Sentinel Lymph node Biopsy
I was diagnosed Invasive Ductal carcinoma on 12/30/13. I don't have any family member or relative who had breast cancer. My mom had lung cancer but she was 70 yrs old and I was so shocked to be diagnosed with cancer at 48. Size of tumors are 2cm and 1cm in a same breast. I have a question about lymph node biopsy. I went to 2 doctors and one doctor told me she will take 1-2 nodes. Other doctor said she won't know how many she will take until surgery. My Canadian friend said when she had surgery, biopsy was done at operation room and doctor only took the one which are necessary. But both doctors said they will need to send it out for biopsy.
I just worry about lymphedema and I want minimum number of node taken out. How many lymph nodes really need to taken out? And what is the chance to get lymphedema after surgery?
Comments
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I had a lumpectomy on 11/22/13 with sentinel node biopsy. First the injections to track the nodes hurt like nothing else, but I think it was necessary. In surgery cancer was found in 4 of 6 sentinel nodes, none in 5 axillary nodes. At surgery they removed a couple, found them to be positive then removed a couple more, they were positive so they took two more. Just kept working through until they got it all. The pathologist was on duty, they also did not get good margins the first time, went in and took more tissue until I was clear. The whole surgery was less than an hour and when I came out I knew they had all the nodes and good margins. No reason to have surgery then to have to wait for pathology results, they should know when they have you open the first time. I am not having any problems with lymphedema at this time, crosses fingers. Hope this answers a few questions.
Patti
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If a sentinel node biopsy is done properly, the surgeon can't know until he or she is operating how many nodes will be removed. It all depends on
how many nodes "light up".The way an SNB works is that injections are
made into the breast prior to the surgery. The
injections are either blue dye or radioactive isotopes or both. Several
injections are made, and they are aimed in different directions. The
dye/isotopes then travel through the breast and move to the lymph nodes
under the arm. The nodes that "light up" with the dye and/or isotopes
are the sentinel nodes. It's not that the dye/isotopes light up nodes
that have cancer. They just light up which ever nodes they enter into.
What is not well understood is that sometimes with an SNB only 1 node needs to be removed but often it's 2 or 3 and it could even be up to 6 or 7.
When a sentinel node biopsy is properly done, the surgeon should remove
all of the nodes that 'light up' from the dye or isotope injections.
If only one node lights up, then only one node needs to be removed. But
if 6 nodes light up, then all 6 nodes need to be removed. If the
dye/isotopes were able to travel so quickly from the injection site in
the breast into 6 nodes, then logically if cancer cells were to travel
from the breast to the nodes, the cancer cells could just as easily
move into any one of those 6 nodes (or all 6). So when 6 nodes light
up, the surgeon can't just pick one to remove. Because of the way that
the nodes are bunched, there is no way to know which node was the
first one that the dye (and cancer cells) would have entered. All 6
nodes must be removed.
So basically the theory of an SNB is that the injected dye/isotopes
will follow the same pathways within the breast to the nodes that cancer
cells would have followed. Therefore whichever nodes are entered into
and lit up by the dye/isotopes injections are the nodes that would be
the most likely to have cancer cells, if any cancer had moved from the
breast to the nodes.An SNB usually is done at the same time as the breast surgery. Sometimes the nodes are sent out for a quick pathology check while the rest of the surgery is going on. If any nodes are found to be positive, more nodes can be removed during the surgery. But even if the nodes are all found to be negative, this is just a quick check, and a more thorough examination of the nodes will be done by the pathologist after the surgery. So the final word on the status of the nodes won't be available until you get your post-surgical pathology report.
As for the risk of lymphedema, I believe that with an SNB, most studies put the risk in the range of 5% - 10%. Of course the risk is at the higher end of that scale if more nodes are removed,however if your SNB injections 'light up' 5 nodes, you really don't want to have your surgeon only remove 2 because in that case the SNB results might not be reliable. If you are going to go through the trouble of having the SNB and putting yourself at risk of lymphedema, you at least want the results to be as reliable as possible.
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Thank you so much for reply. Is it common that pathologist at operation room to do biopsy and will know if it's node is positive right away? Both doctors said biopsy of nodes will be done after work and I will know result later. I just don't want extra nodes to be removed. Maybe I will find doctors who can have node biopsy at the same time as operation.
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I had 5 nodes light up and then 6 removed during surgery. All were negative. The blue dye injection did not hurt. I didn't even know it was done. I have no lymphedema at 6 and 1/2 months post surgery.
