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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_732_Библиотеки_им_академика_М_И_Перельмана

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Fig. 14.6 (Clinical Case 1): (A, B) Preoperative frontal view, left oblique view of a 43-year-old patient
with previous superior left quadrantectomy and immediate reconstruction with submuscular implant and breast advancement flaps through periareolar approach. (C) Preoperative markings showing the mas­topexy planning, the area of AFG and contralateral procedure. (D–F) The patient underwent to delayed BCS reconstruction with bilateral mastopexy, implant change and AFG on the upper pole of the left breast. (E, F) Postoperative (1 year) frontal view, left oblique view following BCS reconstruction with AFG associated with bilateral mastopexy, showing a very good outcome.
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TABLE
Conducted Clinical Studies Concerning Breast Conservative Surgery Reconstruction with Autogenous Fat
14.2
Grafting
Author Year No. pts Mean Age (ys) Timing of Reconstruction Follow-up (months) LR (%)
Petit etal.
Petit etal.
Rietjens etal.
Delay etal.
Semprini etal.
Brenelli etal.42 2014 59 50 Delayed 34 3
Gale etal.
Kronowitz etal.482016 69 NR Delayed 60 1
Garcia etal.
Mestak etal.51 2015 32 53 Delayed 19 2
Biazus etal.
Turnhout etal.
Khan etal.9 2017 35 49 Immediate 36 0
Mirzabeigi etal.332017 20 53 Delayed/Brava 25 0
Munhoz etal. 2018 53 49 Delayed 56 0.5
LR, local recurrence; No. pts, number of patients; NR, not reported; ys, years; Personnal communication.
14
48
10
49
15
13
2011 143 NR Delayed/Immediate 18 13
2013 12 NR Delayed/Immediate 63 2
46
2011 62 NR Delayed 19 1
2007 42 51 Delayed 19 2
50
2014 151 NR Delayed 45 0
2015 35 NR Delayed 34 2
2016 37 55 Immediate 12 0
2015 20 55 Delayed/Immediate 18 0
24
2017 109 55 Delayed 26 0.7
approximately 3–4 weeks, edema in 2–4 months, and the nal result can be observed after 4 months. Local infection may be noted but is infrequent. Infections in the donor area and breast can normally be managed using systemic or local antibiotics with satisfactory outcome. In our clinical experi­ence, no cases of moderate to severe hematoma, pneumo­thorax, and fat embolism were observed.
Long-term complications include microcalcications, fat necrosis, cysts, and contour irregularities in the donor areas. ese complications are more frequently observed when a large volume of AFG is injected and are more common during the learning curve period or when large cannulas are used. Microcalcications are usually easy to identify, and in our experience these image alterations are less frequent in this procedure than in reduction mam­moplasty, which can produce up to 85% of postoperative radiological features.
42,54,55
Microcalcications tend to have a round, regular appearance with a light center and are completely dierent from calcications associated with local relapse and classied as ACR 2 (American College of Radiology). Most breast images associated with AFG are easily recognized as benign lesions by an experienced radiologist.
42,50,54
Donor area complications such as depressions, nodules, and irregularities can be produced by aggressive AFG har­vesting. To avoid these unsatisfactory results, it is important to harvest fat the same way that conventional aesthetic lipo­suction/liposculpture would be performed.20 
Postoperative Care
All patients received intravenous antibiotics, and oral anti­biotics were continued for 48 hours. Immobilization with an occlusive dressing should be used for 3 days to improve scarring. Elastic bands or straps over the grafting areas of the breasts should not be used, to avoid pressure and fat reabsorption. In terms of postoperative care, early massag­ing or mobilization of the breasts should also be avoided for at least three weeks. It is essential for patients to avoid physical activities for a period of time following surgery to minimize the risk of fat necrosis and other complica­tions. As breast edema diminishes, bra tension will require adjustment, and patients are seen at appropriate intervals to evaluate the outcome. e nal result can be observed 3–4 months after AFG procedure, and in case of inadequate correction, supplementary surgeries can be indicated, each 3 or 4 months apart. 
