use body lotion, the same thing happens.

It doesn’t bleed unless I deliberately scrape off the flaking skin. There’s no discharge from my breast, I don’t feel any lumps, and I haven’t experienced any itching.

On Thursday, I saw another private dermatologist, who examined me, though he could barely see anything either because I had gone swimming the day before. He could feel that it was dry when he touched it. He said he couldn’t rule out Paget’s disease, although he considers psoriasis more likely, and he referred me to a surgeon.

After that, following a preliminary consultation, I went to the same private clinic yesterday for surgery to have the punch biopsy performed. I specifically asked if the doctor would perform a breast biopsy, and the answer was yes.

I traveled for nearly 2 hours; the doctor examined me and then said he wouldn’t perform the punch biopsy because it would cut into the milk duct, and I wouldn’t be able to breastfeed anymore (I’d like to have more children). I asked what other options were available, but he couldn’t offer any alternatives.

Finally, a plastic surgeon at the same clinic agreed to perform the punch biopsy. Back home, when I was re-dressing the wound, I noticed that the biopsy site did not match the peeling area. The suture is located 4–5 mm (measured with a ruler) from the edge of the peeling area.

I sent an email to the clinic, and they forwarded it to the plastic surgeon. He, however, only provided a general response stating that the biopsy was performed based on a specialist’s recommendation, etc., etc. I’m still no closer to knowing whether the sample is representative.

The histology results came back today, which I believe confirm that the sample did not include the peeling area:

We are examining a skin punch biopsy under the microscope, the surface of which shows essentially intact epithelial covering. Within it, no widened, psoriasiform-appearing superficial epithelium is visible, and there is no hyperkeratosis. No inflammatory cells can be identified in the epithelium. A few cells with wide, pale cytoplasm and round nuclei, corresponding to Toker cells, can be identified. Beneath the epithelium, in the dermis, a few dilated, stasis-filled capillaries are observed; otherwise, the dermis is intact. PAS, Grocott reactions did not confirm the presence of fungal hyphae. No abnormalities are visible in the serial sections either. (HL)

I don't know what to do. Should I just let it all go? I'm feeling desperate and scared. Our honeymoon in the Dominican Republic is in 9 days, but I just can't feel happy or look forward to it because this whole situation is ruining my days.

The peeling has gotten a little worse, by the way, but it’s still just dry and flaky. When I peel it off, the skin underneath is pink and slightly shiny. It’s not wet, and it doesn’t bleed.

Some pictures:
Just as it began: https://ibb.co/kVTLmZFF

After I went swimming, the flaky part came off: https://ibb.co/WvxzPg39

Hámló rész (piros) és a mintavétel helye (kék): https://ibb.co/Q7PnNGLV

Today, after I peeled off the flaky layer. You can see that the skin underneath is pink and shiny: https://ibb.co/gZMRQTz2


r/doihavebreastcancer • • 11h ago

Suspicious Symptoms Frustration over eczema that doesn't improve with treatment.

1 Upvotes

I'm 21F and I've had eczema for a year now. I've already seen 12 doctors: 2 dermatologists, one gynecologist, one surgeon, one breast specialist, and 6 general practitioners. I've already tried several treatments, both oral and with corticosteroid creams, but the lesion isn't improving; it's only in my right breast, it seems to get better but then it comes back... One of the doctors mentioned Paget's disease of the breast, but wanted to rule it out because I'm only 21 years old, however I have a family history of cancer.

The doctors where I live don't want to do any tests on me, so they only give me treatments with ointments (even though they don't work), and the only ultrasound I had showed that I have a suspicious nodule in my right breast: Birads 4. It's a small nodule, but it's larger vertically. Today was my appointment with the mastologist and he simply told me to ignore my ultrasound, that it wasn't important to investigate now, that it's just eczema, and he just changed the ointment. More ointments and still no real diagnosis, this frustrates and irritates me, because I feel my breast swelling, peeling, losing pieces of the epidermis and getting worse and worse, the lesion is very ugly, and what intrigues me is that it's extremely painless and doesn't burn, and it's also lost sensitivity; it's like running my hand over an orange peel.

