Has anyone had micro fat grafting?

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  • GointoCarolina
    GointoCarolina Member Posts: 753
    edited September 2010

    Kitchenwitch, I think it is wonderful that you saw Dr. Ahn.From what I understand,she does it all, the microfat grafting plus all the flap surgeries.So you will have many options! I do understand about the people who are posting about the microfat grafting being very new as far as reconstruction.I too looked for more info on the clinical trials and could not find any data.Does not mean there isn't any,but I do wish the results were available.I had an appoinment scheduled with Dr. Ahn,but after talking to my insurance company,knew that they were not going to approve out of network coverage for something so new.If I could have referred them to a site with data,it may have helped. I will be seeing Dr. Vasile and Dr. Levine next week to discuss SGAP.I think reconstruction is exciting no matter what method we choose.

  • Renata
    Renata Member Posts: 172
    edited September 2010

    alexandra-aaa, I'm really grateful that you posted about the Brava system and Dr. Khouri. It is not an option for me right now since I had reconstruction with an implant last year but I think it's so promising...I'm glad that there are doctors trying new and less invasive procedures, I can't help but think of my grandaunt who had a halsted mastectomy without reconstruction 60 years ago, I'm glad that doctors tried and created techniques to "reconstruct" a breast (of course I'd be happier if they had found a cure for cancer instead of having to mutilate patients and pray for NED...).

    Your posts in my opinion have been very informative and I hope you continue to join us.

    Best wishes.

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited September 2010

    Kitchen, I'm so glad your meeting with Dr. Ahn went so well! Of course, you'll have to keep us posted!

    Beesie, thanks for weighing in; as usual you provide a great voice of reason. Yes, this procedure is only 5 years old so there aren't 10, 20, 30-year recurrence stats yet. Women who are highly risk-averse or fearful of having breast tissue should not do this procedure.

    That said, I personally am excited about being a pioneer in this procedure. I'm not afraid of having breast tissue, I'm only afraid of having DCIS cells still in me... if I could, I'd be having a second re-excision instead of a mx.

    Even if it's found to double or even triple the risk of recurrence from 2% to 4 or 6% (or whatever), that's a risk I'm SO very willing to take in exchange for the benefits of a much less invasive surgery, fewer incisions, my OWN fat (no foreign objects), no scars on my back or belly, and no lost skin sensation. But whether that trade-off is worth it for something so new is a decision each woman must make for herself.

    Alexandra, I've always enjoyed and appreciated your posts in this thread and want to express my thanks for the information you've shared.

    mdradf, that's hilarious, I had noticed that too. Sounds like someone is trying to help Dr. K. with a "fishing" post to garner a little extra publicity... I think Dr. K is doing just fine on the publicity front without phony posts. Wink

  • NotMyTime2Go
    NotMyTime2Go Member Posts: 34
    edited September 2010

    This has been a happening place for the last couple of days.Laughing I guess it's time I jump in with my two cents. I'm not even going to try to keep track of who said what. But first, if there is someone here posting from Dr. Khouri's office - will you please let us know who you are so we can ask some real questions? I'm constantly tempted to call his office and try to get through with my questions, but then I tell myself to be patient and wait for my ps to learn all the details. Not so cool to do it anonymously, but if your bias is clearly stated, I don't think there's a problem?

    Also, I guess I'm guilty of being one of those who has mostly just posted on this thread. I did join this site a year ago when I was diagnosed, and did a lot of reading, but only posted maybe twice.  I'm not sure why, except that I was overwhelmed and didn't feel like it. This procedure is the first exciting thing I've come across since finding that horrible lump a year ago. If my enthusiasm has comes across as an advertisement, well that's just because I'm enthusiastic. 

    AAA - okay, I did remember you. =) You're very welcome here. I'm grateful for all your research and information. I do want to add that I felt defensive from the ominous tone of some of the posts as well, and was tempted to just back away. I'm real big on surrounding myself with good feelings while trying to heal. Not that I think we want keep blinders on, but I hope this can remain a happy place to visit. 

