Lymphatic Function of the Lower Limb after Groin Dissection for Vulvar Cancer and Reconstruction with Lymphatic SCIP Flap

Anna Amelia Caretto, Gianluigi Stefanizzi, Simona Maria Fragomeni, Alex Federico, Luca Tagliaferri, Valentina Lancellotta, Giovanni Scambia, Stefano Gentileschi, Anna Amelia Caretto, Gianluigi Stefanizzi, Simona Maria Fragomeni, Alex Federico, Luca Tagliaferri, Valentina Lancellotta, Giovanni Scambia, Stefano Gentileschi

Abstract

Inguinofemoral lymphadenectomy, frequently performed for vulvar cancer, is burdened with substantial immediate and long-term morbidity. One of the most disabling treatment-related sequelae is lower limb lymphedema (LLL). The present study aims to describe the wound complications and the severity of LLL in patients who have undergone groin dissection for vulvar cancer and immediate inguinal reconstruction with the Lymphatic Superficial Circumflex Iliac Perforator flap (L-SCIP). We retrospectively reviewed the data of patients who underwent bilateral groin dissection and unilateral inguinal reconstruction with the L-SCIP. The presence and severity of postoperative LLL during the follow-up period were assessed by lymphoscintigraphy and limbs' volume measurement. In addition, immediate complications at the level of the inguinal area were registered. The changes between preoperative and postoperative limb volumes were analyzed by Student's t test. p values < 0.05 were considered significant. Thirty-one patients were included. The mean variation of volume was 479 ± 330 cc3 in the side where groin reconstruction had been performed, and 683 ± 425 cc3 in the contralateral side, showing smaller variation in the treated side (p = 0.022). Lymphoscintigraphy confirmed the clinical findings. Based on our results, inguinal reconstruction with L-SCIP performed at the same time of groin dissection in patients treated for vulvar cancer can provide a significant protective effect on LLL.

Keywords: SCIP flap; groin dissection; gynecologic cancer; inguinal lymphadenectomy; inguinofemoral lymphadenectomy; lymphatic flap; lymphedema; lymphedema prevention; personalized medicine; vulvar cancer.

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(a) Frontal and posterior pre-operative view of an 80-year-old woman undergoing surgery for vulvar cancer, involving bilateral groin dissection and reconstruction of the right inguinal area with L-SCIP. (b) Frontal and posterior view of the same patient one year after surgery. The black arrow indicates the flap skin island at the level of the right groin. The patient shows moderate swelling of the left lower limb (untreated side) and mild swelling of the right limb. (c) The same patient, 4 years after surgery, shows severe swelling of the left lower limb and no swelling of the right limb.
Figure 2
Figure 2
(a) Frontal and posterior pre-operative view of a 77-year-old woman undergoing surgery for vulvar cancer, involving bilateral groin dissection and reconstruction of the right inguinal area with L-SCIP. (b) Frontal and posterior view of the same patient one year after surgery. The black arrow indicates the flap skin island at the level of the right groin. The patient shows moderate swelling of the left lower limb (untreated side) and mild swelling of the right lower limb. (c) The same patient, 5 years after surgery, shows severe swelling of the left lower limb and mild swelling of the right lower limb.
Figure 3
Figure 3
(a) Wound breakdown after groin dissection and reconstruction with L-SCIP flap at the level of the left inguinal area. The white arrow indicates the buried part of the flap, showing granulation tissue after VAC-therapy. The presence of the flap prevented femoral vessels exposure. (b) Postoperative view of the same patient after debridement and primary closure of the wound dehiscence.
