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Postoperative Complications from Breast and Axillary Surgery

Published:October 17, 2022DOI:https://doi.org/10.1016/j.suc.2022.08.007

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      References

        • Bernat J.L.
        • Peterson L.M.
        Patient-Centered Informed Consent in Surgical Practice.
        Arch Surg. 2006; 141: 86-92
        • Browne J.P.
        • Jeevan R.
        • Gulliver-Clarke C.
        • et al.
        The association between complications and quality of life after mastectomy and breast reconstruction for breast cancer.
        Cancer. 2017; 123: 3460-3467
        • Barton M.B.
        • West C.N.
        • Liu I.L.A.
        • et al.
        Complications following bilateral prophylactic mastectomy.
        J Natl Cancer Inst Monogr. 2005; 35: 61-66
        • Seth A.K.
        • Hirsch E.M.
        • Kim J.Y.S.
        • et al.
        Hematoma after mastectomy with immediate reconstruction: an analysis of risk factors in 883 patients.
        Ann Plast Surg. 2013; 71: 20-23
        • Handel N.
        • Cordray T.
        • Gutierrez J.
        • et al.
        A long-term study of outcomes, complications, and patient satisfaction with breast implants.
        Plast Reconstr Surg. 2006; 117: 757-767
        • Almasarweh S.
        • Sudah M.
        • Joukainen S.
        • et al.
        The Feasibility of Ultrasound-guided Vacuum-assisted Evacuation of Large Breast Hematomas.
        Radiol Oncol. 2020; 54: 311
        • O’Hea B.J.
        • Ho M.N.
        • Petrek J.A.
        External compression dressing versus standard dressing after axillary lymphadenectomy.
        Am J Surg. 1999; 177: 450-453
        • Bullocks J.
        • Basu C.B.
        • Hsu P.
        • et al.
        Prevention of Hematomas and Seromas.
        Semin Plast Surg. 2006; 20: 233
        • Srivastava V.
        • Basu S.
        • Shukla V.K.
        Seroma Formation after Breast Cancer Surgery: What We Have Learned in the Last Two Decades.
        J Breast Cancer. 2012; 15: 373
        • Montalto E.
        • Mangraviti S.
        • Costa G.
        • et al.
        Seroma fluid subsequent to axillary lymph node dissection for breast cancer derives from an accumulation of afferent lymph.
        Immunol Lett. 2010; 131: 67-72
        • Van Bemmel A.J.M.
        • Van De Velde C.J.H.
        • Schmitz R.F.
        • et al.
        Prevention of seroma formation after axillary dissection in breast cancer: a systematic review.
        Eur J Surg Oncol. 2011; 37: 829-835
        • Unger J.
        • Rutkowski R.
        • Kohlmann T.
        • et al.
        Potential risk factors influencing the formation of postoperative seroma after breast surgery - a prospective study.
        Anticancer Res. 2021; 41: 859-867
        • Shamley D.R.
        • Barker K.
        • Simonite V.
        • et al.
        Delayed versus immediate exercises following surgery for breast cancer: a systematic review.
        Breast Cancer Res Treat. 2005; 90: 263-271
        • de Oliveira L.L.
        • de Aguiar S.S.
        • Bender P.F.M.
        • et al.
        Men have a higher incidence of seroma after breast cancer surgery.
        Asian Pac J Cancer Prev. 2017; 18: 1423-1427
        • He X.D.
        • Guo Z.H.
        • Tian J.H.
        • et al.
        Whether drainage should be used after surgery for breast cancer? A systematic review of randomized controlled trials.
        Med Oncol. 2011; 28: 22-30
        • Shima H.
        • Kutomi G.
        • Sato K.
        • et al.
        An optimal timing for removing a drain after breast surgery: a systematic review and meta-analysis.
        J Surg Res. 2021; 267: 267-273
        • Faisal M.
        • Abu-Elela S.T.
        • Mostafa W.
        • et al.
        Efficacy of axillary exclusion on seroma formation after modified radical mastectomy.
        World J Surg Oncol. 2016; 14: 1-5
        • De Blacam C.
        • Ogunleye A.A.
        • Momoh A.O.
        • et al.
        High body mass index and smoking predict morbidity in breast cancer surgery: a multivariate analysis of 26,988 patients from the national surgical quality improvement program database.
        Ann Surg. 2012; 255: 551-555
        • Pastoriza J.
        • McNelis J.
        • Parsikia A.
        • et al.
        Predictive factors for surgical site infections in patients undergoing surgery for breast carcinoma.