    Reconstruction is a very personal decision, and any decision needs to be respected. I join those that are pleased to be pioneers, and respect those who aren't comfortable with it. But in my mind the possibility of problems in the future really pales in the face of the problems caused by the other options of the day.

    My surgeon raised the same concerns listed here about this being new, the only study being small (though he did call it legitimate and impressive), and the fact that most of the information out there is in the form of advertisement. But he offered to look into it from a scientific point of view if I was interested. I gave him the go-ahead - and he found information that satisfied him. That was enough for me. 

    Finally, I think it's fair to say that plastic surgeons are a unique group. They're half artists, half scientists, and usually come with an ego. I haven't named my doctor because he doesn't advertise himself and I cringe at the thought of him being maligned like some have. (For instance, if you do a search for Dr. Coleman you'll find a whole bunch of negative info, which was apparently concocted by one dissatisfied patient.)  I would recommend that as a general rule it's a good idea to find a doctor we trust and rely on his advice more than the range of inaccuracies that can be found online. 

    BUT with that said - CrunchyPoodle - I applaud your decision to go ahead with the doctor willing to do it, even if it's not his first choice. I suspect there's some ego issues going on there, but if he can do fat grafting, he ought to be able to handle this, as long as you keep up with wearing the BRAVA device. Sometimes we're faced with less than ideal choices, and we just have to pick the one that feels best for us.

     Okay, enough of my soap box. I appreciate you all!  

  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited September 2010

    NotMyTime, you summarized exactly how I feel about it!

    I join those that are pleased to be pioneers, and respect those who aren't comfortable with it. But in my mind the possibility of problems in the future really pales in the face of the problems caused by the other options of the day.

    And yes, I think patient compliance re: the Brava technique is all-important... thankfully, I work from home and only see customers several hours a week, so I plan to live in mine! LOL

  • mradf
    mradf Member Posts: 398
    edited August 2013

    alexandra-aaa:

    You're right in noting that I'm protective of the forum and it's members, and when you first started it was I who said "You are a new member here and your post does sort of come off as an advertisement for Dr. Khouri and his Brava System."  

    I have found a welcome and supportive home here these past years, and have been helped through some of the most challenging days and nights of my life, including the loss of my sister this year to BC.  No one, and I mean NO ONE else understands us like each other. 

    You've made a good case for why you post here, and you are as welcome as any other member who follows the rules.  Those who should not be here know who they are, and are usually gone in short order.

    Be well, all of us.

    Maria

  • Beesie
    Beesie Member Posts: 12,240
    edited September 2010

    Julia, thanks for replying to my post. As someone who is pretty risk tolerant, I completely understand why you are willing to live with a somewhat higher risk level in order to try this method of reconstruction. I'm not sure that I would do the same thing, but there are decisions that I've made (not taking Tamoxifen, for example) where I know that in making the decision, I am negatively affecting my risk level.  So I get it.  As I've said hundreds of times on this board, we each have to make the decision that is right for us - it doesn't matter at all what someone else would do.  The fact is that I think it's absolutely wonderful that you are willing to be a pioneer on this procedure.  Without women like you, we would never have the 10 year, 20 year and 30 year usage data that we need. 

    I have no issue whatsoever with the decision that you - or anyone else - has made to go ahead with this method of reconstruction.  Quite the contrary, in fact.  I'm eagerly awaiting updates on how it goes.

    The concern I raised in my earlier post was not with anyone who chooses this procedure, but with the discussion itself, here in this thread.  As I mentioned, it sounded as though it was a paid promotion for the Brava system and Dr. Khouri.  Only in the last few posts has there been mention of the fact that this method of reconstruction doesn't have much history behind it so we really don't know whether it will work over the long term.  Only in the last few posts has there been mention of the fact that this method of reconstruction might in fact increase recurrence risk.  Those are pretty important points, but they haven't been discussed up till now.  Newly diagnosed women who are making their reconstruction decision and who are reading this thread would not have known, until the last few posts, that by choosing this method of reconstruction, they are exposing themselves to uncertainty and possible increases in recurrence risk.  If, in knowing this, someone chooses to go ahead with this method of reconstruction, that's terrific.  We need pioneers!   But I worry whenever I see a completely one-sided discussion, talking only about the upsides, without ever mentioning the downsides (or the reverse).  Whether the topic is mastectomies, lumpectomies, radiation, Tamoxifen, reconstruction, etc... there are always positives and negatives.  Up till now, the discussion about the Brava method in this thread has pretty much only talked about the positives - which do sound wonderful - but the fact is that there are some pretty major negatives too.  To be fair to anyone considering this method of reconstruction, those need to be discussed openly.  That was my concern.   

