Division of Plastic and Reconstructive Surgery, Department of Surgery, Keck School of Medicine of USC, Los Angeles, CA 90033, USA.
Correspondence Address: Dr. Alex K. Wong, Division of Plastic and Reconstructive Surgery, Department of Surgery, Keck School of Medicine of USC, 1510 San Pablo Street, Los Angeles, CA 90033, USA. E-mail: Alex.Wong@med.usc.edu
© The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
While amputation was traditionally the only option available for patients with sarcomas of the extremities, chemotherapy, radiation, and advances in microsurgical technique have allowed many patients to undergo limb-salvaging procedures. Given the low incidence and heterogeneity of these tumors, there is currently no standard treatment algorithm for limb reconstruction after large sarcoma resection. Thus, we systematically reviewed the various types of free tissue transfer used for the reconstruction of lower limbs after sarcoma resection. Techniques were described based on anatomic location. This literature review supports free tissue transfer as a safe and acceptable modality for reconstruction after sarcoma resection of the lower limb. It allows for the application of healthy vascularized tissue to the defect while also providing freedom of flap positioning. Flap choice is dependent on tumor and defect size, tissue type and function, as well as donor site availability.
Lower extremity, sarcoma, reconstruction
Soft tissue and bone sarcomas represent about 1% of all adult tumors, affecting 1.8-5 out of every 100,000 people annually. The lower limb is the most common site of sarcoma occurrence, representing 29%-40% of all cases[3,4]. Although amputation was traditionally the only option available for patients with sarcoma of the extremities, recent implementation of a multimodal treatment approach along with advancements in chemotherapy and microsurgical techniques has led to the influx of limb salvage therapy for these cancers[5,6]. Currently, wide tumor excision combined with adjuvant and or neo-adjuvant therapy is the standard of care for the successful treatment of sarcoma of the lower limbs.
Quite often, sarcoma excision results in large anatomical soft tissue deficits with resultant exposure of vital structures such as bones, tendons, and neurovascular bundles, necessitating complex soft tissue reconstruction with vascularized soft tissue transfer thus facilitating further treatments as well as maintaining or regaining structural function and integrity of the limb in question. To this end both pedicled and free tissue transfers have become a central component of lower extremity salvage after resection and chemo-radiation therapy. Recent data has shown that these complex reconstructions have provided faster recovery with adequate soft tissue reconstruction and maintenance of functionality of the limb[2,6-11].
Currently there is no standard treatment algorithm for limb reconstruction after large sarcoma resection. In part this due to the low incidence of these tumors as well as the heterogeneity of extremity sarcoma. This problem is further compounded by the multitude of neo-adjuvant modalities that are used to treat these tumors as well as the timing of the oncological resection. Hence a comprehensive reconstructive approach that maximizes the maintenance of function and aesthetics depends primarily on the location and size of the defects as well as the muscles, tendon, blood vessels and nerves that were extirpated. The goal of this literature review is to therefore outline various author reports published in the current literature describing the various types of free tissue transfer used for the reconstruction of the lower limbs after sarcoma resection.
The PubMed database was used to review literature describing free tissue coverage of the lower extremity following soft tissue sarcoma resection. The entire PubMed library was used dating to 2016. The following search terms were used: “Neoplasms, Connective and Soft Tissue” [Mesh] OR (“sarcoma” [MeSH Terms] OR “sarcoma” [All Fields]) AND (“lower extremity” [MeSH Terms] OR (“lower” [All Fields] AND “extremity”[All Fields]) OR “lower extremity” [All Fields]) AND (“free tissue flaps” [MeSH Terms] OR (“free”[All Fields] AND “tissue” [All Fields] AND “flaps” [All Fields]) OR “free tissue flaps” [All Fields]. All studies published in the English language were included. Articles were excluded if they met the following criteria: exclusively pediatric patients, cadaver subjects, pathology of the pelvic girdle, exclusively pathology related to trauma, pathology related to skin neoplasms, and studies exclusively describing pedicled flaps. Table 1 lists the studies included in this review. Table 2 describes the types of flaps used for lower extremity reconstruction by region.
