MRI causes a can of worms?
Hi all,
Spoke with the nurse the other day and said I was interested in an MRI to make sure all is well on both sides. I have dense "complicated" breasts, left with atypical hyperplasia, radial scar and I thought it was the test to take. She said, "well...it can open a can of worms." So do you do one and open that can of worms, which means what exactly? or not and wonder if all is well? What a terrible predicament for us dense breasted ladies...
I am having an excisional biopsy on the left as well. Thanks for your words of advice.
Comments
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Somebody will probably give a more detailed explanation than I can, but:
MRIs have a tendency to give false-positive results and leads to unnecessary biopsies.
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I have LCIS (and nothing worse) and had an excisional biopsy. A year later, had 2 more biopsies-one inches away from my excisional site (as far as I knew). It ended up being consistent with scar tissue, so the surgeon went all over my breast during the excision.
The subject whether MRIs should be used to SCREEN LCIS (and nothing worse) patients without a strong family history is controversial.
I went to a Major Institution (NCI certified), and they recommended I not get MRI screening, not even a baseline one, because I have so much scar tissue. (I'm not saying I agree with their recommendation.)
Kuchagirl is right - MRIs tend to have a lot of false positives, which leads to unnecessary biopsies. This means that MRIs are quite sensitive to pick up cancer - but they are also sensitive to pick up inflammation or other junk which is not cancer. They often can't tell the difference between the junk and the cancer. Hence the biopsies.
If they do find cancer, they then do often recommend MRIs to plan the size of the surgery, and to monitor the other breast, particularly if they find ILC (also known as The Sneaky One.)
Here's the article that have the 2007 ACS recommendations. This is for breast SCREENING, not diagnosis. http://caonline.amcancersoc.org/cgi/content/full/57/2/75
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the MRI was a huge part of the dx phase for me but it was never suggested until I had been dx'd. I also had dense breasts. Digital mamo would be a good option but the MRI may pick up scar tissue and "other" stuff like menitoned above. The MRI was invaluable for me because we had planned a lumpectomy and it was only after the MRI that we knew that the tumor was too big for that. Mine had lobular features but was dxd as IDC. Doc said the lobular features allowed it to hide..it also showed all the biopsy spots and B9 cysts as well.
I really think that the MRI as a screening tool is questionable..Like PET's they can read a lot of false positives....I guess that's the can of worms she is referring to.
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I thought having an MRI was the standard of care (after BC diasnosis) and had my doc order one. When I went to see the BS he poo pooed me for having the test done as he said it does open a can of worms and now I needed extra biopsies. He assured me these areas were nothing to worry about. (2 questionable areas lit up on the MRI)
HE WAS WRONG.
In the breast with the IDC, there was a cyst there. HOWEVER, IDC was found, after biopsy, in the other breast. I am 61 so opted for BMX. The path report showed another area of DCIS so I have never regretted my decision, nor pestering a doc to please order an MRI.
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Yes that is the question isn't it. I really wish I had an answer for you and me. I too have very busy breasts, my BS has been encouraging me to have a MRI for almost a year now, he's too warned me of the possibilty of hot spots which might require more biopsies. Isn't that what we all look forward to?
I am torn, I have always declined MRI's before, but since my last US showed an area with a thickened cyst wall I have been reconsidering, My BS is very proactive and often reminds me of how easy it would be for something to be hiding amongst my many large cysts. Having a family history of both paternal and maternal grandmothers with hx of breat cancer certainly raises the stakes. I really wish I knew what to do. Being a nurse does not give me any greater insight, however I understand that breast specific gamma imaging is not only sensitive but very accurate. I believe this is a very new technogoly which is not being used to often beacuse of availabilty and cost.
Has anyone had BSGI, I would appreciate more information.
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Hi Ladies,
I hope no one takes offense, but I couldn't resist posting. When I first saw this topic in the Active Topics list, I had to read it. Why? Because I thought it read:
MRI causes worms?
Gotta love my ability to skim titles.... hope it makes ya smile!
C
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C, have another cup of coffee.