  • NotMyTime2Go
    NotMyTime2Go Member Posts: 34
    edited September 2010

    Beesie,

    I totally hear where your'e coming from, but I have to ask for some clarification. In your post you mention the fact that this method may increase recurrence rates. That was a key point for me and my decision. I found some pretty strong evidence to lead me to think there was no reason to expect an increase in recurrence (I wish I had time to track it all down, but it was over the course of several days of research, and came from at least one prestigise (sp?) doctor not affiliated with Dr. Khouri.) I realize nothing is certain without long-term studies, but are you basing that statement on something specific? I'd really like to be pointed in that direction before making the final decision.  Thanks so much for your input!

  • dustylady
    dustylady Member Posts: 37
    edited September 2010

    Wow...I just had my first fat grafting with Dr. Khouri on Friday and today is the first time I have had a chance to look at this board since I returned home.  Lots of activity!  I had a BX in June and was originally going to start wearing the Bravas 4 weeks afterwards (my surgeon cleared me for this).  Then there was a question as to whether I had some residual fluid...so I delayed wearing them for another couple of weeks).  It was a little hard for me to break myself into the BRAVA wear, but you really do get used to them.  I wore them for about 4 weeks prior to surgery.  17 years ago, I had breast cancer in my left breast and had a lumpectomy followed by radiation, so that breast was smaller prior to my BX.  When my surgeon performed the mastectomies, he said that that tissue was not as forgiving as the right breast, due to the previous radiation.  He talked with Dr. Khouri prior to my surgery and did a loose, simple BX, keeping the cleavage line and fold under the breast.  The left fold was not quite as apparent as the right and the skin pocket (for want of a better word) was smaller too...again, due to the previous surgery. 

    Anyway, I am just 6 days post surgery.  I am very impressed at this point.  Originally, Dr. Khouri thought I would need 3 treatments....depending on how this first treatment looks over the next several weeks, I could stop at this point...or have a second treatment.  It really will depend on how my body responds.  After my mastectomies, my left side had one spot that was very dented and I think the skin had tightened a bit on the chest wall.  Dr. Khouri did a very impressive job of lifting out this dent...using only needles. 

     Maybe some of Dr. Khouri's patients sound like commercials because we are just so pleased with what he does for us.  Prior to finding out about him, I was going to go breast free, because the only other two options offered (implants or flap reconstruction) were not appealing to me.  That is why I am so grateful to have found out about Dr. Khouri.   As far as time he spends -- when my husband and I flew down to Miami to check him out, he took at least 2 hours talking with us and answering our questions.  He is extremely dedicated to his work and his patients. 

     As I progress, I will let you all know how it goes!

  • Beesie
    Beesie Member Posts: 12,240
    edited September 2010

    NNT2G,

    No, the good news is that I'm not basing my comment on anything specific.  In my earlier post in this thread, I asked this question: Are there any potential problems with the system in that it may spur the growth of the tiny amounts of breast tissue that remain after a mastectomy.... does this create an increased recurrence or new primary BC risk?   I think it's a reasonable question and I wondered if any testing has been done to determine whether an increase in recurrence risk is a possibility and/or real concern or not.  From what I can gather, no testing has been done.  Julia, in her response to my post, indicated that she's made the decision to go ahead with this reconstruction method and is okay "(e)ven if it's found to double or even triple the risk of recurrence from 2% to 4 or 6%".  So my most recent comments were simply a continuation of this earlier discussion.