        Am Surg. 2021; 87: 68-76
        • McCullough M.C.
        • Chu C.K.
        • Duggal C.S.
        • et al.
        Antibiotic prophylaxis and resistance in surgical site infection after immediate tissue expander reconstruction of the breast.
        Ann Plast Surg. 2016; 77: 501-505
        • Chen C.M.
        • Halvorson E.G.
        • Disa J.J.
        • et al.
        Immediate postoperative complications in DIEP versus free/muscle-sparing TRAM flaps.
        Plast Reconstr Surg. 2007; 120: 1477-1482
        • Sbitany H.
        • Serletti J.M.
        Acellular dermis-assisted prosthetic breast reconstruction: a systematic and critical review of efficacy and associated morbidity.
        Plast Reconstr Surg. 2011; 128: 1162-1169
        • Chang D.W.
        • Barnea Y.
        • Robb G.L.
        Effects of an autologous flap combined with an implant for breast reconstruction: an evaluation of 1000 consecutive reconstructions of previously irradiated breasts.
        Plast Reconstr Surg. 2008; 122: 356-362
        • Thiruchelvam P.T.R.
        • Leff D.R.
        • Godden A.R.
        • et al.
        Primary radiotherapy and deep inferior epigastric perforator flap reconstruction for patients with breast cancer (PRADA): a multicentre, prospective, non-randomised, feasibility study.
        Lancet Oncol. 2022; 23: 682-690
        • Degnim A.C.
        • Throckmorton A.D.
        • Boostrom S.Y.
        • et al.
        Surgical site infection (SSI) after breast surgery: impact of 2010 CDC Reporting Guidelines.
        Ann Surg Oncol. 2012; 19: 4099
        • Viola G.M.
        • Selber J.C.
        • Crosby M.
        • et al.
        Salvaging the infected breast tissue expander: a standardized multidisciplinary approach.
        Plast Reconstr Surg Glob Open. 2016; 4https://doi.org/10.1097/GOX.0000000000000676
        • Gallagher M.
        • Jones D.J.
        • Bell-Syer S.V.
        Prophylactic antibiotics to prevent surgical site infection after breast cancer surgery.
        Cochrane Database Syst Rev. 2019; 9https://doi.org/10.1002/14651858.CD005360.PUB5
        • Bold R.J.
        • Mansfield P.F.
        • Berger D.H.
        • et al.
        Prospective, randomized, double-blind study of prophylactic antibiotics in axillary lymph node dissection.
        Am J Surg. 1998; 176: 239-243
      1. American Society of Breast Surgeons T. Consensus Guideline on Preoperative Antibiotics and Surgical Site Infection in Breast Surgery. Available from: https://www.breastsurgeons.org/docs/statements/Consensus-Guideline-on-Preoperative-Antibiotics-and-Surgical-Site-Infection-in-Breast-Surgery.pdf.

        • Giguère G.B.
        • Poirier B.
        • Provencher L.
        • et al.
        Do preoperative prophylactic antibiotics reduce surgical site infection following wire-localized lumpectomy? A single-blind randomized clinical trial.
        Ann Surg Oncol. 2022; 29: 2202-2208
        • Petersen L.
        • Carlson K.
        • Kopkash K.
        • et al.
        Preoperative antibiotics do not reduce postoperative infections following needle-localized lumpectomy.
        Breast J. 2017; 23: 49-51
        • Kong A.
        • Tartter P.I.
        • Zappetti D.
        The Significance of Risk Factors for Infection in Patients Undergoing Lumpectomy and Axillary Dissection.
        Breast J. 1997; 3: 81-84
        • Alderman A.
        • Gutowski K.
        • Ahuja A.
        • et al.
        ASPS clinical practice guideline summary on breast reconstruction with expanders and implants.
        Plast Reconstr Surg. 2014; 134: 648e-655e
        • Bağhaki S.
        • Soybir G.R.
        • Soran A.
        Guideline for antimicrobial prophylaxis in breast surgery.
        J Breast Heal. 2014; 10: 79
        • Robertson S.A.
        • Jeevaratnam J.A.
        • Agrawal A.
        • et al.
        Mastectomy skin flap necrosis: challenges and solutions.
        Breast Cancer (Dove Med Press). 2017; https://doi.org/10.2147/BCTT.S81712
        • Matsen C.B.
        • Mehrara B.
        • Eaton A.
        • et al.
        Skin flap necrosis after mastectomy with reconstruction: a prospective study.
        Ann Surg Oncol. 2016; 23: 257-264
        • Yabe S.
        • Nakagawa T.
