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KEY POINTS
Because plastic surgeons are increasingly involved in prophylactic, ablative and restorative surgeries related to the breast cancer, it is imperative that they can offer all technical variants of these surgeries (e.g., prophylactic mastectomy), matching patient oncological needs with high cosmetic expectations and understand the implications of the technical choice on future risks and surveillance requirements. The ability to determine adequate margins after presurgical radiation or neoadjuvant chemotherapy; experience in reconstruction in cases with intraoperative or accelerated partial irradiation; ability to manage breast cancer in patients with previous aesthetic surgery; and the ability to supplement tissue rearrangement repairs with small, well-vascularized flaps or alloplastic materials are characteristic of oncoplastic surgeons who are comfortable with all aspects of breast cancer management and who have mastered advanced techniques.
INTRODUCTION
It is difficult to find an example of a multidisciplinary clinical niche showing more rapid growth and greater diversity than breast cancer care.1 In the 1980s, indications for breast reconstruction were liberalized as a result of increasing experience with various procedures, including microsurgery; development of implants, including tissue expanders designed for breast reconstruction; recognition of the beneficial psychological effects of breast reconstruction; and, most importantly, because of the clinical evidence that reconstructive procedures did not negatively affect the result of mastectomy (at that time the mainstay of the primary breast cancer treatment). Breast reconstructive procedures seem
Disclosures: Dr Dobke has no commercial interests and disclosures in connection with the content of this article; however, he is a consultant for Ulthera. Division of Plastic Surgery, University of California San Diego, 200 West Arbor Drive, San Diego, CA 92103-8890, USA E-mail address: mdobke@ucsd.edu Clin Plastic Surg 39 (2012) 465475 http://dx.doi.org/10.1016/j.cps.2012.07.015 0094-1298/12/$ see front matter 2012 Elsevier Inc. All rights reserved.
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not to worsen the incidence of local and distant disease-free or overall survival in patients subjected to either mastectomy or different forms of breast conservation surgery (BCS) that were established in the 1990s. However, the natural evolution of breast cancer development risk assessment, the advances in diagnostic and surveillance methods, and the changes in the design of comprehensive breast cancer management necessitate the ongoing evaluation of reconstructive approaches to ensure that they do not hinder cancer detection or treatment. Similar concerns are shared in the context of aesthetic breast procedures. Many advances stem from past controversies; whether or not to reconstruct was itself recently a controversy. Practice
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guidelines for the management of breast cancer do not include detailed recommendations regarding aesthetic or reconstructive approaches.2,3 Without knowledge of controversies and recognition of advances in oncological breast care, plastic surgery would not be on par, both conceptually and technically, with quality medicine and surgery.1,4 This article shows how current diagnostic and therapeutic advances affect plastic surgery and how advances in plastic surgery affect breast care. of ovarian ablation and other breast cancer risk reducing strategies are underestimated.9 Because plastic surgeons are increasingly involved in both PM and CPM, it is imperative that they can offer all technical variants of PM to match patient oncological needs and understand the implications of the technical choice for future risks and surveillance requirements. Regarding the simple or skin-sparing type of PM, because all types of mastectomy leave some breast tissue behind, subcutaneous mastectomy (in which nipple-areola complex [NAC] is preserved along with a minuscule layer of supporting breast tissue and terminal ducts segments) is associated with a greater risk of development of breast cancer than total mastectomy. More invasive forms of PM should therefore be recommended to highrisk women; however, strict selection criteria have not been established for the patients with breast cancer who are the best candidates for NAC-sparing mastectomy with an acceptably low risk of NAC tumor involvement.10 Total mastectomy, which includes the removal of breast tissue, NAC, and the axillary tail, is generally considered the preferred procedure for PM and is often followed by immediate BR.11,12
IMPACT OF PREVENTIVE, DIAGNOSTIC, AND BREAST MANAGEMENT ADVANCES ON RECONSTRUCTIVE AND AESTHETIC BREAST SURGERY Prophylactic Mastectomy
