Calcifications & Surgical Biopsy

[Soldier37]

I am 37yo.  I had my 1st mamo. at 35.  Calcifications were found on left breast, 2" up and left of my nipple.  Repeated mamo. every 6 mos.  This time they found growth on original calcifications and new microcalcifications.  Did magnified mamo. at hospital.  New clusters run from larger calcifications down to behind my nipple.  Radiologist said I can't have a needle biopsy because of position so I have an appointment for surgical consultation.  The only thing I know from last mamo. is BIRAD 4.  Should I be concerned this is cancer?  Everything I read says only about 1 in 4-5 is malignant.  I have history of other cancers in family but not breast (that I know of).  I used to smoke heavily but not for about a year.  I know you can't diagnose.  I just want to be prepared if cancer is more than a slim chance.

[misawa47]

A related discussion, Stereotactic Biopsy yielded no Calcifications was started.

[Montana girl 06]

xander - I'd try to call the nurse and talk to her about your research. I hadn't heard they couldn't do stereotactics on small breasts, but there's a lot I don't know.

Jackieone - I wore a tight fitting sports bra after my stereotactic and it worked fine. When I went back to work the next day I put my regular bra over my sports bra (to give more shape since most sports bras flatten me) and slipped a small ice pack in between the two bras. Sorry to hear about your calcs. Hope all turns out well.

[boninclyde]

Hello ladies. Just wanted to suggest you start a new post further up on like page one. I think you are 3/4 pages back and sometimes the other ladies here don't read this far back. Jump up to page 1 with us so we can all chime in and try to help.

[Jackieone]

Hi everyone. Just wanted to thank all of you for the fine information. I'm 51 and will have a surgical biopsy on August 21. I have a 2cm area of calcification. I saw the surgeon Thursday and he didn't feel any abnormalities which is good. I also had a softball hit me last year in the same area so I'm 90% sure that its not cancer but better safe than sorry. The surgeon told me to get and wear a loss fitting good support bra. I've never heard of a support bra being loose fitting before. I plan to go the the local Perfect Fit store and see if they can help me with that. He says I'll need to sleep in if for a few days after the surgery. Anyway, I just wanted to let you know that this forum helped me with knowing what questions to ask and calmed my fears.

Thanks,
Jackieone

[xander1218]

I have microcalcifications, BIRAD 4,  and scheduled in a few weeks to see a Surgeon for a  Biopsy Consultation.  Over the phone, the Nurse from the Surgeon's Office, told me I will have a Stereotatic Biopsy.  However, the Surgeon hasn't physicaaly seen me yet and my glorious 32AA breasts.  After doing more research, I just learned that because of my size (or lack there of) I will have to have an Open Surgical Biopsy.   Is this true?  Is this the only Biopsy choice for very small breasted women?

[mimizerr]

How did the sterotatic biopsy go?  I had one last August and it was so painful I saw stars during the procedure.   I had a cluster of cacifications.  The mamo revealed the calcifications were gone after the procedure.  Last month I had a mamo and all was clear.  Last week my breast hurt and I found a hard lump.  I think it is left over from the stereotatic biopsy.  Next time I will just have the surgery.
What are your thoughts on the stereotatic biopsy?

[brittnat]

What were your results from your biopsy?  iam new to all of this, and have a biopsy (mammotone ) tomorrow.

[Montana girl 06]

First, you need to know that I am not a medical professional and talk only from my personal experiences and from what I've read.

I wonder if your clusters of microcalcs are too far apart to biopsy in 1 proceedure. It's also possible that they are too deep and they feel they might not be successful.  This is just a guess.  With my last stereotactic biopsy I had several clusters near enough that they got a good sampling of the area. But, my clusters were not removed entirely.

At your biopsy I would ask why they chose that particular cluster of microcalcs to biopsy and why not the other, and why they felt a biopsy of only 1 cluster would be sufficient. Also, ask if they removed the entire cluster or just sampled it.

