Techniques of pelvic floor defect reconstruction after extended surgeries of rectal cancer
https://doi.org/10.17650/2949-5857-2025-15-3-27-35
Abstract
A significant proportion of patients with colorectal cancer are diagnosed at advanced stages, requiring extensive surgical procedures that create a substantial “dead space” in the pelvic cavity. One of the major complications of such interventions is perineal hernia formation, which significantly affects quality of life by causing pain, urinary dysfunction, bowel obstruction, fistula formation, and ulcerative skin defects.
Currently, various techniques exist for the prevention and management of this complication. Simple perineal wound closure is the most accessible technique; however, in cases of large defects, it does not provide reliable closure and is associated with increased risks of wound dehiscence, infection, and subsequent hernia formation.
Autologous reconstruction of the pelvic floor defect involves the use of flaps based on the rectus abdominis muscle (vertical rectus abdominis myocutaneous flap, VRAM), gracilis muscle (m. gracilis), gluteus maximus muscle (unilateral or bilateral), as well as skin flaps. The V RAM flap demonstrates low incidence of perineal hernias and acceptable survival rates but requires high level of surgical expertise and may not be feasible in laparoscopic approaches or in patients with multiple stomas. Graciloplasty is effective for selected patients, including those undergoing minimally invasive surgery, but it may be associated with a higher complication rates compared to V RAM. The use of gluteus maximus muscle flaps allows for defect reconstruction with good vascularization but carries risks of muscle function impairment and postoperative pain. Skin flaps are less invasive and may reduce the likelihood of hernia formation, though current statistical data remain limited.
Alloplastic reconstruction of the pelvic floor defect is performed using synthetic or biological meshes. Recent studies suggest that biological meshes significantly reduce the incidence of perineal hernias compared to simple wound closure. However, their use substantially increases treatment costs. The application of synthetic materials requires strict isolation of bowel loops from the mesh surface to prevent adhesions and infectious complications; experience with these materials and long-term outcomes remain limited.
Thus, the choice of pelvic floor reconstruction technique depends on defect size, the patient’s overall condition, the surgical team’s expertise, and the availability of necessary materials. A universal “gold standard” has not yet been established. Further multicenter studies and comparative analyses are needed to determine optimal indications for each method and to develop standardized clinical protocols.
About the Authors
А. М. ОzdoevRussian Federation
Aslan Magomedovich Ozdoev
Bld. 1, 1 Novogireevskaya St., Moscow 111123
А. B. Baychorov
Russian Federation
Bld. 1, 1 Novogireevskaya St., Moscow 111123
М. A. Danilov
Russian Federation
Bld. 1, 1 Novogireevskaya St., Moscow 111123
References
1. Blok R.D., Brouwer T.P.A., Sharabiany S. et al. Further insights into the treatment of perineal hernia based on the experience of a single tertiary centre. Colorectal Dis 2020;22(6):694–702. DOI: 10.1111/codi.14952
2. Sayers A.E., Patel R.K., Hunter I.A. Perineal hernia formation following extralevator abdominoperineal excision. Colorectal Dis 2015;17(4):351–5. DOI: 10.1111/codi.12843
3. Blok R.D., Sharabiany S., Stoker J. et al. Cumulative 5-year results of a randomized controlled trial comparing biological mesh with primary perineal wound closure after extralevator abdominoperineal resection (BIOPEX-study). Ann Surg 2022;275(1):e37–e44. DOI: 10.1097/SLA.0000000000004763
4. Musters G.D., Klaver C.E.L., Bosker R.J.I. et al. Biological mesh closure of the pelvic floor after extralevator abdominoperineal resection for rectal cancer: a multicenter randomized controlled trial (the BIOPEX-study). Ann Surg 2017;265(6):1074–81. DOI: 10.1097/SLA.0000000000002020
5. Kreisel S.I., de Jong D.L.C., Hompes R. et al. Perineal hernia repair: multicentre comparative analysis of mesh-only versus mesh combined with tissue flap. Colorectal Dis 2025;27(7):e70159. DOI: 10.1111/codi.70159