Conclusions
Advances in AFG techniques have led to an important improvement in aesthetic outcomes for BCS. is tech­nique is most frequently used in delayed reconstructions and to repair partial breast defects, where thin tissue and irregularities provide inadequate volume/coverage. Most of the complications in our series were minor and did not impact aesthetic outcomes or normal follow-up. e ideal
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aesthetic result must provide a natural contour and achieve adequate symmetry and shape. To achieve these results, sur­geons have increasingly relied on associated maneuvers such as the Coleman technique, closed systems for AFG ltra­tion, and recipient site pre-expansion in selected cases. is chapter presents an overview of the oncoplastic approach to primary and secondary BCS reconstruction with AFG. Ultimate success will depend on proper patient selection and careful intraoperative and postoperative management.
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19. Kaur N, Petit JY, Rietjens M, Mani F, Luini A, Gatti G, etal. Comparative study of surgical margins in oncoplastic surgery and quadrantectomy in breast cancer. Ann Surg Oncol. 2005;12:539–
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21. Munhoz AM, Montag E, Arruda E, Brasil JA, Aldrighi JM, Gem­perli R, etal. Immediate conservative breast surgery reconstruc­tion with perforator aps: new challenges in the era of partial mastectomy reconstruction? Breast. 2011;20(3):233–240.
22. Ho Quoc C, Sinna R, Gourari A, La Marca S, Toussoun G, Delay E. Percutaneous fasciotomies and fat grafting: indications for breast surgery. Aesthet Surg J. 2013;1(7):995–1001. 33.
23. Ho Quoc C, Piat JM, Carrabin N, Meruta A, Faure C, Delay E. Breast reconstruction with fat grafting and BRAVA® pre­expansion: ecacy evaluation in 45 cases. Ann Chir Plast Esthet. 2016;61(3):183–189.
24. Van Turnhout AA, Fuchs S, Lisabeth-Broné K, Vriens-Nieuwenhuis EJC, van der Sluis WB. Surgical outcome and cosmetic results of autologous fat grafting after breast conserving surgery and radiotherapy for breast cancer: a retrospective cohort study of 222 fat grafting sessions in 109 patients. Aesthetic Plast Surg. 2017;41(6):1334–1341.
25. Khouri RK, Rigotti G, Khouri Jr RK, Cardoso E, Marchi A, Rotemberg SC, et al. Tissue-engineered breast reconstruction with Brava-assisted fat grafting: a 7-year, 488-patient, multi­center experience. Plast Reconstr Surg. 2015;135:643–658.
26. Munhoz AM, Montag E, Arruda E, Aldrighi C, Gemperli R, Ald­righi JM, etal. e role of the lateral thoracodorsal fasciocutane­ous ap in immediate conservative breast surgery reconstruction. Plast Reconstr Surg. 2006;117:1699–1709.
27. Munhoz AM, Montag E, Arruda E, Arruda EG, Sturtz GP, Ald­righi C, etal. Outcome analysis of breast-conservation surgery and immediate latissimus dorsi ap reconstruction in patients with T1 to T2 breast cancer. Plast Reconstr Surg. 2005;116:741–
750.
28. Zhu L, Mohan AT, Vijayasekaran A, Hou C, Sur YJ, Morsy M, etal. Maximizing the volume of latissimus dorsi ap in autolo­gous breast reconstruction with simultaneous multisite fat graft­ing. Aesthet Surg J. 2016;36(2):169–178.
29. Largo RD, Tchang LA, Mele V, Scherberich A, Harder Y, Wettstein R, etal. Ecacy, safety and complications of autolo­gous fat grafting to healthy breast tissue: a systematic review. J Plast Recons Surg. 2014;67:437–448.
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30. Gir P, Brown SA, Oni G, Kashe N, Mojallal A, Rohrich R. Fat grafting: evidence-based review on autologous fat harvest­ing, processing, reinjection, and storage. Plast Reconstr Surg. 2012;130:249–260.
31. Saint-Cyr M, Rojas K, Colohan S, Brown S. e role of fat graft­ing in reconstructive and cosmetic breast surgery: a review of the literature. J Reconstr Microsurg. 2012;28(2):98–107.
32. Rosing JH, Wong G, Wong MS, Sahar D, Stevenson TR, Pu LL. Autologous fat grafting for primary breast augmentation: A sys­tematic review. Aesth Plast Surg. 2011;35:882–890.
