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CHAPTER 15 Extreme Oncoplasty
Pre-op Post-op 1.5 years
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Fig. 15.7 Extreme Oncoplasty: 55-year-old female with an 85-mm area of LEFT breast invasive ductal
carcinoma with ductal carcinoma in situ (DCIS) and RIGHT breast 20-mm DCIS. Surgical plan was for LEFT and RIGHT breast wire-directed segmental resection, LEFT Split Reduction (Extreme oncoplasty) and RIGHT Standard Reduction. (Left) Preoperative photo. (Right) 1.5 year postoperative photo after bilat­eral whole breast radiation therapy.
123
Extreme oncoplasty pushes the oncoplastic surgery envelope. Patients seeking an alternative to mastectomy are turning to a modern take on oncoplastic breast sur­gery. e use of standard and modied reduction excisions and oncoplastic reconstruction dramatically increases the probability of complete excision with an acceptable esthetic outcome in most patients seeking breast conser­vation therapy. Moreover, now that the standard for an adequate margin has been relaxed to no ink on tumor for invasive disease,33 the probability of a successful outcome increases.
For selected patients who need a mastectomy based on current standards, such as patients with large multifocal or multicentric tumors, those with small breast size relative to tumor extent, those with locally advanced tumors, or those with a previously irradiated breast that develops local recur­rence or a new cancer, the alternative for some of them may be extreme oncoplasty (Figs. 15.7–15.9). 
Complications and Side Effects
When using plastic oncoplastic approaches, the breast surgeon without plastic surgery training should partner with a plastic reconstructive surgeon to become comfort­able performing the basic techniques. Over time, and with collaboration and practice, the breast surgeon can incre­mentally expand their armamentarium of surgical tools.
Complications when using split reductions and extreme oncoplasty are those that are commonly associated with cosmetic mastopexy and reductions: wound infections, hematoma, fat necrosis, wound breakdown, delayed wound healing, and nipple necrosis.
34
A few of the factors implicated in poor cosmetic results after breast conservation are age >60, T2 or larger tumors, small breast size, re-excision for inadequate margins, improper scar orientation, breast tissue resection greater than 100 cm3 independent of breast size, breast ptosis, tumors located in the central, medial, or lower quadrants, and radiation dose inhomogeneity.
22,35-38
Conclusion
e standard of care for patients with tumors >5 cm or with locally advanced breast cancer is mastectomy due to a lack of supportive data for breast conservation. A blinded, pro­spective randomized trial to conrm the validity of breast conservation for these women is not forthcoming and likely will never be performed. For the patient who desires to avoid mastectomy despite this, thoughtful consideration should be given to the concept of extreme oncoplasty. Extreme oncoplasty oers a balanced solution that allows aggressive tumor clearance with overlying skin but maxi­mizes the potential for an aesthetically pleasing outcome with minimal surgery.
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Pre-op 6 months post-op
Pre-op Post-op 1 year
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Fig. 15.8 Extreme Oncoplasty: 69-year-old with locally advanced left invasive ductal carcinoma at 6:00,
spanning 7 cm. She had an excellent imaging response to neoadjuvant chemotherapy, and underwent left oncoplastic surgery (Wise pattern extreme oncoplasty) and an immediate contralateral reduction. Final pathology showed no residual disease. She completed adjuvant radiotherapy and has an excellent cos­metic result.
Fig. 15.9 A 56-year-old woman with a 60-mm palpable multifocal invasive ductal carcinoma of the right
lateral breast. Underwent neoadjuvant chemotherapy with a partial imaging response, followed by a right breast segmental resection, with immediate oncoplastic reconstruction with a LICAP flap.
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References
1. Vaidya JS, Wenz F, Bulsara M, Tobias JS, Joseph DJ, Keshtgar M, etal. Risk-adapted targeted intraoperative radiotherapy ver­sus whole-breast radiotherapy for breast cancer: 5-year results for local control and overall survival from the TARGIT-A ran­domised trial. Lancet. 2014;383(9917):603–613.
2. Veronesi U, Orecchia R, Maisonneuve P, Viale G, Rotmensz N, Sangalli C, et al. Intraoperative radiotherapy versus exter­nal radiotherapy for early breast cancer (ELIOT): a randomised controlled equivalence trial. Lancet Oncol. 2013;14(13):1269–
1277.
3. Santos G, Urban C, Edelweiss MI, Zucca-Matthes G, de Oliveira VM, Arana GH, etal. Long-term comparison of aesthetical out­comes after oncoplastic surgery and lumpectomy in breast cancer patients. Ann Surg Oncol. 2015;22(8):2500–2508.