One of the most effective options in preventing breast cancer is prophylactic mastectomy (PM). In high-risk patients, PM may be performed as a bilateral procedure; for women undergoing surgical treatment of unilateral breast cancer, there remains much debate about the role of contralateral PM (CPM). Supporters of CPM cite general statistics showing that CPM identifies occult malignancy in approximately 5% of cases and that CPM also decreases the risk of future contralateral breast cancer in more than 90% of cases.4 A woman is considered to be at high genetic risk for the development of breast cancer if she has a BRCA1 or BRCA2 gene mutation or her family history suggests an autosomal dominant pattern of inheritance.5 A woman with breast malignancy who presents at a young age or has relatives affected by breast cancer should consider testing for BRCA1 and BRCA2 mutations. Plastic surgeons counseling patient candidates for breast reconstructive or aesthetic surgeries have to be familiar with breast cancer risk assessment and recommend appropriate work-up (genetic testing, imaging).3,6 Breast cancer reducing strategies, other than PM or CPM, include ovarian ablation, endocrine treatment (eg, tamoxifen), and lifestyle adjustments.6 It is a difficult decision whether to undergo PM or CPM and, from the technical standpoint, timing of these procedures also matters (discussed later). Skeptics point out that the risk of breast cancer in the contralateral breast is overestimated and that breast cancer prevention strategies other than CPM are underappreciated. However, improvements in outcomes of breast reconstruction (BR) and high patient satisfaction rates from both PM and BR (90% range) boost plastic surgeons confidence and lower the threshold for PM/BR recommendation as an option.7,8 Furthermore, in arguing for PM or CPM, it could be claimed that risks and consequences
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Fig. 1. (A) The patient is prepared for SSM and immediate BR in the management of local recurrence after breastconserving surgery and radiation. (B) Latissimus dorsi myocutaneous flap (with small skin paddle to be used for nipple-areola reconstruction in the future) and silicone gel implant were used to reconstruct the left breast.
SSM should be an option is questionable.10,15,16 In properly selected patients with lesions away from distal ducts, results of NAC sparing in the therapeutic setting would be oncologically acceptable if cancerous or high-risk lesions were histologically contiguous, but this has not been shown.17,18 The study examining the incidence of malignant areolar and nipple involvement separately concluded that, because the areola is less frequently involved than the nipple with terminal ducts (approximately 10% of nipples harbored cancerous tissue), only the areola should be spared.19 Subareolar tissue biopsy and extirpation of ducts distant from the nipple may not ensure oncological safety: approximately 6% to 7% of PM specimens harbored occult malignant lesions.20,21 It was stated earlier that the next step in improving aesthetic outcomes of BCS, is to preserve the NAC; however, there is no evidence from comparative studies that patient satisfaction from the NACsparing mastectomy technique is higher than from NAC reconstruction and that the nipple-areola sparing option is cosmetically superior to de novo reconstruction, outweighing the oncological risks of nipple preservation, so the effort to spare nipples is a technical advancement.10 Unavoidable problems such as loss of nipple volume and tone, likely loss of sensitivity, and loss of erectile capability, and healing problems secondary to ischemia (at least 6% in both prophylactic and therapeutic settings) as the result of the nipple-areolasparing technique, support a bias toward simply offering NAC reconstruction as the primary option for a mastectomy candidate.10,17,18 In patients with a significant ptosis (eg, a patient who had a history of significant body weight loss after bariatric surgery), a premastectomy surgical delay of NAC has been suggested, even with mastopexy.17,22
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reduction incisions with a tumor-directed segmental mastectomy (Fig. 2). Lower quadrant tumors can be easily removed via vertical mammoplasty techniques. Both of these techniques allow large tumors in large breasts to be removed with good cosmetic results. In addition, upper outer quadrant tumors can be removed by a single axillary incision for quadrantectomy, axillary clearance, and, if needed for volume restoration, reconstruction with a latissimus dorsi flap.2,2325 In BCS, challenges will lead to technical advances beyond different types of mastopexy. The ability to determine adequate margins, in particular after presurgical radiation or neoadjuvant chemotherapy (resulting in tumor shrinkage); experience in reconstruction in cases with intraoperative or accelerated partial irradiation (both affecting the healing pattern); ability to manage breast cancer in patients with previous breast aesthetic surgery (with and without implants); and ability to supplement tissue rearrangement repairs with small, well-vascularized local flaps (Fig. 3) or alloplastic implants will be the trait of oncoplastic surgeons who are comfortable with all aspects of breast cancer management and who have mastered advanced (ie, diverse and customized) techniques.2,4,17,24,25 Many think that the
Fig. 3. Clinical needs dictate the choice of supplementary small flaps: the indication for the small split latissimus muscle harvested through the mastectomy wound was the need to provide extra implant coverage with thin and bruised mastectomy skin flaps.
