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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1054_Библиотеки_им_академика_М_И_Перельмана

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S. Saha and M. Singhal
long parenchymal pedicles that may be damaged and susceptible to fat necrosis because of radia­tion. Radiation therapy can cause chronic oedema of the irradiated breast, as well as contraction and scarring, causing initial post-operative symmetry to be permanently altered.
21.1.7 Complications
The overall complication rates after reduction ranges between 17% and 24%. The most common
complications are infection (2.8%), suture line dehiscence (4.6%), skin necrosis, fat necrosis (4.3%), partial or complete nipple areolar com­plex necrosis (0.9%), hematoma (0.9%), and seroma (0.6%). Other complications can be
reduced nipple sensation, and asymmetries com­pounded by radiotherapy. Obese patients and regu­lar smokers suffer from higher complication rates. The complication rates of oncoplastic reduction are similar to breast reduction for macromastia for non-oncological reasons as well as oncoplastic methods involving lesser tissue rearrangement.
If adjuvant chemotherapy is recommended, it can begin after the incisions have healed and be followed by radiation therapy. Complications that hinder wound healing may cause chemother­apy or radiation therapy to be delayed.
21.1.8 Oncological andCosmetic
Outcome
In a meta-analysis comprising of 15 studies with a minimum of 2years’ mean/median follow-up, an overall loco-regional recurrence rate of 3.1% and distant recurrence rate of 3.0% was reported [3]. These outcomes are equivalent to those obtained after a partial mastectomy with no reconstruction. In the study by Fitoussi etal., a positive-margin rate of 18.9% and a local recur­rence rate of 6.8% was reported at 5 years of follow-up [4]. In another study by Chakravorty etal. [5] comparing 150 patients who underwent oncoplastic reduction with 440 patients who underwent BCT, the percentage of patients need­ing intervention for positive margins was 14.5%
for BCT compared to 6.6% with oncoplastic reduction.
When the margins of a breast reduction are positive, there is a debate on whether to re­excise or to do a complete mastectomy.
Oncoplastic reduction is thought to cause consid­erable tissue reorganisation, making sufcient margin re-excision more difcult and a comple­tion mastectomy is more likely.
In the meta-analysis by Piper et al. [3], reported rates of re-excision and completion mastectomy were 3.5 and 3.7%, respectively. However, it is imperative to counsel the patients about all possible complications, including the possibility of completion mastectomy as the pat­terns of recurrence may be signicantly altered because reduction surge leads to complete rear­rangement of breast geometry potentially leaving the margins obscure.
In the same meta-analysis comprising of seven studies that reported the cosmetic out­come, more than 90% of patients reported satis­factory or improved outcomes. Breast asymmetry, signicant scarring, and a lack of nipple sensitivity were the most common rea­sons for patients reporting less-than-satisfactory results.
21.2 Contralateral
Symmetrisation
With the rise in breast cancer survival rates and an emphasis on cosmetic and patient-reported outcomes, addressing the contralateral breast has become an important element of breast cancer treatment. As both the breasts contribute to the aesthetic triangle, thus addressing the contralat­eral breast is essential to optimising the overall cosmetic outcome. The advantages of symmetry surgery on the non-disease breast, on the other hand, may be more than just improved aesthet­ics. Occult cancers in the contralateral breast have been discovered in several studies, with an overall rate ranging from 0.16 to 5%. Furthermore, there is evidence that breast reduc­tion reduces the risk of breast cancer in women over the age of 50.
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21.2.1 Factors Determining theNeed andTiming ofContralateral Symmetry Procedure
Various factors affect decision making, such as:
• Age.
• Comorbid status.
• Surgical factors such as type of mastectomy
(skin sparing / Non-skin sparing).
• Type of reconstruction (Autologous vs.
Prosthetic).
• Time of reconstruction (Immediate vs.
Delayed).
• Oncological risk factors.
• Need for adjuvant therapy.
• Pathologies in the contralateral breast.
Descision making
Algorithm
• Pre-surgery breast size and patients’ desired breast size and shape.