        • Oda G.
        • et al.
        Association between skin flap necrosis and sarcopenia in patients who underwent total mastectomy.
        Asian J Surg. 2021; 44: 465-470
        • Chun Y.S.
        • Verma K.
        • Rosen H.
        • et al.
        Use of tumescent mastectomy technique as a risk factor for native breast skin flap necrosis following immediate breast reconstruction.
        Am J Surg. 2011; 201: 160-165
        • Galimberti V.
        • Vicini E.
        • Corso G.
        • et al.
        Nipple-sparing and skin-sparing mastectomy: Review of aims, oncological safety and contraindications.
        The Breast. 2017; 34: S82-S84
        • Robertson S.A.
        • Rusby J.E.
        • Cutress R.I.
        Determinants of optimal mastectomy skin flap thickness.
        Br J Surg. 2014; 101: 899-911
        • Wiberg R.
        • Andersson M.N.
        • Svensson J.
        • et al.
        Prophylactic mastectomy: postoperative skin flap thickness evaluated by MRT, ultrasound and clinical examination.
        Ann Surg Oncol. 2020; 27: 2221-2228
        • Ogawa A.
        • Nakagawa T.
        • Oda G.
        • et al.
        Study of the protocol used to evaluate skin-flap perfusion in mastectomy based on the characteristics of indocyanine green.
        Photodiagnosis Photodyn Ther. 2021; 35 (1): 102401
        • Pruimboom T.
        • Lindelauf A.A.M.A.
        • Felli E.
        • et al.
        Perioperative hyperspectral imaging to assess mastectomy skin flap and DIEP flap perfusion in immediate autologous breast reconstruction: a pilot study.
        Diagnostics (Basel, Switzerland). 2022; 12https://doi.org/10.3390/DIAGNOSTICS12010184
        • Gdalevitch P.
        • Van Laeken N.
        • Bahng S.
        • et al.
        Effects of nitroglycerin ointment on mastectomy flap necrosis in immediate breast reconstruction: a randomized controlled trial.
        Plast Reconstr Surg. 2015; 135: 1530-1539
        • Spruijt N.E.
        • Hoekstra L.T.
        • Wilmink J.
        • et al.
        Hyperbaric oxygen treatment for mastectomy flap ischaemia: a case series of 50 breasts.
        Diving Hyperb Med. 2021; 51: 2
        • Nicholson B.T.
        • Harvey J.A.
        • Cohen M.A.
        Nipple-areolar complex: normal anatomy and benign and malignant processes.
        Radiographics. 2009; 29: 509-523
        • Mallon P.
        • Feron J.G.
        • Couturaud B.
        • et al.
        The role of nipple-sparing mastectomy in breast cancer: a comprehensive review of the literature.
        Plast Reconstr Surg. 2013; 131: 969-984
        • Ahn S.J.
        • Woo T.Y.
        • Lee D.W.
        • et al.
        Nipple-areolar complex ischemia and necrosis in nipple-sparing mastectomy.
        Eur J Surg Oncol. 2018; 44: 1170-1176
        • Zheng Y.
        • Zhong M.
        • Ni C.
        • et al.
        Radiotherapy and nipple–areolar complex necrosis after nipple-sparing mastectomy: a systematic review and meta-analysis.
        Radiol Med. 2017; 122: 171-178
        • Chicco M.
        • Huang T.C.T.
        • Cheng H.T.
        Negative-pressure wound therapy in the prevention and management of complications from prosthetic breast reconstruction: a systematic review and meta-analysis.
        Ann Plast Surg. 2021; 87: 478-483
        • De Martino R.R.
        • Goodney P.P.
        • Spangler E.L.
        • et al.
        Variation in thromboembolic complications among patients undergoing commonly performed cancer operations.
        J Vasc Surg. 2012; 55: 1035-1040.e4
        • Tafur A.
        • Fuentes H.
        • Caprini J.
        • et al.
        Predictors of early mortality in cancer-associated thrombosis: analysis of the RIETE database.
        TH Open Companion J Thromb Haemost. 2018; 2: e158-e166
        • Castaldi M.
        • George G.
        • Stoller C.
        • et al.
        Independent predictors of venous thromboembolism in patients undergoing reconstructive breast cancer surgery.
        Plast Surg (Oakville, Ont). 2021; 29: 160-168
        • Rochlin D.H.
        • Sheckter C.C.
        • Pannucci C.
        • et al.
        Venous thromboembolism following microsurgical breast reconstruction: a longitudinal analysis of 12,778 patients.