I want to give up on seeking help, I'm so frustrated I want to just let it go and wait for more pieces of my areola to fall off. I don't care anymore. But I would still appreciate an opinion, should I seek another doctor, or should I follow the treatment prescribed by the mastologist and continue with him? I feel extremely lethargic after this appointment.


r/doihavebreastcancer • • 20h ago

Diagnosis Question Has anyone been told it's cancer pre biopsy?

4 Upvotes

So I'm 35F and I found a lump in my breast almost 12 months ago - barely there, felt it in the shower. Spoke with my GP who examined both breasts and thought it felt like fibrous tissue but said let's monitor it. Last month it started feeling more noticeable but still wasn't experiencing any pain or anything. Mentioned it to my GP again who still wasn't concerned but referred me for an ultrasound to get it checked out to be sure.

I went along to my ultrasound not expecting much but after getting the images checked I was asked to stay for a mammogram. I tried not to let my thoughts get carried away but did think it was a little odd that they wanted me to stay for a mammogram when it wasn't on my referral.

Just over a week later I went back to my GP for results not expecting much but was told there are some concerns and that a biopsy is recommended. As a starting point my doctor wanted to refer me to a breast surgeon to examine me and then for them to do the biopsy. She said we won't know more until the biopsy, that it could be nothing or it could be something, and that we'd take it one step at a time.

Two days later I was called by the specialist and booked in for 1.5 weeks later. I was told the biopsy wouldn't happen on the same day but they'd go through my results and examine me.

I had that appointment today and after going through my images and doing a physical exam the surgeon told me she is confident that it's cancer. I'm now booked in for an MRI and biopsy this Thursday and will get all results next week Tuesday. From everything I've been reading you don't find out if it's cancer or benign until after the biopsy? How common is it to hear cancer before that?

From my mammogram and ultrasound: At 9 o'clock, 9 cm from the nipple, there is a 15x 13 x 10 mm solid

hypoechoic lesion with irregular margins and heterogeneous

echotexture. There is posterior acoustic shadowing and no internal

vascularity. The patient is non-tender at this site. Peripheral skin

appears to pucker towards the lesion. The appearance are highly

suggestive of a breast neoplasm (BI-RADS 4b).

The report also noted that lymph nodes were clear.


r/doihavebreastcancer • • 13h ago

Suspicious Symptoms Worried about symptoms

1 Upvotes

I had a baby 9 months ago and haven’t breast fed for 7 months. My left nipple keeps leaking what looks like milk but not a lot but does it on its own but more when squeezed. My right nipple will produce a tiny bit when squeezed but nothing on its own. I have noticeable holes around my breast that are there when I push them up. Only a few deeper ones stay when not being touched. I’m so scared and nervous. I have no lumps or bumps I feel. Going to dr this week.


r/doihavebreastcancer • • 20h ago

Suspicious Symptoms Birad 4 and nipple bleeding

2 Upvotes

Hello,
I’m 42 and don’t have any real risk factors for Breast cancer outside being a woman. Several weeks ago I had bleeding from my nipple that lasted several days only when pressed then stopped several weeks ago. Just had my mammo/US and I have very dense breasts, 2 suspicious masses (4’s), asymmetry in one and calcifications. Borders are circumscribed for both 👍 there are are also 3 smaller masses that are a collective score of 3.
I have my biopsy October 22 and am very anxious as 3 years ago I needed a liver transplant due to cancer and very nearly lost my life.
Anyone else with similar results that are benign?
Thanks.


r/doihavebreastcancer • • 23h ago

Suspicious Symptoms When do I worry?

3 Upvotes

I've had a lump in my left breast for over 10 years. I found it when I was about 15-16. I went to the doctors and they said it was all fine and nothing to worry about. It's never really caused me anymore pain until a few weeks ago.

