Abstract
Background
Preservation of the nipple areolar complex (NAC) provides the optimal conditions for immediate breast reconstruction (IBR). Growing evidence suggests the oncological safety of nipple sparing mastectomy (NSM) when neither NAC nor skin is affected by tumor. This paper presents our initial experience performing NSM and IBR in a selected group of patients through the inframammary incision assisted by hydrodissection.
Material and methods
The study includes 20 healthy women, aged 23-53, and referred for bilateral risk-reducing mastectomy. NSM was carried out using inframammary crease incision assisted by hydrodissection followed by IBR with an acellular dermal matrix (ADM) and an implant as presented in the attached video. Exclusions criteria were hypertension, diabetes, active smoking and previous chest radiation therapy. Data was collected retrospectively.
Results
We achieved the reconstructive goal for all 40 breasts (100%). There were no cases of NAC necrosis. Minor complications were registered in two reconstructions (5%), including one case of small partial necrosis and one case of wound dehiscence. The median follow-up was 13 months (range, 1-32 months).
Conclusions
Bilateral risk-reducing NSM and IBR can be successfully achieved through an inframammary crease incision assisted by hydrodissection. Patient selection is the key to a successful outcome.
Keywords: Nipple sparing, mastectomy, reconstruction, acellular dermal matrix (ADM), implant
Introduction
Breast cancer treatment has changed over the last decade from radical mastectomy towards a more conservative surgical approach favoring skin sparing mastectomy (SSM) (1). Patients are more reluctant to accept a loss of their breast when other options exist and are increasingly requesting a combined ablative and reconstructive surgical procedure. Hence, SSM and more recently a nipple-areola sparing mastectomy (NSM) together with immediate breast reconstruction (IBR) are becoming a popular choice when indicated (1-3).
The preservation of the nipple areolar complex (NAC) provides optimal conditions for IBR as opposed to SSM, where the NAC has to be reconstructed in a secondary, often challenging procedure which tends to result in a flattened and dissatisfying appearance of the breast mound (4,5). Growing evidence suggests that NSM is safe to perform when the NAC and skin is not affected by tumor (5-10). We have regularly performed NSM and IBR for the past 4 years on oncologic as well as risk reducing indication.
We present our initial experience performing NSM on a selected group of patients using hydrodissection in combination with an inframammary incision and illustrate the technical aspects of the procedure performed as presented in the attached video (Figure 1).
Material and methods
The study population consisted of 20 women aged 23-53 who were referred after genetic consultation for bilateral risk-reducing mastectomy. Included patients had NSM and IBR using the same method, presented in this paper, at Vejle Hospital in Denmark and Telemark Hospital in Norway between September 2012 and July 2014.
The patients consented to surgery after oral and written information. Patient selection criteria were based on previously reported findings (12), including only healthy patients without major comorbidity. The exclusion criteria were hypertension, diabetes, active smoking and previous chest radiation therapy. Data was collected retrospectively by revision of charts and supplemented by patient interviews when the information was insufficient or ambiguous.
Pre-operative marking
The breast footprint was marked using a permanent marker with the patient in the upright position. The planned inframammary crease incision was then drawn below the nipple extending 8-9 cm laterally. The expected projection of the planned breast reconstruction was estimated from measurements of the breast, degree of ptosis and laxity of the skin.
Surgical technique
The surgical technique is illustrated in the video: “How to perform a NAC sparing mastectomy with an ADM and an implant”.
A preoperative dose of intra venous antibiotics was given as a standard. Following application of local anesthesia, the skin was incised at the inframammary crease marking. The breast gland was dissected of the pectoralis major muscle and thoracic wall in the subglandular plane using a monopolar cautery. The subglandular cavity was subsequently palpated to ensure that this level had been reached in the entire breast circumference. The breast was then infiltrated with a solution of 1 liter NaCl/ 1 mL epinephrine using a blunt tip cannula immediately below the subcutaneous fascia. The non-dominant hand was used to palpate the movement of the cannula ensuring infiltration in the correct plane.
Correct infiltration is paramount and the cannula should slide freely without resistance as this may indicate displacement of the tip into the wrong dissection plane. However the regions lateral and cranial to the NAC contain more fibrous tissue connecting the cutis and subcutis, and can be challenging to infuse correctly.
The dissection of the glandular tissue commenced at the level of the subcutaneous fascia using combined blunt and sharp scissor dissection. The tissue beneath the NAC as well as the fibrous adhesions laterally to the NAC were cut by careful, sharp dissection removing the entire glandular tissue en bloc through the inframammary incision, and marking it for pathologic evaluation in a standard manner.