• Post reconstruction patients’ expectations regarding the size and shape.
• The nancial and social conditions and avail­ability of insurance cover also determine the patient’s decision.
• Surgeon factors such as expertise, preference and availability.
21.2.2 Decision Making Algorithm
Patients with large breast undergoing large vol­ume resection may be categorised into three groups depending on their decision to undergo symmetrisation and its timing:
Indication: Large breast with 20-50% volume
Patient unwilling for
contralateral procedures
Aim to keep diseased
breast as symmetric as
possible normal breast
WLE + appropriate
displacement/replacement
oncoplasty
(level II Oncoplastic Breast Surgery)
excision
Patient willing for
immediate
symmetrisation
procedure
Aim to leave the diseased
breast slightly larger to
precompensate the effect
of radiotherapy
WLE + bilateral breast
reduction (leaving diseased
breast slightly larger)
Patient willing for a delayed
symmetrisation procedure
Aim to provide optimal aesthetics to the
diseased breast after completion of
adjuvant therapy, contraleteral breast is reduced
using the operated breast as template
WLE + ipsilateral breast
reduction + delayed
contralateral symmetrisation
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21.2.3 Rationale
Patient Satisfaction and Patient-Reported Outcome Measures (PROMs) The overall
patient satisfaction is inuenced by the symmetry of both the breasts. Most patients choose to have the normal breast untouched. In patients with symptomatic macromastia, ptosis, hypoplasia and atrophy, surgery on the non-tumourous breast may improve the overall cosmesis.
Restore Symmetry With advances in tech­niques for breast reconstruction and a paradigm shift towards less extirpative procedures and autologous reconstructions. The aim of restoring the diseased breast similar to the volume of a nor­mal breast may be difcult without a balancing procedure on the unaffected breast.
Oncological Considerations A symmetrising mammoplasty allows us to screen for breast can­cer by examining the removed tissue for occult cancers. Occult carcinoma is a rare malignancy. It has been found that 1–5% of the removed breast tissue contains occult cancer. The radio­logical surveillance for breast cancer is not affected by the surgical procedure.
However, the use of implants for symmetrisa­tion has been debated to confound the mammo­graphic ndings of breast cancer. The presence of capsular contracture and calcications may obscure the ndings. Saline implants and sub­muscular placement of implants are easier to image and minimise the obscuring effect of the implant on the breast parenchyma.
Therefore, implant-based reconstructions require balancing surgeries more often than autologous reconstructions.
Immediate vs. delayed The benet of execut­ing the symmetry treatment concurrently with the reconstruction is that it eliminates the need for another operation and general anaesthesia is avoided. It has been proven that immediate reconstruction results in reduced distress and improved psychological outcomes compared to those who have delayed reconstructions. It is axi­omatic that similar outcomes would be expected in delayed symmetrisation procedures.
The proponents of the delayed procedure tout it as a more oncologically and cosmetically ben­ecial procedure because of following reasons:
1. The foremost reason is change in the volume
of the operated breast following radiotherapy, which may lead to size discrepancies if an immediate symmetrisation has been performed.
2. Prolonged operative time may increase the
anaesthetic risks and technical errors.
3. Procedures on the normal breast may double
the risk of complications and potentially delay the commencement of adjuvant therapy.
4. Reoperations for positive margins or recur-
rences may further alter the breast volume.
5. Insurance reimbursements may not cover aes-
thetic surgery and may add to the cost of can­cer surgery.
21.2.5 Conclusion
21.2.4 Technical Considerations
Implant vs. Autologous To match the opposite
breast, one may perform a reduction or an aug­mentation mammoplasty or a mastopexy. Implant base reconstruction is more articial looking, and with advancing age, the normal breast becomes more ptotic compared to the breast with implant.
The advantages of symmetrising surgery on the non-disease breast may be more than just improved aesthetics. Occult cancers in the con­tralateral breast have been discovered in several studies, with an overall rate ranging from 0.16 to 5%. A symmetrising mammoplasty allows us to screen for breast cancer by examining the removed tissue for occult cancers. Implant base
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reconstructions are more articial looking and require symmetrising surgeries more frequently. The timing of the procedure is a matter of debate, however, depends on several patient and surgeon related factors.