Yes, using MRI for screening, even if you have dense breast tissue, apparently does create more problems. My BC was dx'd and treated at a major university hospital that is an NCI-designated comprehensive cancer center. Once my tumor had been dx'd with a US-guided biopsy (it was never seen by mammography--even the digital variety), my BS ordered an MRI to look for other tumors in that breast or in the other one. But, she will not order MRI for monitoring (which is actually screening) now that my BC has been treated. She explained that MRI is too likely to generate false-positive results--thus, unnecessary biopsies. MRI has been "approved" for screening in women at high risk of BC (women who are BRCA-positive, for example), but not for women at "average" risk. Dense breast tissue supposedly increases our risk, but there has not been enough data on how breast density should be measured (objectively) and recorded. She also said MRI is "approved" for evaluating the presence of other tumors in women who have been dx'd with a tumor but have not undergone treatment yet.
My BS is a surgical oncologist; she is a member of the review panel that produced the NCCN guidelines on BC screening. So, she is following those guidelines. My onco is a medical oncologist; she is a member of the review panel that produced the NCCN guidelines on BC diagnosis and treatment. She also says MRI is not an approved method for screening unless there is high risk of BC.
I need to note that the word "approved" is an official term, referring to FDA approval and/or approval by professional oncology organizations. It also (probably) refers to approval by insurance companies, but my insurance company tends to follow the same official, medical guidelines as my doctors follow.
Yes, it's a can of worms for sure.
otter
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ha ha ha...thank you for the laugh C, that was funny. Made my day.
And thank you to everyone else for such informative responses. Interesting. Okay, so what I gleaned from is if AFTER an excisional biopsy one is diagnosed, then they'll order an MRI to make sure there is nothing else. I don't really want to have more biopsies but I hear you Sue...
But if after the excisional biopsy, the findings are the same as the stereo (ADH, Scar, etc)..then they'll skip it and hope for the best. I'll see what my doctor says...one step at a time I guess. The good news is I don't have family history.
I'm going to have to look into that BSGI though, let me know if you find anything out Roo.
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I agree an MRI can open up a can of worms! After my dx of IDC in the right breast I had an MRI that showed 14 lumps between the two breasts. Although they weren't suspicious, I opted to have BMX with reconstruction. My greatest fear was that if the lumps change at all I would need another biopsy and I didn't want to get on that emotional roller coaster again! My final path report from the BMX showed that with the exception of the original cancer everything else was B9. I don't regret the decision for BMX, it has given me a little peace of mind.
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Hi there....
Yes, your are right about the MRI's...lots of false positives.
I remember when I requested to have my breast mri done after I was diagnosed my oncologist sent me and my breast surgeon got really upset...she said to me "now you have just opened Pandora's Box!!"
I did have some false positives due to having an MRI too close to radiation treatment,, I did a repeat MRI 8 months later and both of my breasts were clear.
I still insist that I want a mammo and a breast mri 1x per year. I would rather have more checking then less checking..and would rather be safe than sorry.
Hugs...Kosh
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Alot of false positvies, sure. MRI's are super sensitive and may lead to unneccessary biopsies.. but I credit my latest one for saving my life. I had DCIS in 6/07 - calcifications showed up on a mammo - that's how it was diagnosed. After that dx they did MRI's and mammos on me every 6 months. 15 months later in 11/08, my mammo came back all clear. The MRI on the same day found invasive ductal carcinoma. Had I not had the MRI, the IDC would have remained undetected and allowed to grow. So, if MRI's open up a can of worms.. I'm glad the can was open in my case. I was always told I had dense complicated breasts too. I agree with Kosh... better safe than sorry... we all know how important early detection is.....
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I am having my care at a NCI designated cancer center. My surgical oncologist has me alternate every 6 months between a digital mammogram and an mri. that way I am being screened every 6 months. If something shows up on either the mammogram or mri an ultrasound is done to clarify what was picked up.