Figure 4
Figure 4
This picture shows the two patients of our series affected by postoperative infection. (a,b) Anterior and posterior view of a 57-year-old woman showing lymphangitis of the right lower limb (untreated side) involving the anterior and posterior surface of the thigh 3 months after bilateral groin dissection for vulvar cancer and reconstruction of the left inguinal area with L-SCIP. The black arrow indicates the skin island of the flap. This patient was healed by antibiotic therapy. (c) Postoperative fluid collection and infection at the level of the left inguinal area 1 month after bilateral groin dissection and reconstruction of the right inguinal area with L-SCIP. The black arrow indicates the skin island of the flap in the right groin. This patient was healed by antibiotic therapy and repeated fluid aspiration.

References

    1. Stehman F.B., Bundy B.N., Dvoretsky P.M., Creasman W.T. Early stage I carcinoma of the vulva treated with ipsilateral superficial inguinal lymphadenectomy and modified radical hemivulvectomy: A prospective study of the Gynecologic Oncology Group. Obstet. Gynecol. 1992;79:490–497.
    1. Burke T.W., Levenback C., Coleman R.L., Morris M., Silva E.G., Gershenson D.M. Surgical therapy of T1 and T2 vulvar carcinoma: Further experience with radical wide excision and selective inguinal lymphadenectomy. Gynecol. Oncol. 1995;57:215–220. doi: 10.1006/gyno.1995.1128.
    1. Hinten F., Van den Einden L.C.G., Hendriks J.C.M., Van der Zee A.G.J., Bulten J., Massuger L.F.A.G., Van de Nieuwenhof H.P., De Hullu J.A. Risk factors for short- and long-term complications after groin surgery in vulvar cancer. Br. J. Cancer. 2011;105:1279–1287. doi: 10.1038/bjc.2011.407.
    1. Manci N., Marchetti C., Esposito F., De Falco C., Bellati F., Giorgini M., Angioli R., Panici P.B. Inguinofemoral lymphadenectomy: Randomized trial comparing inguinal skin access above or below the inguinal ligament. Ann. Surg. Oncol. 2009;16:721–728. doi: 10.1245/s10434-008-0216-4.
    1. Madhuri T.K., Tailor A., Butler-Manuel S. Use of neutral plasma coagulation in groin node dissection for vulvar malignancy: A novel technique. Cancer Manag. Res. 2011;3:253–255. doi: 10.2147/CMAR.S19467.
    1. Judson P.L., Jonson A.L., Paley P.J., Bliss R.L., Murray K.P., Downs L.S., Jr., Boente M.P., Argenta P.A., Carson L.F. A prospective, randomized study analyzing sartorius transposition following inguinal-femoral lymphadenectomy. Gynecol. Oncol. 2004;95:226–230. doi: 10.1016/j.ygyno.2004.07.022.
    1. Gupta M.K., Patel A.P., Master V.A. Technical considerations to minimize complications of inguinal lymph node dissection. Transl. Androl. Urol. 2017;6:820–825. doi: 10.21037/tau.2017.06.06.
    1. Yao K., Zou Z.J., Li Z.S., Zhou F.J., Qin Z.K., Liu Z.W., Li Y.H., Han H. Fascia lata preservation during inguinal lymphadenectomy for penile cancer: Rationale and outcome. Urology. 2013;82:642–647. doi: 10.1016/j.urology.2013.05.021.
    1. Kumar V., Sethia K.K. Prospective study comparing video-endoscopic radical inguinal lymph node dissection [VEILND] with open radical ILND [OILND] for penile cancer over an 8-year period. BJU Int. 2017;119:530–534. doi: 10.1111/bju.13660.
    1. Abbas S., Seitz M. Systematic review and meta-analysis of the used surgical techniques to reduce leg lymphedema following radical inguinal nodes dissection. Surg. Oncol. 2011;20:88–96. doi: 10.1016/j.suronc.2009.11.003.
    1. Gentileschi S., Caretto A.A., Tagliaferri L., Salgarello M., Peris K. Skin cancer plastic surgery during the COVID-19 pandemic. Eur. J. Surg. Oncol. 2020;46:1194–1195. doi: 10.1016/j.ejso.2020.04.048.