        Plast Reconstr Surg. 2020; 146: 465-473
        • Londero A.P.
        • Bertozzi S.
        • Cedolini C.
        • et al.
        Incidence and risk factors for venous thromboembolism in female patients undergoing breast surgery.
        Cancers (Basel). 2022; 14https://doi.org/10.3390/CANCERS14040988/S1
        • Konoeda H.
        • Yamaki T.
        • Hamahata A.
        • et al.
        Incidence of deep vein thrombosis in patients undergoing breast reconstruction with autologous tissue transfer.
        Phlebology. 2017; 32: 282-288
        • Lovely J.K.
        • Nehring S.A.
        • Boughey J.C.
        • et al.
        Balancing venous thromboembolism and hematoma after breast surgery.
        Ann Surg Oncol. 2012; 19: 3230-3235
        • Nwaogu I.
        • Yan Y.
        • Margenthaler J.A.
        • et al.
        Venous thromboembolism after breast reconstruction in patients undergoing breast surgery: an american college of surgeons NSQIP analysis.
        J Am Coll Surg. 2015; 220: 886-893
      2. American Society of Breast Surgeons T. Consensus Guideline on Venous Thromboembolism (VTE) Prophylaxis for Patients Undergoing Breast Operations. Available from: https://www.breastsurgeons.org/docs/statements/Consensus-Guideline-on-Venous-Thromboembolism-VTE-Prophylaxis-for-Patients-Undergoing-Breast-Operations.pdf.

        • Pannucci C.J.
        • Swistun L.
        • MacDonald J.K.
        • et al.
        Individualized venous thromboembolism risk stratification using the 2005 caprini score to identify the benefits and harms of chemoprophylaxis in surgical patients: a meta-analysis.
        Ann Surg. 2017; 265: 1094-1103
        • Keith J.N.
        • Chong T.W.
        • Davar D.
        • et al.
        The timing of preoperative prophylactic low-molecular-weight heparin administration in breast reconstruction.
        Plast Reconstr Surg. 2013; 132: 279-284
        • Stevens S.M.
        • Woller S.C.
        • Baumann Kreuziger L.
        • et al.
        Executive summary: antithrombotic therapy for VTE disease: second update of the CHEST guideline and expert panel report.
        Chest. 2021; 160: 2247-2259
        • Kearon C.
        • Akl E.A.
        • Ornelas J.
        • et al.
        Antithrombotic therapy for VTE disease: CHEST guideline and expert panel report.
        Chest. 2016; 149: 315-352
        • Douketis J.D.
        • Spyropoulos A.C.
        • Spencer F.A.
        • et al.
        Perioperative management of antithrombotic therapy: antithrombotic therapy and prevention of thrombosis, 9th ed: american college of chest physicians evidence-based clinical practice guidelines.
        Chest. 2012; 141: e326S-e350S
        • Klifto K.M.
        • Gurno C.F.
        • Major M.
        • et al.
        Pre-, intra-, and/or postoperative arterial and venous thromboembolism prophylaxis for breast surgery: Systematic review and meta-analysis.
        J Plast Reconstr Aesthet Surg. 2020; 73: 1-18
        • Lucci A.
        • McCall L.M.
        • Beitsch P.D.
        • et al.
        Surgical complications associated with sentinel lymph node dissection (SLND) plus axillary lymph node dissection compared with SLND alone in the American College of Surgeons Oncology Group trial Z0011.
        J Clin Oncol. 2007; 25: 3657-3663
        • Kozak D.
        • Głowacka-Mrotek I.
        • Nowikiewicz T.
        • et al.
        Analysis of undesirable sequelae of sentinel node surgery in breast cancer patients – a prospective cohort study.
        Pathol Oncol Res. 2018; 24: 891
        • Meininger A.K.
        • Figuerres B.F.
        • Goldberg B.A.
        Scapular winging: an update.
        J Am Acad Orthop Surg. 2011; 19: 453-462
        • Flávia De Oliveira J.
        • Bezerra T.
        • Carolina A.
        • et al.
        Incidence and risk factors of winged scapula after axillary lymph node dissection in breast cancer surgery.
        Appl Cancer Res. 2009; 29: 69-73
        • Adriaenssens N.
        • De Ridder M.
        • Lievens P.
        • et al.
        Scapula alata in early breast cancer patients enrolled in a randomized clinical trial of post-surgery short-course image-guided radiotherapy.
        World J Surg Oncol. 2012; 10https://doi.org/10.1186/1477-7819-10-86
        • Macchi V.
        • Tiengo C.
        • Porzionato A.
        • et al.