33. Mirzabeigi MN, Lanni M, Chang CS, Stark RY, Kovach SJ, Wu LC, etal. Treating breast conservation therapy defects with brava and fat grafting: technique, outcomes, and safety prole. Plast Reconstr Surg. 2017;140(3):372–381.
34. Coleman SR, Saboeiro A. Fat grafting to the breast revisited: safety and ecacy. Plast Reconstr Surg. 2007;119:775–785.
35. Khater R, Atanassova P, Anastassov Y, Pellerin P, Martinot­Duquennoy V, etal. Clinical and experimental study of autolo­gous fat grafting after processing by centrifugation and serum lavage. Aesthetic Plast Surg. 2009;33:37–43.
36. Rohrich RJ, Sorokin ES, Brown SA. In search of improved fat transfer viability: a quantitative analysis of the role of centrifuga­tion and harvest site. Plast Reconstr Surg. 2004;113:391–395.
37. Mestak O, Sukop A, Hsueh YS, Molitor M, Mestak J, Matejo­vska J, etal. Centrifugation versus PureGraft for fat grafting to the breast after breast-conserving therapy. World J Surg Oncol. 2014;5(12):178.
38. Zhu M, Cohen SR, Hicok KC, Shanahan RK, Strem BM, Yu JC, et al. Comparison of three dierent fat graft preparation methods: gravity separation, centrifugation, and simultaneous washing with ltration in a closed system. Plast Reconstr Surg. 2013;131(4):873–880.
39. ASPRS Ad-Hoc Committee on New Procedures. Report on autologous fat transplantation. Plast Surg Nurs. 1987;7:140–141.
40. Gutowski KA, ASPS Fat Graft Task Force. Current applications and safety of autologous fat grafts: a report of the ASPS fat graft task force. Plast Reconstr Surg. 2009;124:272–278.
41. Gennari R, Griguolo G, Dieci MV, Guarneri V, Tavaniello B, Sibilio A, etal. Fat grafting for breast cancer patients from basic science to clinical studies. Eur J Surg Oncol. 2016;42:1088–1102.
42. Brenelli F, Rietjens M, De Lorenzi F, Pinto-Neto A, Rossetto F, Martella S, etal. Oncological safety of autologous fat graft­ing after breast conservative treatment: a prospective evaluation. Breast J. 2014;20(2):159–165.
43. Schaer A, Scholmerich J, Buechler C. Mechanisms of disease: adipokines and breast cancer - endocrine and paracrine mecha­nisms that connect adiposity and breast cancer. Nat Clin Pract Endocrinol Metab. 2007;3:345–354.
44. Dieudonne MN, Machinal-Quelin F, Serazin-Leroy V, Leneveu MC, Pecquery R, Giudicelli Y, etal. Leptin mediates a prolifera­tive response in human MCF7 breast cancer cells. Biochem Bio- phys Res Commun. 2002;293:622–628.
45. Delay E, Garson S, Tousson G, Sinna R. Fat injection to the breast: technique, results, and indications based on 880 proce­dures over 10 years. Aesthet Surg J. 2009;29:360–376.
46. Rietjens M, De Lorenzi F, Rossetto F, Brenelli F, Manconi A, Martella S, etal. Safety of fat grafting in secondary breast recon­struction after cancer. J Plast Reconstr Aesthet Surg. 2011;64:477–
483.
47. Petit JY, Rietjens M, Botteri E, Rotmensz N, Bertolini F, Curi­gliano G, etal. Evaluation of fat grafting safety in patients with intraepithelial neoplasia: a matched-cohort study. Ann Oncol. 2013;24(6):1479–1484.
48. Kronowitz SJ, Mandujano CC, Liu J, Kuerer HM, Smith B, Gar­vey P, etal. Lipolling of the breast does not increase the risk of recurrence of breast cancer: a matched controlled study. Plast Reconstr Surg. 2016;137:385–393.
49. Gale KL, Rakha EA, Ball G, Tan VK, McCulley SJ, Macmillan RD, etal. A case-controlled study of the oncologic safety of fat grafting. Plast Reconstr Surg. 2015;135:1263–1275.
50. Semprini G, Cattin F, Zanin C, Lazzaro L, Cedolini C, Vaienti L, etal. About locoregional recurrence risk after lipolling in breast cancer patients: our experience. Minerva Chir. 2014;69(2):91e6.