References
1. Clough KB, Kaufman GJ, Nos C, Buccimazza I, Sarfati IM.Improving breast cancer surgery: a classi­cation and quadrant per quadrant atlas for oncoplastic surgery. Ann Surg Oncol. 2010 May;17(5):1375–91.
2. Dafydd H, Roehl KR, Phillips LG, Dancey A, Peart F, Shokrollahi K. Redening gigantomastia. J Plast Reconstr Aesthet Surg. 2011 Feb 1;64(2):160–3.
3. Piper ML, Esserman LJ, Sbitany H, Peled AW.Outcomes following oncoplastic reduction mam­moplasty: a systematic review. Ann Plast Surg. 2016 May;76:S222.
4. Fitoussi AD, Berry MG, Famà F, Falcou M-C, Curnier A, Couturaud B, etal. Oncoplastic breast surgery for cancer: analysis of 540 consecutive cases [outcomes article]. Plast Reconstr Surg. 2010 Feb;125(2):454–62.
5. Chakravorty A, Shrestha AK, Sanmugalingam N, Rapisarda F, Roche N, della Querci Rovere G, et al. How safe is oncoplastic breast conservation? Comparative analysis with standard breast conserving surgery. Eur J Surg Oncol. 2012 May 1;38(5):395–8.
Lipomodelling inBreast Surgery
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DineshThekkinkattil
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22.1 Introduction
Lipomodelling or autologous fat grafting is the removal of fat from one area of patient’s body and re-insertion into the desired recipient site [1]. Several terminologies such as autologous fat transfer, lipomodelling, lipolling, fat grafting, and liposculpture are all in use to describe this procedure. Fat has many properties that render it as an ideal ller: it is autologous, soft, frequently abundant, easily obtainable, repeatable, inexpen­sive, and biocompatible [2]. Autologous fat trans­fer was rst used in breast over a century ago [3]. Work by Delay and Coleman has been pivotal in making this procedure gain popularity [4, 5]. It has become a workhorse for oncoplastic breast surgeons and is a great adjunct tool to improve the aesthetic outcome after surgery.
22.2 Indications
Fat Grafting in Breast Conservation Surgery Main indication for fat transfer is for
correction of contour deformity or volume decit after breast cancer surgery [3] (Figs. 22.1 and
22.2).
D. Thekkinkattil (*) Consultant Oncoplastic Breast Surgeon, Lincoln County Hospital, Lincoln, UK
Fat Grafting in Implant Based Breast Surgery It is a great tool to improve tissue cover
after implant reconstruction specially to address the issue of rippling and camouaging the edges of implant. With increasing popularity of pre­pectoral implant reconstruction, lipomodelling is routinely used to create more natural anatomic upper pole slope mitigating the step-off or rip­pling deformity [68]. In two staged expander implant reconstruction, lipolling is often used at the time of implant exchange to enhance skin ap thickness and tissue cover over implant, cover the edges of implants, and to address any rippling deformity [7, 9]. Lately, hybrid reconstructive techniques are used in breast reconstruction based of tissue expansion followed by serial ses­sions of fat grafting to enhance the autologous subcutaneous compartment along with a small implant to obtain central core, projection and additional volume [10]. In situations where patients experience recurrent prosthetic associ­ated infections, fat transfer has been used to replace the volume after implant removal in suit­able patients [11].
Fat Grafting in Autologous Breast Reconstruction Delayed fat grafting can be
used to augment the volume of autologous ap reconstruction without the use of any prosthetic devices [7]. It is also used avoid any step defor­mity at the transition between tissue aps and the native chest wall. Fat graft is also a useful tool in
© The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2023 S. V. S. Deo (ed.), Breast Oncoplasty and Reconstruction,
https://doi.org/10.1007/978-981-99-5536-7_22
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Fig. 22.1 Lipomoelling to correct post-surgery deformity. Preoperative picture
D. Thekkinkattil
include postmastectomy pain syndrome, capsular contracture pain, and irradiated tissue brosis [1518]. Radiotherapy induces broblast injury, excessive scarring and reduced microcirculation and pleuripotent cells in the grafted fat are postu­lated to improve angiogenesis through paracrine signalling and endothelial recruitment [11].