        Medial and lateral pectoral nerves: course and branches.
        Clin Anat. 2007; 20: 157-162
        • Prakash K.G.
        • Saniya K.
        Anatomical study of pectoral nerves and its implications in surgery.
        J Clin Diagn Res. 2014; 8https://doi.org/10.7860/JCDR/2014/8631.4545
        • Sharp E.
        • Roberts M.
        • Żurada-Zielińska A.
        • et al.
        The most commonly injured nerves at surgery: a comprehensive review.
        Clin Anat. 2021; 34: 244-262
        • Zhu J.J.
        • Liu X.F.
        • Zhang P.L.
        • et al.
        Anatomical information for intercostobrachial nerve preservation in axillary lymph node dissection for breast cancer.
        Genet Mol Res. 2014; 13: 9315-9323
        • Henry B.M.
        • Graves M.J.
        • Pękala J.R.
        • et al.
        Origin, Branching, and Communications of the Intercostobrachial Nerve: a Meta-Analysis with Implications for Mastectomy and Axillary Lymph Node Dissection in Breast Cancer.
        Cureus. 2017; 9https://doi.org/10.7759/CUREUS.1101
        • Vadivelu N.
        • Schreck M.
        • Lopez J.
        • et al.
        Pain after mastectomy and breast reconstruction.
        Am Surg. 2008; 74: 285-296
        • Mansel R.E.
        • Fallowfield L.
        • Kissin M.
        • et al.
        Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial.
        J Natl Cancer Inst. 2006; 98: 599-609
        • Andersen K.G.
        • Aasvang E.K.
        • Kroman N.
        • et al.
        Intercostobrachial nerve handling and pain after axillary lymph node dissection for breast cancer.
        Acta Anaesthesiol Scand. 2014; 58: 1240-1248
        • Gärtner R.
        • Jensen M.B.
        • Nielsen J.
        • et al.
        Prevalence of and factors associated with persistent pain following breast cancer surgery.
        JAMA. 2009; 302: 1985-1992
        • Chappell A.G.
        • Yuksel S.
        • Sasson D.C.
        • et al.
        Post-mastectomy pain syndrome: an up-to-date review of treatment outcomes.
        JPRAS Open. 2021; 30: 97-109
        • Yang A.
        • Nadav D.
        • Legler A.
        • et al.
        An interventional pain algorithm for the treatment of postmastectomy pain syndrome: a single-center retrospective review.
        Pain Med. 2021; 22: 677-686
        • Tokgöz S.
        • Karaca Umay E.
        • Yilmaz K.B.
        • et al.
        Role of intraoperative nerve monitoring in postoperative muscle and nerve function of patients undergoing modified radical mastectomy.
        J Investig Surg. 2021; 34: 703-710
        • Noland S.S.
        • Krauss E.M.
        • Felder J.M.
        • et al.
        Surgical and clinical decision making in isolated long thoracic nerve palsy.
        Hand (N Y). 2018; 13: 689
        • Warner M.A.
        • Blitt C.D.
        • Butterworth J.F.
        • et al.
        Practice advisory for the prevention of perioperative peripheral neuropathies: a report by the American Society of Anesthesiologists Task Force on Prevention of Perioperative Peripheral Neuropathies.
        Anesthesiology. 2000; 92: 1168-1182
        • Zhang J.
        • Moore A.E.
        • Stringer M.D.
        • et al.
        Iatrogenic upper limb nerve injuries: a systematic review.
        ANZ J Surg. 2011; 81: 227-236
        • Rudra S.
        • Roy A.
        • Brenneman R.
        • et al.
        Radiation-Induced Brachial Plexopathy in Patients With Breast Cancer Treated With Comprehensive Adjuvant Radiation Therapy.
        Adv Radiat Oncol. 2020; 6https://doi.org/10.1016/J.ADRO.2020.10.015
        • Jack M.M.
        • Smith B.W.
        • Capek S.
        • et al.
        The spectrum of brachial plexopathy from perineural spread of breast cancer.
        J Neurosurg. 2022; : 1-10https://doi.org/10.3171/2021.12.JNS211882
        • Suami H.
        • Scaglioni M.F.
        Lymphedema Management: Anatomy of the Lymphatic System and the Lymphosome Concept with Reference to Lymphedema.
        Semin Plast Surg. 2018; 32: 5
        • Campisi C.C.
        • Molinari L.
        • Campisi C.S.
        • et al.
        Surgical research, staging-guided technical procedures and long-term clinical outcomes for the treatment of peripheral lymphedema: the Genoa Protocol.