51. Mestak O, Hromadkova V, Fajfrova M, Molitor M, Mestak J. Evaluation of oncological safety of fat grafting after breast-con­serving therapy: a prospective study. Ann Surg Oncol. 2015:776–
781.
52. Waked K, Colle J, Doornaert M, Cocquyt V, Blondeel P. Sys­tematic review: the oncological safety of adipose fat transfer after breast cancer surgery. Breast. 2017;31:128–136.
53. De Decker M, De Schrijver L, iessen F, Tondu T, Van Goet­hem M, Tjalma WA. Breast cancer and fat grafting: ecacy, safety and complications-a systematic review. Eur J Obstet Gynecol Reprod Biol. 2016;207:100–108.
54. Rubin JP, Coon D, Zuley M, Toy J, Asano Y, Kurita M, etal. Mammographic changes after fat transfer to the breast compared with changes after breast reduction: a blinded study. Plast Recon- str Surg. 2012;129:1029–1038.
55. Chala LF, de Barros N, de Camargo Moraes P, Endo E, Kim SJ, Pincerato KM, etal. Fat necrosis of the breast: mammographic, sonographic, computed tomography, and magnetic resonance imaging ndings. Curr Probl Diagn Radiol. 2004;33:106–126.
15
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Extreme Oncoplasty
NIRAV B. SAVALIA, SADIA KHAN, AND MELVIN J. SILVERSTEIN
Introduction
e surgical management of breast cancer has seen a para­digm shift from radical ablation to maximum conservation. e Halstedian radical mastectomy of the late 1800s gradu­ally evolved by 1975 to spare muscle, lymph nodes, skin, and ultimately manifested in the modern-day nipple–areola sparing mastectomy. e 1970s and 1980s brought forth prospective randomized trials supporting breast conserving therapy for tumors 5 cm as a viable alternative to mas­tectomy. Breast conserving therapy was widely adopted and evolved from quadrantectomies requiring wide margins to localized wire-directed excisions requiring merely no ink on tumor. ese advances in breast conservation allowed a cosmetic benet to the patient without sacricing onco­logic care. Unfortunately, many patients were left with post­lumpectomy deformities that compromised the aesthetic goal of the operation. e advent of oncoplastic surgery was led by the awareness of these post-lumpectomy deformities and gradual acceptance of the concept that optimal onco­logic care and breast cosmesis are not mutually exclusive. As a result, post-lumpectomy deformities were not deemed an inevitable or unavoidable outcome and proactive measures to reduce their incidence were encouraged. Oncoplastic sur­gery further advanced breast conservation to allow larger and larger resections, while still maintaining the aesthetic appearance of the breast.
Modern medical therapies, with improved hormonal and chemotherapy, new techniques and protocols in radiation oncology, and a better understanding of the biology of breast cancer, have improved overall and breast cancer specic sur­vival. Naturally, local recurrence rates have improved after both mastectomy and breast conservation. Recent prospec­tive randomized trials have demonstrated local recurrence rates less than 1.5% at 5 years for patients randomized to excision plus whole breast radiotherapy. spective randomized trials studying breast conservation were only conducted for tumors 5 cm. Consequently, women with tumors >5 cm, or those with multicentric or multifocal disease, are often denied breast conservation and are relegated to mastectomy with adjuvant radiotherapy.
1,2
However, pro-
Oncoplastic surgery presents an opportunity to re­examine this paradigm. A successful aesthetic result after oncoplastic surgery largely depends on a favorable tumor­to-breast volume ratio and the application of appropriate tissue rearranging maneuvers. narios is a small tumor in the lower pole of a large breast that is easily addressed with a standard Wise pattern or vertical pattern mammaplasty. However, when tumors are in unfavorable locations, are close to the overlying skin, or involve the skin, these standard techniques can be modi­ed to still allow an oncoplastic reconstruction, albeit with nontraditional scar patterns. Gradually, we have evolved to push the limits of these techniques and apply to them to patients with less favorable tumor:breast volume ratios. With experience, it becomes apparent that even patients with >5 cm tumors, or those with multifocal or multicen­tric disease, can potentially have breast conservation while still achieving excellent cosmetic outcomes. It is particularly tempting when comparing this reconstructive approach to a post-mastectomy reconstruction. Patients with large or locally advanced tumors typically require post-mastectomy radiotherapy. Implant-based reconstruction with radiother­apy is fraught with poor results and higher complication rates. Autologous reconstruction avoids this issue but often requires multiple procedures and long recovery periods. With current data reporting low local recurrence rates, the impetus for defaulting to mastectomy is fading. Although it is unlikely that randomized prospective data will be gath­ered to support breast conservation for >5 cm tumors, there is clear interest in this concept, as evidenced by a growing body of literature dedicated to this topic.