4. Savalia NB, Silverstein MJ. Oncoplastic breast reconstruc­tion: patient selection and surgical techniques. J Surg Oncol. 2016;113(8):875–882.
5. Bleicher RJ, Ruth K, Sigurdson ER, Daly JM, Boraas M, Ander­son PR, etal. Breast conservation versus mastectomy for patients with T3 primary tumors (>5 cm): a review of 5685 Medicare patients. Cancer. 2016;122(1):42–49.
6. Zucca Matthes AG, Uemura G, Kerr L, Matthes AC, Michelli RA, Folgueira MA, etal. Feasibility of oncoplastic techniques in the surgical management of locally advanced breast cancer. Int J Surg. 2012;10(9):500–505.
7. Bogusevicius A, Cepuliene D, Sepetauskiene E. e integrated evaluation of the results of oncoplastic surgery for locally advanced breast cancer. Breast J. 2014;20(1):53–60.
8. Emiroglu M, Sert I, Karaali C, Aksoy SO, Ugurlu L, Aydin C. e eectiveness of simultaneous oncoplastic breast surgery in patients with locally advanced breast cancer. Breast Cancer.
2015.
9. Vieira RA, Carrara GF, Scapulatempo Neto C, Morini MA, Brentani MM, Folgueira MA. e role of oncoplastic breast con­serving treatment for locally advanced breast tumors. A matching case-control study. Ann Med Surg (Lond). 2016;10:61–68.
10. Silverstein MJ, Savalia N, Khan S, Ryan J. Extreme oncoplasty: breast conservation for patients who need mastectomy. Breast J. 2015;21(1):52–59.
11. Silverstein MJ. Radical mastectomy to radical conservation (extreme oncoplasty): a revolutionary change. J Am Coll Surg. 2016;222(1):1–9.
12. Macmillan RD, McCulley SJ. Oncoplastic breast surgery: what, when and for whom? Curr Breast Cancer Rep. 2016;8(2):112–
117.
13. Boetes C, Veltman J, van Die L, Bult P, Wobbes T, Barentsz JO. e role of MRI in invasive lobular carcinoma. Breast Cancer Res Treat. 2004;86(1):31–37.
14. Chagpar AB, Killelea BK, Tsangaris TN, Butler M, Stavris K, Li F, etal. A randomized, controlled trial of cavity shave margins in breast cancer. N Engl J Med. 2015;373(6):503–510.
15. Silverstein MJ, Mai T, Savalia N, Vaince F, Guerra L. Oncoplas­tic breast conservation surgery: the new paradigm. J Surg Oncol. 2014;110(1):82–89.
16. Piper M, Peled AW, Sbitany H. Oncoplastic breast surgery: cur­rent strategies. Gland Surg. 2015;4(2):154–163.
17. Wise RJ. A preliminary report on a method of planning the mammaplasty. Plast Reconstr Surg (1946). 1956;17(5):367–375.
18. Chang E, Johnson N, Webber B, Booth J, Rahhal D, Gannett D, etal. Bilateral reduction mammoplasty in combination with lumpectomy for treatment of breast cancer in patients with mac­romastia. Am J Surg. 2004;187(5):647–651.
19. Newman LA, Kuerer HM, McNeese MD, Hunt KK, Gurtner GC, Vlastos GS, etal. Reduction mammoplasty improves breast conservation therapy in patients with macromastia. Am J Surg. 2001;181(3):215–220.
20. Spear SL, Pelletiere CV, Wolfe AJ, Tsangaris TN, Pennanen MF. Experience with reduction mammaplasty combined with breast conservation therapy in the treatment of breast cancer. Plast Reconstr Surg. 2003;111(3):1102–1109.
21. Hudson DA. A modied excision for combined reduction mam­moplasty and breast conservation therapy in the treatment of breast cancer. Aesthetic Plast Surg. 2007;31(1):71–75.
22. Foersterling E, Golatta M, Hennigs A, Schulz S, Rauch G, Schott S, etal. Predictors of early poor aesthetic outcome after breast­conserving surgery in patients with breast cancer: initial results of a prospective cohort study at a single institution. J Surg Oncol. 2014;110(7):801–806.
23. Silverstein MJ, Savalia NB, Khan S, Ryan J, Epstein M, DeLeon C, etal. Oncoplastic split reduction with intraoperative radiation therapy. Ann Surg Oncol. 2015;22(10):3405–3406.