|Abramson et al.||1997||Free tissue transfer + radiotherapy|
|Cordeiro et al.||1994||Free tissue transfer + bone reconstruction|
|Serletti et al.||1998||Free tissue transfer|
|Heiner et al.||1993||Free tissue transfer|
|Barner-Rasmussen et al.||2009||Free tissue transfer|
|Leow et al.||2005||Free tissue transfer + bone reconstruction|
|Momeni et al.||2011||Free tissue transfer|
|Muramatsu et al.||2011||Free tissue transfer|
|Ng et al.||2008||Free tissue transfer|
|Zbuchea||2016||Free tissue transfer|
|Nahabedian et al.||1999||Free tissue transfer|
|Vaienti et al.||2013||Free tissue transfer|
|Cadenelli et al.||2015||Free tissue transfer|
|Baxter et al.||2007||Free tissue transfer|
|Miyamoto et al.||2014||Free tissue transfer|
|Lee et al.||2004||Free tissue transfer + radiotherapy|
|Choudry et al.||2008||Free tissue transfer|
|Saito et al.||2010||Free tissue transfer + bone reconstruction|
|Zweifel-Schlatter et al.||2006||Free tissue transfer|
|Hong et al.||2005||Free tissue transfer|
|Weichman et al.||2015||Free tissue transfer|
|Agostini and Agostini||2009||Free tissue transfer|
|Cribb et al.||2010||Free tissue transfer|
|Brenner and Rammelt||2002||Free tissue transfer|
|Medina et al.||2014||Free tissue transfer|
|Struckmann et al.||2014||Free tissue transfer|
|Zaretski et al.||2004||Bone reconstruction|
|Capanna et al.||1993||Bone reconstruction|
|Beris et al.||2011||Bone reconstruction|
|Yajima and Tamai||1994||Bone reconstruction|
|Duffy et al.||2000||Bone reconstruction|
|Ruch and Koman||1997||Bone reconstruction|
|Mastorakos et al.||2002||Bone reconstruction|
|Enneking et al.||1993||Nerve reconstruction|
|Doi et al.||1998||Nerve reconstruction|
|Doi et al.||1999||Nerve reconstruction|
|Fortner et al.||1977||Vascular reconstruction|
|Tsukushi et al.||2008||Vascular reconstruction|
|Nishinari et al.||2015||Vascular reconstruction|
|Wortmann et al.||2017||Vascular reconstruction|
|Rosenthal et al.||1993||Radiotherapy|
|O’Sullivan et al.||2004||Radiotherapy|
|Baldini et al.||2013||Radiotherapy|
|Arbeit et al.||1987||Radiotherapy|
|Shiu et al.||1984||Radiotherapy|
|O’Sullivan et al.||2002||Radiotherapy|
|Cheng et al.||1996||Radiotherapy|
|Kunisada et al.||2002||Radiotherapy|
|Davis et al.||2005||Radiotherapy|
|Townley et al.||2013||Radiotherapy|
|Chao et al.||2012||Radiotherapy|
|Hidalgo et al.||1992||Radiotherapy|
|Brennan et al.||1987||Radiotherapy|
|Ormsby et al.||1989||Radiotherapy|
|Hidalgo and Carrasquillo||1992||Radiotherapy|
|Spierer et al.||2003||Radiotherapy|
|Sadrian et al.||2002||Radiotherapy|
|Pisters et al.||1996||Outcomes|
|Popov et al.||2000||Outcomes|
|Penna et al.||2011||Outcomes|
|Lopez et al.||2015||Outcomes|
Types of flaps used for lower extremity reconstruction based on region
|Authozr||Year||Regions described||Flaps described|
|Cordeiro et al.||1994||Thigh||LD|
|Knee and proximal leg||LD|
|Mid and distal leg||RA|
|Barner-Rasmussen et al.||2009||Foot||LD|
|Lower Leg||Radial forearm|
|Leow et al.||2005||Thigh||LD|
|Knee||RA (free + pedicled)|
|Middle third of the leg|
|Momeni et al.||2011||Lower leg||ALT|
|Muramatsu et al.||2011||Thigh||LD|
|Pedicled medial gastrocnemius|
|Ng et al.||2008||Lateral Posterior Thigh||ALT|
|Zbuchea et al.||2016||Knee||Lateral genicular artery flap|
|Cadenelli et al.||2015||Knee||Advancement propeller perforator ALT|