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Is it common that pathologist at operation room to do biopsy and will know if it's node is positive right away? Both doctors said biopsy of nodes will be done after work and I will know result later.
Nao, were the doctors saying that the surgery on the nodes, i.e. the actual removal of the nodes will be done later?
Or were they saying that the pathology work on the nodes will be done later?
It's the surgeon who performs the SNB and surgically removes the nodes. It's the pathologist who takes the nodes, once removed by the surgeon, and analyses the nodes under a microscope to see if there are any cancer cells in the nodes.
The sentinel node biopsy surgery itself normally is done by the surgeon at the same time as the lumpectomy or mastectomy. Then the assessment of the nodes is turned over to the pathologist. As I explained in my previous post, sometimes a preliminary assessment of the nodes is done by the pathologist while the surgery is underway, but the more thorough assessment is not done until later. So the final pathology on the nodes cannot be known until after the surgery - whether a quick assessment is done during surgery or not. That quick assessment is just a preliminary finding.
For women who are unlikely to have positive nodes, this preliminary pathology assessment sometimes is skipped. That's what happened in my case. As my surgeon explained it, because my risk of nodal involvement was so low, if my nodes were to be found to have cancer, there probably would only be a very small amount of cancer. And in that case, the quick pathology assessment could easily miss finding the cancer. So my surgeon didn't feel that the quick pathology assessment would yield reliable results in my case and therefore he didn't want to waste the pathologist's time. He felt that it was better to have the pathologist do just the one more thorough analysis of the nodes after the surgery was done. While I would have liked to have preliminary results from the surgery, once I understood that those results wouldn't be final and would be pretty meaningless, I was fine to wait.
Not having this assessment done during surgery doesn't mean that you will have more nodes removed. It's the opposite. If the quick pathology assessment of the sentinel nodes is done while you are in surgery and if any of the nodes are found to be positive, then more nodes may be removed. But if no assessment is done, then the only nodes that will be removed during the surgery are the sentinel nodes, the nodes that 'light up' from the dye/isotope injections. And you can't reduce the number of nodes that light up - that's determined by the biology of your body.
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I have heard that most patients have their lymph node biopsies done at surgery. My surgeon scheduled my sentinel node biopsy before my surgery because I only wanted to do reconstruction if I could start when I had the bilateral mastectomy. Three nodes lit up and were removed, all negative with clear margins. The oncologist confirmed that I won't need radiation and I got the green light to visit with the plastic surgeon to go over my options. Two weeks later I had the bilateral mastectomy and started reconstruction.
Bottom line, my surgeon listened to me. My other docs appreciated that he went ahead with the SLN biopsy because it gave us all a better idea of what were dealing with before surgery. I have NO regrets!! Oh...and no pain for me either. I think they gave me Vicodin or something to chill me out when they injected the dye.
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My surgeon did the lumpectomy first but when she found 2mm of IDC, she has now scheduled the SNB for 2/20. I was given a lidocane patch that I have to put on about 6 hours before they inject the dye/isotopes - I'm hoping that the injections won't hurt. I've been very lucky in the pain department so far on this journey (very little pain during the biopsy, minute pain during the guide wire insertion and absolutely no pain after the lumpectomy), so I'm hoping to continue that track record.
My surgeon did say that she would do the quick path exam/report during surgery, even though she thinks there is only a 5% chance that mine has spread - I'd be okay either way, but it will be nice to get the initial report right after surgery -- I'll have to give my husband the question in writing so he remembers to ask her (and have him write down her answer so he doesn't muck it up)!
Good luck!
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Pokemom, just to add one point of clarification about your situation for Nao, I want to point out that you went into your lumpectomy surgery with a preliminary diagnosis (from a needle biopsy) of DCIS. With DCIS, a sentinel node biopsy usually isn't considered necessary - those who are reading who don't have DCIS might not know this. So that's why you didn't have an SNB done at the time of your lumpectomy. But when your lumpectomy uncovered some invasive cancer, an SNB became necessary and had to be scheduled as a separate surgery.
Nao, in your case, it's already known prior to your surgery that you have invasive cancer so there is no reason why the SNB would not be done at the same time as your lumpectomy surgery.
