Calcifications

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Hi,

In February I found a lump in my left breast. I went to my GP who found another lump and was referred to the Breast Clinic on the 2 week pathway.

I had an appointment later that week. The consultant found another lump in my right breast and said he thought they were cysts. Unfortunately, the mammogram wasn’t working so I was unable to have further tests until 10 days later. 

As soon as the radiologist did the mammogram on my left breast I knew something was wrong. She told me that she had seen something that they would want to look at on the ultrasound. I had my ultrasound with core and fine needle biopsies. They told me that they drained a cyst too. 

When I got home I received a phone call to say that they hadn’t got the area that they needed and booked me in for a stereotactic mammogram 3 weeks later. They told me that they found 15mm of  micro calcifications.

I went for my Stereotactic Mammogram and after an hour of being twisted and turned they explained to me that they could not go ahead with the biopsy but would send me for an MRI. I was too traumatised to ask any questions, I just wanted to get out of there.

I found out that the original lump was a cyst with a bigger cyst next to it that was drained and was bloody with inflammation. There was also a complex fibroadenoma next to it, luckily both benign.

I had my MRI and heard nothing for weeks then received a letter for another Stereotactic mammogram. Unfortunately, again they were unable to biopsy due to the central location of the calcifications. I’ve been told that they have rated the calcifications as M3 and the suggestion is to monitor at 6 months then a year. They are discussing my case at multi disciplinary this week.

 I know that it may not be cancer and if it is it’s very early but I am so anxious that they haven’t been able to biopsy and now I just have to wait to see if  it is cancer and it grows. It’s been 3 months of awful waiting and not knowing and I feel like I am in exactly the same position as I was 3 months ago. I just don’t know what to do.

  • Hi  , what a horrible time you’ve had, no wonder you don’t know what to do. And you’ve had so long not knowing whether you might have cancer or not, with a very difficult ending, as it’s still not a definite sign off. I’ve had some of the conditions you’ve mentioned but they’ve never presented themselves all at the same time! I don’t know whether hearing about my fibroadenoma, cysts and calcifications will help and I’m a bit of a rambler, but here goes! 

    Over a period of around 30 years I’ve had a few breast clinic referrals. I’ll only mention the most recent - in my 40s, a lump which the consultant thought was ‘very suspicious’. Needle biopsy and core biopsy came back as atypical but inconclusive. It was evicted (lumpectomy) and turned out to be a fibroadenoma. Phew. A few years later, lumps in the other breast. Inconclusive mammogram but an ultrasound some weeks later showed just cysts. They were left alone as not bothersome. Then at 59, I found ‘thickening’ which was cancer. They told me straight away at the clinic after mammogram and ultrasound, thankfully all on the same day as it’s now a one stop shop, instead of having to wait for lots of different appointments often at different hospitals! I’m now over 6 years post diagnosis, so far, so good. It has been mentioned that I’ve got calcifications, possibly in both breasts, but they compare each mammogram with the previous one and they seem to be stable and not of concern. I had annual mammograms for 5 years but am back on routine monitoring now. 

    So, I’m going to hope that, in your case, the things that needed identifying have been, and that the micro calcifications turn out to be of no concern. I am guessing that you will feel anxious, though, and very understandably, until you hear back from the MDT. Then somehow, if you’re on a 6 month recall, you’ll get through that time and it will hopefully be further reassurance. Keep posting here, if it’s helpful. It’s a very supportive forum, a great place to offload and ask questions. Sending love and a big virtual hug, HFxx

    HappyFeet1 xx
    Don’t be afraid to cry. It will free your mind of sorrowful thoughts. – Hopi
  • Thank you for your reply  please don’t worry about rambling as I do it too and reading other people’s experiences does help so much.

    Im so sorry about your cancer diagnosis but pleased that 6 years on things (touch wood) are going well for you. You have certainly had your fair share of visits to the breast clinic! And been through so much over the years.

    It has been an awful time especially with such a long period of tests without an answer. And, like you say, no definitive sign off either way. That’s what I’m really struggling with, the not being able to biopsy and no answer. I question what I would feel like if in 6 months the cells have grown. I read that 80% of women with M3 calcifications biopsied are benign but I keep thinking what if I’m in that 20% especially as I’m already in a really low number of women who they cannot biopsy. I keep trying to stick to the positive but feel like I’m wrestling with the accepting the unknown.

    Its all been a big shock and unnerved me, going for one lump that was a cyst (thank goodness) but then finding these other problems that I had no idea about. But, also it was my first mammogram. I’m thankful that it was done as I wouldn’t have been entitled to screening for another 6 years. I know the hospital have done everything they can, including an MRI.

    Thank you for taking the time to reply. You much love and a hug too