|Baxter et al.||2007||Knee||Gastrocnemius|
|Miyamoto et al.||2014||Knee||Deep inferior epigastric artery perforator flap|
|Lee et al.||2004||Thigh||RA|
|Choudry et al.||2008||Lower leg||Soleus|
|Saito et al.||2009||Ankle||LD|
|Composite LD + scapular bone|
|Free scapular flap|
|Zweifel-Schlatter et al.||2006||Tibia||Lateral arm fasciocutaneous flap|
|Scapular fasciocutaneous flap|
|Hong et al.||2005||Lower leg||ALT|
|Weichman et al.||2015||Foot||Adipofascial ALT|
|Cribb et al.||2010||Ankle||Radial forearm|
|Brenner et al.||2002||Foot||Fasciocutaneous radial forearm|
|Medina et al.||2014||Foot||Modified radial forearm fascial flap|
|Struckmann et al.||2014||Foot||Gracilis|
|Medial plantar artery|
|Zaretski et al.||2004||Femur||Free vascularized fibula flap ± allograft|
|Tibia||Free double-barreled fibula|
|Capanna et al.||1993||Femur||Free vascularized fibula flap + allograft|
|Beris et al.||2011||Femur||Free vascularized fibula ± allograft|
|Tibia||Free double-barreled fibula|
|Yajima and Tamai||1994||Femur||Twin-barrelled vascularized fibular graft|
|Duffy et al.||2000||Femur||Free vascularized fibula|
|Rush and Koman||1997||Tibia||Fibula-flexor halluces longus osteomuscular flap|
|Mastorakos et al.||2002||Tibia||LD|
|Doi et al.||1998||Lower leg||Gracilis + motor nerve|
|Doi et al.||1999||Thigh||LD + motor nerve|
|Lower leg||Gracilis + motor nerve|
Several factors must be taken into consideration when approaching reconstruction of the thigh. Primarily, malignant sarcomas of the femur are generally challenging to treat because radical resection of the tumor often requires simultaneous resection and reconstruction of the major femoral vessels. Tumor proximity to critical neurovascular structures is particularly of concern in the adductor compartment, where outcomes are generally poor, with high local recurrence rate, high complication rates and short long-term survival.
The first report of reconstruction of major vessels was by Fortner et al. for the treatment of seven patients with sarcoma involving the iliac and femoral vessels. In their study, 3 out of 7 patients underwent vascular reconstruction with polyester or vein grafts, resulting in less postoperative complications and edema compared to the remaining 4 patients who did not undergo vascular reconstruction. In a series by Muramatsu et al., 12 out of 14 patients requiring arterial reconstruction underwent femoropopliteal reconstruction using a contralateral greater saphenous vein (GSV) graft ranging from 12-30 cm, while the 2 who required femoroinguinal reconstruction received expanded polytetrafluoroethylene (ePTFE). Twelve of their 15 patients additionally required venous reconstruction of the superficial vein, deep femoral vein, and greater saphenous vein, which was also done using a GSV or ePTFE graft. Of these patients, 6 had received free latissimus dorsi flaps, while the remaining patients received pedicled flaps. In the patients who were reconstructed using free flaps, the only complications were leg edema and mild lymphedema, which the authors attributed to ischemic reperfusion or venous/lymphatic insufficiency. The use of a myocutaneous flap in combination with an autologous vein graft also results in decreased postoperative infection rates, treatment of lymphedema and fistula, and increased graft patency rates.