    I have found information on the internet that suggests that for women who use this method for breast enhancement, the new breast tissue that develops is at no greater risk of BC than any other breast tissue.  But I have found no information on testing done with women who've had mastectomies.  So the bad news is that it appears that we just don't know whether there is an increased risk of recurrence or not.  What we do know is that no matter how good our surgeons are, there always will be tiny amounts of breast tissue left after a mastectomy. This is why it's possible to have a recurrence after a mastectomy. In women who use the BRAVA system for breast augmentation, the system seems to spur the growth of breast tissue. Therefore does that mean that women who've had mastectomies may end up with more breast tissue after using this  reconstruction method?  And if there is more breast tissue, is there is a greater risk of recurrence and/or the development of a new BC?  Or, in spurring the growth of breast tissue, if there are a few rogue cancer cells left in the breast tissue after the mastectomy, might this system of reconstruction encourage the growth of these cells?  Could that lead to a greater risk of recurrence?

    I think these are reasonable and logical questions.  Without any testing having been done, there seems to be no way to know if this is a real concern or not.  Hopefully it's not, but from what I can gather, it's going to be the women who are pioneers who will be the ones who test this out and answer these questions for the rest of us.

    As I said in my original post, if anyone has information on this, please share.

  • alexandra-aaa
    alexandra-aaa Member Posts: 50
    edited September 2010

    I know this isn't the source you're looking for the information from, nor is it a controlled study of any kind, but it was all I could find on BRAVA and cancer risk/recurrance.

    But I just wanted to remind everyone, that "normal" BRAVA use for expansion is worn 10 hrs (tho more is recommended) per night for minimum 10 weeks (again, longer is recommended for greater growth). 

    For pre-surgical expansion, it is typically only worn for around 4 weeks. (I wore it for 11 because it was that long from my consult to surgery and I have the patience of a gnat!! I also kind of hoped that it might provide some additional growth from additional wear.)

    Post op recommendations are now 4-6 weeks for 10 hours/night, and then gradually tapering down for a few more weeks. It was recommended that I wear them 12-16 weeks, but sometimes it seems the protocol has been changing as it goes along (perhaps finding better/worse results with different criteria?), or else being tailored to individual patients situations and conditions.

    Point though, it sounds like when used solely for reconstruction, they're not worn enough hours or enough weeks to cause tissue growth. Only swelling pre-op and continued (less) swelling post-op, just to keep the blood supply rich and healthy for the newly transplanted fat to "take".

    (None of what I said is necessarily fact - just my interpretation. I'd love to see some long term stats on some of Dr. Khouri's reconstruction patients, if they're any different than the general population. I wonder if he keeps track and does follow-up....I'll try to find out since I have a never ending list of questions for him, lol!)

  • Beesie
    Beesie Member Posts: 12,240
    edited September 2010

    aaa,

    Thanks for the link.  I have read that information before.  Everything discussed there has to do with whether the Brava system may cause cancer or promote the development of cancer.  It seems not to, which is great.  This is important information for those who are undergoing breast enhancement. 

    From my understanding/interpretation however, the information provided has no bearing on what the Brava system may do to someone who has had breast cancer and who may have rogue cancer cells still left in her breast.  Nowhere on the Brava site can I find anything about safety for reconstruction patients.  To me, the absence of this information is glaring.  That's what I find worrisome.  That's not to say that there is a problem but it seems to me to be a pretty obvious question and a pretty obvious topic for them to cover off, and the fact that they don't suggests that they have no information at all about this.

  • GointoCarolina
    GointoCarolina Member Posts: 753
    edited September 2010

    Does anyone know anything about the clinical trial? I am wondering how many women it involved, how long it will follow them,will they still need mammograms or maybe MRIs?And when exactly did it start and end?And I am still not clear on how the Brava works with reconstruction, does it stretch out the skin and the fat is put in,then stretched again and more added?Was anyone here in the trial?

  • Beesie
    Beesie Member Posts: 12,240
    edited September 2010

    Here's the webpage with info on the clinical trial:

    http://www.clinicaltrialssearch.org/breast-reconstruction-and-augmentation-with-brava-enhanced-autologous-fat-micro-grafting-nct00466765.html

    It's only 50 women and it appears that they are being followed for only 1 year.  While the trial was started in November 2004 and was supposed to end in November 2008, the website indicates that they are still recruiting.

