December 2011 Surgeries - want to wait together?

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  • QuinnCat
    QuinnCat Member Posts: 3,456
    edited January 2012

    Chrissilini- that's good news. Can I ask you what size your tumor was, since our dx is very similar (though I haven't had surgery yet, just SNB)??  Oops - I just asked the same question as CookieMonster Smile

  • Blessings2011
    Blessings2011 Member Posts: 4,276
    edited January 2012

    Awesome news, chrissilini!

    CookieMonster - looking forward to your post....

     Kam170 - Can't remember - do you have another surgery date scheduled?

  • Nicole55
    Nicole55 Member Posts: 37
    edited January 2012

    Hello Ladies,

    As I can see everyone is going fine :-)  I received my pathology report yesterday and everything is clear as the surgeon told be after the surgery.  The margin is clear and i will see the oncologist next week.  Don't plan to go back to work until march, after 4 weeks of radiations.

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    Kam170 - In my search for info on Chrissilini I looked back through this thread and she didn't say the size but did say that it was less than 1 cm. Mine was 1.1 cm.

    I imagine that Chrissilini will give us more info but I'm leaving for the MO's office in about 45 minutes so I wanted more info.

    Happy Friday everyone!

    -Judy

  • chrissilini
    chrissilini Member Posts: 313
    edited January 2012

    No problem, ask away. According to my path report' which I am looking at right now:



    histologcal grade- well dfferentiated (mo said that was good)

    tubule formation: 1/3

    nuclear pleomorphism: 2/3

    mitosis: 1/3 (less than 10 per 10 HPF)

    total score: 4/9

    size of invasive component: 0.7 cm measured microscopically

    tumor focality:single focus

    extent of invasion: nipple neg for malignancy

    margins: neg

    greater than 1cm to all margins

    lymph-vascular invasion: not identifiied

    dcis: cribiform aand micropapillary types with mod to high nuclear grade with necrosis

    comprisess >75% of tumor volume

    estrogen positive(34%), progesterone receptor positive (97%) her-2/neu(+1) by immunohistochem

    >1cm to all margins

    TNM stage:pT1bN0---mo said this was really good along with the hormone pos status



    right breast was benign with fibrocystic changes including adenosis, adenomatoid changes, microcyst formation,apocrine metaplasia and fibrosis. Sounds like a recipe for future ugliness, doesn't it?



    Hope this helps and wasn't too much info.I have to look up the meanings of some of this stuff everytime I look at it. She did tell me when tumor size is less than 1cm they really look at benefits vs risks. Good luck.

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    Chrissilini...you got an awesome oncologist!

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    Thanks Chrissilini - sadly my IDC was 1.1 cm so I'm guessing that Tamox. is in my future. :(

    Sigh, on well. 

    Thanks for the info. Now it's time to go get dressed - it all seems to take so much longer now a days, I just move so much slower (something about a hip to hip incision can do that to you, I guess).

    -Judy

  • QuinnCat
    QuinnCat Member Posts: 3,456
    edited January 2012

    Chrissilini - Am I wrong about this?? Looks like your initial dx was Grade 3 and now it is possibly Grade 2??

    Blessings - yes, my surgery is postponed from previous Dec 13 (lump) to Jan 20 (BMX) due to BRCA.

    Anyone? - Chrrisilini's "lymph vascular invasion" negative - this seems like a biggee to me??  Does anyone now the real signficance of this one thing, medically?

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    doesn't negative lympth vascular invasion mean it's no mets?

  • exbrnxgrl
    exbrnxgrl Member Posts: 12,424
    edited January 2012

    Eve,

    Hang in there. We all heal at different rates but it often takes more time and patience than anticipated. I hate the narcotic pain killers too but they did their job when needed. Sleep is very healing and a mastectomy is major surgery.

    Caryn

  • QuinnCat
    QuinnCat Member Posts: 3,456
    edited January 2012

    I'm not sure evebarry...at the least it might mean the lesion didn't have a blood supply? Seems to me, after negative nodes,this could be very important, but I'm finding things in my original pathology report that spell doom that my new treatment center says "why the heck did that pathologist even mention that!  That means so little."

  • CarolAnn6
    CarolAnn6 Member Posts: 44
    edited January 2012

    Hi Ladies -

    I just got back from my first Oncologist meeting.  