Aesthetically, reconstruction of the thigh requires a large flap with muscle bulk that can eliminate dead space while providing adequate contour. The use of a free rectus abdominis flap has been reported to be particularly successful for this purpose[6,10]. The latissimus dorsi flap, which is thin, large with a long vascular pedicle, ± neurotization has also been used for large defects of the thigh[6,10]. The use of the anterior lateral thigh (ALT) flap for large thigh defects, particularly of the posterior thigh, has also been reported.
Obtaining adequate soft tissue coverage of the knee remains challenging for many plastic surgeons, not only because of the biomechanics of the knee, but also due to exposure of vital structures as well as the joint space[16-18]. Rotational muscle flaps or myocutaneous flaps such as gastrocnemius or reverse anterior lateral thigh flaps have been the mainstay for the reconstruction of tumors in this location. These flaps usually have low donor - site morbidity. However more complex defects may require the use of free tissue transfer. In these cases the deep-seated recipient popliteal vessels of the knee can make microvascular anastomosis difficult, an autologous vein graft loop can be used and the distal SFA and SFV can be used as recipient vessels if there is an extended field of neoadjuvant radiation.
Multiple donor sites have been successful used in free flap coverage of knee defects. These include latissimus dorsi, rectus abdominis, and scapula flaps. When there is a large contour defect in the popliteal fossa that does not require much filling of the muscular space, Leow et al. have also described the use of a free mini-transverse rectus abdominis (TRAM) myocutaneous flap.
In many cases where complex reconstruction of the knee region is needed, salvage of the popliteal artery, which can often be involved in the disease process, becomes critical. This has traditionally been accomplished using a combination of a local gastrocnemius flap with an interpositional vein graft. However, Miyamoto et al. described two cases of successful one-stage reconstruction of complex knee defects including the popliteal artery using a free flow-through ALT flap. Although the use of a deep epigastric artery perforator flap has also been used for these situations, this flap is often too bulky and provides a less aesthetic option.
In the distal leg, dead-space obliteration is generally not a concern and the use of bulky musculocutaneous flaps, such as TRAM flaps, can result in significant contour deformities. As a solution, several authors describe the ALT flap as a preferred method for distal lower extremity defects following sarcoma resection, given the easy ability to reshape the flap[11,22]. In a series by Barner-Rasmussen et al., 73 patients with soft tissue tumors located predominantly in the distal leg received 75 free-flap procedures with a 95% flap survival rate and a 97% limb salvage rate. A majority of the flaps used were latissimus dorsi flaps (72%) and ALT flaps (12%). The rectus abdominis and latissimus dorsi flaps as well as free scapula flaps have been described for this region by Cordeiro et al. with an overall success rate close to 90%. Other flaps commonly used in the lower leg are the radial forearm flap, gracilis flap, tensor fascia lata flap, and fibula flap.
Several factors must be taken into account when reconstructing oncologic defects of the ankle and foot. In addition to considering the need for adjuvant radiotherapy, the soft tissue of this area is very thin and must provide a smooth surface for the tendons underneath. Traditional flaps used to cover defects of the distal third of the foot have included the rectus abdominis, latissimus dorsi, gracilis, and rectus femoris flaps. Free scapular and ALT flaps have also been used with adequate results. Muscle flaps provide excellent coverage, and while they are initially quite bulky for this region, they flatten significantly with time as they atrophy. Thus fasciocutaneous flaps have been described as a successful alternative with superior contouring[25,26].