24. Bartelink H, Fentiman I, Lerut T, Mignolet F, Olthuis G, Syl­vester R, et al. Randomized clinical trial to assess the value of breast-conserving therapy in stage I and II breast cancer, EORTC 10801 trial. J Natl Cancer Inst Monogr. 1992;(11):15–18.
25. Veronesi U, Saccozzi R, Del Vecchio M, Ban A, Clemente C, De Lena M, etal. Comparing radical mastectomy with quadran­tectomy, axillary dissection, and radiotherapy in patients with small cancers of the breast. N Engl J Med. 1981;305(1):6–11.
26. Lichter AS, Lippman ME, Danforth Jr DN, d’Angelo T, Stein­berg SM, DeMoss E, etal. Mastectomy versus breast-conserving therapy in the treatment of stage I and II carcinoma of the breast: a randomized trial at the national cancer institute. J Clin Oncol. 1992;10(6):976–983.
27. Fisher B, Bauer M, Margolese R, Poisson R, Pilch Y, Redmond C, etal. Five-year results of a randomized clinical trial compar­ing total mastectomy and segmental mastectomy with or with­out radiation in the treatment of breast cancer. N Engl J Med. 1985;312(11):665–673.
28. Fisher B, Anderson S, Bryant J, Margolese RG, Deutsch M, Fisher ER, et al. Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. N Engl J Med. 2002;347(16):1233–1241.
29. Veronesi U, Cascinelli N, Mariani L, Greco M, Saccozzi R, Luini A, etal. Twenty-year follow-up of a randomized study compar­ing breast-conserving surgery with radical mastectomy for early breast cancer. N Engl J Med. 2002;347(16):1227–1232.
30. Cochrane R, Valasiadou P, Wilson A, AlGhazal S, Macmillan R. Cosmesis and satisfaction after breastconserving surgery correlates with the percentage of breast volume excised. BJS. 2003;90(12):1505–1509.
31. Al-Ghazal S, Blamey R, Stewart J, Morgan A. e cosmetic out­come in early breast cancer treated with breast conservation. Eur J Surg Oncol. 1999;25(6):566–570.
32. Moody A, Mayles W, Bliss J, A’Hern R, Owen J, Regan J, etal. e inuence of breast size on late radiation eects and asso­ciation with radiotherapy dose inhomogeneity. Radiother Oncol. 1994;33(2):106–112.
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33. Moran MS, Schnitt SJ, Giuliano AE, Harris JR, Khan SA, Horton J, et al. Society of Surgical Oncology–American Soci­ety for Radiation Oncology consensus guideline on margins for breast-conserving surgery with whole-breast irradiation in stages I and II invasive breast cancer. Int J Radiat Oncol Biol Phys. 2014;88(3):553–564.
34. Iwuagwu O. Additional considerations in the application of oncoplastic approaches. Lancet Oncol. 2005;6(6):356.
35. Munshi A, Kakkar S, Bhutani R, Jalali R, Budrukkar A, Dinshaw KA. Factors inuencing cosmetic outcome in breast conserva­tion. Clin Oncol (R Coll Radiol). 2009;21(4):285–293.
36. Taylor ME, Perez CA, Halverson KJ, Kuske RR, Philpott GW, Garcia DM, etal. Factors inuencing cosmetic results after con­servation therapy for breast cancer. Int J Radiat Oncol Biol Phys. 1995;31(4):753–764.
37. Hennigs A, Hartmann B, Rauch G, Golatta M, Tabata­bai P, Domschke C, et al. Long-term objective esthetic out­come after breast-conserving therapy. Breast Cancer Res Treat. 2015;153(2):345–351.
38. Waljee JF, Hu ES, Newman LA, Alderman AK. Predictors of breast asymmetry after breast-conserving operation for breast cancer. J Am Coll Surg. 2008;206(2):274–280.