  • mormor1
    mormor1 Member Posts: 136
    edited August 2013

    I skimmed things, so hope I am following this correctly...I don't know all the answers but will tell you what I know.

    I was in the government clinical trial.  I started in June 2008 and I think I was one of the last ones to finish after my last grafting in Jan. 09  I had multiple MRI's...before, during and after.  My last one was April 2010 and it was totally clear (read by a very highly esteemed radiologist in Boston, I believe).  That was about 2 years from when I started using the Brava.

    MRI's are very sensitive and I think if this was causing any kind of cancer growth, it would show up after 8 months of Brava wear and then another year and 4 months later.  I also had a clear mammogram on both breasts May 2010.

     I just checked the web site and didn't see anything about still recruiting.  A friend of mine who recently had this done was not offered to be in the clinical trial. This is what they have under clinical trials on the web site:  Oops... I guess I can't post it, but people are welcome to check it out at miamibreastcenter.com under clinical trials.  Dr. Khouri is very well esteemed in his work in the U.S. and Europe.  If I missed the part about recruiting, please correct me.

    There are risks and unknowns with whatever surgical choices are made.  I was much less afraid of the unknowns for this procedure than the risks of other procedures both during the surgery and down the line   As it has been said though, tha is my take. obviously there are going to be women finding different choices to be what is right for them.  There are pros and cons to this option that women do need to consider, just as there are with other options. 

    with all due respect for the various opinions expressed,

    wisconsin randi

  • GointoCarolina
    GointoCarolina Member Posts: 753
    edited September 2010

    On the clinical trial page,it does say they are still recruiting,but they don't update those pages very often.If there were 50 women,how many had reconstruction and how many augmentation?I think the concern with the cancer growth is that from what I have read(and someone please correct me if I am wrong)most are very slow growing,so it would need several years of follow up to be sure.I guess part of what I do not understand is if this has had the clinical trial and been approved, why is the Brava system not covered by insurance?

  • lago
    lago Member Posts: 17,186
    edited September 2010

    This video just posted today on the Chicago Tribune online:

    Don't Lose It, Use It: Fat Transfer
    http://www.wgntv.com/news/medicalwatch/wgntv-fat-transfer-sept23,0,4107332.story

  • NotMyTime2Go
    NotMyTime2Go Member Posts: 34
    edited September 2010

    I'm going to take Beesie's concerns to my ps. Based on our conversation in the past, I think I know what his answer will be, but I'll refrain from posting it until I talk to him. I'm hoping to hear some feedback from others as well.

    But before I talk to him, I'm wondering if those of you who have done this can answer a question for me - was your first procedure done in a hospital? Was it outpatient? And how long were you in the surgical room?

    The reason I ask is that I'm anxious to get started as soon as I can, especially since I have expanders in and apparently won't need to start with the BRAVA device until after the first surgery. But my surgeon isn't getting the training until the end of October, and he schedules two months out for surgery. So I called his assistant to see if I could get on his schedule, and she said she has no idea what kind of room he'll need or how long he'll need it, and he won't know till he gets back. Which means waiting probably until the end of December (and that means probably January). So if I can figure out how to get a room scheduled now I'd be really happy. I'm crossing my fingers it's something he can just do in his office, but that's probably a bit too optimistic.

    Finally, I think I can address the question of why the BRAVA isn't paid for by insurance. I know from my experience with lymphedema that manufacturers have to jump through a bunch of hoops to get any device approved to where it's considered a "medical device" and approved by insurance companies. I tried to for many months to get my insurance to pay for a pump that does lympathic drainage. It was recommended by my doctor and my therapist, and has all kinds of studies proving it works, but it hasn't passed through the approval maze and my insurance wouldn't budge. So I don't find it so odd that they won't pay for a boob suction cup device.  =)

  • GointoCarolina
    GointoCarolina Member Posts: 753
    edited September 2010

    I just did a search  on the FDA site under medical devices  for Brava,I was thinking I could find something about where they stood in the approval process.All I found was a couple of reports that  women experienced blisters and another had an allergic reaction.Not many,I think three total.These women were using it for enhancement though.My concern is that my skin over my mastectomy is so sensitive that it is possible I could not use it.I think someone here tried it in the doctor's office and it was painful for her.Wonder if they would refund the money if that happened after you had used it for a bit or if you had a reaction and could not continue?.

