Anyone from Hamilton Ont, know a good surgeon!!!

paulachiz
paulachiz Member Posts: 14

Hi All,

Hi had my first appt with the surgeon my family doctor referred me to, and I wasnt very comfortable with him.  I would like to see some one else and see what there personality is like as well as there view on DCIS. 

I have read that it is a non-invasisve cancer and he is just telling me It is not cancer.

Comments

  • Moderators
    Moderators Member Posts: 25,912
    edited January 2013

    Hi Paulachiz,

    You may also want to reach out to the members in the Canadians forum for their recommendations.

    Hope this helps!

    --The Mods

  • paulachiz
    paulachiz Member Posts: 14
    edited January 2013

    Thank you, how do i get to the candian forum

  • Moderators
    Moderators Member Posts: 25,912
    edited January 2013

    Just click the link we provided in our last post :)

  • Deirdre1
    Deirdre1 Member Posts: 1,461
    edited January 2013

    You might also touch base with Beesie  she is in Toronto but seems to have a great deal of knowledge about the Canadian Health System..  Best of luck and please know there is a great deal of information on the DCIS site BECAUSE of Beesie (and others) postings... 

  • paulachiz
    paulachiz Member Posts: 14
    edited January 2013

    Thank you, I have been talking with Beesie prior to my diagnosis, and that is why i am confused he said i did not have cancer, but will be scheduled for an MRI immediately and stated i would be having a lumectomy within 2 weeks and he also has to biopsy another area that they did not do during my last biopsy.  I am just looking for another doc for  second opinion in Hamilton.  I will contact Beesie and see if she knows of any.

    I appreciate your response.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2013

    paulachiz, I'm sorry to hear that you got the DCIS diagnosis, although going into your biopsy with a BIRADs 5, it was unfortunately the most likely result. I was hoping you'd be one of the 5% with a benign result! I'm glad though that the biopsy has only found DCIS. Hopefully when you have surgery the final diagnosis will remain pure DCIS.

    I'm sorry that you ran into a surgeon who doesn't consider DCIS to be breast cancer. Most doctors do consider DCIS to be the earliest stage of breast cancer but there are some doctors who choose to call DCIS a pre-cancer.  As much as I disagree with that, I do understand the logic behind it.  

    The issue is in how one defines cancer. The definition of cancer often includes 3 criteria (from the National Cancer Institute: What Is Cancer?):

    1) Abnormality of the cells

    2) Uncontrolled growth of the cells

    3) Invasiveness/the ability to metastasize

    DCIS cells are virtually fully formed cancer cells. But DCIS cells are confined to the milk ducts in the breast and do not have the ability to break through the duct or survive/thrive outside of the duct; therefore DCIS is not "invasive" and cannot move beyond the breast.  For those who believe that the definition of cancer includes invasiveness/the ability to metastasize (i.e. the ability of the cancer cells to move to a secondary location in the body away from the main source of the cancer), DCIS does meet that criteria and that's why there are those who say that DCIS is not cancer.  

    Here's the big "BUT". Where there is DCIS, there could be invasive cancer. This means that a preliminary diagnosis of DCIS doesn't mean that DCIS is all that is present.  Until all the affected breast tissue is analysed, it can't be known if the diagnosis is pure DCIS or whether some invasive cancer is also present.  In about 20% of cases where DCIS is diagnosed via a needle biopsy, some invasive cancer is later found during the surgery.  Even when this doesn't happen, it only takes one small biological change for a DCIS cell to acquire the ability to break through the milk duct and metastasize. It's the same DCIS cell (with minor biological changes) that moves from the duct into the open breast cancer and becomes an invasive cancer cell. This is why it's important that  every DCIS cell be surgically removed and/or killed off (with rads or hormone therapy).  If any DCIS cells remain in the breast, there can be a recurrence and in 50% of cases, the recurrence is not found until the DCIS has progressed to become IDC (invasive cancer). It's for these reasons that most doctors do consider DCIS to be a pre-invasive cancer, i.e. the earliest stage of breast cancer. 

