Ask plastic surgeon Scott Sullivan, M.D., your recon questions!

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  • CarlaR333
    CarlaR333 Member Posts: 2
    edited January 2017

    Hi MQY,


    I hope I am posting this message correctly. I just joined. Sorry to hear about your situation. No one ever talks about lymphedema until you have it. My doctors barely mentioned it, and I had never even heard of it before I got cancer. I was wondering if the reconstruction made your lymphedema worse? I have it in my left arm and am worried about it getting worse because of the surgery. Did the doctors tell you it would make it worse, better, or neutral before you had it? Thank you so much.

  • SeattleBound
    SeattleBound Member Posts: 48
    edited January 2017

    Very frustrated!!This topic site is very frustrating to read. Suggest that the info I found in one post by moderators be included in the main area so we will understand that the doctor's answers are not posted here, but instead, certain questions are chosen by the moderators and appear elsewhere in a blog topic. I had to read through many posts before finding that information. The doctor's answers were excellent, but clearly, there can be many months before a question is answered.

  • moni22
    moni22 Member Posts: 4
    edited January 2017

    Agreed. This website is very frustrating. I don't know if my question was ever answered as I do not have the time to sift through the many pages on here.

    Would be great to have a much more user friendly website.

    I'm 3 weeks post-op from DIEP if anyone wants to chat.


    Blessings to you all for 2017

  • Moderators
    Moderators Member Posts: 25,912
    edited January 2017

    Thank you all for posting your questions -- our apologies for not being more clear with how these questions would be handled. We have now updated the opening post to give a clearer definition of how this thread will be used. We are currently working with Dr. Sullivan to select questions for the next blog.

    Thank you for your patience and for your participation in this matter.

    --The Mods

  • Binney4
    Binney4 Member Posts: 8,609
    edited January 2017

    Carla and MQY, how about hopping over to the "Lymphedema" board here and posting your questions there--lots of women there who have dealt with reconstruction and lymphedema and would be able to share their experience and discoveries with you. Scroll down on the "Jump to a Forum" feature (above left) and click on "Lymphedema", then click on the GO button.

    Gentle hugs,
    Binney

  • Mariangel43
    Mariangel43 Member Posts: 136
    edited April 2017

    Dr. Scott: Hello, thanks for giving us the opportunity of having a forum where we can express our worries and concerns.

    My first question is why BSs cut nerve terminals of the breast skin which is not removed?

    Second, PSs when inserting the implants do not remove the excess skin from a former biopsy and leave those skin folds next to the recon breast. Why the folds are not part of the recon?

    Third, I received my implant on Dec. 8 and had a piece of areola and nipple transplant from left breast. It's almost a month and the sutures haven't dissolved on their own. Can I remove them?

  • Mariangel43
    Mariangel43 Member Posts: 136
    edited January 2017

    Dr. Scott, I asked my PS about the possibility of having an allergic reaction to implants. He said that silicon implants he used do not provoke allergic reactions. Is that true or not?

    I developed capsule contracture around the TE in four months. I am worried about developing it with the implant. What is the probability if I already had capsule contracture?

    Thanks in advance

  • bethesue14
    bethesue14 Member Posts: 2
    edited January 2017

    I'm brand new to this forum, very happy I found you! I had DCIS in 1999 with lumpectomy and radiation. The doc misread the dx and gave me "extra" radiation, which has caused 18 years of fibrosis until my breast essentially disappeared. I had hormone receptive tumor in the other breast 5 years ago with lumpectomy and radiation with a much better result. I recently decided to have breast reconstruction; I'm 68 years old and a widow, but I was tired of being angry with the doc.

    Anywho, I'm dealing with pain from tissue expander and asked the plastic surgeon if I could have fill of 60 ml every 2 weeks instead of every week, as I have 3 days of pain requiring oxycodone to function. He said the expander might "close up" if I went to 2 weeks and I've not found a report of this anywhere or any mention of it. I'm wondering if this is just his schedule that he wants to stick to or if this is a valid caution. Thanks!

  • Moderators
    Moderators Member Posts: 25,912
    edited January 2017

    Hi Bethesue14-

    Congrats on your decision to have reconstruction! You may want to post your question in our reconstruction forum as well, lots of great info and knowledgeable members there who might be able to offer some insight on filling your expanders on a slightly modified schedule: https://community.breastcancer.org/forum/44.