  • dustylady
    dustylady Member Posts: 37
    edited September 2010

    pandazankar:  I started wearing it about 4-6 weeks after the BX and I was concerned about it too, but for the most part...on my body, it rested on the perimeters of the mastectomy and actually felt good in the middle part that was being suctioned out.   Except for an area on my left side where I had a lumpectomy about 18 years ago, and virtually nothing but skin and bones was left....the Brava on that side rested on a nerve, I think, but after a while, I was able to adjust the positioning....it would be interesting to find out if they would provide a refund if you can't wear them, though. 

    NotMyTime2Go:  My procedure was done in a hospital....outpatient....I think my surgery was around 3 or so hours under general anesthesia and several hours recovery....but every case will vary depending on the situation.

  • whippetmom
    whippetmom Member Posts: 6,920
    edited August 2013

    Brava system for sale on Houston craigslist...

    http://houston.craigslist.org/hab/1971263456.html

    This Ft. Worth plastic surgeon uses the Brava system, http://www.usaplasticsurgery.com/brava.html and his website contains information regarding the use and benefits of the BRAVA domes.  His comments on the website are exclusively related to the BRAVA device.  This is what he states about those women for whom the Brava system would not be appropriate. 

    Are there women who should not use the system?

    "Most healthy women can wear the system. Women who should not use the BRAVA System include pregnant and lactating women, those with a history of breast cancer, those who have had a mastectomy, and those under the age of 18 years (or those whose natural breast development is not complete)"

    He then responds to a FAQ regarding the "initial" BRAVA "clinical trials"...

    Can you describe the clinical trials?The initial clinical trials involved 17 women ranging in age from 18 to 40. Some were mothers and others had never had children. Five women were dropped from the trial due to noncompliance with the visitation protocol. Their initial cup sizes were AA, A, or B. All of the women grew approximately one-cup size and they were satisfied with their results. They agreed to use a medically accepted birth control method for the duration of the study and comply with stringent protocol requirements. Volunteers were excluded from the study for the following reasons: positive urine test for pregnancy; breastfeeding; a history of breast surgery or disease; severe breast tenderness and swelling related to menstruation, trauma or pain; presence of a breast mass; severe drooping of the breast; history of chronic dermatitis, and use of hormonal therapy besides birth control pills..
  • CrunchyPoodleMama
    CrunchyPoodleMama Member Posts: 1,220
    edited August 2013

    I'm hoping to talk a different plastic surgeon in metro ATL into trying this technique. One thing he didn't understand was what is the point in doing an initial fat graft at the time of the mastectomy (before there is breast tissue structure to support it). He thought the fat would just drain right out via the drains.

    Does the initial fat graft (if done the same day as mx) "take" at all, or is that really just so the patient has a breast mound and it isn't so shocking after the mx? This plastic surgeon tried several times to call Dr. Khouri but got a busy signal every time.

    BTW, if anyone has a direct phone number for Dr. Khouri that my doctor could try, I would appreciate if you could PM it to me... thanks so much!

    whippetmom, that does sound alarming on first read, but actually it just sounds like an overly cautious plastic surgeon who has no interest in (or possibly doesn't even know about) the applications for mastectomy patients. He's speaking for his own practice's policies, not the safety of the device for those applications. 

    The pregnancy exclusion alarmed me, but since he's only treating non-mastectomy patients, of course that makes sense.