    1. Benoit L., Boichot C., Cheynel N., Arnould L., Chauffert B., Cuisenier J., Fraisse J. Preventing lymphedema and morbidity with an omentum flap after ilioinguinal lymph node dissection. Ann. Surg. Oncol. 2005;12:793–799. doi: 10.1245/ASO.2005.09.022.
    1. Rodriguez J.R., Fuse Y., Yamamoto T. Microsurgical Strategies for Prophylaxis of Cancer-Related Extremity Lymphedema: A Comprehensive Review of the Literature. J. Reconstr. Microsurg. 2020;36:471–479. doi: 10.1055/s-0040-1710047.
    1. Gentileschi S., Servillo M., Garganese G., Fragomeni S., De Bonis F., Cina A., Scambia G., Salgarello M. The lymphatic superficial circumflex iliac vessels deep branch perforator flap: A new preventive approach to lower limb lymphedema after groin dissection-preliminary evidence. Microsurgery. 2017;37:564–573. doi: 10.1002/micr.30142.
    1. Gentileschi S., Caretto A.A., Servillo M., Stefanizzi G., Alberti C., Garganese G., Fragomeni S.M., Federico A., Tagliaferri L., Moroni R., et al. Feasibility, indications and complications of SCIP flap for reconstruction after extirpative surgery for vulvar cancer. J. Plast. Reconstr. Aesthet. Surg. 2021;13:1748. doi: 10.1016/j.bjps.2021.11.005.
    1. Bracaglia R., D’Ettorre M., Gentileschi S., Mingrone G., Tambasco D. “Kris knife” brachioplasty after bariatric surgery and massive weight loss. Aesthet. Plast. Surg. 2013;37:640–642. doi: 10.1007/s00266-013-0101-9.
    1. D’Ettorre M., Gniuli D., Bracaglia R., Tambasco D., Mingrone G., Gentileschi S., Massi G. Micro- and macroscopic structural modification of subcutaneous adipose tissue after bariatric surgery. Aesthet. Plast. Surg. 2012;36:213–214. doi: 10.1007/s00266-011-9762-4.
    1. Gentileschi S., Bracaglia R., Garganese G., Gallucci V., Corrado G., Pacelli F., Scambia G. Immediate definitive prosthetic reconstruction in patients with ptotic breasts. Ann. Plast. Surg. 2013;70:144–148. doi: 10.1097/SAP.0b013e3182367bfd.
    1. Gerken A.L.H., Herrle F., Jakob J., Wei ß C., Rahbari N.N., Nowak K., Kar C. Definition and severity grading of postoperative lymphatic leakage following inguinal lymph node dissection. Langenbecks Arch. Surg. 2020;405:697–704. doi: 10.1007/s00423-020-01927-7.
    1. Tartaglione G., Rubello D. The evolving methodology to perform limb lymphoscintigraphy: From rest to exercise acquisition protocol. Microvasc. Res. 2010;80:540–544. doi: 10.1016/j.mvr.2010.09.003.
    1. Gentileschi S., Servillo M., Albanese R., De Bonis F., Tartaglione G., Salgarello M. Lymphatic mapping of the upper limb with lymphedema before lymphatic supermicrosurgery by mirroring of the healthy limb. Microsurgery. 2017;37:881–889. doi: 10.1002/micr.30247.
    1. Gentileschi S., Servillo M., Salgarello M. Supramicrosurgical lymphatic-venous anastomosis for postsurgical subcutaneous lymphocele treatment. Microsurgery. 2015;35:565–568. doi: 10.1002/micr.22478.
    1. Executive Committee of the International Society of Lymphology The diagnosis and treatment of peripheral lymphedema: 2020 Consensus Document of the International Society of Lymphology. Lymphology. 2020;53:3–19.
    1. Kleinhans E., Baumeister R.G., Hahn D., Siuda S., Bull U., Moser E. Evaluation of transport kinetics in lymphoscintigraphy: Follow-up study in patients with transplanted lymphatic vessels. Eur. J. Nucl. Med. 1985;10:349–352. doi: 10.1007/BF00251310.