        J Surg Surg Res. 2020; 6: 041-050
        • Cortina C.S.
        • Yen T.W.F.
        • Bergom C.
        • et al.
        Breast cancer-related lymphedema rates after modern axillary treatments: How accurate are our estimates?.
        Surgery. 2022; 171: 682-686
        • Naoum G.E.
        • Roberts S.
        • Brunelle C.L.
        • et al.
        Quantifying the impact of axillary surgery and nodal irradiation on breast cancer-related lymphedema and local tumor control: Long-term results from a prospective screening trial.
        J Clin Oncol. 2020; 38: 3430-3438
        • DiSipio T.
        • Rye S.
        • Newman B.
        • et al.
        Incidence of unilateral arm lymphoedema after breast cancer: a systematic review and meta-analysis.
        Lancet Oncol. 2013; 14: 500-515
        • McLaughlin S.A.
        • Brunelle C.L.
        • Taghian A.
        Breast cancer–related lymphedema: risk factors, screening, management, and the impact of locoregional treatment.
        J Clin Oncol. 2020; 38: 2341
        • Galimberti V.
        • Cole B.F.
        • Zurrida S.
        • et al.
        Axillary dissection versus no axillary dissection in patients with sentinel-node micrometastases (IBCSG 23-01): a phase 3 randomised controlled trial.
        Lancet Oncol. 2013; 14: 297-305
        • Cortina C.S.
        • Kong A.L.
        ASO author reflections: the evolving multidisciplinary management of the axilla in mastectomy patients.
        Ann Surg Oncol. 2021; : 1-2https://doi.org/10.1245/S10434-021-10585-Y
        • Cortina C.S.
        • Bergom C.
        • Craft M.A.
        • et al.
        A national survey of breast surgeons and radiation oncologists on contemporary axillary management in mastectomy patients.
        Ann Surg Oncol. 2021; 28: 5568-5579
        • Cortina C.S.
        • Kong A.L.
        Comment on “women could avoid axillary lymph node dissection by choosing breast-conserving therapy instead of mastectomy.
        Ann Surg Oncol. 2021; 28: 772-773
        • Morrow M.
        • Jagsi R.
        • Chandler M.
        • et al.
        Surgeon attitudes toward the omission of axillary dissection in early breast cancer.
        JAMA Oncol. 2018; 4: 1511-1516
        • Donker M.
        • van Tienhoven G.
        • Straver M.E.
        • et al.
        Radiotherapy or surgery of the axilla after a positive sentinel node in breast cancer (EORTC 10981-22023 AMAROS): a randomised, multicentre, open-label, phase 3 non-inferiority trial.
        Lancet Oncol. 2014; 15: 1303-1310
        • Giuliano A.E.
        • Ballman K.V.
        • McCall L.
        • et al.
        Effect of axillary dissection vs no axillary dissection on 10-year overall survival among women with invasive breast cancer and sentinel node metastasis: the ACOSOG Z0011 (Alliance) randomized clinical trial.
        JAMA. 2017; 318: 918-926
        • McDuff S.G.R.
        • Mina A.I.
        • Brunelle C.L.
        • et al.
        Timing of lymphedema after treatment for breast cancer: when are patients most at risk?.
        Int J Radiat Oncol. 2019; 103: 62-70
        • Basta M.N.
        • Wu L.C.
        • Kanchwala S.K.
        • et al.
        Reliable prediction of postmastectomy lymphedema: the risk assessment tool evaluating lymphedema.
        Am J Surg. 2017; 213: 1125-1133.e1
        • Armer J.M.
        • Ballman K.V.
        • McCall L.
        • et al.
        Factors associated with lymphedema in women with node-positive breast cancer treated with neoadjuvant chemotherapy and axillary dissection.
        JAMA Surg. 2019; 154: 800-809
        • Husted Madsen A.
        • Haugaard K.
        • Soerensen J.
        • et al.
        Arm morbidity following sentinel lymph node biopsy or axillary lymph node dissection: a study from the Danish Breast Cancer Cooperative Group.
        Breast. 2008; 17: 138-147
        • McLaughlin S.A.
        • DeSnyder S.M.
        • Klimberg S.
        • et al.
        Considerations for clinicians in the diagnosis, prevention, and treatment of breast cancer-related lymphedema, recommendations from an expert panel: part 2: preventive and therapeutic options.
        Ann Surg Oncol. 2017; 24: 2827-2835
        • Stout Gergich N.L.
        • Pfalzer L.A.
        • McGarvey C.
        • et al.
