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DOI: 10.1055/a-2616-4532
Characterization of Soft Tissue Reconstruction Following Chordoma Resection

Abstract
Background
Chordomas are rare, malignant bone tumors of the axial skeleton. Soft tissue reconstruction is often needed postextirpation to reduce the risk of peritoneal content herniation. The purpose of this study is to describe presurgical factors associated with postchordoma resection reconstruction and evaluate postoperative outcomes.
Methods
We retrospectively reviewed patients who underwent reconstruction postexcision of chordomas derived from the lumbar or sacral regions at a single institution between 2012 and 2023. Wilcoxon rank sum test, chi-square test, Fisher's exact test, and Kruskal–Wallis test were used to compare outcomes based on reconstruction method.
Results
Among 68 patients who met the inclusion criteria, 67 underwent sacrectomy. Patients primarily received gluteus muscle (GM) flaps (n = 36, 53%). Vertical rectus abdominus myocutaneous (VRAM) and paraspinous muscle (PSM) flaps were the second most common, each used in 12 patients (18%). Eight patients (12%) underwent reconstruction with fasciocutaneous local flaps only. GM and VRAM flaps were primarily used to reconstruct defects at the level of the sacrum (n = 47, 98%) while PSM flaps were used for lumbar (n = 7 [58%]) and sacral (n = 5 [42%]) reconstruction, respectively. The median tumor volumes were 468 cm3 (271–1,592) for VRAM flaps, 92 cm3 (12–246) for GM flaps, 77 cm3 (34–239) for PSM flaps, and 25 cm3 (16–86) for non-muscle reconstruction; tumor volume was significantly greater in patients who underwent VRAM flap reconstruction. Median defect diameter managed by VRAM flaps was significantly longer compared with GM flaps (33 [30–46] cm vs. 22 [15–30] cm, respectively; p = 0.001). VRAM and PSM flap reconstruction were more often associated with hardware placement (p < 0.01). Median follow-up was 34 months. Neither reconstruction type nor hardware placement was associated with the incidence of postoperative complications.
Conclusion
We found that surgical reconstruction following chordoma resection varied depending on the chordoma spinal level, tumor volume, and defect diameter. Complication rates were similar among the included reconstructive options.
Note
This study was presented at the Plastic Surgery The Meeting (PSTM 2024); Northeastern Society of Plastic Surgeons (NESPS 2024).
* These senior authors contributed equally to this work.
Publication History
Received: 26 November 2024
Accepted: 07 May 2025
Article published online:
12 June 2025
© 2025. Thieme. All rights reserved.
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References
- 1 Barber SM, Sadrameli SS, Lee JJ. et al. Chordoma-current understanding and modern treatment paradigms. J Clin Med 2021; 10 (05) 1054
- 2 Pillai S, Govender S. Sacral chordoma : A review of literature. J Orthop 2018; 15 (02) 679-684
- 3 Baratti D, Gronchi A, Pennacchioli E. et al. Chordoma: natural history and results in 28 patients treated at a single institution. Ann Surg Oncol 2003; 10 (03) 291-296
- 4 Scampa M, Tessitore E, Dominguez DE. et al. Sacral chordoma: A population-based analysis of epidemiology and survival outcomes. Anticancer Res 2022; 42 (02) 929-937
- 5 Sharma R, Mukherjee D, Arnav A, Shankaran R, Agarwal VK. Surgical and functional outcomes of en bloc resection of sacral chordoma: A retrospective analysis. Indian J Surg Oncol 2021; 12 (04) 750-758
- 6 Connors SW, Aoun SG, Shi C, Peinado-Reyes V, Hall K, Bagley CA. Recent advances in understanding and managing chordomas: An update. F1000Res 2020; 9: 713
- 7 Zuckerman SL, Bilsky MH, Laufer I. Chordomas of the skull base, mobile spine, and sacrum: An epidemiologic investigation of presentation, treatment, and survival. World Neurosurg 2018; 113: e618-e627
- 8 Jing L, Wang G. Giant recurrent sacral chordoma. World Neurosurg 2019; 122: 96-97
