I had a stereotactic for calcifications in 1/06. At 6 month follow-up radiologist #1 recommended a stereotactic for new pleomorphic
clustersCluster headaches of calcifications. Surgeon agreed I could wait 3 months for a follow-up mammogram instead of biopsy. Radiologist #2 read 3 month follow-up mammo and there was very
littleLittle noses decongestant
Little tummys change; again recommended a stereotactic. On biopsy day Radiologist #3 said he found the
clustersCluster headaches to be similar and due to
benignBenign ear cyst or tumor
Benign positional vertigo condition, not pleomorphic as Radiologist #1 stated,probably caused by biopsy in Jan. I have possible fibroadenomas of similar form in same quadrant.Radiologist #3,surgeon and I decided not to do the stereotactic but follow-up in 6 months.Most of breast would have to be removed to take out all “suspicious” areas plus margins so surgeons are not jumping at excisional biopsy
1)Is it true breast cancer does not initially appear in several areas of the breast at once but rather in just 1
spotBirthmarks - pigmented
Liver spots
Measles, koplik spots - close-up
Mongolian blue spots? 2) When SIMILAR
clustersCluster headaches of calcifications appear at once are they considered likely benign?
3)When similarly formed lumps (possible fibroadenomas) appear at once are they considered less likely to be cancerous than if only one lump appeared?
4)Can new clusters of calcifications be caused by a previous biopsy? My new calcifications are not located bythe marker from previous biopsy but are in same quadrant.
5)Does my combination of similar clusters of calcifications PLUS similar lumps appearing in 6 months in same quadrant as biopsies sound like a benign condition, or do these calcifications plus lumps indicate greater suspicion for cancer?Thank you
breastcancer.org
under support and community click on discussion boards
then main forum index
scroll down to Help me get through treatment, click there
see my post under bonnienclyde or you can post your on questions
If you scroll down on the main forum index again to Research News and Discussion I also posted same question there.
Again hope this helps.
This is the first posting I have made on this site. I have been reading all your posts for a few days, and I admire all of you... your courage. I was told a few days ago that I have an area w/ microcalcifications and after a diagnostic mammo, I need a stereotactic biopsy. After numerous phone calls I still haven't been able to even find out what info my primary doc needs to schedule the appt. Very frustrating, and I feel invisible. Anyhow, the radiologist who read the diagnostic mammo said I had the option of having an excisional biop or the stereotactic. He said that pathologists like as much tissue as they can get. Well, it's not their body, and at this point, I definitely feel that a core needle biop is the way to go. However, it is really scary, the waiting, not knowing. I think I am doing OK, but just the weirdest things will set off the tears. I woke up in the middle of the night a couple days ago from a nightmare in which I was on the table having the biopsy, and I was covered with sweat and feeling like I was going to throw up. I guess my stress over this is a little deeper than what I thought. I just wanted to say that reading all of your posts: your insights and experiences, have helped me feel grounded.
Another question for anyone... since the diagnostic mammogram, I have had a lot of soreness in that breast, especially the nipple. They really used a lot of compression, so much that I had redness for about 12 hours. Is this common? I still can't touch that nipple, and it's been 6 days. Thanks.
Anxiously awaiting a reply.
I totally understand what you are going through. I found out 11/1 that my last mammo (a digital mammo, taken on 10/20) showed a new cluster of microcalcifications. I have my sterostatic biopsy tomorrow. I'm not sure how long it will take to get the results back. I had to wait almost 2 weeks from hearing about the resutls of my mammo to get in to have the biopsy. So waiting until 11/20 is not really that bad. If they were really concerned that it was something that needed to be biopsied immediately, you'd be in the next day.
I know it is hard to wait. I will be thinking of you and hoping for the best.
Donna
Michelle
bat - yes, waiting is the hardest. If it turns out cancerous (remember the odds are in your favor that it will be BENIGN) calcification biopsies typically find a very early cancer or precancer. I know it's impossible not to worry...but I've always had to wait several weeks for my biopsies and there won't be much change in that amount of time. I'll keep you in my prayers also.
Thanks for your help.
Thinking of ya
Michelle
Thank you for asking. The biopsy itself went well and wasn't nearly as bad as I anticipated. As far as pain, I didn't really experience any.
The radiologist that did the biopsy showed me the microcals on the mammogram film. I have 6, loosely clustered. I had an ultrasound beforehand and the radiologist told me they didn't find a mass. The doctor said that my microcals "looked" benign, but that at the same time, they are "on the border," and they really didn't know for sure. He assured me that if it were something, that is was caught very early. He also said that 2/3 of these biopsies are benign.
So I won't know anything official for 3-5 more days (business days). I feel much better now that the biopsy is done, and feel that I am ready for the diagnosis, whatever it might be.
Thank you, again, for asking.
Donna
Michelle
MontanaGirl and VermontGirl, I feel for what you are going through and will send my prayers your way.