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Oncoplastic Variations Based on Tumor Location
ALBERT LOSKEN
Introduction
e type of reconstruction used for partial mastectomy defects depends on (1) the size of the resection, (2) the size of the breast, and (3) the location of the tumor. Tumor loca­tion on the breast and relative to the nipple–areolar complex is critically important. A recent study of 350 patients dem­onstrated that the maximal volume of tissue resected with lumpectomy without resulting in unacceptable aesthetic and functional outcomes of decreased quality of life were 18–19% in the upper-outer quadrant, 14–15% in the lower quadrant, 8–9% in the upper-inner quadrant, and 9–10% in the lower inner quadrant.1 Tumor location not only can predict the potential for a cosmetic deformity, but it also can help determine the type of reconstruction required to ll the partial mastectomy defect. Women with smaller breasts are more often amenable to ap type volume replace­ment reconstructions, whereas women with larger or more ptotic breasts are better candidates for volume displace­ment techniques. Adhering to strict algorithms is dicult because every case is dierent. Being familiar with the vari­ous reconstructive tools will allow reconstruction of almost any partial mastectomy defect. e oncoplastic reduction and mastopexy techniques can reconstruct a tumor in any location. any breast defect, the type of pedicle and type of skin pat­tern might dier depending on the tumor location. Flaps can also reach any tumor location; however, some aps are better suited for certain locations than others.
Problem Areas in Oncoplastic Reconstruction
Partial reconstruction works well in lower quadrants of the breast.5 ese areas are adjacent to suitable volumes of breast parenchyma that can be transposed or rotated into a nearby defect. e upper and superomedial quadrants of the breast are relatively volume decient and are often not close to suitable pedicles that may be used as volume ll­ers. e supra-areolar area from the upper anterior axillary
2-4
Although principles are essentially the same for
fold laterally across to the manubriosternal junction medi­ally is often challenging to reconstruct. is area often requires local aps or autoaugmentation techniques to ll the defects. Central defects can also be challenging because they potentially interfere with blood supply to the nipple– areolar complex and, when not lled appropriately, will lead to nipple retraction and resultant deformity. It is important to keep in mind that when the defect is extensive with little remaining breast tissue, completion mastectomy and imme­diate reconstruction is often the more appropriate option.
1. Volume Displacement Techniques
Breast-reshaping procedures all essentially rely on advance­ment, rotation, or transposition of an area of the breast to ll a small- or moderate-sized defect. is absorbs the volume loss into a smaller breast. In its simplest form, it entails mobilizing the breastplate from the area immediately around the defect in a breast ap advancement technique.6 ese procedures are indicated in women with small- to medium-sized breasts where the resection does not lead to any signicant volume alteration that might cause breast asymmetry. A contralateral symmetry procedure is typically not required.
Perhaps the most popular and versatile breast-reshaping options are the mastopexy or reduction techniques.7 e ideal patient is one where the tumor can be excised within the expected breast reduction specimen in medium to large or ptotic breasts where sucient breast parenchyma remains following resection to reshape the mound. is means that any tumor location within the standard Wise pattern resection tissue is ideal for this approach. Kronowitz etal describe seven areas or zones of the breast that can be used to determine pedicle location.3 e most dicult locations to treat are superomedial areas, where lack of adjacent breast volume tends to limit reconstructive options; women with large lower poles and cleavage are easier to manage in this area. High upper pole tumors can also be problematic unless a ap of breast tissue can be incorporated into an inferior pedicle as a pennant ap rotated up into the defect from below.
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ABC
G
Fig. 16.1 This 50-year-old female with a left lower pole breast cancer underwent a generous 120-gram
tumor resection including breast tissue and skin. Her lower pole defect is within the resection pattern for Wise resection. A superomedial pedicle was performed with a total resection of 320 grams on the left and 360 grams on the right. Her result is shown 5 months postoperatively and before irradiation therapy.
H I
Lower quadrant tumors in women with larger breasts are ideally suited for the oncoplastic approach.5 Some of the original descriptions of oncoplastic reduction techniques were in tumors located inferiorly. Quadrantectomy type resections are possible, removing skin and parenchyma from this location, reshaping the breast using a superior or superomedial pedicle (Fig. 16.4). Inferior and midline tumors can be reconstructed using the vertical pattern in smaller- to moderate-sized breasts. A superiorly based pedicle can be used to reposition the nipple, and this then results in a very familiar defect because it is the location where tissue is resected in a vertical pattern breast reduction or mastopexy. e medial and lateral pillars are then pli­cated to ll the defect and lift the breast with a similar pat­tern being performed on the other side. e breast surgeon will often have the luxury of removing skin along with the
FED
tumor resection if this falls within the proposed preopera­tive markings (Fig. 16.1).