    Regardless of what a doctor calls DCIS, the treatment is the same.  So the MRI and lumpectomy that your surgeon is proposing would be the same whether he calls DCIS a cancer or a pre-cancer.  Still, I can appreciate why you would prefer to see another surgeon. Unfortunately I don't know of any surgeons in Hamilton.  I do recall reading some posts from women who've been treated at the Juravinski Cancer Centre. If you put "Juravinski" in the search box on this site, you'll find some of the women treated there, and you may be able to contact them via PM (if they are still coming to the board). If you are willing to travel a bit, there are lots of women on the board who've gone to Trillium in Mississauga and I'm sure you could get the names of recommended surgeons from them.  I could even recommend a surgeon there too, although he's a surgical oncologist and does not specialize exclusively on breast cancer.  Sorry I can't be more helpful on that. 

  • Myleftboob
    Myleftboob Member Posts: 1,469
    edited January 2013

    Hi Paulachiz

    Because my GP is in Oakville (long story LOL) but I live in Brampton, she referred me to Dr. Rosario who operates out of Oakville-Trafalgar.  I found him to be an excellent surgeon.  While it was obvious via the mammo that there was widespread DCIS in my breast, there was also 2 obvious areas that looked like more.  For this reason he recommended an immediate radical mastectomy.  As it turned out via the pathology report, there were 3 small IDC tumors, but the results were great from a margin perspective.  He was very no nonsense but very professional and addressed any concerns I had prior to surgery even if it was an evening phone call.  He even called me during his family vacation to give me a verbal on the path results when they came in.  I was very gratefull for that.  My mastectomy scar is super smooth and any nurses or doctors that have looked at it since remark on how nice it is.  As for my MO at Credit Valley Hospital whom I really liked, he's of the opinion that DCIS is a pre cancer too.  I told him, cancer is cancer no?  As far as I'm concerned its not to be taken lightly AT all.  I know someone personally that didn't take it seriously, dropped out of further treatment after a double mastectomy figuring she had given up enough and was diagnosed recently with mets to lungs and bones.  While I was dragged into chemo kicking and screaming (not literaly LOL) and had to receive Herceptin for a year AND take Tamoxifen for now anyway, I'm glad I did it.  Bestof luck to you and please join us on the Canadian thread oo, great bunch of ladies there.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2013

    Right after I posted and signed off, I thought "Oakville!" I know that there are women on the board who've been treated at Oakville-Trafalgar and that's closer to Paulachiz than Mississauga.  Myleftboob, I'm glad you found this post and chimed in!

    I do want to provide one point of clarification about DCIS treatment. If someone with DCIS has a bilateral mastectomy, standard of care guidelines suggest that no further treatment is required. With pure DCIS, there should be no risk of distant metastasis (unless there was a misdiagnosis or an occult invasion) and there is usually only about a 1% - 2% risk of a local recurrence (assuming adequate margins from the mastectomy). Most oncologists, and all treatment guidelines that I've ever seen, say that such a low risk does not warrant any further treatment. But that doesn't mean that anyone who goes this route can stop being diligent. If there is a local recurrence, and if it's not found while it's still DCIS, that changes the whole diagnosis and prognosis. And that's how someone with DCIS could end up with mets. It's rare - most studies put the the long term survival rate for those diagnosed with pure DCIS at 98% - 99% - but it can happen. 

  • Scottiee1
    Scottiee1 Member Posts: 2,329
    edited January 2013

    If you go to the Canadian thread and/or 2013 survivors.....there is one member there who comes from Hamilton.

  • Joanne_53
    Joanne_53 Member Posts: 1,477
    edited January 2013

    My bc was Nicole Hodgson who is an Oncological Surgeon. She works out of juravinsky cancer centre. I loved her.