- 9 Yadav SK, Kunal K, Kantiwal P, Rajnish RK, Elhence A, Gupta S. Sacrococcygeal chordoma-illustrative cases and our experience. Int J Burns Trauma 2023; 13 (03) 110-115
- 10 Berra LV, Armocida D, Palmieri M. et al. Sacral nerves reconstruction after surgical resection of a large sacral chordoma restores the urinary and sexual function and the anal continence. Neurospine 2022; 19 (01) 155-162
- 11 Kolz JM, Wellings EP, Houdek MT, Clarke MJ, Yaszemski MJ, Rose PS. Outcomes of recurrent mobile spine chordomas. J Am Acad Orthop Surg 2023; 31: e278-e286
- 12 Kerekes D, Goodwin CR, Ahmed AK. et al. Local and distant recurrence in resected sacral chordomas: A systematic review and pooled cohort analysis. Global Spine J 2019; 9 (02) 191-201
- 13 Chang DW, Friel MT, Youssef AA. Reconstructive strategies in soft tissue reconstruction after resection of spinal neoplasms. Spine 2007; 32 (10) 1101-1106
- 14 Triolo JC, Buchs NC, Tessitore E. et al. Sacral defect reconstruction using double pedicled gracilis muscle flap combined with gluteal fasciocutaneous rotation flap. Plast Reconstr Surg Glob Open 2022; 10 (05) e4329
- 15 Vartanian ED, Lynn JV, Perrault DP. et al. Risk factors associated with reconstructive complications following sacrectomy. Plast Reconstr Surg Glob Open 2018; 6 (11) e2002
- 16 Houdek MT, Bakri K, Tibbo ME. et al. Outcome and complications following vertical rectus abdominis myocutaneous flap surgery to reconstruct sacrectomy defects. Plast Reconstr Surg 2018; 142 (05) 1327-1335
- 17 Kim JE, Pang J, Christensen JM. et al. Soft-tissue reconstruction after total en bloc sacrectomy. J Neurosurg Spine 2015; 22 (06) 571-581
- 18 Deskoulidi P, Stavrianos SD, Mastorakos D. et al. Anatomical considerations and plastic surgery reconstruction options of sacral chordoma resection. Cureus 2023; 15 (04) e37965
- 19 Charlson ME, Carrozzino D, Guidi J, Patierno C. Charlson Comorbidity Index: A critical review of clinimetric properties. Psychother Psychosom 2022; 91 (01) 8-35
- 20 Gallia GL, Haque R, Garonzik I. et al. Spinal pelvic reconstruction after total sacrectomy for en bloc resection of a giant sacral chordoma. Technical note. J Neurosurg Spine 2005; 3 (06) 501-506
- 21 Asaad M, Rajesh A, Wahood W. et al. Flap reconstruction for sacrectomy defects: A systematic review and meta-analysis. J Plast Reconstr Aesthet Surg 2020; 73 (02) 255-268
- 22 Miles WK, Chang DW, Kroll SS. et al. Reconstruction of large sacral defects following total sacrectomy. Plast Reconstr Surg 2000; 105 (07) 2387-2394
- 23 Diaz J, McDonald WS, Armstrong M, Eismont F, Hellinger M, Thaller S. Reconstruction after extirpation of sacral malignancies. Ann Plast Surg 2003; 51 (02) 126-129
- 24 Ramirez OM, Swartz WM, Futrell JW. The gluteus maximus muscle: experimental and clinical considerations relevant to reconstruction in ambulatory patients. Br J Plast Surg 1987; 40 (01) 1-10
- 25 Ramirez OM, Hurwitz DJ, Futrell JW. The expansive gluteus maximus flap. Plast Reconstr Surg 1984; 74 (06) 757-770
- 26 Weitao Y, Qiqing C, Songtao G, Jiaqiang W. Use of gluteus maximus adipomuscular sliding flaps in the reconstruction of sacral defects after tumor resection. World J Surg Oncol 2013; 11: 110
- 27 Maricevich M, Maricevich R, Chim H, Moran SL, Rose PS, Mardini S. Reconstruction following partial and total sacrectomy defects: an analysis of outcomes and complications. J Plast Reconstr Aesthet Surg 2014; 67 (09) 1257-1266
- 28 Koh PK, Tan BK, Hong SW. et al. The gluteus maximus muscle flap for reconstruction of sacral chordoma defects. Ann Plast Surg 2004; 53 (01) 44-49
- 29 Garvey PB, Rhines LD, Feng L, Gu X, Butler CE. Reconstructive strategies for partial sacrectomy defects based on surgical outcomes. Plast Reconstr Surg 2011; 127 (01) 190-199
- 30 van Wulfften Palthe OD, Houdek MT, Rose PS. et al. How does the level of nerve root resection in en bloc sacrectomy influence patient-reported outcomes?. Clin Orthop Relat Res 2017; 475 (03) 607-616