    1. Latchford S., Casley-Smith J.R. Estimating limb volumes and alterations in peripheral edema from circumferences measured at different intervals. Lymphology. 1997;30:161–164.
    1. Gentileschi S., Servillo M., De Bonis F., Albanese R., Pino V., Mangialardi M.L., Valente I., Garganese G., Scambia G., Salgarello M., et al. Radioanatomical Study of the Pedicle of the Superficial Circumflex Iliac Perforator Flap. J. Reconstr. Microsurg. 2019;35:669–676. doi: 10.1055/s-0039-1693144.
    1. Tagliaferri L., Di Stefani A., Schinzari G., Fionda B., Rossi E., Del Regno L., Gentileschi S., Federico F., Valentini V., Tortora G., et al. Skin cancer triage and management during COVID-19 pandemic. J. Eur. Acad. Dermatol. Venereol. 2020;34:1136–1139. doi: 10.1111/jdv.16529.
    1. Santonocito C., Concolino P., Lavieri M.M., Ameglio F., Gentileschi S., Capizzi R., Rocchetti S., Amerio P., Castagnola M., Zuppi C., et al. Comparison between three molecular methods for detection of blood melanoma tyrosinase mRNA. Correlation with melanoma stages and S100B, LDH, NSE biochemical markers. Clin. Chim. Acta. 2005;362:85–93. doi: 10.1016/j.cccn.2005.05.031.
    1. Baas P.C., Schraffordt Koops H., Hoekstra H.J., van Bruggen J.J., van der Weele L.T., Oldhoff J. Groin dissection in the treatment of lower-extremity melanoma. Short-term and long-term morbidity. Arch. Surg. 1992;127:281–286. doi: 10.1001/archsurg.1992.01420030043008.
    1. Serpell J.W., Carne P.W., Bailey M. Radical lymph node dissection for melanoma. ANZ J. Surg. 2003;73:294–299. doi: 10.1046/j.1445-2197.2003.t01-1-02622.x.
    1. de Vries M., Vonkeman W.G., van Ginkel R.J., Hoekstra H.J. Morbidity after inguinal sentinel lymph node biopsy and completion lymph node dissection in patients with cutaneous melanoma. Eur. J. Surg. Oncol. 2006;32:785–789. doi: 10.1016/j.ejso.2006.05.003.
    1. Stuiver M.M., Westerduin E., ter Meulen S., Vincent A.D., Nieweg O.E., Wouters M.W. Surgical wound complications after groin dissection in melanoma patients-a historical cohort study and risk factor analysis. Eur. J. Surg. Oncol. 2014;40:1284–1290. doi: 10.1016/j.ejso.2014.01.019.
    1. Butler C.E. Treatment of refractory donor-site seromas with percutaneous instillation of fibrin sealant. Plast. Reconstr. Surg. 2006;117:976–985. doi: 10.1097/01.prs.0000200619.26559.c3.
    1. Teiche P.E., Pauer W., Schmid N. Use of talcum in sclerotherapy of pelvic lymphoceles. Tech. Urol. 1999;5:52–53.
    1. Hiramatsu Y., Yoshimatsu K., Yokomizo H., Fujimoto T., Otani T., Matsumoto A., Osawa G., Watanabe K., Umehara A., Isohata N., et al. A case of successful treatment with OK-432 administration into lymphatic cyst formed after resection of rectal cancer. Gan Kagaku Ryoho. 2008;35:2162–2164.
    1. Huang J., Yu N., Wang X., Long X. Incidence of lower limb lymphedema after vulvar cancer: A systematic review and meta-analysis. Medicine. 2017;96:e8722. doi: 10.1097/MD.0000000000008722.