    Two lymph nodes taken, both negative, I have DCIS, LDIS and IDC.  They belive that with my UMX that they removed all of the IDC - no residual in left breast.   All clear margins. 

    He is recommending Hormonal Therapy. 

    My Oncotopy DX is not back yet.. if low score, no Chemo.  High Score, then I receive Chemo.  A middle score is most likely no-Chemo. 

    No need for Radiation. 

    I will still need to keep my right breast in check....Mammo every 6mos or yearly.  I sometimes second guess my decision to have a Uni vs. Bi.  There is a probable chance that I have LCIS in other breast and I will need to keep an eye on it.  For now, my right breast is still staying. 

    I am extremely happy with the good news that I have received and my MO believes that my Oncotype DX results will be low.  So, good to go with just HT. 

    I want to once again say that these posts have been with me daily.  I have looked forward to the messages I see here in the December surgery postings.  I love reading your messages and I love seeing your progress.  Much love to all of you!

    Carol Ann

  • QuinnCat
    QuinnCat Member Posts: 3,456
    edited January 2012
    Congrats Carol Ann - node negative!  I'm sure you are relieved. Smile  No radiation is huge too!
  • CharB22
    CharB22 Member Posts: 310
    edited January 2012
    Chrissilini - that is awesome, awesome news!!! A GREAT way to start 2012!
  • CharB22
    CharB22 Member Posts: 310
    edited January 2012
    Congrats to you too, Carol Ann for no node involvement!
  • Ginger48
    Ginger48 Member Posts: 1,978
    edited January 2012

    Sounds like some good news was heard today...wondering about you Cookie?

    FYI- this is info on lymph vascular invasion from an abc news report:

    Question:What Does Vascular Invasion Mean?

    Answer: Before a cancer can spread to the rest of the body, it has to get into the channels that go through the rest of the body; that's lymph channels or blood channels, particularly the venous system. If the cell gets into the veins, it can go to the heart, and the heart can pump those cells to the rest of the body; and it might grow in those places.

    Diagnosis and Screening

    One of the indicators that we have that cells have a tendency to go into the vascular system and to spread to the rest of the body is called 'vascular invasion.' And when we see, under the microscope, cells that are actually getting into blood vessels, this gives us some indication that these cells may have a tendency to spread; and we should use drugs that kill cells wherever we find them that goes through the blood stream, such as hormone therapies and chemotherapies.

    I am exhausted after a day in preshcool and climbed in bed at 5pm.

  • chrissilini
    chrissilini Member Posts: 313
    edited January 2012

    Thanks for that info Ginger. The neg lymph-vascular means that there was no evidence that the cancer had entered the vascular/lymph systems. Therefore, less likely that any cancer has traveled and set up camp somewhere else.

    As far as the grade, not sure. I think overall there is so much in the path reports that it gets so confusing. Main points, in my opinion, size, lymph node involvement and whether in vascular tissue.

    Great news CarolAnn.

    Cookie... I didn't have the surgery you did but I still find everything takes longer. Although I've healed well, the te's have taken quite a bit getting used to. Just seems like everything moves and feels differently. Maybe it's all in my head. Maybe I'm just savoring every moment. Maybe a little of both. Never know what your onc will sy. Wishing the best for you and everyone. Brighter days are ahead.

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    I know my final surgical report said no vasuclar invasion and 0 node involvement...at least in the 4 nodes taken. But, my oncologist said as she studied the biopsy pictures that it looked as if there might be vasclar invasion with the initial biopsy of 2 C. I need to ask her if it's on the initial biopsy report. I didn't read it. It seems that if there is no evidence of vasular invasion or node involvement then the mx is treatment enough for stage 1 cancer.

    How do you determine if you are stage 1a or stage 1b? I figured I'm stage 1a in that there is no node involvement or vasular evidence.

    Mid January I'll meet with my oncologist who will explain my pathology report as it is difficult to understand it all. I am happy that the cancer didn't spread outside the breast area.  

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    OK, I'm finally home. After the MO appt. we picked up DS and headed to the in-laws and then out to dinner. But here I am, at last, sorry to keep you all waiting.

    As I knew from before, margins are clear, nodes (from Oct. surgery) were clear as well and Oncotype was low (14) so I'm still in the no rads no chemo camp.