In May '08 a mammogram picked up a cancerous 8mm tumor but showed nothing else of concern.Luckily, the BS ordered an mri that picked up another area of suspicion that turned out to be DCIS. None of the tests are perfect but each has its place
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my oncologist used that expression too ----that an MRI would "open Pandora's box" --referring to the possibility of unecessary biopsies and the ensuing anxiety that goes along with them. But I told him I was willing to take that risk rather than have something invasive missed (I'm high risk from the combination of LCIS and family history)----I've had some suspicious "spots", but everything's been clear on the f/u mammo or US.
Anne
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C, that was pretty funny. I guess MRI's don't cause worms but definately cause indigestion.
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I am another person who had IDC diagnosed after a MRI.
My initial diagnosis was DCIS; I had calcifications that showed up on a mammogram. I had a lumpectomy and SNB. In addition, my surgeon felt a dimple on the underside of my breast during a pre operative exam. So he removed the tumor that was causing the dimple. It turned out to be IDC, 8 mm. Later when I read the radiologist's reports, it turned out that there was a shadow in my initial mammogram, but it didn't show up on a diagnostic mammogram and the area was not biopsied. 1+ for my surgeon.
When I met with my medical oncologist after my first diagnosis, he said that he didn't think a MRI was necessary as there were too many false positives. I didn't argue with him. However, when I had my initial appointment with the radiation oncologist, she asked me to get an MRI, to check for the extent of disease. I had the MRI; there were four suspicous areas. The radiologist was able to biopsy three of the areas, after I had an ultra sound to confirm the MRI results. One of the areas was IDC, 1.2 cm. 1+ for the radiation oncologist. 1- for my medical oncologist.
I recommend anyone who is dx with bc get an MRI to check for the extent of disease; you may have to have additional biopsies, but you will have a more complete picture before deciding on surgery. -
As a new reader I cannot let this one pass without a comment. I credit MRI with saving my life. I have had fibrocystic disease for 30+ years and have had yearly mammograms, multiple ultrascans, biopsies x 2 (both B9), unsuccessful needle aspiration attempts, etc., etc., etc. My 85 year old mother was diagnosed with ILC last year in July. She had a mastectomy and is doing great, even with positive nodes.
I had a diagnostic mammogram with ultrasound in Oct. 2009 and was told to return in a year for a screening. I am so thankful for having a GYN who wouldn't stop. Because of my long history of troublesome issues and my mother's newly diagnosed cancer, she encouraged me to have the MRI. I knew about false positives but I'd rather have a biopsy and be told that it was nothing rather than have cancer that would go undetected. I was also told that if I didn't plan to follow-up with biopsy if the MRI was positive, that I should not have it in the first place. Makes sense.
My cancer was on the edge of a papilloma with mixed ductal and lobular features. My surgeon, one of the best at Markey Cancer Center in Lexington, said that MRI gave me a two year jump; it would have taken (in his opinion) that long for it to show up on mammogram. I was also told that I had an angel watching over me. Once a diagnoses is made, a treatment plan can be formulated.. that can help save lives. I hope my story will help someone who is trying to make a decision and let's not ignore our guardian angels. Hugs to all who live with this hateful disease.
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I am also another one who credits the MRI with saving my life. I have a strong family history of BC and had regular mammograms and some ultraounds for 15 years. I had dense breasts so there was always that caveat on the mammogram results. After I turned 50, my doctor ordered an MRI, as a baseline, he said. Turns out that I had two areas of IDC that were not picked up on a mammogram six months before. He said that they probably wouldn't have shown up for a year. I encourage anyone with dense breasts and a family history to push for an MRI.
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I had my first MRI (reluctantly) on friday. I have very busy breasts and was concerned that the MRI would lead to even more aspirations and biopsies.
I thank this forum and the many of you ladies who shared your results from your MRI. I was given the courage to go through with the test, which I did friday. I recieved my report yesterday and to my surprise was actually given a BIRADS 2 rating ( usually given BIRADS 3 or 4)
For now I have some peace of mind. Having a family history and having dense fibrocystic breasts with large cysts requires close survellance.
May we all be B9.
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or not... i had an mri with contrast and a bsgi which both came back birads 2 - benign. i had an excisional biopsy last week and my results are idc stage la. there were no hot spots on either mri or bsgi. my cancer is only 3mm, which is very small and may be why it didn't enhance on the tests. my doctor also told me that no test is l00% accurate.