At our institution, oncoplastic reconstruction is oered to all patients whenever technically feasible. Extreme onco- plasty is the term applied to a specialized concept for a breast conserving operation, using oncoplastic techniques, in a patient who, in most physicians’ opinions, requires a mastectomy. Extreme oncoplasty applies to breast con­servation using a reduction mammaplasty technique in patients with larger lesions, with the goal of clear surgical margins, while maintaining or improving the cosmetic out­come. ese lesions are generally large, >5 cm, multifocal,
3,4
One of the simplest sce-
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or multicentric tumors. ey may be locally advanced, and many will have positive lymph nodes. Most of these patients will require radiation therapy, even if they are treated with mastectomy.
10,11
Oncoplastic reconstruction generally yields a cosmetic result superior to a mastectomy with immediate reconstruc­tion and radiation therapy. ere is less operative and post­operative morbidity with extreme oncoplasty, fewer surgeries required, and nally, radiation therapy is far kinder to breast conservation than to mastectomy with reconstruction.
10,11
Patient Selection
e ideal patient for extreme oncoplasty is a woman with a large breast, who desires a smaller breast, who desires breast conservation, and has disease limited to a single quadrant, with limited comorbidities. Naturally, not all patients meet every one of the criteria, and many decisions are made on a case-by-case basis. Neoadjuvant chemotherapy is often utilized to downstage a patient and convert from obliga­tory mastectomy to potential breast conservation. e over­riding theme is that if a method of reconstruction with a volume-displacing technique is possible, regardless of the aforementioned criteria, then the patient is a candidate. e value of extreme oncoplasty is in its ability to condense sur­gical therapy. e patient will undergo the ablative surgery, immediate reconstruction, and immediate contralateral breast surgery within a 3-hour outpatient operation. e recovery is usually rapid, similar to the recovery process of a reduction mammaplasty, and there are no additional recon­structive procedures necessary. Although most patients are treated with volume displacement oncoplasty, occasionally a volume replacement technique involving local fasciocu­taneous aps (e.g., LICAP) may be utilized. Regional or distant tissue transfer techniques for oncoplastic reconstruc­tion are usually not utilized, given the uncertainty of margin status at the time of reconstruction. Delayed partial breast reconstruction with autologous methods is another option; however, these patients may be better suited for mastec­tomy if they are considering this signicant investment in reconstruction. 
Preoperative History and Consideration
Oncoplastic surgery requires a multidisciplinary approach and thorough preoperative planning. Multidisciplinary planning requires discussion, at minimum, with the onco­logic surgeon, radiologist, and plastic surgeon; however, other team members should be included as well. Onco­plastic surgery requires a philosophy that the appearance of the breast after tumor excision is important. All preop­erative imaging tests must be carefully evaluated and inte­grated with information about the pathological subtype, tumor size, location in relation to the nipple, skin quality, and patient preferences. Other concerns include invasive lobular cancers that may be larger on the microscopic level than expected based on initial imaging, extensive in situ
components with similar risk for understaging on imaging. Also, radiation eects on the size and shape of the ipsilateral breast compared with the contralateral side undergoing a symmetry procedure must be considered.
A common misconception is that the goal of breast
reconstruction is to create the “perfect breast.” e goal should be to achieve an outcome that best suits the patient’s goals for reconstruction and desires for nal breast appear­ance, while still considering the primary goal of treating the cancer. e reconstructive plan can be formulated only after analysis of the tumor size and location; the preoperative breast shape, size, and degree of ptosis; and understanding the patient’s oncologic and reconstructive desires. e ideal is to minimize the amount of surgery, recovery period, risk of complications, and surgical failure rates, while maximiz­ing the desired aesthetic and oncologic outcome.