    I asked if endocrine therapy (ET) was necessary even though I had the UMX. The MO said that while all of the BC is gone from the breast, the ET is to take care of any cancer cells that might have escaped and gone elsewhere. Becuase if they set up shop elsewhere, THEN you're in big trouble. She also said that if it had only been DCIS, then no ET would be necessary, but since there was a bit of IDC, we do the ET.

    I asked when I had to start and she said that it was a marathon not a sprint so whenever I was ready I could start, but it didn't need to be right away, I could wait until I felt closer to 100%. She gave me a few options: Tamox. or Luprin (sp?) injections monthly with an AI, or ooph with an AIl. AI is usually used with post menopausal patients, but if we supress estrogen (or remove the ovaries), then I could do AI as well. I think that Tamox is my best bet. She also said that the tamox or other treatments lower my chance of mets (cancer settling somewhere else) by about 50% which seems pretty good to me.

    I asked who was in charge of my TX and BC care, it's her and I asked about mammo/MRI and she said that yearly on both would be good. I've got dense breasts and so mammo misses about 15% of BC in dense breasts, but that MRI helps reduce that 15% to much lower.

    She also mentioned that my last blood draw (while I was in the hospital) showed very low hemoglobin. It is not unusual, but she wants me to get another blood draw just to make sure that it's come back up. I'll do that next week on Friday when I have to go see the GYN anyway (for Tamox. screening).

    It was a good visit. Oh, she also did a breast exam. Getting to the breast took some work, I had on a button down shirt, the abdominal binder, a t-shirt for under the binder and a bra. Ha! She said that the breast looked amazing being only 3 weeks out from surgery.

    I think that covers it all. It sounds like Carol Ann and I heard much of the same information from our MOs

    Have a great evening and weekend!

    -Judy

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    evebarry - the only difference between 1A and 1B is that in 1B there are micromets and 1A there are none. Stage 1 is the tumor is less than 2 cm. Got that info from cancer.org.

    -Judy

  • Blessings2011
    Blessings2011 Member Posts: 4,276
    edited January 2012
    CookieMonster - thanks for posting even after a full day! A lot of what you heard today was what I heard a week ago; the difference being that I am about ten years post-menopausal. Sounds like you have a very good doc!!!
  • Ginger48
    Ginger48 Member Posts: 1,978
    edited January 2012

    eve- they thought they saw vascular invasion on my initial biopsy as well but it was not in the final pathology and they said that is the one they go by. Not sure why it would be on one and not the other but I trust my drs.

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    Thanks Ginger, thats why I put stage 1a. Although if they put the biopsy of 2 C. 1.7, and about the same for the final report the actual tumor would had been greater than 2 C. So the the surgical report rules making me a stage 1a dx. I prefer being the lesser because it has a better prognosis.

  • Beesie
    Beesie Member Posts: 12,240
    edited January 2012

    Eve, what do you mean when you say that "the surgical report rules" make you a stage IA? 

    I know that in determining the tumor size for staging purposes, if the tumor is multi-focal and there are two (or more) separate tumors, the size of all the tumors is not supposed to be added together to determine the tumor size and staging.  Instead, it's the size of the largest of the tumors that is used for staging purposes.  However if you have a single tumor that is partially removed in one surgery but the margins aren't clear and then the rest of that tumor is removed in another surgery, my understanding is that the size of the tumor for staging purposes will be the combined size from the two surgeries.  That is the reality of the size of the tumor.  That fact that it wasn't all removed during one surgery really isn't relevant.  

    Was the area of cancer that was removed during your mastectomy part of the same tumor as what was removed during your lumpectomy, or was it a separate area of cancer?

    I completely understand that you prefer to be Stage IA because it has a better prognosis but if that turns out to not be the reality of the situation, you would want to know, right?  So it's probably worth talking to your oncologist about. Same thing with the vascular invasion. My understanding is that if something is definitively found (actually found, not just speculated) during a biopsy or lumpectomy but then the same thing is not found during a subsequent lumpectomy, re-excision or mastectomy, that doesn't mean that what was found in the first place never happened and isn't incorporated into the staging and/or treatment plan.  In my case, my microinvasion of IDC was found during my excisional biopsy.  No further invasions were during my mastectomy - that was DCIS only.  But my staging is Stage I and not Stage 0, because of that microinvasion.  And the discussions with my oncologist about my prognosis and any subsequent treatments all considered the fact that I had that microinvasion and did not have pure DCIS.  So in my case, my diagnosis was based on the combination of my surgeries and in fact more so on my excisional biopsy than my mastectomy. 