technical challenges of partial BR frequently exceed those of complete mound reconstruction. Specifics of the technical advances of partial BR are presented by Dr M. Hamdi elsewhere in this issue.26 BCS, subsequent tissue rearrangement, and delivery of small flaps may result in the site of the original tumor not being located under the scar. In addition, focal tissue necrosis and change in tissue density, especially if implants are used, may cause the surveillance imaging to be difficult.24,27 Therefore, marking the location of the original lesion site for surveillance or further treatment (eg, radiation) should be a part of state-ofthe-art approaches (Fig. 4).
Fig. 2. Simple reconstructive scenario: T1 breast cancer with the lesion cranial to the NAC. Following excision, the defect was repaired using a Wisepattern, inferior pedicle breast reduction technique. However, a major consideration when choosing the repair is the extent of excision volume and the need to provide breast symmetry.22 Therefore, the patient underwent breast reduction on the contralateral side.
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Fig. 4. One of the useful breast biopsy or cancer site markers before and after hydration (HydroMark, Biopsy Sciences, Clearwater, FL). It is visible under ultrasound, mammogram, and magnetic resonance imaging. The marker, which is inserted in nonhydrated form, expands in situ as it becomes hydrated, increasing in length and diameter after it is deployed. As it enlarges it becomes fixed within the site where it is deployed.
cancers has been a topic of controversy for years.4,28,29 The appropriate extent of axillary dissection, whether axillary dissection alone is sufficient to control the disease, whether axillary irradiation could suffice, and how the morbidity of axillary surgery can effectively be minimized remain unknown and are the subjects of clinical research. Prevention or treatment of upper extremity lymphedema following mastectomy and axillary node dissection is presented by colleagues from Dr C. Beckers group elsewhere in this issue. Sentinel lymph node biopsy (SNB), in which the first node draining a specific tumor is isolated and removed, is a technique that has become the standard in breast cancer management.30 Aesthetic surgeons were questioning whether previous breast augmentation and pectoralis major muscle releases would change lymphatic functioning and affect axillary or pectoral area nodes. It seems that SNB can be performed in patients with augmented breasts with low false-negative results regardless of the surgical approach (transaxillary, inframammary, periareolar) and trauma to breast lymphatics.31,32 Certain reconstructive procedures, such as transfer and passage of the latissimus dorsi myocutaneous flap through the axillary region, affects the ability to follow with periodic axillary physical examinations; lymphoscintigraphy in case of local recurrence; or detection of the rare, but possible, axillary recurrence, and a plastic surgeon has to be aware of potential pitfalls and be able to design breast care so that clinical objectives are met.28,32
Fig. 5. Lesions in the upper/inner breast quadrant are aesthetically challenging.22 The patient is shown after superomedial lumpectomy to the right breast, sentinel node biopsy, and radiation. This location is difficult to correct with a laterally based small flap such as the lateral intercostal artery perforator flap. Options: fat grafting, bat-wing full-thickness excision, and rotation of the glandular flap (with contralateral surgery for symmetry); however, the patient has chosen completion mastectomy and reconstruction with a transverse rectus abdominis myocutaneous (TRAM) flap.