12
At our institution, the oncologic breast surgeon assumes the role of “leader” to guide the team and ensure excellent communication among all team members. During the rst visit we generate a surgical plan, called the “Flight Plan,” that summarizes the diagnosis, includes photos of the patient’s chest and relevant imaging, and lists the plan of action lead­ing up to and including the planned operation (Fig. 15.1). e surgical plan is given to the patient, as well as distrib­uted to all team members, and updated as the patient moves through the consultation process.
Preoperative work-up should include a full history and physical, paying close attention to prior breast surgery and location of prior surgical incisions. Breast imaging should include a combination of mammogram, ultrasound, and breast magnetic resonance imaging (MRI). MRI can often better determine extent of disease in mammographically subtle ndings and has improved sensitivity for invasive lobular carcinoma.13 
Indications and Contraindications
Historically, women were commonly left feeling maimed after breast cancer surgery when a lumpectomy cavity was left to form a seroma that later resorbs, leading to deforma­tion after radiation therapy (Fig. 15.2). In a typical lumpec­tomy, an incision is made over the tumor, the tumor is removed, and no specic eort is made to ll the defect left with remaining breast tissue. Even when surrounding breast tissue is used to ll with a small local tissue ap advance­ment, this can still lead to puckering or dimpling when the patient is out of the supine position and sitting or standing upright. Unfortunately, as many as 36% of simple excisions fail to achieve adequate margins in a single operation, lead­ing to re-excision, worsening cosmesis, and conversions to mastectomy.14 Oncoplastic surgery, using a reduction mam­maplasty, allows removal of the tumor but also prevents undue distortion of the breast by allowing the defect to be lled with remaining breast tissue.
Oncoplastic surgery can be performed in tandem with a lumpectomy in most cases where the tumor is 5 cm. Extreme oncoplasty can be considered when women with
SURGEON NAME
DATE
PATIENT NAME
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Diagnosis: 61F presents with LEFT BREAST mass spanning 30x34x20mm on MRI at 2:00 6cm from Nipple - Invasive Ductal Carcinoma Grade 3, SBR 8/9 ER+ 100% PR+100% HER2 NEG Ki67 10%. FH: Sister and
Maternal Aunt with Breast CA.
CHAPTER 15 Extreme Oncoplasty
PATIENT MRN
119
LEFT Breast Invasive Ductal CA - Clinical Stage cT2N0, Stage IIA
PLAN:
1. Genetic Testing - PENDING
2. Medical Oncology Consultation
3. Radiation Oncology Consultation
4. Plastic Surgery Consultation for LEFT breast oncoplastic Split Reduction with contralateral mastopexy for symmetry
5. SURGICAL PLAN: LEFT BREAST wire directed segmental resection,
LEFT axillary sentinel lymph node biopsy with possible axillary lymph node dissection
Fig. 15.1 Surgical plan sheet that includes summary of pathology and imaging findings, involved con-
sultants, and proposed surgical plan. This plan goes with the patient through their journey and can be adjusted as needed when the treatment plan changes.
tumors >5 cm are seeking an alternative to mastectomy, when oncologically feasible. In either case, oncoplastic sur­gery allows for breast conserving therapy with a better cos­metic result.
15,16
Oncoplastic surgery should be considered in all patients who are candidates for surgical treatment of breast cancer. 
Operative Approach
e workhorse of oncoplastic surgery at our institution is performed with the inverted T or Wise pattern as the pre­ferred incisional approach for the mammaplasty.17 is versatile technique is the ideal option for women with preoperative macromastia. skin pattern and nipple–areolar complex (NAC) pedicle are designed preoperatively to allow for resection of the tumor
18-20
Based on tumor location, a
and lling of the tumor cavity defect with the remaining breast tissue. is technique can also be applied to tumors that fall outside the Wise pattern by shifting tissue and rotating the reduction pattern.21 e wide amount of skin excised allows for correction of ptosis, exposure to the entire breast, the ability to widely resect tissue from any quad­rant, and signicantly reduce overall breast volume to aid radiation dose homogeneity. Once the amount of required tissue resection is determined on the ipsilateral side, the contralateral breast is reduced to match as a symmetrizing procedure.