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    Beesie, I admit it is a little confusing. My bs said I was stage 1. I wasn't for sure if I was stage 1a or stage 1b. I haven't yet spoken to my oncologist and for sure will discuss this with her. Someone said to me that the final pathlogy report said unless it is greater than 2 C it is stage 1a that is if there are no micromets or vasular invasion. For that reason I reasoned I'm stage 1a. The original biopsy took out 2C by 1.8 of idc with the her2+++ (and a small amount of high grade dcis) and left what they thought to be .5 C. The oncologist said something about vasuclar invasion in regard to the biopsy report...but the final pathology report showed no vasular invasion. But, the surgical mx showed the remainder of the tumor left was about the same as the biopsy...about 2 C by 1.8 x 1C ... something like that. So, I figured it's less than 2 C without mets which would put me in the 1a catergory. It was noted that it was a palitable mass. If you put the two together than the tumor would be almost 4 C making me a stage 2. My bs surgeon only considered the final pathology report in determining my prognosis. So can I say more?

    In March my idc, mucious grade 1 cancer was also dx as idc stage 1. But, the recent cancer also written up as stage 1 is a more serious cancer in that it is grade 3, idc, with the her2+++ and larger tumor...yet both are stage 1a.

    I am ok with it being stage 1a in that the prognosis is good either way.  If it's not perhaps they should change how they dx the final pathology or maybe the surgeon should leave the dx to the oncologist who considers the biopsy along with the surgical biopsy ... because mine was the same tumor.

  • Hindsfeet
    Hindsfeet Member Posts: 2,456
    edited January 2012

    How long do you need to rest after a mastectomy with reconstruction? It's been a few weeks and I still have the drain. I want the drain removed but the surgeon won't remove it until it stops draining so much...so I do almost nothing for now hoping the rest will heal the wound and stop the drain thing.

    I feel trapped...can't drive or do much. This is all part of the healing process...just wonder how much longer until life returns to normal?

  • gabe2011
    gabe2011 Member Posts: 33
    edited January 2012

    So glad to read everyone is getting good onc reports. I had my bmx last Wednesday came home on Friday. I am with evebarry if I had not had the bmx it would have been impossible to talk me into this again. I have been miserable since. I came home with 4 drains. I have been in so much pain since home. Thursday my BS removed two of my drains which made it a little more comfortable but then yesterday it starting hurting so much I couldn't stand even a shirt touching me. I was crying so hard when I called my husband at work he thought I had done something.  I went to the er they said it didn't look infected and after 3 shots of morphine or two toradol it finally took the worst of the pain away.they changed my pain meds and that seems to be helping some.

    Today it is not as bad but still painful. I know it has only been 10 days but I guess I thought it wouldn't be this bad. I feel like such a baby. I go to the ro on Tuesday and the mo on Wednesday and the BS on Thursday (he might take out the other two drains). Has anyone gone to PT? How soon after surgery do you go for that?

    evebarry I don't think life ever goes back to normal after a cancer diagnosis does it? My BS told me not to plan on doing anything for 4-6 weeks after surgery. 

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    gabe2011 and evebarry - I'm so sorry things are rough. It would be great if after the surgery everything would immediately return to normal. Sadly, it does not.

    eve - I can't drive either and that's difficult, but I totally get WHY I'm not allowed to drive even though I'm not on pain meds. I hope that after Monday I do get to drive again.

    gabrielle - I'm learning all kids of stuff about meds for me that I didn't know because I've so rarely taken anything - mostly I'm finding allergies - chloraprep and clindamycin - those have been rashy, itchy experiences, sadly. File all this info away though, who knows when you might need it next.

    Hang in there and hopefully a new comfortable normal will eventually settle for us all, but I supposed it'll take some time.

    (HUGS!!)

    -Judy

  • Bogie
    Bogie Member Posts: 286
    edited January 2012

    I would like to join the December Surgery Forum.



    bilateral mastectomy with reconstruction 12/20/11



    Original DX DCIS Grade 3' Stage 0

    After Surgery Invasive 1.5 cm tumor Stage 1, Grade 3 per pathology report misses on all tests

  • CookieMonster
    CookieMonster Member Posts: 1,035
    edited January 2012

    Welcome Bogie! I added you to the list. Hope you're healing well.

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