If the inverted T or Wise pattern reduction or mastopexy is planned, the technique is similar. Resection is performed either with or without skin within the Wise pattern mark­ings. e nipple is then moved up on a superiorly based ped­icle, and the remaining dermatoglandular tissue is resected from around the lower pole, and the oncoplastic reduction is completed. If additional tissue is resected from around the tumor defect, it is important to mark the specimen because this will then become the new margin. If signicant pto­sis exists, and the tumor is inferior and a superiorly based pedicle is not possible, then this becomes more challeng­ing. Autoaugmentation techniques are often not required for central lower pole defects because the nature of these techniques will often have sucient remaining breast tissue
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to fall into place lling the defect without having to rear­range parenchyma.
8
Inferolateral tumors are best closed with a superomedial pedicle incorporating an accessory ap of inferior central tissue to rotate into the lateral defect if indicated. If a supe­riorly based pedicle is not possible due to signicant ptosis, then an inferior or centrally based pedicle can be used and shifted medially to enhance perfusion to the nipple. True inferolateral defects often do not require autoaugmenta­tion techniques, but when they do, extended superomedial pedicles can be used to rotate and ll an area of volume void when indicated. e nipple pedicle is extended and the glandular tissue is de-epithelialized and rotated laterally.
Inferomedial tumors are also often very amenable to superior or superomedial pedicles. e defect will often lie in the Wise pattern markings, and completing the reduc­tion will reshape the breast mound. If an inferior pedicle is needed, it can also be shifted laterally and used to move the nipple and ll the defect. Autoaugmentation techniques are similarly not often needed but can be performed using an extended superolateral pedicle if indicated.
Upper quadrant tumors result in defects that can be more challenging to reconstruct. ese defects are outside the Wise pattern markings, which makes skin and parenchyma removal dicult. e vast majority will be lumpectomy type defects and are often best lled with an inferior or central pedicle (Fig. 16.2, upper). When sucient glandular tissue remains above the nipple–areolar complex on an inferior pedicle, this can be used to ll the central upper defects. If not, it will be important to mobilize some upper pole tissue to ll the defect and provide upper pole fullness. e higher the tumor on the chest wall and the thinner the patient, the more dicult this becomes. If there is a paucity of available tissue, glandular “wings” of parenchyma from the lateral and medial upper quadrants can be mobilized to help close the defect. is is often not possible, and subsequently auto­augmentation techniques are used to ll the dead-space and maintain shape. Extended superomedial pedicles in women with medium-sized and ptotic breasts and upper or upper­outer quadrant defects will often provide good reconstruc­tion. A vertical reduction technique is performed creating medial and lateral pillars. e lower pole breast tissue is kept as an extension of the superomedial pedicle and transferred to ll the upper or outer quadrant defect. e breast is then shaped by closing the pillars inferiorly. A similar technique can be performed for upper-inner quadrant defects using an extended superolateral pedicle.
ese upper-outer quadrant defects in women with large breasts who undergo a Wise pattern reduction can also be lled using the secondary dermatoglandular pedicle. If a superomedial pedicle is used to reposition the nipple, and volume is needed to ll an upper-outer defect, then a sec­ondary inferolateral pedicle can be created to ll the defect. e pedicle is fashioned to t the defect and made smaller or larger depending on the demands. is is often safer than extending the primary pedicle as it preserves better perfused dermatoglandular tissue with less risk of fat necrosis.
Larger quadrantectomy defects, especially above the nipple, can be incorporated into a batwing mastopexy or elliptical-type incision and provide preservation or improve­ment of shape and elevation of the ptotic breast along with the tumor resection. A similar mirror image resection is often performed on the opposite side for symmetry. Addi­tional mastopexy options exist for oncoplastic breast con­servation.6 e donut mastopexy allows a breast segment to be removed through a periareolar incision and is useful for segmentally distributed cancers in the upper or lateral portion of the breast. e batwing mastopexy involves a full thickness excision of lesions deep within the breast centrally or adjacent to the nipple–areolar complex. e two similar half-circle incisions with angled wings on either side of the areolar allow advancement of the broglandular tissue to close the defect. Because this removes sucient breast tis­sue and skin to alter the size of the breast and nipple posi­tion, a similar contralateral lift is occasionally required to achieve symmetry. Additionally, if the patient is a candidate for breast conservation therapy (BCT) and has multiple areas that need to be resected, as long as sucient tissue remains, remodeling techniques can be used in a similar fashion.