6. Sharabiany S., Brouwer T.P.A., Kreisel S.I. et al. Mesh, flap or combined repair of perineal hernia after abdominoperineal resection – a systematic review and meta-analysis. Colorectal Dis 2022;24(11):1285–94. DOI: 10.1111/codi.16224
7. Kono T., Tsurita G., Yazawa K., Shinozaki M. Ileal strangulation by a secondary perineal hernia after laparoscopic abdominoperineal rectal resection: a case report. Int J Surg Case Rep 2017;33:107–11. DOI: 10.1016/j.ijscr.2017.02.005
8. West N.P., Anderin C., Smith K.J. et al. Multicentre experience with extralevator abdominoperineal excision for low rectal cancer. Br J Surg 2010;97(4):588–99. DOI: 10.1002/bjs.6916
9. Garuba F.O., McPhie J.M., Anolik R.A. et al. Perineal hernia as a sequela of anal reconstruction surgeries in perianal Crohn’s disease. Radiol Case Rep 2023;18(11):3988–92. DOI: 10.1016/j.radcr.2023.08.071
10. Kumar H., Ng S.C., Chua J.Y.J., Raaj C. Deadly if missed: a case of recurrent perineal hernia mimicking as perineal cellulitis following abdominoperineal resection. World J Colorectal Surg 2019;8(2):58–60. DOI: 10.4103/WJCS.WJCS_7_19
11. Kreisel S.I., Sharabiany S., Rothbarth J.et al. Quality of life in patients with a perineal hernia. Eur J Surg Oncol 2023;49(12):107114. DOI: 10.1016/j.ejso.2023.107114
12. Blok R.D., Musters G.D., Borstlap W.A.A. et al. Collaborative Dutch Snapshot Search Group. Snapshot study on the value of omentoplasty in abdominoperineal resection with primary perineal closure for rectal cancer. Ann Surg Oncol 2018;25(3):729–36. DOI: 10.1245/s10434-017-6273-9
13. Peirce C., Martin S. Management of the perineal defect after abdominoperineal excision. Clin Colon Rectal Surg 2016;29(2):160–7. DOI: 10.1055/s-0036-1580627
14. Woodfield J., Hulme-Moir M., Ly J. A comparison of the cost of primary closure or rectus abdominis myocutaneous flap closure of the perineum after abdominoperineal excision. Colorectal Dis 2017;19(10):934–41. DOI: 10.1111/codi.13690
15. Sharabiany S., Blok R.D., Lapid O. et al. Perineal wound closure using gluteal turnover flap or primary closure after abdominoperineal resection for rectal cancer: study protocol of a randomised controlled multicentre trial (BIOPEX-2 study). BMC Surg 2020;20(1):164. DOI: 10.1186/s12893-020-00823-7
16. Sinna R., Alharbi M., Assaf N. et al. Management of the perineal wound after abdominoperineal resection. J Visc Surg 2013;150(1): 9–18. DOI: 10.1016/j.jviscsurg.2013.02.001
17. Nakamura T., Sato T., Hayakawa K. et al. Risk factors for perineal wound infection after abdominoperineal resection of advanced lower rectal cancer. Ann Med Surg (Lond) 2017;15:14–8. DOI: 10.1016/j.amsu.2017.01.024
18. Pai V.D., Engineer R., Patil P.S. et al. Selective extra levator versus conventional abdomino perineal resection: experience from a tertiary-care center. J Gastrointest Oncol 2016;7(3):354–9. DOI: 10.21037/jgo.2015.11.05
19. Wiatrek R.L., Thomas J.S., Papaconstantinou H.T. Perineal wound complications after abdominoperineal resection. Clin Colon Rectal Surg 2008;21(1):76–85. DOI: 10.1055/s-2008-1055325
20. Mathes S.J., Bostwick J. A rectus abdominis myocutaneous flap to reconstruct abdominal wall defects. Br J Plast Surg 1977;30(4):282–3. DOI: 10.1016/0007-1226(77)90118-7
21. Mathes S.J., Nahai F. Classification of the vascular anatomy of muscles: experimental and clinical correlation. Plast Reconstr Surg 1981;67(2):177–87. PMID: 7465666
22. Kent I., Gilshtein H., Montorfano L. et al. Perineal reconstruction after extralevator abdominoperineal resection: differences among minimally invasive, open, or open with a vertical rectus abdominis myocutaneous flap approaches. Surgery 2021;170(5):1342–6. DOI: 10.1016/j.surg.2021.05.027
23. Black A.J., Karimuddin A., Raval M. et al The impact of laparoscopic technique on the rate of perineal hernia after abdominoperineal resection of the rectum. Surg Endosc 2021;35(6):3014–24. DOI: 10.1007/s00464-020-07746-7
24. Sunesen K.G., Buntzen S., Tei T. et al. Perineal healing and survival after anal cancer salvage surgery: 10-year experience with primary perineal reconstruction using the vertical rectus abdominis myocutaneous (VRAM) flap. Ann Surg Oncol 2009;16(1):68–77. DOI: 10.1245/s10434-008-0208-4
25. Kapur S.K., Butler C.E. Vertical rectus abdominis myocutaneous flap for perineal reconstruction. In: Flaps and Reconstructive Surgery, 2nd ed. Elsevier, 2017. Pp. 471–482.