    Feel free to start a new topic there, if you don't see one where you think your question is a good fit!

    The Mods

  • anotherNYCGirl
    anotherNYCGirl Member Posts: 1,033
    edited January 2017

    bethesue, - My radiated side was much more uncomfortable than the non radiated side. My fills were reduced to 25 ml on that side, and were at least 2 weeks apart!

  • bethesue14
    bethesue14 Member Posts: 2
    edited January 2017

    Thanks for the info. I'm definitely going to 2 weeks and maybe reduce fills. What's the rush, anyway. I've lived with this for almost 20 years! I've had radiation on both sides, but only need expander for one.

  • Cooljewels
    Cooljewels Member Posts: 4
    edited February 2017

    I had a mastectomy on my right breast, this is a recurrence, my 1st surgery on my right breast on 7/2010 was a lumpectomy with 18 to 20 lymph nodes removed 1 positive. I was diagnosed with a recurrence on 10/2016, had surgery on 12/12/16 Stage 1A, no nodes positive.  My question is I am having swelling in my right breast a few days after my drains were removed, my PS tried to aspirate my breast and nothing came out, he tried several areas on my right breast, my PS sent me to the hospital to have a drain put in because he thought there was a abscess or infection, and I had no symptoms of either of these, the Radiologist at the hospital said only a small amount of fluid in breast and it was under my TE so he could not install drain and thought it would cause me to get an infection. Now my right breast has swelled more it looks like almost have a normal breast.  What can I do?

  • FreeYourMelons1
    FreeYourMelons1 Member Posts: 3
    edited May 2017

    im wondering can you do a diep flap and fat graphing to make a full breast at same time during same surgery procedure?

  • Nanpop
    Nanpop Member Posts: 75
    edited May 2017

    My TE's were put in Oct 2016 after bilateral mx. I developed a hematoma in right breast and had new TE put in two days later and it had to be replaced.

    I'm having radiation on chest wall for left breast with intermamery nodes. I will most Likely need DIEP or SIEA. However that breast was sewn in a straight line using alloderm instead of being rounded. It liooks higher than right breast and is painful.

    Is this a common problem that can easily be fixed or do I need to see a reconstruction specialist especially after radiation?

    My PS doesn't think it will be able to be fixed so that it looks like the right. Where do you find specialists that have experience with fixing thus


  • LettyF
    LettyF Member Posts: 43
    edited August 2017

    Hello Dr. Sullivan,

    I go for another fill tomorrow and plan to speak with my plastic surgeon about this but would like your opinion. My last fill (100ccs left breast and only 70ccs in the right which is where the cancer was) my doctor said I may very well end up with two different implant sizes. I don't understand how I can have more saline in the left expander and it still looks so much smaller than the right. I currently have 600ccs in the left and 570ccs in the right but the right looks so much larger. I had my dbl mastectomy 2/17 and expanders placed 5/17. I'm wondering if there is a slow leak in the left????? I don't have any pain or discoloration but there is definitely a size difference. I look forward to hearing your thoughts, is this normal or happen often?

    Thank you,

  • kae_md99
    kae_md99 Member Posts: 621
    edited August 2017

    Hello Dr. Sullivan,

    i have pre pecs TE's ,400 cc. i was small to begin with ( cup A) and my PS mentioned putting a bigger implant.i want to go small, maybe 300-320 and the 400 feels so heavy on me.is it possible to have smaller implants than TE's at the exchange.Thank you.

  • Moderators
    Moderators Member Posts: 25,912
    edited November 2017

    Hi all --

    Although it turns out that Dr. Sullivan was unable to participate due to scheduling, the Center enlisted three of his colleagues in microsurgery to respond to a selection of your questions. Visit the Q&A series to read insights from Craig Blum, M.D., F.A.C.S.; M. Whitten Wise, M.D.; and Chris Trahan, M.D., F.A.C.S. Please see blog below!

    Surgeons Answer Your Breast Reconstruction Questions, October 30, 2017



  • MTwoman
    MTwoman Member Posts: 2,704
    edited October 2017

    Thanks to the Mods and the Team at the Center for Restorative Breast Surgery!

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