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Thank you everyone for sharing knowledge and experience! I spoke to my doctor's assistant and she said there will be a pathologist in operation room if the surgery is for mastectomy. But for lumpectomy I will know the result later, she also told me that it's very rare to get lymphodema for my case but I have been unlucky for last few years and just worried. My other doctor said node biopsy is not always accurate and does not change mortality rate, she takes only 1 or 2 ...so why do I want to risk? But many people are saying they checked if nodes are positive or negative right at surgery...
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Hi all
A bit of clarification between frozen section or pathology specimen analysis done during surgery and permanent pathology which is when the tissue is placed in formalin for preservation and then sent to pathology for much more detailed study.
This may be more than you ever wanted to know but it is kind of interesting
In the first situation the tissue is taken (breast tissue, nodes) and sent "fresh" to the pathologist- some hospitals have the satellite pathology lab right in the operating room, others its a few floors away. The pathologist can prepare several "sections" using a cryo type machine then examine the tissue under the microscope real time- they can usually communicate with the surgeon either by phone, by video or by getting up and walking in the OR in some cases. If they want more tissue it can be taken at that time with more "frozen sections" done. Once that happens the specimen either comes back to the OR and/or they take more tissue all which is then put in preservative and back to the pathology lab. Specimens frequently are tagged and labeled for geographic orientation with sutures with descriptions of where they were obtained from. These are the tissues they can send out for Oncotype or for other opinions etc. They are preserved and will be around for a while.
In many many cases the surgeon is comfortable with the results of the frozen section and what he sees and feels depending on if the mass can be seen/felt. I don't know the stats but the frozen section findings "usually" correlate with the permanent pathology in my experience- but not always-. I have been in surgery a long time and I have seen frozen sections that look okay and the permanent pathology reveals something different- this is true for breast as well as other tumors.
Hope you find this a bit informative about something you don't typically get to "see" Its a process with all that running back and forth
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Nao,
I appreciate that you want to avoid lymphedema, but I'm assuming that first and foremost, you want to ensure that you are properly diagnosed and get all the appropriate treatments to treat your breast cancer .
If you are thinking "so why do I want to risk?" the SNB, then you might as well tell your doctor to not bother having your removed breast tissue analysed by pathology. Because not having the SNB, and not knowing if you are node positive or node negative, has as much effect on your diagnosis and treatment plan as not knowing the pathology of your cancer.
"My other doctor said node biopsy is not always accurate and does not change mortality rate" My advice is to not go with this doctor. SNBs - if properly done - have a very high accuracy rate. However if it's the surgeon's policy to only remove 1 or 2 nodes regardless of how many nodes are lit up by the dye/isotope injection, then the SNB is not being properly done and that will impact the accuracy.
And to say that having an SNB and knowing one's nodal status doesn't impact the mortality rate is, frankly, absurd. If you find out that you have several positive nodes, it will change your treatment plan, possibly quite significantly (chemo vs. no chemo, for example) and that can save your life. Alternately, if you find out that you are node negative, it may mean that fewer treatments are necessary, avoiding over-treatment and having to deal with the side effects of these extra treatments.
What has been shown to be true is that if a patient has an SNB and is found to be node positive, and if the patient will be having chemo, then there is no survival benefit to having any more nodes removed, i.e. doing an axillary node dissection in addition to the SNB. And this is the reason why it really doesn't matter if the nodes are checked during surgery. The only reason to check the nodes during surgery is to allow the surgeon to remove more nodes, i.e. do the axillary node dissection, while the surgery is underway, if it's found that the SNB nodes are positive. But if you don't want more nodes removed than necessary, you probably wouldn't want to have the axillary node dissection done anyway. So this means there is absolutely no reason to have your nodes checked while you are in surgery.
wyo, I've been on this board a long time, and I've seen lots of situations where the SNB nodes are sent for a frozen section while surgery is underway and come back clean, only to find when the permanent pathology is done that there is a small amount of cancer in one or more of the nodes. Larger amounts of cancer in the nodes will be found by a frozen section but when dealing with something as small as micromets, it's easy to miss. Usually when this happens, the nodal involvement is micromets or an area of cancer just slightly larger.
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agreed with beesie. most BS now firstly removed the sentinel nodes (3 of them) first. if they're negative, no more nodes will be removed. and if there's positive nodes, depends how many, the doc will usually perform full axillary node dissection. i asked an onco, she told me, for lack of a better description, those nodes are like those seeds in a squash, the doctor could only scoop out the colored ones (bc of the dye injection). the nodes actually branch out, hence the dye to trace the cancer cells. surgeons can't pick and chose what nodes to take after the sentinel nodes dissection.