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quality, with reduction of problems related to scarring and capsular contracture, and improved contour modeling (axillary tail, cleavage, inframammary crease) can be provided.35 Expansion of indications for postmastectomy radiotherapy may affect the timing and reconstructive options available, possibly decreasing the use of immediate reconstruction, especially with implants.36,37 Delayed BR, even with microsurgically transferred free transverse rectus abdominis myocutaneous (TRAM) flaps, was recommended for those undergoing adjuvant radiotherapy because of the increased rate of complications such as fat necrosis, loss of flap volume, fibrosis, and flap contracture.38 However, for immediate BR, it is not always known whether subsequent radiotherapy will follow. Given the significant rate of postradiation complications affecting the aesthetic outcomes, saline inflatable, and, in particular, volumeadjustable implants seem to be a more logical implant choice for reconstruction of the breast mound in the initial (perhaps temporary) stage of reconstruction before radiotherapy. Reduction of an implant volume (temporary or permanent, as needed) may be helpful in the management of pain or wound healing problems, whereas temporary overexpansion may be helpful in preventing or managing effects of radiation fibrosis.39 In previously augmented breasts, radiotherapy has been shown to be as effective as for nonaugmented breast cancer. However, more than 50% of patients develop capsular contracture following radiotherapy and the likelihood of revisions is high.32 Autologous tissue BR seems to be the preferred immediate breast mound reconstruction option for women with a significant probability of postmastectomy radiotherapy by reconstructive surgeons (Fig. 6).2,32,38 Little evidence exists regarding concerns that chemotherapy might affect healing and that both induction and adjuvant chemotherapy may affect results of reconstructive procedures. Induction chemotherapy slightly prolonged the interval to postoperative chemotherapy in patients with locally advanced breast cancer in BR; however, no effect on survival associated with this delay was reported.40,41 Immediate BR seemed not to delay the start of adjuvant chemotherapy; however, the rate of surgical complications was approximately 15% to 24% compared with 4% to 5% in nonreconstructed patients.4244 approaches. Although there is consensus that surgical reconstructive procedures do not negatively affect results of mastectomy, questions are raised whether new emerging reconstructive modalities such as fat transfer, stem cells, and tissue engineering affect malignancy risks. It seems that, in postmastectomy patients who received radiotherapy, autologous fat grafting, in addition to traditional tissue expander and implant reconstruction, leads to better clinical reconstructive outcomes with the creation of the neosubcutaneous tissue, accompanied by improved skin quality of the reconstructed breast without capsular contracture and without negative impact on oncological outcome. The concept of fat injection to the breast was not accepted until recently. Some propose tissue pretreatment with fat (before delayed reconstruction with implants in irradiated tissue), which seems to reduce the radiationinduced complication rate.45 Beneficial effects of fat transfer (healing of radiolesions or helping to prevent radiation-related problems) is attributed to the angiogenic capacity of preadipocytes, or stem cells in the fat. Preliminary experimental and clinical studies indicate that autologous fat enriched with adipose tissuederived stem cells injected to correct limited (postlumpectomy or postradiation) breast defects, or seeded on scaffold structures to form mini-implants, may be useful in BR. Studies are underway to show that fat-derived stem cells taken from a patient with breast cancer behave biologically no differently than those from healthy women.46,47 Preliminary studies have to led to investigations to address, for example, whether stem cells affect epithelial cell line breast cancer recurrence, how they affect breast stroma, whether patients with BRCA1 and BRCA2 (and other risk-determining gene mutations) respond differently than patients who are BRCA1/2 negative to stem cell engrafting and transdifferentiation, and whether clonal expansion is a prerequisite for malignancy formation.47
ADVANCES IN BREAST CANCER TREATMENT: NEW PITFALLS AND CONCERNS Oncological Follow-Up and Imaging of the Reconstructed Breast
There are no standard practice guidelines for follow-up and imaging of the reconstructed breast.48 Mammographic surveillance after BCS is recommended. However, difficulties associated with interpretation of mammograms after local surgery, radiotherapy, and adjuvant chemotherapy can be expected.27,49 Differential diagnosis may be difficult because of residual hematoma, seroma, fat necrosis, skin and fascia
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Fig. 6. (A) The patient is shown after modified radical mastectomy, radiation treatment, and following completion of chemotherapy. There was no evidence of local recurrence or systemic disease. (B) For large volumetric needs, TRAM flap seemed to be the best option. Autologous fat of the TRAM flap seems to increase in bulk as the patient (who was taking tamoxifen) gained some body weight, maintaining satisfactory symmetry between the left reconstructed and the right intact breast. (C) Good symmetry of breast mounds on arms abduction.