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debnyc
did you request the biopsy or was it on the advice of your BS. Since having the MRI I have not yet returned for a f/u with my BS. I have many large palpable cysts that did light up but they considered to be in the benign spectrum, now you have me wondering.
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I am another one whose life was actually saved by an MRI...my mammo was clean, the palpation by oncologist, OB/GYN, and BS was fine. On a whim, my onc said let's try an MRI just to be super sure. I was violently opposed. Ick, tiny tube, 40 minutes. My onc just said give it a whirl, even ultra sound was clear. He was OK with waiting six months anyway. On a whim, my husband and I decided just to go and get it anyway and get it done. (I had had previous BC and spent 5 years on tamoxifen. No one thought it'd be anything but another tool in the arsenal, not even my onc.
Well, a big old 1.5 cm. tumor, hiding deep in chest wall. Unseeable by mammo and unpalpable by human hands. If I had not had that MRI, I'd be telling a different tale.
So get one. It could literally save your life. (BTW I was node negative, early stage IDCIS, good oncotype, clear blood markers. No sign of this thing.
It's worth it.
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p.s. "the can of worms" is true, unfortunately. There are many false positives with MRI, no where near as many as there were even two years ago, but these false positives can lead to unnecessary worry and biopsies.
But wouldn't you rather find out and be absolutely sure? As with the combo of mammo and MRI you can be really safe.
Good luck. This is why I was opposed to it, too. As you can read my tale................
xoxo
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hi roorooep,
i had:
birads 4 mammo and ultrasound
benign stereotactic biopsy
fna biopsy with atypia
negative mri and bsgi
my breast surgeon and pcp both told me that the negatives do not cancel out the positives and that diagnosis is based on findings of multiple tests. since i did have the positive fna, the only way to know for sure was to have the excisional biopsy. unfortunately, now i need to go back for re-excision and sentinel node biopsy.
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MRI is the only screening tool that showed the 9 CM ILC beast that was hiding in my right breast. I had a small cluster of microcalcifications on a mammo ( after 15 years of faithfully getting my mammos, and sighing with relief every time I was told it was all clear!) which when biopsied showed ILC.
I have an MRI on remaining breast every year. So far every thing has been clear, but if something shows up that needs a biopsy I say bring it on!
This actually brings me to question about MRI's. Is it true that microcalcifications (which in my case was a small area of DCIS) are not seen on MRI?
One of the reasons I ask this is that I am scheduled for unilateral DIEP in October. I had a clear MRI in May, but I am not due for another Mammogram until December. I am thinking I might want to have the mammo early in case there are some microcalcs that were not picked up in May. Since DIEP is a one shot deal, if there is anything funny going on in my left breast I want to know, because in that case it is gone!
Cyndi
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My sister had a lump not seen on mammogram. Biopsy revealed cancer. She was going to have a lumpectomy but surgeon said to have an MRI, "just in case". The MRI revealed additional areas of DCIS in both breasts so she had a dbl mst. She would have gone untreated if not for that MRI.
I get MRIs (and mammograms) now and they schedule them within 5-7 days of my period to reduce the false positives. I'm told timing and an excellent radiologist who reads these all day can reduce the false positives.
Best of luck!
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Everything everyone said about MRI "opening a can of worms" and producing false positives is true.
There's an article about this if you care to read it:
In Newly Diagnosed Early Breast Cancer, MRI May Cause More Harm Than Good
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hi "debnyc"
thanks for the info.
roorooep
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Having an MRI probably saved my life. I had a palpable lump for at least 4 years (I felt it, the doctors repeatedly said it was "nothing"). I am an "A" cup, very lean and it was right at the surface, so I was able to easily feel it. It didn't show on mammo (even on the day of my surgery) or on sonogram, but it showed on the MRI - a 8mm lump. It was a very slow growing tubulolobular, which (as I understand it) generally does not show up on mammos. I'm slated for MRIs 2x a year - and I will go into that tube with not a single complaint (which will thrill the radiologist, I'm sure). Better to potentially have a couple of false alarms that to miss the opportunity of an early diagnosis.
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