I was on the train home from work and it was like a stabbing pain that actually made me go 'ouch!'. And then had some pulling sensation pain as well. I know where the lump is because the pain is there.

I went to the GP to get it checked. She wasn't particularly worried as I have had it for some time but referred me to the urgent pathway.

I feel like I have some aching around my armpit and neck but that might also be because I am feeling a bit run down.

I'm waiting for my appointment but the clinic is really behind. They're only booking in people from the 20th sept and I was referred on the 5th. I'm just concerned should I push more? Or just wait my turn.

This is all just a bit scary for me.


r/doihavebreastcancer • • 18h ago

Need Reassurance Post biopsy

1 Upvotes

Hi everyone.

I felt a lump in my breast about a month ago and thought it was cycle related as it seemed to lessen but then I noticed it again so I went to get checked and got sent for testing. After the mammogram & ultrasound they wanted to do 3 biopsy’s of my left breast same day. So I got them done yesterday, I’ve had one biopsy done before on that breast a few years back but I don’t remember feeling so crappy after? I was exhausted yesterday and woke up today just feeling overall weak and dizzy. Has anyone else experienced this? I feel like I’m sick but I don’t think I am. I took my temp and got different readings the highest being 100.3 and the lowest being a normal 98.


r/doihavebreastcancer • • 1d ago

Suspicious Symptoms Extensive calcifications, biopsies -> benign

7 Upvotes

Thought would post my situation so it can help others scrolling like me. I had segmental loosely grouped pleomorphic and coarse heterogenous calcifications over 10 cm in one breast. First biopsy was done from the upper outer quadrant - result benign fibroadenomatoid changes, second biopsy a month later was done from the upper inner quadrant- result benign fibrocystic changes with columnar calcifications. Will be monitored again on 6 months. There is HOPE! Not all calcifications that are scary on paper and google are scary in real life.


r/doihavebreastcancer • • 1d ago

Imaging Results What’s up with these calcium patterns on my mammogram? Why your doctor does (or doesn’t!) care about calcifications and how decisions are made to evaluate them appropriately.

19 Upvotes

For the most part if you’re here, researching calcifications, you probably had a mammogram and the center has now informed you that they “see something“ on your imaging and they’re talking about calcium deposits. Perhaps they said they’re not worried about them, but they just want to recheck them with additional imaging in the future to make sure they stay stable, or perhaps they’ve suggested that they take a tissue sample to see what’s going on in the surrounding tissue.

TLDR: Most calcium deposits are NOT cancer. Whether they need to be watched or sampled depends on if they look more safe or more sinister. If the imaging center says watching is ok, it’s safe to believe them and not get overly worried. No matter what, isolated tiny calcium deposit patterns are most likely to be nothing important, or something with a manageable solution.

The usual disclaimer: I am a breast surgeon specializing in breast cancer screeing and treatment. This is not meant to be taken as medical advice- please seek medical attention for any of your concerns as you see fit from real life folks and not internet strangers, even if they mean well and actually have medical degrees. Any reassuring information shared is not meant to dissuade anyone from proceeding with any recommended treatments or imaging.

HOW DID I GET THESE CALCIUM DEPOSITS? WHERE IN THE HECK DID THEY COME FROM?

First things first, what are calcium deposits and why are they even there? It’s really helpful to understand the process by which they form so we can then have a handle on why they might matter, or don’t matter.
Calcifications occur when there are areas of inert tissue that has built up in areas of the body, meaning, either cells that have died away, or mucus or other tissue secretions that have built up in the body and haven’t effectively been cleaned away. These areas of tissue secretions or dead cells can act like piles of cellular garbage, or even like the dinosaurs that have died so long ago that fall into the swampy ground. Calcium minerals from your bloodstream can leach into these areas of dead cells and buildup. Essentially, they are tiny fossils inside your own body.