Central tumors have in the past been considered rela­tive contraindications to BCT; however, with the oncoplas­tic approach in women with macromastia, the tumor and nipple–areolar complex can be widely excised and recon­structed using a variety of techniques.9 e mound can be remodeled in the inverted T-closure pattern, similar to breast amputation reduction techniques. e nipple is then reconstructed later using the reconstruction technique of choice (Fig. 16.3). Another option if the tumor is located more superiorly or lateral is to perform a central ellipti­cal excision of skin, nipple, and parenchyma, and mirror image contralateral reduction for symmetry. A third option includes creation of a skin island on a dermatoglandular pedicle to rotate into the central defect to allow for shape preservation and nipple reconstruction (Fig. 16.7). e breast is marked preoperatively for an inverted T or a verti­cal approach depending on breast size, and the skin island is brought in from inferior or medial (Fig. 16.4).
In situations where the resection is central and the nipple–areolar complex can be spared, then parenchymal tissue can be mobilized during the reduction technique to provide breast tissue beneath the nipple to provide shape. One example includes de-epithelialized inferior pedicle with medial and lateral tissue rotated around in a similar fashion to that described for the massive weight loss breast (Fig. 16.5).
Medial and lateral defects are similarly treated. Medial and upper inner quadrant defects can often be lled with a broad inferior pedicle if sucient volume persists (Fig.
16.6). Women with smaller breasts who have small- or
medium-sized defects in the medial or lateral locations that are not adequately lled with surrounding breast tissue are best lled with the extended pedicle. e tissue that is typi­cally removed when creating the medial and lateral pedicles
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A
C
B
D
E
Fig. 16.2 This is a 65-year-old female with DCIS in the upper quadrant of her left breast. Preopera-
tive markings following guidewire placement show plan for possible superomedial reduction. Following removal of a 100-gram partial mastectomy, the plan was changed to perform an inferior pedicle given the extent of tumor resection. An additional 200 grams were removed around an inferior pedicle on the left, and a similar inferior pedicle reduction (350 grams) was removed from the right breast. Her result is shown 2 years following completion of radiation therapy with good upper pole shape and symmetry.
F
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A
B
C
Fig. 16.3 This 43-year-old woman had a tumor beneath her nipple on the left resulting in significant
nipple–areolar retraction. She had a wide resection with breast amputation on the left and a reduction on the right. Eventual nipple reconstruction and areolar tattoo on the left results in good shape and symmetry.
A
D
Fig. 16.4 This patient did not want to undergo skin sparing mastectomy (SSM) and reconstruction
despite having a subareolar tumor-elected breast preservation. Given proximity, she had resection of the nipple–areolar complex with her partial mastectomy. An inferior pedicle was created leaving a skin island appropriately located for nipple areolar replacement. She is shown after completing irradiation therapy.
B
E
C
F
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A
C
Fig. 16.5 This 33-year-old woman with stage III breast cancer had an excellent response to preoperative
chemotherapy and desired breast conservation (A). To minimize the potential for a poor cosmetic result with a defect in the upper pole, she underwent a right wire-guided lumpectomy (100 grams) (B, C) with simultaneous bilateral breast reduction (total volumes, 250 grams left and 150 grams right). The nipple was moved on an inferiorly based dermatoglandular pedicle with the central attachments intact, and used in part to fill the upper pole volume void. Her result is shown at 1 year following completion of right breast radiation therapy (D).
B
D
in a vertical breast reduction or mastopexy is preserved as an extension to the superiorly based pedicle. It is rotated with the nipple to the proposed location and used to ll the defect (Fig. 16.7). e medial and lateral glandular pillars are then plicated in the usual manner. is tissue can also be used to ll superior defects or, if necessary, with a Wise pattern. Larger, lateral, or upper-outer quadrant defects in women with larger breasts, however, would require two pedicles. Once the defect is examined, a superomedial pedicle is created, and the nipple is rotated into the desired position. An inferiorly based lateral dermatoglandular ped­icle is de-epithelialized and created based on how much is anticipated to ll the defect. e residual dermatoglandular tissue is then resected, and the breast mound is shaped in
the usual fashion. e secondary pedicle can then indepen­dently be cut to size and placed into the defect (Fig. 16.8). Medial defects are also amenable to a superolateral pedicle (Fig. 16.9). is can be extended and used to ll the defect in an autoaugmentation fashion in women without su­cient local tissue to ll the defect. e medial quadrant is aesthetically sensitive, and a lack of sucient volume ll will result in BCT contour irregularities.
2. Volume Replacement Techniques Partial mastectomy defects in women with small to medium breasts are often dicult to reconstruct.10 Women with large tumor-to-breast ratios and women with small to moderate breasts who have insucient residual breast tis­sue for rearrangement require partial reconstruction using