Fig. 22.2 Lipomodelling to correct post-surgery defor­mity. Post-operative picture
volume augmentation in ap reconstruction of breast and is particularly useful if explantation of implant is needed due to complications [11, 12].
Fat Grafting for Whole Breast Reconstruc­tion Recent studies have also shown that pri-
mary reconstruction using fat graft alone is possible in the appropriate subset of patients [13]. External expansion by application of vac­uum via a specially designed bra (BRAVA LCC,Miami,FL) is usually used to facilitate large volume fat transfer in this setting [14].
Therapeutic Indications of Fat Grafting Pro-
posed therapeutic applications of lipomodelling
Fat Grafting in Aesthetic Breast Sur­gery Lipolling is extensively used tool in aes-
thetic and cosmetic breast surgery. Lipomodelling is extensively used for correction of breast asym­metry, tuberous breasts, chest wall deformities [19]. Breast augmentation can also be achieved only by fat transfer in appropriate patients [20]. It is also used to improve appearance after masto­pexy and reduction procedures and to address the effects of capsular contracture [21, 22].
22.2.1 Informed Consent
A detailed consultation and discussion about the potential complications both at the donor site and recipient sites should be carried out and docu­mented. It is important to make patients aware of the potential need for multiple serial sessions under general anaesthetic to achieve the desired outcome. Pre- and post-operative photographs are helpful to monitor the progress as well as use­ful in decision making process.
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22.2.1.1 Preoperative Assessment
Patient should be t and prepared for multiple procedures mostly under general anaesthesia. Smoking increases fat resorption. Bleeding dis­orders and anticoagulant treatment increases risk of bleeding and bruising. Patient should have adequate donor site to harvest fat without incur­ring damage to underlying structures. Patient should be counselled for impact of lipomodelling on future breast imaging (it can cause changes such as fat necrosis, oil cysts, calcications) and may at times necessitate biopsy. Patient should be counselled for donor site deformities such as numbness, skin dimpling, fat necrosis, rarely damage to underlying structures. Patients should also be aware of variable degree of resorption after lipomodelling. Most of the studies suggest up to 30% resorption at 1 year after the procedure.
22.2.2 Technique
Lipomodelling has three main stages.
1. Harvesting
2. Processing
3. Fat injection
Successful outcome depends on the technique of harvesting, preparing, and harvesting the fat. There is no agreement among clinicians as to the ideal method for the harvesting and handling of grafts.
22.2.3 Harvesting
Common donor sites used are anterior abdominal wall, anks or saddlebags, thighs, or knees. There is no clear relationship proven in literature for adipocyte viability and donor sites [23].
Harvesting mainly done by syringe or vacuum aspiration. Low negative pressure vacuum aspira­tion helps to harvest larger volume of fat. High vacuum pressures of conventional liposuction may cause structural disruption in up to 90% of adipocytes. Coleman technique uses a 3 mm
blunt cannula attached to 10 ml of Luer–Lock syringe. Slight negative pressure is applied by manually withdrawing the plunger [24].
Harvesting can be by ‘Dry’ or ‘Wet’ method. In wet harvesting donor site is usually inltrated with a solution containing local anaesthetic and adrenaline and causes hydrodissection and enlarges the target fat layer facilitating aspiration [21]. It is associated with less pain and bruising.
In dry method tumescent solution is not used and can lead to more pain at donor site. Studies have shown that local anaesthetic and adrenaline used in wet technique does not alter adipocyte viability or uptake [25].