26. Kim E., Fernando C., McCombie A. et al. Abdominal and perineal hernia rates following vertical rectus abdominis myocutaneous (VRAM) flap reconstruction – a supraregional experience. J Plast Reconstr Aesthet Surg 2022;75(4):1158–63. DOI: 10.1016/j.bjps.2021.11.002
27. Diener M.K., Voss S., Jensen K. et al. Elective midline laparotomy closure: the INLINE systematic review and meta-analysis. Ann Surg 2010;251(5):843–56. DOI: 10.1097/SLA.0b013e3181d973e4
28. Bosanquet D.C., Ansell J., Abdelrahman T. et al. Systematic review and meta-regression of factors affecting midline incisional hernia rates: analysis of 14 618 patients. PLoS One 2015;10(9):e0138745. DOI: 10.1371/journal.pone.0138745
29. Temperley H.C., Shokuhi P., O’Sullivan N.J. et al. Primary closure versus vertical rectus abdominis myocutaneous (VRAM) flap closure of perineal wound following abdominoperineal resection – a systematic review and meta-analysis. Ir J Med Sci 2024;193(1):123–32. DOI: 10.1007/s11845-024-03651-3
30. Pickrell K.L., Broadbent T.R., Masters F.W., Metzger J.T. Construction of a rectal sphincter and restoration of anal continence by transplanting the gracilis muscle: a report of four cases in children. Ann Surg 1952;135(6):853–62. DOI: 10.1097/00000658-195206000-00006
31. Graham J.B. Vaginal fistulas following radiotherapy. Surg Gynecol Obstet 1965;120:1019–30. PMID: 14269833
32. Orticochea M. A new method of total reconstruction of the penis. Br J Plast Surg 1972;25(4):347–66. DOI: 10.1016/s0007-1226(72)80077-8
33. Bartholdson L., Hulten L. Repair of persistent perineal sinuses by means of a pedicle flap of musculus gracilis. Case report. Scand J Plast Reconstr Surg 1975;9(1):74–6. DOI: 10.3109/02844317509022861
34. Coelho J.A.J., McDermott F.D., Cameron O. et al. Single center experience of bilateral gracilis flap perineal reconstruction following extra-levator abdominoperineal excision. Colorectal Dis 2019;21(6):910–6. DOI: 10.1111/codi.14654
35. Jenkins E., Humphrey H., Finan C. et al. Long-term follow-up of bilateral gracilis reconstruction following extra-levator abdominoperineal excision. J Plast Reconstr Aesthet Surg 2023;76:198–207. DOI: 10.1016/j.bjps.2022.10.025
36. Chong T.W., Balch G.C., Kehoe S.M. et al. Reconstruction of large perineal and pelvic wounds using gracilis muscle flaps. Ann Surg Oncol 2015;22:3738–44. DOI: 10.1245/s10434-015-4435-1
37. Johnstone M.S. Vertical rectus abdominis myocutaneous versus alternative flaps for perineal repair after abdominoperineal excision of the rectum in the era of laparoscopic surgery. Ann Plast Surg 2017;79(1):101–6. DOI: 10.1097/SAP.0000000000001137
38. Stein M.J., Karir A., Ramji M. et al. Surgical outcomes of VRAM versus gracilis flaps for the reconstruction of pelvic defects following oncologic resection. J Plast Reconstr Aesthet Surg 2019;72(4):565–71. DOI: 10.1016/j.bjps.2018.12.044
39. Eseme E.A., Scampa M., Viscardi J.A. et al. Surgical outcomes of VRAM versus gracilis flaps in vulvo-perineal reconstruction following oncologic resection: a proportional meta-analysis. Cancers (Basel) 2022;14(17):4300. DOI: 10.3390/cancers14174300
40. Singh M., Kinsley S., Huang A. et al. Gracilis flap reconstruction of the perineum: an outcomes analysis. J Am Coll Surg 2016;223(4):602–10. DOI: 10.1016/j.jamcollsurg.2016.06.383