- 31 Dasenbrock HH, Clarke MJ, Bydon A. et al. Reconstruction of extensive defects from posterior en bloc resection of sacral tumors with human acellular dermal matrix and gluteus maximus myocutaneous flaps. Neurosurgery 2011; 69 (06) 1240-1247
- 32 Glatt BS, Disa JJ, Mehrara BJ, Pusic AL, Boland P, Cordeiro PG. Reconstruction of extensive partial or total sacrectomy defects with a transabdominal vertical rectus abdominis myocutaneous flap. Ann Plast Surg 2006; 56 (05) 526-530 , discussion 530–531
- 33 Manrique OJ, Rajesh A, Asaad M. et al. Surgical outcomes after abdominoperineal resection with sacrectomy and soft tissue reconstruction: Lessons learned. J Reconstr Microsurg 2020; 36 (01) 64-72
- 34 Huang W, Hu X, Cai W. et al. Soft-tissue reconstruction with pedicled vertical rectus abdominis myocutaneous flap after total or high sacrectomy for giant sacral tumor. J Plast Reconstr Aesthet Surg 2024; 91: 173-180
- 35 Lasso JM, Pinilla C, Vasquez W, Asencio JM. The effect of intraoperative radiotherapy on healing and complications after sacrectomy and immediate reconstruction. Ann Plast Surg 2021; 86 (06) 688-694
- 36 Atomura D, Makiguchi T, Nakamura H. et al. Sacral and rectal necrosis after carbon ion radiotherapy reconstructed with transpelvic rectus abdominis flap. Plast Reconstr Surg Glob Open 2020; 8 (06) e2885
- 37 Garvey PB, Rhines LD, Feng L, Gu X, Butler CE. Reconstructive strategies for partial sacrectomy defects based on surgical outcomes. Plast Reconstr Surg 2011; 127 (01) 190-199
- 38 Junge K, Krones CJ, Rosch R, Fackeldey V, Schumpelick V. Mesh reconstruction preventing sacral herniation. Hernia 2003; 7 (04) 224-226
- 39 Fourney DR, Rhines LD, Hentschel SJ. et al. En bloc resection of primary sacral tumors: classification of surgical approaches and outcome. J Neurosurg Spine 2005; 3 (02) 111-122
- 40 Ooi A, Foo L, Tan BK, Ng SW. Massive sacral chordoma resection and reconstruction with a combination of pedicled and free flaps. J Reconstr Microsurg 2015; 31 (01) 76-78
- 41 Brault N, Qassemyar Q, Bouthors C, Lambert B, Atlan M, Missenard G. [A giant sacral chordoma resection and reconstruction with a gluteal perforator flap, a case report and literature review]. Ann Chir Plast Esthet 2019; 64 (03) 271-277
- 42 Durden F, Wang D, Mendel E, Tiwari P. Reconstruction of a large external hemipelvectomy defect after chordoma resection using a 5-component chimeric rotational flap. Ann Plast Surg 2015; 74 (01) 74-79
- 43 Garvey PB, Clemens MW, Rhines LD, Sacks JM. Vertical rectus abdominis musculocutaneous flow-through flap to a free fibula flap for total sacrectomy reconstruction. Microsurgery 2013; 33 (01) 32-38
- 44 Leach GA, Pflibsen LR, Roberts AD. et al. Meningomyelocele reconstruction: Comparison of repair methods via systematic review. J Craniofac Surg 2023; 34 (07) 2040-2045
- 45 Massaad E, Patel SS, Sten M. et al. Pedicled omental flaps for complex wound reconstruction following surgery for primary spine tumors of the mobile spine and sacrum. J Neurosurg Spine 2024; 41 (02) 283-291
- 46 Felsenreich DM, Gachabayov M, Ritter E, Bergamaschi R. En-bloc excision of sacral squamous cell carcinoma with immediate reconstruction. Updates Surg 2024; 76 (03) 1099-1103
- 47 van Wulfften Palthe ODR, Tromp I, Ferreira A. et al. Sacral chordoma: a clinical review of 101 cases with 30-year experience in a single institution. Spine J 2019; 19 (05) 869-879
- 48 Mikula AL, Pennington Z, Lakomkin N. et al. Risk factors for sacral fracture following en bloc chordoma resection. J Neurosurg Spine 2023; 39 (05) 611-617
- 49 Radaelli S, Stacchiotti S, Ruggieri P. et al. Sacral chordoma: Long-term outcome of a large series of patients surgically treated at two reference centers. Spine 2016; 41 (12) 1049-1057
- 50 Yolcu Y, Wahood W, Alvi MA. et al. Evaluating the role of adjuvant radiotherapy in the management of sacral and vertebral chordoma: Results from a national database. World Neurosurg 2019; 127: e1137-e1144
- 51 Angelini A, Pala E, Calabrò T, Maraldi M, Ruggieri P. Prognostic factors in surgical resection of sacral chordoma. J Surg Oncol 2015; 112 (04) 344-351