thickening, increased and nonhomogeneous soft tissue density in the breast, microcalcifications, and implants. Breast tissue rearrangement for reconstructive purposes or increased density secondary to tissue compression caused by breast aesthetic augmentation implants may result in an even higher rate of false-positive and falsenegative mammograms. Some institutions have adopted screening mammography after implant or autologous tissue reconstruction, thus enabling the same mammographic look of the skin, chest wall, and remaining breast tissue as for a women who has not had a mastectomy, whereas others prefer magnetic resonance imaging (MRI) even for screening purposes in these situations.27,50 A reported case of local recurrence involving flap tissue reaffirms the notion of a need for diligent
Box 1 Case 1. A 23-year-old nulliparous woman who tested positive for BRCA2 Her mother and grandmother had prophylactic mastectomies 20 years ago because of family history. A 32-year-old maternal aunt succumbed to breast cancer. A 28-year-old maternal cousin was recently diagnosed with breast cancer. There was a high odds ratio and relative risk for breast cancer.3 Options: careful observation (understanding that the reliability of mammograms may be poor in a young patient with glandular, dense breasts), oophorectomy (systemic consequences unknown at such young age), tamoxifen (long-term benefit and systemic consequences unknown), bilateral prophylactic mastectomy (which was ultimately her choice; Fig. 7).
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Fig. 7. (A) The patient before prophylactic bilateral mastectomy that included the NAC. (B) Status post immediate BR using tissue expanders followed by permanent implants and subsequent nipple-areola reconstruction (frontal view). (C) Same patient after reconstruction (lateral view). (D) Good symmetry in athletic outfit with attractive collete . de
oncological follow-up and evaluation even of the tissue delivered to the breast area.51 For difficult radiated reconstruction contrastenhanced MRI or positron emission tomography scanning enables differentiation of recurrent tumors from scars or fat necrosis.27,52 In a study comparing the sensitivity and specificity of clinical examination, screening ultrasound, and screening MRI in detecting local recurrence in patients who underwent mastectomy for invasive breast cancer, the sensitivity and specificity for clinical examination were poor (70% and 35.2% respectively) but could be significantly improved by the use of ultrasound (90% and 88.2% respectively) or MRI (100% and 100% respectively). Considering that ultrasound is an inexpensive and easily repeatable procedure, and because most recurrences occur in the quadrant of the original tumor, directed, focused, frequent ultrasound follow-up examination may be warranted.52
Box 2 Case 2. A 45-year-old woman with multiple, metachronous left breast T1N0 invasive lobular cancer lesions Treated several times with lumpectomy and radiation. Developed another lesion of the left breast and declined the recommendation and offer of prophylactic mastectomy on the right side. A few years later she developed lobular carcinoma of the right breast and underwent mastectomy. Breast reconstruction was performed using latissimus dorsi as opposed to earlier TRAM myocutaneous unit, resulting in an unfavorable outcome. Although the patient was well informed about her options, her decisions were oncologically and cosmetically suboptimal.8 This patient exemplifies the need for early identification of those who are at high risk of developing breast cancer, as well as the importance of patient education (Fig. 8).