    1. Tagliaferri L., Lancellotta V., Casà C., Fragomeni S.M., Ferioli M., Gentileschi S., Caretto A.A., Corrado G., Gui B., Colloca G.F., et al. The Radiotherapy Role in the Multidisciplinary Management of Locally Advanced Vulvar Cancer: A Multidisciplinary VulCan Team Review. Cancers. 2021;13:5747. doi: 10.3390/cancers13225747.
    1. Bracaglia R., D’Ettorre M., Gniuli D., Gigliofiorito P., Gentileschi S., Mingrone G. Morbidly obese patients undergoing bariatric and body contouring surgery: Psychological evaluation after treatments. J. Plast. Reconstr. Aesthet. Surg. 2011;64:1246–1248. doi: 10.1016/j.bjps.2011.04.001.
    1. Ferro M., Deodato F., Macchia G., Gentileschi S., Cilla S., Torre G., Padula G.D., Nuzzo M., Massaccesi M., Valentini V., et al. Short-course radiotherapy in elderly patients with early stage non-melanoma skin cancer: A phase II study. Cancer Investig. 2015;33:34–38. doi: 10.3109/07357907.2014.998835.
    1. Bracaglia R., Tambasco D., D’Ettorre M., Gentileschi S. “Inverted-Y”: A modified vest-over-pants abdominoplasty pattern following bariatric surgery. Aesthet. Plast. Surg. 2012;36:1179–1185. doi: 10.1007/s00266-012-9956-4.
    1. Bracaglia R., D’Ettorre M., Gentileschi S., Tambasco D. “Vest over pants” abdominoplasty in post-bariatric patients. Aesthet. Plast. Surg. 2012;36:23–27. doi: 10.1007/s00266-011-9767-z.
    1. Micheletti L., Bogliatto F., Massobrio M. Groin lymphadenectomy with preservation of femoral fascia: Total inguinofemoral node dissection for treatment of vulvar carcinoma. World J. Surg. 2005;29:1268–1276. doi: 10.1007/s00268-005-7745-9.
    1. Catalona W.J. Modified inguinal lymphadenectomy for carcinoma of the penis with preservation of saphenous vein: Technique and preliminary results. J. Urol. 1988;140:836. doi: 10.1016/S0022-5347(17)41838-6.
    1. Sommariva A., Pasquali S., Rossi C.R. Video endoscopic inguinal lymphadenectomy for lymph node metastasis from solid tumors. Eur. J. Surg. Oncol. 2015;41:274–281. doi: 10.1016/j.ejso.2014.10.064.
    1. Taussig F.J. Cancer of the vulva: An analysis of 155 cases [1911e1940] Am. J. Obstet. Gynecol. 1940;40:764–779. doi: 10.1016/S0002-9378(15)30802-4.
    1. Daseler E.H., Anson B.H., Reimann A.F. Radical excision of the inguinal and iliac lymph glands: A study based upon 450 anatomical dissections and upon supportive clinical observations. Surg. Gynecol. Obstet. 1948;87:679–694.
    1. Way S. Carcinoma of the vulva. Am. J. Obstet. Gynecol. 1960;79:692–697. doi: 10.1016/0002-9378(60)90626-8.
    1. Rouzier R., Haddad B., Dubernard G., Dubois P., Paniel B. Inguinofemoral dissection for carcinoma of the vulva: Effect of modifications of extent and technique on morbidity and survival. J. Am. Coll Surg. 2003;196:442–450. doi: 10.1016/S1072-7515(02)01895-1.
    1. Jorgensen M.G., Toyserkani N.M., Thomsen J.B., Sorensen J.A. Surgical site infection following lymph node excision indicates susceptibility for lymphedema: A retrospective cohort study of malignant melanoma patients. J. Plast. Reconstr. Aesthet. Surg. 2018;71:590–596. doi: 10.1016/j.bjps.2017.11.026.
    1. Ravi R. Morbidity following groin dissection for penile carcinoma. Br. J. Urol. 1993;72:941–945. doi: 10.1111/j.1464-410X.1993.tb16304.x.