Although the versatile ALT flap has also been used in the past, the amount of adipose deposit in this flap can be addressed by primary thinning via a supra-fascial dissection or secondary procedure using mechanical lipectomy. A third approach was described by Weichman et al. where they reported a series using an adipofascial ALT flap with a split thickness skin graft to cover dorsal foot defects on three patients after sarcoma resection. In addition to its superior contour, the fascial plexus of the adipofacial flap is stronger than that of the thinned ALT, and the extra fascia can be used to reconstruct local tendons.
The fasciocutaneous radial forearm flap has also been reported to have good results in reconstruction of the foot and ankle, providing normal contour and durable stability[29,30]. Unfortunately however, it can result in significant donor-site morbidity and occasional bulkiness. Thus, Medina et al. proposed a using a radial forearm fascial free flap for dorsal foot defects and reported its use in a patient with wound dehiscence following sarcoma resection and radiation therapy, with no resulting complications or contour defects. Another flap that can provide excellent results in the ankle if the size of the defect permits is the temporalis fascia free flat.
In contrast to the dorsum of the foot, reconstruction of the weight-bearing sole of the foot requires strong soft tissue that is resistant to pressure, weight, and stress. Struckmann et al. covered heel defects in 12 patients with a variety of free flaps including latissimus dorsi, gracilis, lateral arm, ALT, and parascapular free flaps. They found that myofasciocutaneous flaps had the best functional results, followed by adipocutaneous and muscle flaps with split-thickness skin grafts, while fasciocutaenous flaps had the lowest outcomes. However there was no significant difference between specific flap type.
For bone reconstruction, the flap is chosen based on specific patient needs including location of the lesion, level of activity of the individual, need for adjuvant therapy, and growth potential. The most commonly harvested bone flap is the free fibula flap, which can be used in three major reconstructive ways: traditional vascularized fibula flap, vascularized fibula flap combined with an allograft, and vascularized double-barreled fibula.
The traditional vascularized fibula flap as a bony replacement is indicated in areas that endure lighter loads or when reinforcement of weak areas is needed. The free fibula flap with an allograft, which was first described by Capanna et al. in 1993, involves the insertion of the vascularized fibular graft into the intramedullary canal of an allograft, which is then used to fill the bony defect. This flap provides strength and stability early on, making it ideal for anatomical locations where high forces are applied. For areas that must withstand intermediate stress loads, the free double-barreled fibula flap is typically chosen. This flap allows for twice the volume of the fibula to be substituted with the same number of microvascular anastomoses. It is generally indicated for femur and proximal tibia reconstruction as well as reconstruction of the tibia of younger patients who are physically active[35,36]. Additionally for radiation-induced long-bone fractures, the vascularized fibula can also be osteotomized longitudinally and used as an onlay graft. The fibula can also be harvested as a combined osteocutaneous flap for composite defects of the lower extremity[6,10].
An additional osteomuscular flap that has been reported to have good outcomes for coverage after distal tibial osteosarcoma resection is the fibula-flexor hallucis longus osteomuscular flap. Saito et al. also describe adequate aesthetic and functional outcomes with the use of a free composite graft of latissimus dorsi and scapular bone as well as a free osteocutaneous scapular-parascapular flap. Finally, in cases of allograft bone reconstruction of the lower extremities, soft tissue flap coverage using latissimis dorsi and rectus abdominis flaps has been shown to maximize limb salvage.
Radical sarcoma resection often leads not only to extensive soft tissue defects, but also suboptimal degrees of functionality secondary to damage to surrounding nerves. Functional outcomes following conventional limb-sparing procedures reported in the literature have been close to 75%.
Reinnervated muscle transfer, which has been extremely valuable in a number of reconstructive procedures, may also become necessary in patients with sarcoma resection. Doi et al. describe a patient with synovial sarcoma of the anterior compartment of the lower leg who received a gracilis flap to cover the defect. The motor nerve of the gracilis was sutured to the motor branch of the tibialis anterior muscle from the peroneal nerve, resulting in gradual increase in power and range of toe and ankle extension postoperatively. In a second series by Doi et al., reinnervated latissimus dorsi transfer was used to improve or supplement knee flexion or extension by connecting to the sciatic or femoral nerve at the time of reconstruction.