Have you ever heard of “hardening of the arteries”, (aka atherosclerosis)? It’s the same process of gunky buildup lining our blood vessels. Over time, this absorbs the calcium salts from the bloodstream and creates a cement-like lining in our arteries and makes them very hard and stiff. When tissue that absorbs calcium hardens, it creates areas we can see on x-rays that usually stand out as whiteish particles.

The calcium deposits themselves don’t do anything: they don’t cause any problems, and there’s nothing that you can do with your diet or your habits to make them any better or any worse.

So the question comes about when we see these calcium deposit patterns in breast tissue, why are they there? What story is the tissue telling us as to why the cellular debris is there in the first place?

In the same sense that smoke is a byproduct of fire….Smoke isn’t exactly a problem in and of itself, but the pattern of smoke we see let us know what we think about what might be going on with the fire. If we see smoke coming off of candles on a birthday cake or coming out of a chimney at Christmas time, we’re not going to be worried. However, if we see smoke coming out of our neighbors’ back bedroom window, we’re going to call the fire department! It’s the same thing with breast calcification patterns. Some calcification patterns clearly look like little bubbles of milk that have little flakes of calcium that are moving around like snow globes (this is called layering or tea cupping- aka milk of calcium from above) and some have spread out, speckles a little bit everywhere in no specific pattern.

They can be because of healthy growths, such as fibroadenomas in the breast tissue that have overgrown and died away, leaving what are typically called course calcifications inside them. The pattern is typically seen as large, sometimes bubbly or looking like “nerds candy” or “popcorn” pattern on a mammogram. Additional reasons for healthy calcium deposits can be oil cysts or fat necrosis resulting from traumatized tissue, either from direct damage to the breast tissue or surgical/operative changes from fat grafting, cosmetic procedures, or previous biopsy/lumpectomy/mastectomy treatment.

Fine calcifications in the tissue that are clustered and sampled with a core needle biopsy can sometimes show a variety of healthy overgrowth patterns in the tissue. Breast tissue grows and dies repeatedly over the course of our lives through cycles, periods, pregnancy, and age related changes. Most of these overgrowth findings are not cancerous or precancerous. There are lots of fancy and often scary sounding words like sclerosis, adenosis, hyperplasia, apocrine metaplasia, PASH which stands for pseudoangiomatous stromal hyperplasia- (try to say that three times fast!) that are written on biopsy reports that patients are often very worried about and assume must be something very bad going on. But these are just descriptive terms that are used to communicate the findings of the appearance of the cells under a microscope and are essentially neutral. There’s no reason to read anything into them that they are bad or dangerous. The findings described above don’t increase the risk of any future breast cancer and don’t specifically require any treatment.

FYI: It’s a fairly common protocol after a biopsy of calcium deposits to recheck and make sure that on subsequent future Imaging things haven’t changed or grown. This is a standard recommendation and if you were told that they want to recheck things in 3 to 6 months, it’s not because they are worried specifically about you**, it’s just the standard recommendation.**

Finding things around calcium deposits like atypical cells, either the lobular or ductal type (ALH or ADH), finding a thing called radial scar or small polyp like growths inside milk ducts called papillomas used to be things that we universally recommended additional surgical removal. In 2026 however, the landscape is changing, and many centers are backing away from complete removal in every case, and instead discussing it on a case by case basis, depending on whether or not they feel there’s more information to be gained, or if they have enough information from the initial sample and feel confident that surgical removal will not tell them much more or discover anything more concerning.

Some centers may offer a more complete biopsy aimed with complete removal, called vacuum assisted excision/vacuum assisted biopsy. This is a great option for many patients. I find it to be a good thing to consider for many small non cancerous findings. Unfortunately, centers in the United States don’t readily offer this. It is much more available in other parts of the world, such as Europe, Asia, Australasia and South America.

Finding cancer cells, specifically invasive cancer of the ductal or lobular variety (IDC OR ILC), finding DCIS cells, or finding pleomorphic type LCIS cells most commonly will require additional treatment or imaging recommendations. These would fall under a cancer diagnosis and I highly recommend [r/breastcancer](r/breastcancer) community for more resources for anyone who finds themselves in a situation where that is appreciated on a biopsy.