The cavity was inspected and palpated to ensure that the ablative surgery had been performed correctly and any excess tissue underneath the subcutaneous fascia was removed, guided by vision. A subdermal, avascular dissection plane is readily found beneath the areola. The underside of the NAC was checked by eversion through the inframammary crease to make sure that no glandular tissue remnants were left behind. In all cases, the underside of the nipple was biopsied for separate histopathology and finally the cavity was checked for sufficient hemostasis.
The skin quality and viability was evaluated prior to reconstruction. The pectoralis major muscle insertion was released inferomedially using a monopolar cautery, as for a dual-plane breast augmentation, to allow partial muscular coverage of the implant.
Extended implant coverage was created using a hammock of acellular dermal matrix (ADM) (12,13). The ADM was sutured to the inferior edge of the muscle and the desired position of the inframammary crease. Implant selection was based on breast footprint measurements, skin quality, as well as the patient’s wishes for size and projection. Two drains were placed, one at the inframammary crease and the other pointing towards the axilla. The reconstruction was finalized suturing the skin in two layers using absorbable 3-0 sutures.
Drains were removed when the daily output was less than 20 mL. Oral antibiotics were administered until all drains were removed. After discharge, patient follow-up was conducted in the outpatient clinic.
Results
We achieved the reconstructive goal for all 40 breasts (100%) (Figure 2). There were no cases of NAC necrosis, neither partial nor complete. Minor complications were registered in two reconstructions (5%), one case of small partial necrosis and one case of wound dehiscence.
The ADMs used were 8×16 cm in 24 breasts and 8×20 cm in 14 breasts according to the size needed for the selected implant (Figure 3). Permanent silicone implants were used in most patients 18/20 (90%). In the remaining cases we used expander implants 2/20 (10%). The mean implant size at the time of reconstruction was 450 cc (range, 225-700 cc).
Four women in this series (20%) had either a great degree of ptosis or macromastia too large for IBR. They received a reduction mammoplasty 3 months prior to the subsequent NSM and IBR. The combined pre-reduction mammoplasties and subsequent NSM and IBR were all achieved without complications (Figure 4).
The median follow-up was 13 months (range, 1-32 months).
Discussion
We have performed risk-reducing NSM and IBR since 2011 using hydrodissection in combination with different incisions and approaches. In this series focusing on the inframammary crease approach, reconstructive goals were achieved in all of the planned cases without any major complications. Two minor complications occurred; in the first case, ADM’s were not available and the reconstruction was achieved using silicone implants and marionette suture fixation of the pectoralis muscle over the implant upper pole, as previously described by Spear et al. (14) (Table 1). The patient suffered compression necrosis of the lower pole due to the tight bandage covering the sutures. She made an uneventful recovery in 3 weeks. In the other case the patient developed a blister due to wound dehiscence at the inframammary crease. The wound margins were revised under sterile conditions and the patient made a full and uneventful recovery.
Table 1. Bilateral risk reducing NSM using hydrodissection in women with no co-morbidity.
Patient | Age (years) | Hammock type | Hammock size | Implant type | Implant size (cc) | Drain days | Complications minor/major | Outcome achieved | Follow up months |
---|---|---|---|---|---|---|---|---|---|
1 | 28 | None | - | Silicone | 300 | 14 | Mi | Y | 32 |
2 | 39 | ADM | 8×16 | Silicone | 300 | 13 | None | Y | 31 |
3 | 30 | ADM | 8×16 | Silicone | 550 | 12 | None | Y | 30 |
4 | 49 | ADM | 8×16 | Becker50/50 | 400 | 14 | None | Y | 21 |
5 | 49 | ADM | 8×16 | Silicone | 225 | 15 | None | Y | 20 |
6 | 46* | ADM | 8×20 | Silicone | 475 | 14 | None | Y | 16 |
7 | 45 | ADM | 8×20 | Expander | 550 | 21 | None | Y | 15 |
8 | 41 | ADM | 8×16 | Silicone | 440 | 21 | None | Y | 12 |
9 | 53 | ADM | 8×20 | Silicone | 555 | 12 | None | Y | 11 |
10 | 49 | ADM | 8×20 | Silicone | 475 | 11 | Mi | Y | 10 |
11 | 40 | ADM | 8×16 | Silicone | 475 | 14 | None | Y | 9 |
12 | 38 | ADM | 8×16 | Silicone | 325 | 12 | None | Y | 8 |
13 | 45* | ADM | 8×16 | Silicone | 420 | 15 | None | Y | 8 |
14 | 34 | ADM | 8×16 | Silicone | 440 | 11 | None | Y | 7 |
15 | 32 | ADM | 8×16 | Silicone | 420 | 7 | None | Y | 6 |
16 | 38* | ADM | 8×20 | Silicone | 590 | 12 | None | Y | 5 |
17 | 43 | ADM | 8×20 | Silicone | 515 | 9 | None | Y | 3 |
18 | 42 | ADM | 8×16 | Silicone | 440 | 14 | None | Y | 3 |
19 | 47* | ADM | 8×16 | Silicone | 440 | 14 | None | Y | 2 |
20 | 50 | ADM | 8×20 | Silicone | 700 | 11 | None | Y | 1 |
*, pre-reduction 3 months prior to NSM. NSM, nipple sparing mastectomy; ADM, acellular dermal matrix.