41. Whitaker I.S., Karavias M., Shayan R. et al. The gracilis myocutaneous free flap: a quantitative analysis of the fasciocutaneous blood supply and implications for autologous breast reconstruction. PLoS One 2012;7(5):e36367. DOI: 10.1371/journal.pone.0036367
42. Coquerel-Beghin D., Milliez P.Y., Auquit-Auckbur I. et al. The gracilis musculocutaneous flap: vascular supply of the muscle and skin components. Surg Radiol Anat 2006 Dec;28(6):588-95. doi: 10.1007/s00276-006-0150-8
43. Thiele J.R., Weber J., Neeff H.P. et al. Reconstruction of perineal defects: a comparison of the myocutaneous gracilis and the gluteal fold flap in interdisciplinary anorectal tumor resection. Front Oncol 2020;10:668. DOI: 10.3389/fonc.2020.00668
44. Fricke A., Rassner M., Kiefer J. et al. Donor-site morbidity of free muscle and perforator flaps: comparison of the gracilis muscle flap and the anterolateral thigh flap. J Reconstr Micros 2017;33(7):526–32. DOI: 10.1055/s-0037-1602724
45. Purnell C.A., Lewis K.C., Mioton L.M. et al. Donor-site morbidity of medial and lateral thigh-based flaps: a comparative study. Plast Reconstr Surg 2016;4(11):e1012. DOI: 10.1097/GOX.0000000000001012
46. Baird W.L., Hester T.R., Nahai F., Bostwick J. Management of perineal wounds following abdominoperineal resection with inferior gluteal flaps. Arch Surg 1990;125(11):1486–9. DOI: 10.1001/archsurg.1990.01410230080014
47. Davison E., Allan A.Y., Kang N. The use of gluteus maximus to restore the function of the pelvic diaphragm in the reconstruction of the pelvic outlet after abdomino-perineal resection: a case series. Eur J Plast Surg 2023;46:1219–25. DOI: 10.1007/s00238-023-02127-4
48. Rubio G.A., Askari M. Bilateral gluteus maximus myocutaneous flap. In: Eds. T.A. Tran, Z. Panthaki, J. Hoballah, S. Thaller. Operative dictations in plastic and reconstructive surgery. Cham: Springer, 2017. 150 p. DOI: 10.1007/978-3-319-40631-2_150
49. Gultekin S., Gartrell R., Lu L. et al. Outcomes of perineal reconstruction with inferior gluteal artery myocutaneous flaps and primary closure following abdominoperineal resection. ANZ J Surg 2022;92(11):2968–73. DOI: 10.1111/ans.17769
50. Bowers C., Chandrasekar B., Dargan D. et al. Partial myocutaneous gluteal flap for perineal reconstruction of extralevator abdominoperineal defects: a single surgeon series of 49 cases in 8 years, and a modification of the technique. J Plast Reconstr Aesth Surg 2022;75(1):125–36. DOI: 10.1016/j.bjps.2021.06.007
51. Faur I.F., Clim A., Dobrescu A. et al. VRAM flap for pelvic floor reconstruction after pelvic exenteration and abdominoperineal excision. J Pers Med 2023;13:1711. DOI: 10.3390/jpm13121711
52. Horch R.E., Hohenberger W., Eweida A. et al. A hundred patients with vertical rectus abdominis myocutaneous (VRAM) flap for pelvic reconstruction after total pelvic exenteration. Int J Colorectal Dis 2014;29:813–23. DOI: 10.1007/s00384-014-1868-0
53. Gielen A.H.C., Colier E., Qiu S.S. et al. Surgical outcomes of gluteal VY plasty after extensive abdominoperineal resection or total pelvic exenteration: research highlight. Langenbeck’s Arch Surg 2023;408:157. DOI: 10.1007/s00423-023-02896-3