        Preoperative assessment enables the early diagnosis and successful treatment of lymphedema.
        Cancer. 2008; 112: 2809-2819
        • McNeely M.L.
        • Magee D.J.
        • Lees A.W.
        • et al.
        The addition of manual lymph drainage to compression therapy for breast cancer related lymphedema: a randomized controlled trial.
        Breast Cancer Res Treat. 2004; 86: 95-106
        • Schmitz K.H.
        • Ahmed R.L.
        • Troxel A.
        • et al.
        Weight lifting in women with breast-cancer-related lymphedema.
        N Engl J Med. 2009; 361: 664-673
        • Schaverien M.V.
        • Asaad M.
        • Selber J.C.
        • et al.
        Outcomes of vascularized lymph node transplantation for treatment of lymphedema.
        J Am Coll Surg. 2021; 232: 982-994
        • Tummel E.
        • Ochoa D.
        • Korourian S.
        • et al.
        Does axillary reverse mapping prevent lymphedema after lymphadenectomy?.
        Ann Surg. 2017; 265: 987-992
        • DeSnyder S.M.
        • Yi M.
        • Boccardo F.
        • et al.
        American society of breast surgeons’ practice patterns for patients at risk and affected by breast cancer-related lymphedema.
        Ann Surg Oncol. 2021; 28: 5742-5751
        • YANG E.
        • LI X.
        • LONG X.
        Diagnosis and treatment of axillary web syndrome: an overview.
        Chin J Plast Reconstr Surg. 2020; 2: 128-136
        • Koehler L.A.
        • Haddad T.C.
        • Hunter D.W.
        • et al.
        Axillary web syndrome following breast cancer surgery: symptoms, complications, and management strategies.
        Breast Cancer (London). 2019; 11: 13
        • O’Toole J.
        • Miller C.L.
        • Specht M.C.
        • et al.
        Cording following treatment for breast cancer.
        Breast Cancer Res Treat. 2013; 140: 105-111
        • Fourie W.J.
        • Robb K.A.
        Physiotherapy management of axillary web syndrome following breast cancer treatment: discussing the use of soft tissue techniques.
        Physiotherapy. 2009; 95: 314-320
        • Cohen-Hallaleh R.B.
        • Smith H.G.
        • Smith R.C.
        • et al.
        Radiation induced angiosarcoma of the breast: outcomes from a retrospective case series.
        Clin Sarcoma Res. 2017; 7: 15
        • Kleinerman R.A.
        • Tucker M.A.
        • Tarone R.E.
        • et al.
        Risk of new cancers after radiotherapy in long-term survivors of retinoblastoma: an extended follow-up.
        J Clin Oncol. 2005; 23: 2272-2279
        • Mito J.K.
        • Mitra D.
        • Barysauskas C.M.
        • et al.
        A Comparison of outcomes and prognostic features for radiation-associated angiosarcoma of the breast and other radiation-associated sarcomas.
        Int J Radiat Oncol Biol Phys. 2019; 104: 425-435
        • Deutsch M.
        • Safyan E.
        Angiosarcoma of the breast occurring soon after lumpectomy and breast irradiation for infiltrating ductal carcinoma: a case report.
        Am J Clin Oncol. 2003; 26: 471-472
        • De Smet S.
        • Vandermeeren L.
        • Christiaens M.R.
        • et al.
        Radiation-induced sarcoma: analysis of 46 cases.
        Acta Chir Belg. 2008; 108: 574-579
        • Smith T.L.
        • Morris C.G.
        • Mendenhall N.P.
        Angiosarcoma after breast-conserving therapy: Long-term disease control and late effects with hyperfractionated accelerated re-irradiation (HART).
        . 2014; 53: 235-241https://doi.org/10.3109/0284186X.2013.819117
        • Sharma A.
        • Schwartz R.A.
        Stewart-treves syndrome: pathogenesis and management.
        J Am Acad Dermatol. 2012; 67: 1342-1348
        • Bernia E.
        • Rios-Viñuela E.
        • Requena C.
        Stewart-treves syndrome.
        JAMA Dermatol. 2021; 157: 721
        • Araco A.
        • Caruso R.
        • Araco F.
        • et al.
        Capsular contractures: a systematic review.
        Plast Reconstr Surg. 2009; 124: 1808-1819
        • Namnoum J.D.
        • Largent J.
        • Kaplan H.M.
        • et al.
        Primary breast augmentation clinical trial outcomes stratified by surgical incision, anatomical placement and implant device type.