  • pearlcap
    pearlcap Member Posts: 11
    edited September 2010

    Hi,

    I'm new here.  I'm having part of my breast taken out for ADH, possibly DCIS in a few weeks and wondered if fat grafting can fix the dents afterwards.  I have three large areas and was already told that my breast would be dented afterwards since I have small breasts.  I visited a plastic surgeon and he said he could do a fat graft but it would not be the same.  I thought I could see some pictures but as it turned out the office didn't have any fat grafting pictures for lumpectomy.  Is there anyone out there who had this done and can they fix it 100%? Is it still slightly indented afterwards? I'm trying to decide if in addition, I should take out some benign areas that feels lumpy out (the surgeon is leaving that up to me.)  I'm not talking about the Brava or the Cytori procedures but plain fat transfer.  Thanks in advance

  • whippetmom
    whippetmom Member Posts: 6,920
    edited September 2010

    pearlcap:  Fat graft transfer can be used to fill in defects after lumpectomy - especially as you describe, "slight indentations."  I would personally want a plastic surgeon who is experienced with FGT for breast reconstruction.  It might take two or even three separate FGT procedures to accomplish this....it might take only one.  The "100%" guarantee though....I don't think you will find any plastic surgeon to make such a promise.

  • lago
    lago Member Posts: 17,186
    edited September 2010

    I agree with wippetmom. Be wary of any PS that gives 100% guarantee. A good PS will tell you what the complications might be… even if they are remote a good surgeon is required to let you know. I think that is part of the board certifications rules.

  • pearlcap
    pearlcap Member Posts: 11
    edited October 2010

    Thank you Whippetmom and lago.  I'm having surgery in two weeks and maybe a fat transfer sometimes next year.  I'll let the board know my experience with fat grafting if that helps anyone.  Thanks for your responses.

      

  • Sarnie123
    Sarnie123 Member Posts: 15
    edited October 2010

    FAT TRANSFER, THIS IS WHAT MY SURGEON TOLD ME.....

    My surgeon offered me fat transfer recently after having a lumpectomy, I thought this would be great - but when I went back a few weeks later, he said because I'd had radiotherapy and chemo I couldn't have fat transfer.  He said there may still be cancer cells still in my body and if transferred to my breast could cause cancer?  

    He has now offered me reduction in my left breast and right mastopexy, I just don't know whether to go ahead with this....friends say leave well alone, whats your experience?

  • lago
    lago Member Posts: 17,186
    edited October 2010

    What, I never heard that?!

    I know my surgeon is planning on doing some fat transfer with my implants. He knows I'm doing chemo and might do rads. I would get a 2nd opinion on this. I would also ask your oncologist what s/he thinks about this.

  • Sarnie123
    Sarnie123 Member Posts: 15
    edited October 2010

    Thanks I will, perhaps he has changed his mind and does not want to this procedure....

  • pearlcap
    pearlcap Member Posts: 11
    edited October 2010

    I have a life science/medical background (not in breast research) and have been reading some research on fat grafting since I've been thinking of doing this post lumpectomy surgery.  This is what I found out.  Although fat grafting/transfer has been done for many years in Europe, its use in reconstructive surgery is still controversial in the US.  There are two main issues.  First, there has been fear that some of the fat transferred will die (necrosis), causing calcification and interfering with accurate detection of cancer.  Both my physicians at Memorial Sloan and references to studies I looked at indicated (Plastic Surgeon Societies continue to be against fat grafting for breast augmentation) that radiologists are able to distinguish between calcification from fat necrosis (cell death) and breast cancer.  As far as I am concerned, this is not an issue for good radiologists.  The second issue is whether stem cells from fat grafting will induce growth of tumor cells.  This is the more important issue and we still need more data; but thus far, the data suggest that the transferred fat cells may promote active tumor cells but not dormant cancer cells (see link below).  This is a personal decision but what one should consider is whether there is a risk that there may be unknown cancer cells left behind that may induce tumor growth through the fat grafting/transfer.  The perfect situation is to wait a few years of cancer free diagnosis before getting a fat graft.  Personally, I am going to reassess my situation after surgery.  I have to see what my breast look like and read more research.   If I get a fat transfer, I will let the board know the outcome.

    (http://www.upmc.com/MediaRelations/NewsReleases/2010/Pages/Fat-Stem-Cells-Breast-Reconstruction-Dormant-Cancer.aspx)

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