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Fig. 8. (A) Status post multiple breast-conserving surgeries and repeated radiation for lobular carcinoma lesions of the left breast. The patient developed another lesion, was admitted for completion mastectomy, and had reconstruction using a pedicled TRAM flap. (B) Five years later, the same patient developed lobular carcinoma of the right breast, which was treated by mastectomy and latissimus dorsi myocutaneous flap and implant reconstruction. Use of the TRAM unit on the left side necessitated a different type of reconstruction on the right side with an overall suboptimal cosmetic result.
The plastic surgeon who performs BR must become skilled in and attentive to the follow-up examination of the patient who has breast cancer. Anything suspicious or worrisome must be further examined. An aesthetic surgeon has to be committed to the same standards despite implant augmentation of breasts not increasing the risk of breast cancer or worsening prognosis if breast cancer does develop, and self-examination and clinical breast examination being as effective as in the nonaugmented breast.3,32 In contrast, the surgical oncologist must not assume that new areas of thickening, fullness, mass, pain, skin change, and so forth are just caused by the BR; these findings should be treated with the same level of cancer suspicion as the same findings in the nonreconstructed breast.
of patients subjected to breast care by plastic surgeons. This article presents cases that show the impact of patient education; the impact of the multispecialty breast team on management decisions, both satisfactory and less satisfactory; and the role of plastic surgery doctoring and surgical techniques in resolving breast cancer problems (Boxes 1 and 2).
Box 3 Key technical advances in plastic surgery for breast cancer Adaptation of existing mammoplasty techniques for oncoplasty purposes and development of techniques to serve quadrant per quadrant reconstruction needs Development of new locoregional flaps such as the lateral intercostal perforator flap Development of small perforator free flaps Development of techniques for transfer of fat and fat enriched with adipose tissuederived stem cells for correction of breast defects Microlymphatic surgery for the treatment of upper extremity lymphedema Use of acellular dermal matrices
ILLUSTRATIVE CASES
The plethora of problems and concerns that have to be addressed by plastic surgeons practicing breast surgery, either aesthetic or reconstructive, has to be addressed with long-term patient wellness in mind. Understanding of the breast cancer biology, risk stratification, and changing principles of surgical and nonsurgical management of breast cancer is essential to ensure the oncological safety
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The focus on individualization and customization of approaches, as well as an evidence-based approach, has become the technical standard of aesthetic and reconstructive breast surgery. The merits of surgical techniques are interlaced with breast cancer risk stratification, diagnostic and surveillance issues, and selection and sequencing of the best treatment modalities. The key technical considerations and skills acquisition to ensure the necessary versatility in a modern breast plastic surgeon are listed in Box 3.