I am new to the forum (41, Connecticut, married, 2 boys 15 and 10, full-time legal assistant) and have been reading through the posts on this Board for the last 3 days. I come here with tears in my eyes reading and feeling for what people are going through. Those who are patiently waiting for the testing, those who are currently going through the disease, those who have survived the disease, those who are going through the aftermath of regaining their lives.
I want all of you to know how wonderful you are answering questions and giving so generously of yourselves and your own stories have been a source of inspiration and hope, lifting our spirits and helping to alleviate our fears.
On 11/7, I had my mammogram (last mammogram was March 2004). I received a phone call on 11/13 from Radiology saying that they found a dense mass in my left breast (I have saline breast implants since June 1999). They have scheduled me for an Ultrasound 3 weeks from now and they cannot get me in any sooner. The anxiety is so bad, I can't eat, sleep or focus at work. I have not told my parents or my best friends. I don't want to get everyone worried at this point and don't want a lot of drama. I called Radiology today to see if there were any cancellations to squeeze me in, but no cancellations and they don't do waiting lists. My husband is so upset that we have to wait weeks, that he scheduled an appointment for in New York City tomorrow 11/16 for an Ultrasound (and Biopsy if needed). I am picking up the paperwork today from the Radiologists to bring with me since I haven't seen it myself as of yet.
Although my grandmother had breast cancer at age 78 (and spread throughout her body quickly, not sure if it started in the breast or other area, by the time they detected it was too far gone and she died 3 months after it be detected.) There is no one else in my family that has had cancer.
I apologize if I am rambling, but there are so many thoughts racing through my head and I am trying not to think the worst, but at the same time, I am one of those people who likes to be in control and wants to be prepared for the worst possible outcome.
Thanks for listening. :)
Good luck
Bat42563, I can't find the web page you wrote about, or maybe it is a posting, for "stereotactic breast biopsy"
Thanks
I did the same thing, I went to NYC, and didn't wait, my doctor didn't calll me for about 4 days, when I already met with a suregeon and made my biopsy appointment. Again, you have to be your own advocate.
Your reports sound like they may be fine. If you read about scattered calcs are benign. I believe from what some friends say that have implant, its one of the side effects.
You are going to be fine too. We are all praying!!
You are in a similiar mode as me, had my biopsy Monday, and have to wait a few days.
However, my cluster too was a bit scattered, but it was a cluster.
It is a relief when that part is done, and then the waiting.
Please keep us posted.
Anyway, I got the stomach flu today (kids brought it home from school). So I can't think of much other than holding food down. I'm SO GLAD I wasn't sick during my bx yesterday - that would have been awful. So sometimes things work out the right way.
Donna
I had something similar happen to me about 3 years ago. They found a mass on my mammogram and I had to go back for a diagnositic mammo and an ultrasound, then consult with a breast surgeon. The tests showed that it was a cyst and everything turned out okay. My maternal grandmother got breast cancer, too, and died from it (mainly from lack of treatment, it WAS treatable and not aggressive, but that is another story!)
I remember that time being extremely stressful (like what I am going through now). It was almost surreal. Everyone is different regarding who they tell and how much they talk about it. Personally, I find talking about it makes it less scary, but some women don't like to talk about it. That's what makes this forum so nice - you can "talk" about it but remain anonymous.
Your husband is a gem for taking things into his own hands and scheduling the US and possible bx for you. My H took things into his own hands, too, recently, when I was scared about my BIRAD 4 mammo and recommended bx. He called and made the appointment for me. It is nice to know that husbands love us so much at times like this.
Take care and hoping for the best for you.
Donna
Everyone is in my prayers.
Montana Girl: Thank you....
I just received my results...benign, I want to thank everyone for being so wonderful, I will be on this forum continually, it has changed my life and helped me through this ordeal...
GOD BLESS US BEAUTIFUL STRONG WOMEN!!!!
I met with my surgeon on 11/9. I got a copy of my mammography. He pointed out to me that it stated "geographic area of multiple calcifications laterally in right breast." He did indicate that geographic is better than cluster, however he did say he has been wrong before. The earliest I could have the biopsy done was on the 22nd and we were going to be on the road for Thanksgiving so I will be having the stereotactic on the 27th. Today, I shared with my mom and one of my dear friends that is a nurse at the hospital where I will be having the procedure done, that I am having a biopsy. I have not really wanted to talk to anyone about it other than my husband. I really did not want to give the situation any life.
Sometimes I am really up and if I am alone-it can be very scarey. The unknown and all. I haven't said anything to my children. Ages 18 and 15. I figure I will decide after the biopsy.
I just wanted to say hell'o. I think of you all and pray for you. This forum has been such a help for me. I kind of drop in and out of threads, as I will join one and the thread will close. Regarding husbands, my has been great and has done his best to let me show and share my fear and he has been extremely supportive. He truly is a great guy.
God Bless and thank you for letting me vent.
Donna
You, too Arcmurd! Thanks for sharing this with us. I'm very happy for both of you.
That is fantastic news. Enjoy your Thanksgiving with your family.
And thankyou again for your comforting words. This is the best site.
Donna