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I would take saving my life over the possibility of developing lymphadema. I had 4 nodes taken out and fortunately they were clear. I'm out over 4 years and I could possibly get lymphadema but I'm very comfortable with my decision. Please know that I am not minimizing lymph.
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From my experience last week, I wasted time worrying over the pain of the isotope injection! I made the mistake of googling it and read that it was painful then noticed the post was from 2004. The actual injection was about 10 seconds of a tolerable burning sensation. For me it was uneventful in the grand scheme of everything else going on.
My BS estimates a 2% chance of lymphedema for each LN removed. I had 3 SLN removed so by his theory I have a 6% chance, but I considered that all secondary and let him do what needed to be done. As everyone else has said, the priority is to get an accurate picture of your situation. My BS also had the "preliminary" testing done during my surgery to reduce the likelihood of a second surgery for more tissue/nodes. My final path report agreed with the preliminary so no second surgery.
Nao - Good luck with your decision on which BS to go with, I hope you find a sense of confidence with one of them!
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I have Rhumatoid Arthritis, auto immune disease and now I was diagnosed with cancer I can't use my medication (will lower immune system) and I started to have pain. I can't deal with lymphodema on top of rheumatoid arthritis. It will lower my QOL. Also yesterday I had a call from BS that they found suspicious enhancement (abnormality) in both of my breast from MRI, one is as big as 4 cm and scheduled for biopsy with MRI. Since radiology department is jam packed I have to wait until 2/20 for that biopsy. So many things to worry about...
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Nao, I completely understand why you feel you do about the SNB. I'm so sorry to hear about the MRI findings. Please check in here for support and perhaps they can get you in sooner. I hope so.
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Nao, I am so sorry to hear what you're going through.
I too, have Rheumatoid, I was Dx with it about 17years ago.
I was Dx with DCIS and decided to have a Mx, 13 months ago. My surgeon explained that it would be "remiss" of him if he didn't do a SNB at the time. It was a case of 1or2 nodes to make sure there was no invasion, against taking no nodes, then finding invasion in the final Pathology, and having to do a full Axillary clearance which would greatly increase the possibility of LE.
Try not to jump too far ahead, The waiting game is a terrible thing and we have all experienced the negative thoughts that go with it.
I am confused about your RA drugs, have you been told not to take anything? There are several of us with RA on these boards, you may want to search and chat! take care, and let us know how you're doing.
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I felt like I needed more info before surgery and got insurance to approve a PET scan the day before. My boob and armpit lit up, so I knew it was in the nodes, just not how many. My surgeon said they never heard of it getting approved like that. But what if it was in the ovaries or somewhere else? Shouldn't we get as much info before going under to make a complete decision? PET scans can't and don' show everything, but it is a tool.
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chicopeach, PETs normally are given to check for distant metastasis in situations where the diagnosis indicates that this is a risk. So whereas PETs are often not given to women with small early stage cancers (where the risk of mets is low), they are usually given to women who have more advanced diagnoses. However to my understanding, PETs usually aren't used to diagnose/assess the breast cancer or nodal involvement prior to surgery - MRIs are used more often for that. One big concern about PETs is the amount of radiation, and for that reason, if another form of imaging can serve the same role, that is generally preferred.
As you indicated, PETs (and MRIs) unfortunately don't catch everything. So in the case of the nodes, if there is only a small amount of cancer in one or several of the nodes, the PET or MRI most likely wouldn't show it. And for that reason, I don't think there is any surgeon who would say that an SNB isn't necessary because the PET or MRI showed the nodes to be clear. The surgeon would say that the SNB is needed regardless, because there still could be nodal involvement despite having a clear scan.
I agree that it's important for the surgeon (and the patient, of course) to have as much information as possible prior to surgery. In my case, the MRI indicated that my DCIS appeared to cover a larger area than what showed on the mammogram, and that led to my decision to have a MX instead of a lumpectomy - although to be fair, both my first opinion surgeon and my second opinion surgeon told me that they felt that a MX was the best approach because it was likely that my DCIS was widespread; the MRI just confirmed their suspicions. If I had not had the MRI, the extent of DCIS would have been uncovered by the surgery. Your PET scan may have told you in advance that you had nodal involvement, but if you had not had the PET, the SNB would have provided the same information the next day when you had surgery.
In the end, it's only surgery that can provide a definitive diagnosis, either of the nodes or of the extent of cancer in the breast.
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