11. Meijers-Heliboer H, Van Geel B, Van Putten WL. Breast cancer after prophylactic mastectomy in women with a BRCA 1 or BRCA 2 mutation. N Engl J Med 2001;345(3):15964. 12. Simmons RM, Osborne MP. Prophylactic mastectomy. Breast J 1997;6(3):3729. 13. Nair A, Jaleel S, Abbott N, et al. Skin-reducing mastectomy with immediate implant reconstruction as an indispensable tool in the provision of oncoplastic breast services. Ann Surg Oncol 2010; 17(9):24805. 14. Linford AJ, Meretoja TJ, von Smitten KA, et al. Skinsparing mastectomy and immediate breast reconstruction in the management of locally recurrent breast cancer. Ann Surg Oncol 2010;17(6):166974. 15. Babiera G, Simmons R. Nipple-areola complex sparing mastectomy: feasibility, patient selection, and technique. Ann Surg Oncol 2010;17(3):S2458. 16. Laronga C, Robb GL, Singletary SE. Feasibility of skin-sparing mastectomy with preservation of the nipple-areola complex. Breast Diseases 1998;9: 1257. 17. Jensen JA, Orrigner JS, Giuliano AE. Nipple-sparing mastectomy in 99 patients with a mean follow-up of 5 years. Ann Surg Oncol 2011;18(6):166570. 18. Spear SL, Willey SC, Feldman ED, et al. Nipplesparing mastectomy for prophylactic and therapeutic indications. Plast Reconstr Surg 2011; 128(5):100514. 19. Simmons RM, Brennan M, Christos P. Analysis of nipple/areolar involvement with mastectomy: can the areola be preserved? Ann Surg Oncol 2001; 9(2):1658. 20. Filho P, Capko D, Barry JM, et al. Nipple-sparing mastectomy for breast cancer and risk-reducing surgery: the Memorial Sloan-Kettering Cancer Center experience. Ann Surg Oncol 2011;18(11):311722. 21. Reynolds C, Davidson JA, Lindor NM, et al. Prophylactic and therapeutic mastectomy in BRCA mutation carriers: can the nipple be preserved? Ann Surg Oncol 2011;18(11):31029. 22. 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(3):57281. 23. Bong J, Parker J, Clapper R, et al. Clinical series of oncoplastic mastopexy to optimize cosmesis of large-volume resections for breast carcinoma. Ann Surg Oncol 2010;17(12):324751. 24. Clough KB, Kaufman GJ, Nos C, et al. Improving breast cancer surgery: a classification and quadrant per quadrant atlas for oncoplastic surgery. Ann Surg Oncol 2010;17(5):137591. 25. Shrotria S. Single axillary incision for quadrantectomy, axillary clearance and immediate reconstruction with latissimus dorsi. Br J Plast Surg 2001; 54(2):12831.
REFERENCES
1. Zannis VJ. Presidential address: 2010. The American Society of Breast Surgeons. There is no boring in breast surgery. Ann Surg Oncol 2010; 17(3):S197201. 2. Rosson GD, Magarakis M, Shridharani SM, et al. A review of the surgical management of breast cancer: plastic reconstructive techniques and timing implications. Ann Surg Oncol 2010;17(7):1890900. 3. Sharabi SE, Bullocks JM, Dempsey PJ, et al. The need for breast cancer screening in women undergoing elective breast surgery: and assessment of risk and risk factors for breast cancer in young women. Aesthet Surg J 2010;30(6):82131. 4. Boughey JC, Mittendorf EA, Solin LJ, et al. Controversies in breast surgery. Ann Surg Oncol 2010; 17(3):S2302. 5. Mielnicki LM, Asch HL, Asch BB. Genes, chromatin, and breast cancer: an epigenetic tale. J Mammary Gland Biol Neoplasia 2001;6(2):16982. 6. Schragg D. Life expectancy gains from cancer prevention strategies for women with breast cancer and BRCA1 or BRCA2 mutations. JAMA 2000; 283(5):61724. 7. Frost M, Hoskin TL, Hartman LC, et al. Contralateral prophylactic mastectomy: long term consistency of satisfaction and adverse effects and the significance of informed decision-making, quality of life, and personal traits. Ann Surg Oncol 2011;18(11):31106. 8. Lee CN, Belkora J, Chang Y, et al. Are patients making high-quality decisions about breast reconstruction after mastectomy. Plast Reconstr Surg 2011;127(1):1826. 9. Arrington A, Tuttle T. Author reply: contralateral prophylactic mastectomy overtreatment: expectations from personal genomics for tailored breast cancer surgery. Ann Surg Oncol 2010;17(3):940. 10. Wagner JL, Fearmonti R, Hunt KK, et al. Prospective evaluation of the nipple-areola complex sparing mastectomy for risk reduction and for early-stage breast cancer. Ann Surg Oncol 2012; 19(4):113744.
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