    Joanne

  • Myleftboob
    Myleftboob Member Posts: 1,469
    edited January 2013

    Beesie



    I understand what your saying. In this case she was ER+ and wanted to continue with having kids vs taking tamoxifen. I'm praying that she's stays stable now that she's on it. I have a neighbor as well that opted out of chemo and tamoxifen after her LX. Its an individual choice I know just as it is doing everything that's recommended.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2013

    Myleftboob, Tamoxifen normally would not be recommended after a BMX for DCIS even if someone is ER+. In fact I was ER+ and I had a UMX for DCIS-Mi and my oncologist recommended against Tamoxifen for me, although he would have prescribed it if I'd asked. He explained that the benefit would have been protection of my remaining breast rather than any meaningful recurrence risk reduction because after a BMX for DCIS, recurrence risk is already so low. 

    I'm wondering if the person you are referring to had invasive cancer in addition to DCIS. That's usually the case if additional treatments are recommended after a BMX. If the diagnosis included invasive cancer, that can completely change the risk/benefit equation for Tamoxifen and make Tamoxifen very worthwhile. And with invasive cancer, there is of course a risk of mets, which someone with pure DCIS would not face. 

    Whatever the original diagnosis, I share your hope that she does remain stable now. 

  • paulachiz
    paulachiz Member Posts: 14
    edited January 2013

    Hi Ladies, and thank you for your responses!!!

    Beesie again thanks with your knowledge on DCIS.  I feel like I have been hit by a stun gun, there is so much I want to say/ask, but when i sit at the computer nothing comes out.

    I am waiting for my MRI date and he also stated that I "guess" once he is in doing the biopsy there is an area behind the nipple that he said he was going to stick in this hook thing and grab that tissue to test.

    I am so confused, what i will do is contact my family dcotor and see if she can refer me to Dr Nicole Hodgson. I would still like to hear what she has to say.  But the surgeon said I would have the lumpectomy within the next 2-3 weeks,

    Should I do that now prior to the mri or wait until i have the results of that??????????

    Again thanks for listening

  • Joanne_53
    Joanne_53 Member Posts: 1,477
    edited January 2013

    Paulachiz, get your family doc to get you in ASAP with Dr. Hodgson. She works from the cancer centre. She is wonderful and very knowledgable of breast cancer. She will do your surgery. Get your questions ready for her. I would wait until you could get in to see her and let her send you for more tests.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2013

    I agree with Joanne.  Ask for the referral to Dr. Hodgson right away, before the MRI.  

    The good news with DCIS is that you have time to do your research and find the doctors you want.  DCIS needs to be removed, but you don't need to rush into surgery. A short delay, even a couple of months, isn't a problem. 

    I think it's a very good idea to have the MRI - my MRI results really helped me with my surgery decision (I had a single mastectomy).  MRIs sometimes show a larger area of concern than what shows on the mammogram image and it's good to know that before having surgery.  If you are having the MRI at Juravinski, then it probably makes sense to let it be scheduled, since Dr. Hodgson will be able to access the results.  But if the MRI is at a different facility, then I'd suggest waiting for your appointment with Dr. Hodgson so that she can schedule it at Juravinski. 

    What you should be sure of is that your surgery is not scheduled with the other surgeon.  If you know you don't want to work with him, there's no point in scheduling the surgery.  And you really want the MRI results beforehand anyway, so that you have a better idea of what you are dealing with and so that you can be comfortable that a lumpectomy is a viable option. 

    Good luck getting in to see Dr. Hodgson quickly. And I hope you like her as much as Joanne does!

  • Joanne_53
    Joanne_53 Member Posts: 1,477
    edited January 2013

    Paulachiz,

    Rdrunner on the Canadian thread has Dr. Hodgson too so you could send her a PM. I am sure you will be happy.

  • owlwatcher
    owlwatcher Member Posts: 130
    edited January 2013

    I agree with the prior posting about getting the MRI prior to surgery. That is what my doctors did before the surgical procedure.

  • owlwatcher
    owlwatcher Member Posts: 130
    edited January 2013

    I agree with the prior posting about getting the MRI prior to surgery. That is what my doctors did before the surgical procedure.