We prefer the inframammary crease approach which in our experience results in a more optimal reconstruction. This technique may appear challenging at first, however, plastic surgeons are familiar with both the inframammary approach and the subglandular dissection. Consequently, the procedure is a joint team effort performed simultaneously by a breast surgeon and a plastic surgeon. This teamwork leads to an ongoing and important discussion about skin thickness, trying to balance ablative and reconstructive surgery in a way which ensures removal of sufficient tissue, and at the same time sustaining blood supply for the remaining skin flaps for reconstruction. When we are able to identify the superficial fascia, we use this as our dissection plane. However, as described recently in a review by Robertson et al., the superficial fascia is readily identified in just 56% of patients (15). When the fascia is not well identified the dissection plane is based on team experience. We have not measured the thickness of the skin flaps of the studied patients. However, we found that the skin flaps varied between patients and we estimate the variation was between 4 to 8 mm.
The most recent and largest reported series on NSM by Colwell et al. based on 500 procedures supports our findings stating the importance of patient selection and that inframammary crease incision persistently produces better results and fewer complications (16). A lateral inframammary crease incision in combination with hydrodissection, similar to our technique, has been described earlier by Blechman et al. (17). Our incision is more medially placed and the patient sample more homogenous.
It seems that skin and nipple survival can be optimized by correct patient selection and lower the risk of reconstructive failure and cancer recurrence (9,12,18,19). Oncological safety is an important issue when performing NSM and IBR. However, risk-reducing NSM and IBR can be regarded oncologically safe (6,8). Reported evidence, after 5-15 years follow-up, shows that there does not seem to be an increased risk of recurrence in patients treated by the nipple sparing technique compared to other approaches. Thus the procedure does not seem to increase the risk of tumor recurrence or decreased survival compared to other ablative methods (6-10). The use of ADM in primary breast reconstruction is well established and as in other techniques, patient selection is a key element to a successful result (12,13). The most important selection criteria are breast size and comorbidity as described above. A large ptotic breast cannot be reconstructed using this NSM technique in a satisfactory manner. Pre-shaping or the pre-reduction/mastopexia can be offered to patients undergoing risk-reducing procedures as a safe alternative as described by Spear et al. (20). Pre-shaping seems to cause a delayed effect by increasing the dermal vascularity of the NAC, which increases the chance of survival after the subsequent mastectomy and reconstruction (21).
Conclusions
Bilateral risk-reducing NSM and IBR can be performed successfully through an inframammary crease incision in combination with hydrodissection. Critical patient selection is the key to a successful outcome.
Acknowledgements
Disclosure: The authors declare no conflict of interest.