        J Plast Reconstr Aesthet Surg. 2013; 66: 1165-1172
      3. Lapid O., Noels E.C., Meijer S.L., et al., Pathologic findings in primary capsulectomy specimens: analysis of 2531 patients, Aesthet Surg J, 34 (5), 2014, 714-718.

        • Doren E.L.
        • Miranda R.N.
        • Selber J.C.
        • et al.
        U.S. epidemiology of breast implant-associated anaplastic large cell lymphoma.
        Plast Reconstr Surg. 2017; 139: 1042-1050
        • McCarthy C.M.
        • Loyo-Berríos N.
        • Qureshi A.A.
        • et al.
        Patient registry and outcomes for breast implants and anaplastic large cell lymphoma etiology and epidemiology (PROFILE): initial report of findings, 2012-2018.
        Plast Reconstr Surg. 2019; 143 (3S A Review of Breast Implant-Associated Anaplastic Large Cell Lymphoma): 65S-73S
        • Clemens M.W.
        • Jacobsen E.D.
        • Horwitz S.M.
        2019 NCCN Consensus guidelines on the diagnosis and treatment of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL).
        Aesthet Surg J. 2019; 39: S3-S13
        • Helms R.L.
        • O’Hea E.L.
        • Corso M.
        Body image issues in women with breast cancer.
        . 2008; 13: 313-325https://doi.org/10.1080/13548500701405509
        • Cornell L.F.
        • Mussallem D.M.
        • Gibson T.C.
        • et al.
        Trends in sexual function after breast cancer surgery.
        Ann Surg Oncol. 2017; 24: 2526-2538
        • Rosenberg S.M.
        • Dominici L.S.
        • Gelber S.
        • et al.
        Association of breast cancer surgery with quality of life and psychosocial well-being in young breast cancer survivors.
        JAMA Surg. 2020; 155: 1035-1042
        • Campbell-Enns H.
        • Woodgate R.
        The psychosocial experiences of women with breast cancer across the lifespan: a systematic review protocol.
        JBI Database Syst Rev Implement Reports. 2015; 13: 112-121
        • Janowski K.
        • Tatala M.
        • Jedynak T.
        • et al.
        Social support and psychosocial functioning in women after mastectomy.
        Palliat Support Care. 2020; 18: 314-321
        • Ng E.T.
        • Ang R.Z.
        • Tran B.X.
        • et al.
        Comparing quality of life in breast cancer patients who underwent mastectomy versus breast-conserving surgery: a meta-analysis.
        Int J Environ Res Public Health. 2019; 16: 4970
        • Aerts L.
        • Christiaens M.R.
        • Enzlin P.
        • et al.
        Sexual functioning in women after mastectomy versus breast conserving therapy for early-stage breast cancer: a prospective controlled study.
        Breast. 2014; 23: 629-636
        • Parker P.A.
        • Youssef A.
        • Walker S.
        • et al.
        Short-term and long-term psychosocial adjustment and quality of life in women undergoing different surgical procedures for breast cancer.
        Ann Surg Oncol. 2007; 14: 3078-3089
        • Anderson C.
        • Islam J.Y.
        • Elizabeth Hodgson M.
        • et al.
        Long-term satisfaction and body image after contralateral prophylactic mastectomy.
        Ann Surg Oncol. 2017; 24: 1499-1506
        • Parker P.A.
        • Peterson S.K.
        • Shen Y.
        • et al.
        Prospective study of psychosocial outcomes of having contralateral prophylactic mastectomy among women with nonhereditary breast cancer.
        J Clin Oncol. 2018; 36: 2630-2638
        • Guarino A.
        • Polini C.
        • Forte G.
        • et al.
        The Effectiveness of Psychological Treatments in Women with Breast Cancer: A Systematic Review and Meta-Analysis.
        J Clin Med. 2020; 9https://doi.org/10.3390/JCM9010209
        • Didier F.
        • Radice D.
        • Gandini S.
        • et al.
        Does nipple preservation in mastectomy improve satisfaction with cosmetic results, psychological adjustment, body image and sexuality?.
        Breast Cancer Res Treat. 2009; 118: 623-633
        • Wei C.H.
        • Scott A.M.
        • Price A.N.
        • et al.
        Psychosocial and sexual well-being following nipple-sparing mastectomy and reconstruction.
        Breast J. 2016; 22: 10-17
        • Tevlin R.
        • Brazio P.
        • Tran N.
        • et al.
        Immediate targeted nipple-areolar complex re-innervation: Improving outcomes in immediate autologous breast reconstruction.
        J Plast Reconstr Aesthet Surg. 2021; 74: 1503-1507