My experience with surgeons is that they are often not eager to remove a large area unless they really feel core biopsy is not adequate. I've had 2 different surgeons choose not to remove the large area recommended by the radiologist because it would remove about 1/3 of my breast and become a major surgery.

Please remember that most microcalcifications (even those biopsied) are benign. I wish you well with your biopsy.

[Bay area girl]

I would like some comments about this. I am 53 with this being my first call back on a mamogram.   I have a core biopsy scheduled 2 days from now on one of 2 similar cluster amorphic microcalcifications on the right breast.  I got a birad 4 classifications but the dictor said in the report that they were faint and hard to see and that is why the biopsy.  I insisted that both clusters be biopsied and removed but the doctor said emphatically that that would be removing too much tissue and if I wanted both removed I should go to a breast surgeon.  I read every forum comment on core biopsies and I noticed that many had more than one cluster biopsied.  I am going ahead with the initial biopsy but I am of couse concerned and frightened.  Any  comments?

[Montana girl 06]

How are you doing? Did you need more treatment after your surgery, or did they feel they removed everything? Haven't heard from you in awhile and just wonder how you're doing.

[stresscase123]

Get it checked out for peace of mind, if there is *any* question, IMO.

For the record, I had my baseline mammo and was given a BiRADS score of 3 for calcifications.  The radioloigst suggested I have a biopsy, since we had no history on the calcs, but also told me waiting 6 months was an option, since it was highly likely to be benign.  I went ahead with the biopsy, and lo and behold was diagnosed w/DCIS!

Regardless of BiRADS, if the techology exists to rule something in or out, we should take advantage of it.  The benefits of early diagnosis far outweigh the inconvenience/risks of an unnecessary biopsy, IMO!

[lasimon]

Thanks Montana girl.  I'm praying that everything goes good also- my test is on Friday the 13th-:(  but hey- never had anything bad happen before on this date so I hope that the trend continues!

Have a great 4th of July!!!

[Montana girl 06]

I recommend you get an actual copy of the radiology report so you have as much info as possible. It would be a good idea to ask for a copy after every mammogram so YOU can follow your reports and not just leave it in the doctor's hands. It is fairly common for women (whether they have family history or not) to get a notice that they should come back in 6 months to check an area that is probably benign, but since they're not certain they want to keep an eye on it. It's also fairly common for radiologists to follow somewhat suspicious findings in the breast and not even let the patient know! Since they said come back in 6 months I'm guessing the radiologist gave it a BIRADS 3 rating on a scale of 1-5. That means it's highly unlikely it will be cancer. But, with your family history it's great that your doctor is moving forward with an MRI. I just want you to know that MRI's have a fair number of FALSE positives. I really hope you get some answers, because I know how scary it is to just wait and wonder if you have cancer. I hope all goes well with your MRI.

[lasimon]

I went for my mammogram a few weeks ago and I was asked to come back for some additional pictures for my right breast- ( I have family history of breast cancer also- Mother at 37 and an aunt also ) When I had the additional pictures done the radiologist said that everything is fine but they want to have me come back in 6 months for another mammogram.  After this I received a letter in the mail from the place where my Mammogram was done and they used the term you "PROBABLY" dont have cancer but you need to come back in 6 months for a recheck- I called my Dr who was to get the information and wanted to understand what the word"probably" meant???  I could have cancer or I don't?? really felt uneasy about the letter just leaving it as is.  My Dr. Then called back and sent a referral for and MRI to be done.  Is this letter common for woman to get with high risk of cancer history in family?  Just curious if I am overreacting.....

Thanks in advance for any advice!!!

[Montana girl 06]

Thanks for keeping us posted. I'm glad your biopsy is scheduled soon so you can get some answers. I hope you join the benign group.

[blkw]

Thanks for the advice and reply. I'm new here. I've been trying to do some of my own research (which is probably making me more nervous instead of helping) but can't find the answer to this question.  I got it posted this morning.
Thanks again and best regards to you,
-blk

[Montana girl 06]

I hope all goes well. Keep us posted.