While arterial reconstruction is always indicated after limb-sparing surgery to prevent ischemia, the need for venous reconstruction is not as well-established, as venous ligation compromise the limb. Studies showing high occlusion rates have led to debates regarding the benefits of venous revascularization. Additionally, there have been reports of symptoms of severe venous insufficiency such as edema, claudication, and hyperpigmentation after reconstruction.
A large series of lower limb soft tissue sarcoma resection with arterial and venous reconstruction was conducted by Nishinari et al. in 25 patients. Graft occlusion rates were found to be significantly greater in patients who received synthetic grafts vs. those who received saphenous vein grafts (P = 0.02), which is consistent with the results of other studies. However occlusion rates were not different between arterial and venous reconstruction and there was no association between prior radiotherapy and graft occlusion. Wortman et al. reported one-year patency rates of venous bypass grafts to be 65%, with high numbers of overall bypass-related complications including thrombosis and emboli as well as infections. Common wound complications that occur are wound healing difficulties, infections, and lymphatic fistulas.
Surgery with wide margins alone can be implemented to treat sarcoma of the extremities that is subcutaneous or intramuscular, small in size, or low in grade. However, if the resected margin is close, or if there is extramuscular involvement, surgery must be combined with adjuvant radiotherapy. For those that are high-grade or large in size, neoadjuvant chemotherapy must also be considered. The need for additional therapy is often a determining factor in flap selection, as wound-healing difficulties can delay the onset of adjuvant therapy and negatively affect long-term survival.
Radiotherapy may be administered either pre- or postoperatively with similar local control and overall survival rates. The concern with radiation therapy is the complications it causes with wound healing. Reported complications have ranged from 33%-44% in the past, with severe morbidity in 22%-27% of patients[48-50]. Abramson et al. however only reported a 12.5% wound complication rate, including a patient who developed radiation necrosis and required a second free tissue transfer months after his initial treatment.
While preoperative radiotherapy results in higher rates of wound complications[51-53], patients treated with postoperative radiotherapy experience more long-term fibrosis, edema and joint stiffness. The National Cancer Institute of Canada (NCI Canada) conducted a randomized control trial comparing wound complications in patients who received preoperative vs. those postoperative radiotherapy and found that 35% of those in the preoperative group had major wound complications compared to 17% of those in the postoperative group. O’Sullivan et al. found higher rates of wound complications and reoperations in patients who received preoperative radiation. However a larger percentage of patients with wound complications in the postoperative radiation group required other invasive procedures.
Townley et al. compared patients with preoperative irradiation to a control group who received no radiation and found similar microvascular complication rates such as those requiring intra-operative revision or flap reexploration or loss. Though wound healing complications were more common in the group who received radiation, the ultimate outcomes were similar between both groups. Some factors associated with wound complications in sarcoma patients who receive preoperative radiation are tumor size > 10 cm, tumor proximity to skin surface < 3 mm, and current smoking status.
Chao and associates compared complication rates between patients receiving neoadjuvant and adjuvant irradiation and found no significant difference in perioperative complication rates or rates of salvaged pedicle thrombosis between the two groups. However, the rate of total free flap loss was lower in patients receiving neoadjuvant radiation, suggesting that the introduction of new, well-vascularized tissue counteracts the effects of the radiation. The authors also attributed this finding to the fact that higher doses and larger fields of irradiation are involved with adjuvant therapy, and with neoadjuvant therapy, irradiated tissue may be excised during tumor resection. Additionally, they found that late recipient-site complications (occurring > 30 days after surgery) occurred more frequently in patients who received adjuvant radiation (26.1% vs. 6.8%, P = 0.0006), although the reoperation rate following these complications was similar between the groups. Because wound complications are generally treatable without resulting in permanent damage, preoperative radiotherapy is preferred by many practitioners.