22
e need to be certain of the anterior tumor margin led our group to develop the Split Reduction. e main strength of the Wise pattern is the independence of the skin resection and the parenchymal resection. e parenchymal reduction does not need to follow the skin reduction pattern; the end
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Fig. 15.2 A 60-year-old female who presented with concerns about
the appearance of her right breast subsequent to lumpectomy and radiotherapy 5 years prior.
goal is creation of a breast mound over which the skin can be re-draped. For an aesthetic breast reduction, it is desir­able to place the scars in the least visible areas. us, the Wise pattern is designed to limit the scars to the circumare­olar border, the vertical midline of the breast, and the infra­mammary crease. For oncoplastic breast surgery, we do not need to limit ourselves to this ideal skin pattern. Because the need for tumor clearance trumps this aesthetic ideal, we may modify the traditional Wise pattern to displace a hidden scar from the medial or lateral infra mammary fold onto the visible breast, directly over the tumor, in favor of clearing the anterior margin in lesions close to the skin. is modication, that we term a Split Reduction, allows deni­tive clearance of the anterior (skin) margin or access to a lesion that falls out of the standard Wise pattern. e end result is resection of a comparable amount of skin as a tra­ditional Wise pattern with maintenance of a similar, cone­shaped skin envelope but higher visibility of the scar. In our opinion, this trade-o is acceptable, because the alternative of a close or involved anterior margin leading to mastec­tomy is avoided (Fig. 15.3).
Fig. 15.3 A 48-year-old female with a 30-mm LEFT breast invasive ductal carcinoma close to the lateral
skin on preoperative imaging. Surgical plan was for LEFT breast wire-directed segmental resection and LEFT axillary sentinel lymph node biopsy through a LEFT Split Reduction and contralateral mastopexy for symmetry. (Left) Preoperative photos. (Right) 1 week postoperative photos showing in the LEFT breast— radial incision in the upper outer quadrant that represents the “split” or “Z” pattern incision. In the RIGHT breast, the standard Wise pattern inverted T scar is seen.
Pre-op Post-op 1 week
CHAPTER 15 Extreme Oncoplasty
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e Wise pattern mammaplasty requires the creation of three triangles: vertical, medial, and lateral. e inferior borders of all three triangles are incorporated into the infra­mammary fold incision, limiting the scars to the circum­areolar border, the vertical midline of the breast, and the inframammary fold (Fig. 15.4). e pedicle for the NAC is chosen based on the tumor location: superior, medial, lat­eral, inferior, or central. Tumors located in the inferior pole can be easily incorporated in this pattern, with the overlying skin, through a standard Wise pattern. e vertical pillars are then plicated and the NAC inset into the keyhole. If the NAC cannot be saved, a nipple can be reconstructed imme­diately or as a delayed procedure. is technique allows the lower pole and central tumors to be easily excised along with the overlying skin to avoid a close or positive anterior margin. When the tumors are located in areas that do not
naturally fall within a standard Wise pattern, two options exist. e rst is to perform a standard Wise pattern tech­nique and elevate skin aps to reach the distant tumor. is is acceptable if the tumor is deep and the anterior margin is not felt to be of concern. However, for most cases when the tumor is located outside the Wise pattern, our preferred alternative is to excise the tumor with the anterior skin mar­gin to decrease the need for re-excision or mastectomy with close or positive margins. For tumors located in the upper outer or upper inner quadrants, the Wise pattern may be recongured to include the tumor with the overlying skin in a split reduction.
When the tumor is in the upper central breast, the split occurs at the apex of the keyhole rather than along the verti­cal limbs of the pattern (Fig. 15.5). If the NAC is involved by tumor, the central excision of breast tissue is incorporated into an inverted T mammaplasty that allows for reshaping and immediate NAC reconstruction. In a split reduction, the lateral or medial triangle of the Wise pattern is not positioned at the base of the breast but advanced cephalad to a position directly overlying the tumor (Fig. 15.6). e medial or lateral vertical limb of the inverted T is split on the side of the tumor excision to accommodate the higher position of the medial or lateral triangle.
10,11,23
During the reconstruction, second­ary and tertiary pedicles may also be employed to allow for maximal preservation of volume and to reconstruct excisional defects. Videos 15.1–15.4 demonstrate the authors’ various approaches to standard and extreme oncoplasty. 