References
- 1.Fisher B.From Halsted to prevention and beyond: advances in the management of breast cancer during the twentieth century. Eur J Cancer 1999;35:1963-73. [DOI] [PubMed] [Google Scholar]
- 2.Ballard TN, Momoh AO. Advances in breast reconstruction of mastectomy and lumpectomy defects. Surg Oncol Clin N Am 2014;23:525-48. [DOI] [PubMed] [Google Scholar]
- 3.Simmons RM, Adamovich TL. Skin-sparing mastectomy. Surg Clin North Am 2003;83:885-99. [DOI] [PubMed] [Google Scholar]
- 4.Laronga C, Lewis JD, Smith PD. The changing face of mastectomy: an oncologic and cosmetic perspective. Cancer Control 2012;19:286-94. [DOI] [PubMed] [Google Scholar]
- 5.Djohan R, Gage E, Gatherwright J, et al. Patient satisfaction following nipple-sparing mastectomy and immediate breast reconstruction: an 8-year outcome study. Plast Reconstr Surg 2010;125:818-29. [DOI] [PubMed] [Google Scholar]
- 6.Piper M, Peled AW, Foster RD, et al. Total Skin-Sparing Mastectomy: A Systematic Review of Oncologic Outcomes and Postoperative Complications. Ann Plast Surg 2013. [Epub ahead of print]. [DOI] [PubMed] [Google Scholar]
- 7.Munhoz AM, Aldrighi CM, Montag E, et al. Clinical outcomes following nipple-areola-sparing mastectomy with immediate implant-based breast reconstruction: a 12-year experience with an analysis of patient and breast-related factors for complications. Breast Cancer Res Treat 2013;140:545-55. [DOI] [PubMed] [Google Scholar]
- 8.Stanec Z, Zic R, Budi S, et al. Skin and Nipple-Areola Complex Sparing Mastectomy in Breast Cancer Patients: 15-Year Experience. Ann Plast Surg 2014;73:485-91. [DOI] [PubMed] [Google Scholar]
- 9.Colwell AS, Tessler O, Lin AM, et al. Breast reconstruction following nipple-sparing mastectomy: predictors of complications, reconstruction outcomes, and 5-year trends. Plast Reconstr Surg 2014;133:496-506. [DOI] [PubMed] [Google Scholar]
- 10.Poruk KE, Ying J, Chidester JR, et al. Breast cancer recurrence after nipple-sparing mastectomy: one institution’s experience. Am J Surg 2014. [Epub ahead of print]. [DOI] [PubMed] [Google Scholar]
- 11.Gunnarsson GL, Børsen-Koch M, Wamberg P, et al. How to perform a NAC sparing mastectomy using an ADM and an implant. Asvide 2014;1:363. Available online: http://www.asvide.com/articles/363 [DOI] [PMC free article] [PubMed]
- 12.Gunnarsson GL, Børsen-Koch M, Arffmann S, et al. Successful breast reconstruction using acellular dermal matrix can be recommended in healthy non-smoking patients. Dan Med J 2013;60:A4751. [PubMed] [Google Scholar]
- 13.Salzberg CA. Focus on technique: one-stage implant-based breast reconstruction. Plast Reconstr Surg 2012;130:95S-103S. [DOI] [PubMed] [Google Scholar]
- 14.Spear SL, Sher SR, Al-Attar A. Focus on technique: supporting the soft-tissue envelope in breast reconstruction. Plast Reconstr Surg 2012;130:89S-94S. [DOI] [PubMed] [Google Scholar]
- 15.Robertson SA, Rusby JE, Cutress RI. Determinants of optimal mastectomy skin flap thickness. Br J Surg 2014;101:899-911. [DOI] [PubMed] [Google Scholar]
- 16.Colwell AS, Gadd M, Smith BL, et al. An inferolateral approach to nipple-sparing mastectomy: optimizing mastectomy and reconstruction. Ann Plast Surg 2010;65:140-3. [DOI] [PubMed] [Google Scholar]
- 17.Blechman KM, Karp NS, Levovitz C, et al. The lateral inframammary fold incision for nipple-sparing mastectomy: outcomes from over 50 immediate implant-based breast reconstructions. Breast J 2013;19:31-40. [DOI] [PubMed] [Google Scholar]
- 18.Moyer HR, Ghazi B, Daniel JR, et al. Nipple-sparing mastectomy: technical aspects and aesthetic outcomes. Ann Plast Surg 2012;68:446-50. [DOI] [PubMed] [Google Scholar]
- 19.Dent BL, Small K, Swistel A, et al. Nipple-areolar complex ischemia after nipple-sparing mastectomy with immediate implant-based reconstruction: risk factors and the success of conservative treatment. Aesthet Surg J 2014;34:560-70. [DOI] [PubMed] [Google Scholar]
- 20.Spear SL, Rottman SJ, Seiboth LA, et al. Breast reconstruction using a staged nipple-sparing mastectomy following mastopexy or reduction. Plast Reconstr Surg 2012;129:572-81. [DOI] [PubMed] [Google Scholar]
- 21.Jensen JA, Lin JH, Kapoor N, et al. Surgical delay of the nipple-areolar complex: a powerful technique to maximize nipple viability following nipple-sparing mastectomy. Ann Surg Oncol 2012;19:3171-6. [DOI] [PubMed] [Google Scholar]