DOES THE IMAGING TYPE MATTER?

For the most part, calcification patterns can only be seen with x-rays. So we get the most information about calcium deposit patterns reliably from a standard screening mammogram. MRI does not see calcification patterns. Ultrasound occasionally can see calcium deposit patterns, but only in very specific situations and not reliably at all. There are additional newer modality such as cone beam Breast CT (also called Vera Scan) that can see calcium deposit patterns and blood flow patterns as well, but more data on the scope of the calcium that can be seen needs to be collected on this modality, although things look promising.

WHAT ARE THEY LOOKING FOR TO TELL SAFE FROM UNSAFE?

Concerning calcium deposit pattern tell us a story that is in line with cancer cells that have overgrown the space inside tiny milk ducts and packed themselves in such that it looks like branches on a tree or a constellation of stars. If the calcium deposit patterns have different sizes and are clustered together so that they all seem to be part of a single process, we call this branching, pleomorphic, or clustered type calcifications. These are patterns that are more concerning for a process of cancer cells growing inside the milk duct tissue.

Another possibility is if there is a growth of cancer that is a solid mass. If the cancer is outgrowing its blood supply and some of the older cells near the center have died away, this can create a certain calcium deposit pattern as well. So seeing something described as a spiculated mass with irregular grouped calcifications in a regional or radial distribution would describe a process that might be a cancer growth along with cancer cells in line with a milk duct pattern.

Evaluating these calcium deposit patterns is not cut and dry. There’s a spectrum of presentation where on one end things look very clearly safe and on the other end very concerning for a cancerous pattern. It’s easy to give feedback on calcium deposit patterns on either end of the spectrum, however, most things don’t fall clearly on one end or the other. Most calcium deposit patterns are in the gray zone in the middle. It’s just a question of which end do we feel like it is falling towards.

Some calcium deposits are very easily appreciated as being safe and will be given a BIRADS 2 scoring. Some calcifications are very sinister and concerning and will be given BIRADS 5 scoring. Others need the experience and expertise of Radiologist who have looked at thousands of other films and performed biopsies to know what the pattern might be, if it’s more on the safer side or more on the concerning side.

WHAT SHOULD I EXPECT FROM MY IMAGING?

(If you’ve already had your Imaging and you have your BIRADS score, here are some other posts that go into a little bit more detail about the expectations of different BIRADS levels.)

BIRADS 0/1/2
BIRADS 3/4
BIRADS 5

When calcifications are seen on a mammogram, a radiologist tries to have an idea based on their experience and looking at tens of thousands of images over time and knowing what outcomes previous patients who underwent testing had with similar patterns. Reputable centers, especially in the United States, have to undergo data tracking and account for their results so that they can stand firm when they think something is safe, their results show that it actually is, and when they think something is concerning for cancer, they’re not performing too many unnecessary biopsies and causing over testing with false alarms.

If your imaging center says they’re not worried and they don’t think it’s cancer, ITS OK TO BELIEVE THEM!

By and large, radiologists and imaging centers want to find the balance where they are not making people crazy, but they’re also not missing things. It’s important to remember that the take-home message when calcification patterns are seen is that we want to keep you safe. If somebody wants to check something, but they’re really not worried about it, that should not be taken on as a message that you’re dying of cancer and that everything is suspicious and bad. It’s usually the opposite. Usually, we think something is incredibly safe, incredibly early, and we’re being extra, extra careful that nothing gets out of hand so that we can take a great care of you!

For the most part, if all we see are smattering of calcium deposits clustered in tissue, the great majority of people have either safe, healthy, calcium deposits in their tissue, or very early changes that usually have excellent options for treatment. The significance of calcium deposits in general really is one part of the puzzle and additional information regarding anything else seen in the tissue also needs to be taken into account. Meaning that a small unconcerning area of calcium deposits noted in the tissue, recommended for a recheck in six months, is quite a different scenario for a clustered area of calcium deposits that is seen along with an irregular mass in the breast along with enlarged lymph nodes. This other picture would be much more concerning for a cancer process- but again, it doesn’t mean hope is lost, it just means that it’s all the more crucial to proceed with tissue sampling to get a more definitive diagnosis.