    1. Bracaglia R., D’Ettorre M., Gentileschi S., Tambasco D. Was the surgeon a satisfactory informant? How to minimize room for claims. Aesthet. Surg. J. 2014;34:632–635. doi: 10.1177/1090820X14528504.
    1. Nirmal T.J., Gupta A.K., Kumar S., Devasia A., Chacko N., Kekre N.S. Tensor fascia lata flap reconstruction following groin dissection: Is it worthwhile? World J. Urol. 2011;29:555–559. doi: 10.1007/s00345-011-0706-z.
    1. 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;15:373–380. doi: 10.4048/jbc.2012.15.4.373.
    1. Gentileschi S., Servillo M., Garganese G., Simona F., Scambia G., Salgarello M. Versatility of pedicled anterolateral thigh flap in gynecologic reconstruction after vulvar cancer extirpative surgery. Microsurgery. 2017;37:516–524. doi: 10.1002/micr.30077.
    1. Gentileschi S., Servillo M., Garganese G., Fragomeni S., De Bonis F., Scambia G., Salgarello M. Surgical therapy of vulvar cancer: How to choose the correct reconstruction? J. Gynecol. Oncol. 2016;27:e60. doi: 10.3802/jgo.2016.27.e60.
    1. Yamamoto T., Daniel B.W., Rodriguez J.R., Kageyama T., Sakai H., Fuse Y., Tsukuura R., Yamamoto N. Radical reduction and reconstruction for male genital elephantiasis: Superficial circumflex iliac artery perforator [SCIP] lymphatic flap transfer after elephantiasis tissue resection. J. Plast. Reconstr. Aesthet. Surg. 2021;5:1748. doi: 10.1016/j.bjps.2021.08.011.
    1. Di Sipio T., Rye S., Newman B., Hayes S. Incidence of unilateral arm lymphoedema after breast cancer: A systematic review and meta-analysis. Lancet Oncol. 2013;14:500–515. doi: 10.1016/S1470-2045(13)70076-7.
    1. Jorgensen M.G., Toyserkani N.M., Sorensen J.A. The effect of prophylactic lymphovenous anastomosis and shunts for preventing cancer-related lymphedema: A systematic review and meta-analysis. Microsurgery. 2018;38:576–585. doi: 10.1002/micr.30180.
    1. Boccardo F., Casabona F., De Cian F., Friedman D., Villa G., Bogliolo S., Ferrero S., Murelli F., Campisi C. Lymphedema microsurgical preventive healing approach: A new technique for primary prevention of arm lymphedema after mastectomy. Ann. Surg. Oncol. 2009;16:703–708. doi: 10.1245/s10434-008-0270-y.
    1. Kaciulyte J., Garutti L., Spadoni D., Velazquez-Mujica J., Losco L., Ciudad P., Marcasciano M., Lo Torto F., Casella D., Ribuffo D., et al. Genital Lymphedema and How to Deal with It: Pearls and Pitfalls from over 38 Years of Experience with Unusual Lymphatic System Impairment. Medicina. 2021;57:1175. doi: 10.3390/medicina57111175.
    1. Lo Torto F., Kaciulyte J., Mori F.L., Frattaroli J.M., Marcasciano M., Casella D., Cigna E., Losco L., Manrique O.J., Nicoli F., et al. Microsurgical lymphedema treatment: An objective evaluation of the quality of online information. J. Plast. Reconstr. Aesthet. Surg. 2021;74:637–640. doi: 10.1016/j.bjps.2020.11.033.
    1. Nacchiero E., Maruccia M., Vestita M., Elia R., Marannino P., Giudice G. Multiple lymphatic-venous anastomoses in reducing the risk of lymphedema in melanoma patients undergoing complete lymph node dissection. A retrospective case-control study. J. Plast. Reconstr. Aesthet. Surg. 2019;72:642–648. doi: 10.1016/j.bjps.2019.01.023.

Source: PubMed

3
Subscribe