54. Haapamaki M.M., Pihlgren V., Lundberg O. et al. Physical performance and quality of life after extended abdominoperineal excision of rectum and reconstruction of the pelvic floor with gluteus maximus flap. Dis Colon Rectum 2011;54(1):101–6. DOI: 10.1007/DCR.0b013e3181fce26e
55. Hodea F.-V., Hariga C.-S., Bordeanu-Diaconescu E.-M. et al. Assessing donor site morbidity and impact on quality of life in free flap microsurgery: an overview. Life 2025;15:36. DOI: 10.3390/life15010036
56. Sharabiany S., van Dam J.J.W., Sparenberg S. et al. A comparative multicenter study evaluating gluteal turnover flap for wound closure after abdominoperineal resection for rectal cancer. Tech Coloproctol 2021;25(10):1123–32. DOI: 10.1007/s10151-021-02496-7
57. Sharabiany S., Blok R.D., Lapid O. et al. Perineal wound closure using gluteal turnover flap or primary closure after abdominoperineal resection for rectal cancer: study protocol of a randomised controlled multicentre trial (BIOPEX-2 study). BMC Surg 2020;20(1):164. DOI: 10.1186/s12893-020-00823-7
58. Chavan R., Saklani A.P., Desouza A.L. et al. V-Y gluteal advancement fasciocutaneous flap for reconstruction of perineal defects after surgery for anorectal cancers: a single-center experience. Indian J Surg Oncol 2021;12:241–5. DOI: 10.1007/s13193-021-01311-x
59. Riva C.G., Kelly M.E., Vitellaro M. et al. A comparison of surgical techniques for perineal wound closure following perineal excision: a systematic review and network meta-analysis. Tech Coloproctol 2023;27:1351–66. DOI: 10.1007/s10151-023-02868-1
60. Smart N.J., Pathak S., Boorman P., Daniels I.R. Synthetic or biological mesh use in laparoscopic ventral mesh rectopexy: a systematic review. Colorectal Dis 2013;15(6):650–4. DOI: 10.1111/codi.12219
61. Giugale L.E., Baranski L.A., Meyn L.A. et al. Preoperative pelvic floor injections with bupivacaine and dexamethasone for pain control after vaginal prolapse repair: a randomized controlled trial. Obstet Gynecol 2021;137(1):21–31. DOI: 10.1097/AOG.0000000000004205
62. Tao Y., Han J.G., Wang Z.J. Comparison of perineal morbidity between biologic mesh reconstruction and primary closure following extralevator abdominoperineal excision: a systematic review and meta-analysis. Int J Colorectal Dis 2021;36(5):893–902. DOI: 10.1007/s00384-020-03820-7
63. Ahmad N.Z., Abbas M.H., Al-Naimi N.M.A.B., Parvaiz A. Meta-analysis of biological mesh reconstruction versus primary perineal closure after abdominoperineal excision of rectal cancer. Int J Colorectal Dis 2021;36(3):477–92. DOI: 10.1007/s00384-020-03827-0
64. Maspero M., Heilman J., Otero Piñeiro A. et al. Techniques of perineal hernia repair: a systematic review and meta-analysis. Surgery 2023;173(2):312–21. DOI: 10.1016/j.surg.2022.10.022
65. Shi H., Wang R., Dong W. et al. Synthetic versus biological mesh in ventral hernia repair and abdominal wall reconstruction: a systematic review and recommendations from evidence-based medicine. World J Surg 2023;47:2416–24. DOI: 10.1007/s00268-023-07067-5
66. Rampado S., Geron A., Pirozzolo G. et al. Cost analysis of incisional hernia repair with synthetic mesh and biological mesh: an Italian study. Updates Surg 2017;69:375–81. DOI: 10.1007/s13304-017-0453-9