22.2.4 Fat Processing
The most used methods to prepare fat grafts are sedimentation, ltering, washing, and centrifuga­tion. This is necessary as harvested fat contains blood, collagen bres, blood, and debris in addi­tion to adipocytes. These elements can cause inammation at the graft site and can be detri­mental to the grafted fat. Blood can accelerate degradation of fat. Comparative studies investi­gating the effects of fat processing with centrifu­gation, washing and ltration have showed no signicant difference in fat retention [1].
In Coleman technique fat is centrifuged at 3000 rpm for 3 min. After centrifugation three layers are observed: rst layer of oil, second layer of concentrated adipocytes and bottom layer of blood, tissue uid. Middle layer is used to graft [2]. Recently commercially available lipoaspira­tion systems are available to process the fat by selectively washing lipoaspirate while draining superuous tumescent uid, free lipids, and debris (Figs.22.3, 22.4 and 22.5).
22.2.5 Fat Grafting
Major limiting step in successful fat grafting is oxygen diffusion and factors which can impair revascularisation of grafted fat. The grafted fat must be distributed in three-dimensional fashion to create microdroplets that do not coalesce [26].
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D. Thekkinkattil
Normally small stab skin incisions are made to insert the cannula and fat is injected in small ali­quots and in different layers in three-dimensional lattice format. Fat is injected only during with­drawal of cannula and is fanned out to varying depths in soft tissue to avoid excessive interstitial pressure at the recipient site and overcrowding of transplanted adipocytes [27] (Fig. 22.6). Attempting to graft more is counterproductive and should take care to avoid overlling, other­wise there will be risk of fat necrosis and oil cysts [28]. Fat is mainly grafted using blunt cannula. However, grafting fat into scarred tissues may
Fig. 22.3 Puregraft ltration system for fat grafting
Fig. 22.5 Lipolter
gravity decanting system
Fig. 22.4 Vacuum assisted system for fat grafting. (Microaire Liposuction and Lipolter System)
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Fig. 22.6 Cannulae used in fat grafting
163
necessitate release of the scar prior to grafting. A large bore needle or sharp tipped V cannulae can be used to break the scar tissue to facilitate lipo­modelling [29] (Fig. 22.6). This technique is called three- dimensional ligamentous band release or ‘Rigottomy’ [29].
It is natural to have a proportion of fat grafted gets lost by resorption and this occurs usually within rst 4–6months after the procedure [30]. Delay described this loss as ‘twice 30% rule’­30% of the fat is lost during the liposuction and centrifugation and another 30% is lost in the rst 4months following resorption [30].
Insufcient vascularisation, inammatory response to the grafted fat and cellular damage due to mechanical stresses have been associated with fat resorption. Overlling can lead to increased tissue pressure, poor capillary perfu­sion, and poor retention. Patient related factors such as smoking can also inuence retention of fat graft. Patients may be dissatised if lipolling leads to further contour irregularities due to over or under correction of the defect [31].
Several studies have been conducted to nd ways to improve the viability of adipocytes by using growth media, nutrients as part of process-
ing procedure. Unfortunately, heterogeneity in the methodology and use of combination of agents make it difcult determine clinical appli­cability [32].
22.2.6 Complications
Mostly the procedure is safe, and incidence of complications are less frequent and mostly are minor.
Donor site complications are bruising, swell­ing, haematoma, paraesthesia, donor site pain, infection, hypertrophic scars, contour irregulari­ties, and damage to underlying structures due to intraperitoneal or intramuscular penetration of cannula.
Lipolling in breast can cause fat necrosis, oil cysts, and calcication especially when large vol­ume is injected into a single area or injected to poorly vascularised areas [33]. It can lead to pal­pable masses of fat necrosis. Agha etal. suggested that complication rate after fat transfer was 7.3% and fat necrosis accounted for 62% of these com­plications [34]. Sometimes these changes can be difcult to differentiate from local recurrence and
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may warrant additional imaging or biopsy in 3–15% of patients. Post- lipomodelling calcication can be seen in 0.7%–4.9%. Hence patients should be counselled about the impact of fat grafting on future breast imaging and the pos­sible need for biopsies to assess alterations. Injecting fat in the recipient site can also cause damage to surrounding structures such as chest wall, pleura, and implant. This can potentially lead to pneumothorax or loss of implant.