  • Myleftboob
    Myleftboob Member Posts: 1,469
    edited January 2013

    Good luck Owlwatcher in getting in to see her!



    Beesie

    You always give such good explanations of everything. Honestly I though DCIS could be ER/PR, HER+

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2013

    Myleftboob, DCIS can be ER+/PR+/HER2+. It often is. But the treatment protocol for DCIS is different than the treatment protocal for invasive cancer, even if they are both ER+/PR+/HER2+.  Herceptin, as one example, is not even approved for women with DCIS.  AIs are not approved yet either.  Tamoxifen is, but after a BMX for DCIS, Tamox is not generally considered to be necessary because there is usually only a 1%-2% risk of local recurrence and no risk of mets. DCIS, no matter how aggressive the pathology, cannot metastasize. So DCIS has a different risk profile than invasive cancer. That's why the treatment protocol is different and that's why usually no additional treatment is recommended if someone with DCIS has a BMX. 

  • netty46
    netty46 Member Posts: 296
    edited January 2013

    I have read stories on this board of women with dcis who had it in nodes. There are also some who even Went to

    stage4. I believe dcis patients should get chemo.

  • netty46
    netty46 Member Posts: 296
    edited January 2013

    Bessie is correct dcis is cancer.breast cancer.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2013

    netty, there are a lot of women on this board who state their diagnosis to be DCIS when in fact their diagnosis includes a combination of DCIS + IDC. I can't count the number of times I've seen "DCIS Stage I" as someone's diagnosis, or even Stage II or Stage III. Or someone might write that they have "invasive DCIS".  None of those diagnoses actually exist.  Pure DCIS is always Stage 0 and it is never invasive. That's not a judgement or opinion on my part; that's the actual definition of DCIS.  So this means that anyone who is Stage I or higher does not have pure DCIS.  They might have some DCIS along with their IDC, but their stage and diagnosis is based on the IDC.

    What often happens is that someone might have a preliminary diagnosis of DCIS based on a biopsy.  Then some invasive cancer is found during surgery, however the surgeon or oncologist never explains that the diagnosis has changed.  This is why we see so many women who state DCIS as being their diagnosis when it's really not. 

    By definition, DCIS is confined to the milk ducts and cannot move into the nodes or the bloodstream.  If nodes are found to be positive with a finding of only DCIS in the breast, it means one of two things:

    1) The cancer was accidentally placed in the nodes by a surgical instrument.  This is harmless, since the DCIS cells will not continue to grow and thrive in a situation like this. Usually accidental placement is assumed to be what happened when only isolated tumor cells (ITC) or micromets are found in the nodes.  Numerous studies have shown that there is no difference in prognosis between those who have pure DCIS and those with DCIS who are found to have ITC or micromets. 

    2) There was an "occult" invasive cancer in the breast that was never found, and some cancer cells from that invasive cancer moved into the nodes. Occult invasions are rare, and happen almost exclusively in situations where there was a large amount of very aggressive (grade 3, comedonecrosis) DCIS.  In most cases where positive nodes are found, a second very thorough check of the breast tissue pathology in fact uncovers a small area of invasion, so it's no longer "occult".  

    For someone initially diagnosed with DCIS, the presence of anything more than ITC in the nodes, whether an invasion was found in the breast tissue or not, immediately changes the diagnosis from DCIS Stage 0 to either IDC Stage Ib (if all that is found is micromets) or IDC Stage II (for anything more than micromets).

    The rate of lymph node invasion that is found with "pure" DCIS (i.e. when an invasive component is not previously or subsequently found in the breast) is actually very low:

    Ductal carcinoma in situ and sentinel lymph node metastasis in breast cancer

    Ductal carcinoma in situ (DCIS) and biopsy of the sentinel lymph node

    Since this is the DCIS forum and a lot of women newly diagnosed with DCIS may be reading, I thought it was important to clarify the information about DCIS and nodal involvement.  

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