Fig. 15.4 Photo representing the typical incisions for a standard Wise
pattern reduction. Surgical scars outlined in inframammary crease, periareolar border, and vertical midline of the breast.
Fig. 15.5 A 56-year-old female with an 18-mm LEFT breast ductal carcinoma in situ (DCIS) close to skin
on preoperative imaging. Surgical plan was for LEFT breast wire-directed segmental resection and intra­operative radiation therapy, LEFT Split Reduction (Split from the keyhole) and contralateral mastopexy for symmetry. (Left) Preoperative photo with approximate tumor location marked. (Middle) and (Right) 2 year postoperative photo outlining split reduction scar oriented radially from the keyhole to remove skin over the lesion.
Outcome
e rationale for breast conserving therapy comes from a group of prospective randomized trials performed in the
24-27
1970s. was 5 cm. When breast preservation is performed in
In these trials, the maximum tumor size allowed
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Fig. 15.6 Split Reduction: 58-year-old female with a 36-mm LEFT breast invasive ductal carcinoma. Sur-
gical plan was for LEFT breast wire-directed segmental resection, LEFT Split Reduction and contralateral mastopexy for symmetry. (Left) Preoperative photo with approximate tumor location marked. (Middle) and (Right) 5 year postoperative photo, after whole breast radiation therapy, outlining split reduction scar in upper outer quadrant to remove skin over the lesion.
patients with tumors larger than 5 cm, there are no prospec­tive randomized data to support it. Nevertheless, in clinical practice, it is commonly done. When breast conservation was rst adopted, the recurrence rates were higher for those randomized to breast conservation therapy compared with mastectomy. Despite higher local recurrence rates, survival at 20 years was similar.
28,29
Surgeons and patients have long accepted a higher local recurrence rate in exchange for a better aesthetic and sensory outcome and a happier patient with no decrease in survival.
Our institution’s experience with extreme oncoplasty and standard oncoplastic surgery is outlined in Table 15.1. In the extreme series, 88% of tumors with a mean size of 74 mm were excised with no ink on tumor. Only six patients of 200 (3%) patients who attempted to save their breast after being advised to have a mastectomy were converted to mastectomy after nal pathology was reviewed. All six had multiple positive or close margins. An additional 16 patients (8%) underwent re-excision and then continued on with breast conservation and radiation therapy. Eight patients (4%) have developed a local recurrence.
Breast conservation can generally be done in one operation
erative pain, and it is less expensive for the patient as multiple operations and procedures are avoided. ere is no foreign body and no donor site. It is more functional when compared with mastectomy and allows patients to keep their natural breast shape and sensation. e patient often has a better per­ceived body image.
30,31
Additionally, breast cancer patients with macromastia present a challenge for radiation oncolo­gists planning for whole breast radiation therapy. A larger more pendulous breast often requires higher energy photos to ensure delivery to a deeper depth of tissue. is leads to hot spots of radiation and can lead to signicant toxicity to the skin and tissue.32 For these reasons, if it is technically pos­sible and oncologically reasonable, we should consider breast conservation as the rst option for our patients.
TABLE
Comparison of Wise Pattern Reduction
Mammoplasty (Standard Oncoplasty),
15.1
Including Patients with Split Reductions, Versus Extreme Oncoplasty
Standard
Variable
N 500 200
Mean Sample
Weight
Mean Tumor Span 22 mm 74 mm
No Ink on Tumor 97% 88%
Margin 1 mm 90% 70%
Re-excision 3% 8%
Mastectomy 1% 3%
Median Follow-up 28 months 20 months
Any Local
Recurrence
Oncoplasty
141 grams 201 grams
3% 4.1%
Extreme Oncoplasty
Whether for standard or extreme cases, it is important to maintain a multidisciplinary approach. ere are many patients who are relegated to mastectomy as the only option, simply due to an erroneous judgment that a defor­mity would inevitably result with breast conservation. ese patients are referred for plastic surgical consultation with a plan for mastectomy already in place. e plastic surgeon will then counsel the patient regarding post-mastectomy reconstruction, and an oncoplastic approach may never be discussed. Improved communication and a mindset that breast conservation should not be ruled out before plastic surgery consultation may allow many women to escape the default mastectomy.