Fat Grafting and Oncological Safety Main oncological concerns raised against lipomodel­ling was based on its oncogenic potential and interference with tumour surveillance [28]. There have been hypotheses suggested regard­ing safety of lipomodelling include the risk of recurrence secondary to increased growth fac­tors that promote re vascularisation and interac­tion of growth factors produced by adipocytes and progenitor cells with cancerous cells in a paracrine fashion [35, 36]. Numerous studies have conrmed comparable local, regional, and distant recurrence rates with and without fat transfer [3739]. Furthermore, advancement in radiology permits better differentiation between post lipomodelling changes and neoplastic cal­cications [40, 41]. Consensus is that the lipo­moelling procedure is oncologically safe and does not signicantly increase cancer recur­rence [42].
22.2.7 Post-Operative Care
Patients are usually advised to wear supportive garments for both donor site and breast in the post-operative period and this helps to reduce the discomfort and bruising. Routinely patients will not need any post-operative antibiotic cover.
References
1. Kakagia D, Pallua N. Autologous fat grafting: in search of the optimal technique. Surg Innov. 2014;21(3):327–36.
2. Coleman SR. Structural fat grafts: the ideal ller? Clin Plast Surg. 2001;28(1):111–9.
3. Agarwal K, Mistry M. Autologous fat trans­fer for breast surgery. Br J Hosp Med (Lond). 2017;78(8):448–52.
4. Coleman SR. Structural fat grafting: more than a permanent ller. Plast Reconstr Surg. 2006;118(3 Suppl):108S–20S.
5. 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(5):360–76.
6. Sbitany H. Important considerations for per­forming Prepectoral breast reconstruction. Plast Reconstr Surg. 2017;140(6S Prepectoral Breast Reconstruction):7S–13S.
7. Katzel EB, Bucky LP.Fat grafting to the breast: clini­cal applications and outcomes for reconstructive sur­gery. Plast Reconstr Surg. 2017;140(5S Advances in Breast Reconstruction):69S–76S.
8. Highton L, Johnson R, Kirwan C, Murphy J. Prepectoral implant-based breast reconstruction. Plast Reconstr Surg Glob Open. 2017;5(9):e1488.
9. Hammond DC, O’Connor EA, Scheer JR.Total enve­lope fat grafting: a novel approach in breast recon­struction. Plast Reconstr Surg. 2015;135(3):691–4.
10. Stillaert F, Lannau B, Van Landuyt K, Blondeel PN. The Prepectoral, hybrid breast reconstruction: the synergy of Lipolling and breast implants. Plast Reconstr Surg Glob Open. 2020;8(7):e2966.
11. Khouri RK Jr, Khouri RK. Current clinical appli­cations of fat grafting. Plast Reconstr Surg. 2017;140(3):466e–86e.
12. Thekkinkattil DK, Salhab M, McManus PL.Feasibility of autologous fat transfer for replace­ment of implant volume in complicated implant­assisted latissimus dorsi ap breast reconstruction. Ann Plast Surg. 2015;74(4):397–402.
13. Stark RY, Mirzabeigi MN, Vonderhaar RJ, Bucky LP.Utilizing large volume fat grafting in breast recon­struction after nipple sparing mastectomies. Gland Surg. 2018;7(3):337–46.
14. Khouri RK, Rigotti G, Khouri RK Jr, 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(3):643–58.
15. Turner A, Abu-Ghname A, Davis MJ, Winocour SJ, Hanson SE, Chu CK. Fat grafting in breast recon­struction. Semin Plast Surg. 2020;34(1):17–23.
16. Caviggioli F, Maione L, Forcellini D, Klinger F, Klinger M. Autologous fat graft in postmas­tectomy pain syndrome. Plast Reconstr Surg. 2011;128(2):349–52.
17. Papadopoulos S, Vidovic G, Neid M, Abdallah A. Using fat grafting to treat breast implant cap­sular contracture. Plast Reconstr Surg Glob Open. 2018;6(11):e1969.