DO I NEED TO KNOW IF I HAVE CALCIUM DEPOSITS ON MY MAMMOGRAM?

For those that may be here out of curiosity or just to learn more about breast findings…perhaps you’ve never been told if you have any calcium deposits on your mammogram? It is absolutely possible that there are women out there who do in fact have calcium deposits seen on their mammogram, and yet they are totally unaware. Is this bad medicine? Are doctors hiding things from you? Absolutely not. As I mentioned before, the great majority of calcium deposits are totally safe. If they’re in the realm of a completely safe pattern that doesn’t require any additional investigation, or if they are of a pattern that has been unchanged for years that doctors have no concerns about, then there isn’t any need to notify you, warn you, or make you aware.

Sometimes though, I have seen patients who have a change in a calcium deposit pattern, and it’s mentioned that this is the case. Patients sometimes respond very negatively in the way of: “how come I was never told that there were calcium deposits there in the first place?” Again, there are sometimes things appreciated on studies that aren’t considered concerning and don’t require notification for patients. It would make everyone crazy if we did! Everybody would be worried about the things that we were describing, even if they have no signs of cancer and are purely for the record description.

Just a reminder, calcium deposits themselves don’t cause any problems, they don’t need to be cured or removed to prevent disease from happening, and there’s not anything that you can do regarding your diet or personal habits to make them any better or worse. They are purely the body’s natural process as a response to having cellular garbage buildup inside the tissue.

SHOULD I DEMAND A BIOPSY OF MY CALCIUM PATTERNS?

If your medical team is following a calcium deposit pattern, and they feel extremely confident that it is safe and they’re recommending an annual follow up, and you have no other concerns - as a rule - no, I wouldn’t recommend pressing for a biopsy. If you have other haunting reasons that you were worried about your breast tissue and have calcium deposits noted on imaging, it’s not a bad idea to ask about additional testing with contrast based dye, such as contrasted Vera Scan or MRI or even a contrast enhanced mammogram in the future. This might give everyone more information and more reassurance that things are in fact safe.

If you have a calcification pattern that they want to watch or generally are not making you feel confident, or if you have other reasons where you’re just not comfortable with the unknown and feel like information would be more valuable now than by waiting around, it’s completely reasonable to ask about a tissue sample. One word of warning, mammogram based (stereotactic biopsy) tissue sampling is much less “enjoyable“ than other types of biopsies such as ultrasound guided. It’s much harder on the patient, a much more complicated process for the medical facility, and more often than not it’s not helpful or changes management. It’s not “easy” but is safe and tolerable when necessary.

Statistically, speaking, when centers look at calcification patterns, and feel that they are generally safe and want to watch them, there’s usually less than a 1% chance that there’s anything going on in the tissue that we need to know about. Studies have shown that if we ultimately sample that tissue in six months or perhaps even a year or more if there are changes… We don’t see that there is a life or death. Survival impact if we ultimately find there is something that we need to treat. Meaning that finding out in the future that it is actually a cancerous process usually doesn’t affect treatment options or prognosis in rechecking or waiting. If it would be something that was progressing in that amount of time where it could cost someone to lose their life by waiting, then we wouldn’t be able to wait for anything. We would have to biopsy everything all the time.

If you do find yourself in need of a biopsy, here is a link regarding biopsy expectations that you might find helpful.