[Soldier37]

Hi everyone!  I had my consultation with the surgeon today.  I feel so much better!  I'm having a stereotactic biopsy next Tuesday.  He gave me the same percentages as most of you - "...85% of cases similar to your circumstances are benign".  I am also glad I don't have to have an open biopsy.  Hopefully, I'll know for sure by the end of next week.  I really think everything is going to be alright.  I'll pass on the good news to you when I get it.  Hope you all are doing well. Thanks for all the support.

-Soldier

[Soldier37]

Thanks to everyone for all the info.  I got my report today but it was only one page and not very descriptive.  Most of the information I got from the nurse after my appointment wasn't even on it.  Do they do a summary report or something?  I wanted to see it so I could ask questions tomorrow.  My BIRAD rating wasn't even on it nor were any of the measurements of the clusters.  One thing I did see is that if I have a family history, the radiologist thinks this could be more of an indication of malignancy.  The only problem is that my mom died at 52 with colon cancer.  She had something in her breast but since she refused further treatment for the colon cancer, she never did anything about the spot on her breast.  I have no idea whether it could have been something or not.  I guess I'll see tomorrow what the surgeon thinks.

[boninclyde]

Well I guess I'll butt in. I have been scolded and I have scolded some on this site. I had to learn patience. It is most of the time a mis-interpretation and we don't mean to harm anyone. We only try to help. We appreciate being corrected. We are all here to learn. Lizzie has been a great help on here and has helped alot of people. Thank you all who post so much for taking your time to help.

[japdip]

Hi .... I believe there isn't a difference due to the age of the patient. If you would like an answer from the Cleveland Clinic Professional you should ask your question as a post rather than just a comment. They never read the comments; just the original post. I know it's difficult to get on the forum but if you try at different times of the day (and even late at night) you will eventually be able to post. They reset at different times each day to give those in different time zones an opportunity to post.

[lizziecee]

I truly apologise if I said anything incorrect.... I would not purposely mislead anyone with this awful disease.  When I had my 3rd mammo at 58 yrs, at a travelling van in the isolated place I live, I had a BIRADS 4 - then I was recalled to a breast care centre where my surgeon said that a BIRAD 4 was highly suspicious of malignancy - perhaps by the mammo which I eventually saw, that showed a black mass, which was spiculated. I may be in a minority of BIRADS stage 4. that was dx with breast cancer,  but at least it was picked up. I just wanted to detail my own experience and let Soldier realise how important the score is/was.

I eventually was dx with a 2 cm invasive tumour and spread to the lymph nodes
I apologise to anyone I upset by my post.
Liz.

[blkw]

You mention the percentage of biopsy of calificatioin clusters that are cancer vs. benign. Does this percentage vary by age? I'm 37 and having a calification cluster biop this Thursday (my mother also had breast cancer), I'm wondering if the percentage of non-cancer findings is higher over 50/under 50 or over 40/under 40. Thanks,

[Avidhiker]

I am a breast cancer survivor.  In April of 2006, my mammo was given a BIRAD of 4 which I know for a fact means "suspicious abnormality".  A biopsy was recommended.  I had microcalcifications spread out over too large an area for any needle biopsy.  I had an excisional biopsy and unfortunately mine turned out to be malignant.  At the time, I asked my surgeon the chances of this happening and he advised that 15% turn out to be malignant.  This, of course, means that 85% of the time it is not.  Since April of 2006, perhaps these percentages have fallen or risen.  My surgeon has 33+ years of breast surgery and diagnosing and treating breast diseases.  I believe what he tells me.  

By the way, I also know for a fact that a BIRAD 5 rating is "highly suggestive of malignancy".  A BIRAD 6 is after the biopsy and means "known biopsy-proven malignant".

To soldier37:  GO ASAP FOR YOUR BIOPSY!  If it is cancer, it will be EARLY and that is the most important issue.  Good luck.