Brachytherapy, another form of adjuvant therapy, is a method of administering radioisotopes directly into a surgical wound to treat residual tumor. Addition of brachytherapy to surgical excision has been shown to reduce tumor recurrence rates from 14% to 4%. Brachytherapy was initially administered during the immediate postoperative period and resulted in high rates of wound complications. Waiting until at least the 5th postoperative day is associated with significantly lower rates. In a study by Lee et al., brachytherapy was initiated about 7 days after free tissue transfer and resulted in a 29% complication rate, including partial-thickness skin necrosis, venous thrombosis necessitating flap exploration, kinking of the brachytherapy catheters, and partial flap skin loss. Hidalgo et al. described 3 patients who were treated with adjuvant brachytherapy 7-10 days postoperatively with no wound-healing complications. Although considered typically safe, the number of wound complications requiring reoperation has been shown to be higher with brachytherapy than with external beam radiation therapy. Preoperative intraarterial chemotherapy is another option and has been shown to have no effect on free flap results.
Because of the prolonged surgical time and extensive periods of bed rest combined with immunosuppresive therapy following sarcoma resection, surgical treatment of these tumors is generally associated with high numbers of postoperative complications. Lopez et al. found that patients who received combined pedicled + free flaps after sarcoma resection had significantly higher wound complications rates compared to patients who received just one, although systemic complications were distributed equally between all groups.
Recurrence rates are generally high following flap reconstruction after resection of advanced, high-grade sarcomas. Popov et al. found a statistically significant correlation between recurrence and extracompartmental tumor location (P < 0.01) and large tumor size (> 4 cm) (P < 0.01). Postoperative wound complications can also lead to amputation following tumor resection and flap reconstruction.
As wide local excision has become the most commonly accepted approach to the surgical treatment of sarcomas, reconstructive surgical techniques become crucial to the success of this line of therapy. Although pedicled flaps have been traditionally preferred for oncologic resections, their use is sometimes precluded by the use of neoadjuavant radiation as well as the size of the defect left after the resection. The need to re-establish function also makes the use of a pedicle/local flap less optimal. Several recent studies have reported successful functional and aesthetic results using free tissue transfer as the main modality for reconstruction after sarcoma resection of the limb[6,7,56]. Free tissue transfer allows for the application of healthy vascularized tissue to the defect while also providing freedom of flap positioning as well as avoidance of stretching or kinking of the vasculature. Studies of sarcoma resection and free tissue reconstruction have reported high success rates, with complication rates ranging between 2%-22%[7,64,65] and limb salvage rates close to 100%[6,57,64,65]. Flap choice is dependent on tumor and defect size, tissue type and function, as well as donor site availability, thus resulting in numerous different treatment options. Given the low incidence and prevalence of lower extremity sarcomas as well as the heterogeneity of the sarcomas and their respective neo-adjuvant treatments, there are currently no clear treatment guidelines or specific algorithms for the reconstruction of soft tissue defects following oncologic resection. The lack of significant case volume makes it difficult for any single institution to conduct a study comparing the success rates of various flaps, and although a systematic review would be helpful, the innate nature of the pathology also leads to a paucity of literature consisting largely of studies describing small numbers of isolated cases. This descriptive review however attempts to provide an overview of the various reconstructive options that are available, as well as the considerations that must be taken into account when treating patients with soft tissue defects of the lower limb following sarcoma resection.
Performed the literature search and reviewed the articles: Azadgoli B, Perrault DP
Drafted the manuscript: Azadgoli B
Revised the manuscript: Carre AL, Wong AK
Reviewed the manuscript and approved its final version: all authorsFinancial support and sponsorship
None.Conflicts of interest
There are no conflicts of interest.Patient consent
Not applicable.Ethics approval
© The Author(s) 2018.
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