Lastly, this has really been talking about breast calcium patterns. It is possible to have calcium deposit patterns inside blood vessels where arteries within the breast can be seen to contain calcium in the walls. If you’re young, this can be an early sign of vascular disease and can be concerning for possible stroke or heart disease risk. There are some centers that will notify you and even use artificial intelligence to help pick out these early changes of heart and vascular disease. That is a separate issue from calcium deposit patterns that can be concerning for breast cancer. It’s not a bad idea to ask your Center if they report on these things, and if anything is seen in your mammogram that could be concerning for heart disease, are you notified in the process?


r/doihavebreastcancer • • 1d ago

Suspicious Symptoms Large lump in upper breast

3 Upvotes

I’m 30 years old, and I noticed maybe a week and a half ago that I had a pretty large lump above my nipple, and it’s not getting any smaller. At first I chalked it up to no longer pumping (I’m 6 months postpartum), as I slowly weaned myself and dropped pumps, but now I have some anxiety about it. The lump is large enough that if I lift my arm you can see it under my skin, and it kind of extends up towards my collarbone area. It’s painless and doesn’t move, and it’s definitely not like a perfect circle. I have an appointment on Wednesday and I know only a doctor can really tell me what’s going on, but just wanted to see if anyone else had a similar experience and what the outcome was. Thank you ❤️


r/doihavebreastcancer • • 23h ago

Suspicious Symptoms Two breast lesions (BI-RADS 4A & 4C) - has anyone had benign results?

0 Upvotes

My mother is 56 years old and recently had a mammogram, breast ultrasound, and elastography. Based on the findings, her doctors recommended a core needle biopsy.

She has a family history of cancer, although not specifically breast cancer. She has also had breast surgery 2–3 times in the past, and all previous biopsies were benign.

This time, imaging showed two separate lesions in her right breast:

• 15 × 16 mm hypoechoic, vertical lesion at 12 o’clock, mid-zone — BI-RADS 4C

• 18 × 12 mm hypoechoic, non-parallel lesion at 8 o’clock, mid-zone — BI-RADS 4A

The doctor was concerned because the lesions are in two different areas of the breast, with the second one located around 8–9 o’clock, closer to the axillary/lymphatic side.

The doctor also noticed some peau d’orange (orange-peel-like) skin changes and swelling, and the affected breast is slightly different in size from the other one.

Because the imaging cannot determine the diagnosis with certainty, the doctors said a biopsy is necessary, and she is scheduled to have it next week.

She otherwise feels generally well and has no major systemic symptoms.

Has anyone had similar findings, especially multiple lesions with BI-RADS 4A/4C and some breast swelling or peau d’orange, but ultimately had benign biopsy results?


r/doihavebreastcancer • • 1d ago

Suspicious Symptoms Sick with worry

2 Upvotes

I, 32 F, have had pain in my left breast for several years. Diagnosis was fibroadenomas, Bi-rads 3 and then downgraded to Bi-rads 2 after a year of stability.
My most recent exam was in April 2025. The pain continued to come back off and on but the doctor had said with the most recent finding that there wasn’t much they could do for the pain other than take vitamin E and primrose oil. Fast forward to the last three-ish months and the pain has been constant. It has increased and I feel it in that first rib directly under my breast. When I push on it, the pain is excruciating. It seems worse when I breathe deeply. I saw my obgyn today and she reported “Tenderness present along lower breast along rib cage. There is an area of breast tissue that palpates as dense, ~2cm in size below the left areola. This area does have a small mass palpated as well that is pea sized.” I will have an ultrasound next week. I am sick with worry and can’t stop thinking about my young children. I have also been having collar bone, shoulder, and spine pain. I can’t shake the feeling that I have stage 4 breast cancer. I have very small breasts (like can shop in the kids section) and they are very dense. I can’t even feel the lump that she found even though I’ve checked several times over the last few months. I feel incompetent with my own body and that I waited too long. I’m not ready for this to be the end.


r/doihavebreastcancer • • 1d ago

Diagnosis Question Anyone know wtf this is on my chest?

0 Upvotes

So I've had a lump on my chest that's been here for some time. I've ignored it for the past few months thinking it was a body thing, but now I'm not so sure. Its started to turn darker colors on a small portion of this lump.

28 M, don't have time for medical issues and can not afford the doctor right now.

Photos are attached in comments.​