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ORIGINAL ARTICLE Table of Contents   
Year : 2009  |  Volume : 43  |  Issue : 4  |  Page : 403-407
Limb conservation in extremity soft tissue sarcomas with vascular involvement


Department of Surgical Oncology, Govt Royapettah Hospital, Chennai, India

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Date of Web Publication23-Sep-2009
 

   Abstract 

Background: The major neurovascular involvement and large primary tumors are indication of amputation. The present study is an attempt to explore the feasibility of a limb salvage surgery in extremity sarcoma cases with major vessel involvement. Oncological outcomes and surgery-related morbidities are compared with those reported in literature.
Materials and Methods: A retrospective review of all limb salvage surgeries done in our department between 2005 and 2008 was done and four cases of extremity sarcoma of lower limb involving femoral vessels analyzed. Interpretation of data from these cases, along with review of literature, is done.
Results: In all these cases a wide monobloc excision was done adhering to oncological principles. This required resection of superficial femoral artery alone in two cases, resection of superficial femoral artery along with common femoral vein and femoral nerve in another, and of common femoral vein alone in yet another. Reconstruction was done in all these cases with reversed long saphenous vein graft. Histopathology of resected margins was free of tumor in all the four patients. One patient developed local recurrence and one developed distant metastsis. Two were disease free for one year with good functional limb, one has been disease-free for three years and another was disease-free at two years, after which he defaulted further follow-up. One patient developed arterial blowout which required ligation of common femoral artery which resulted in gangrene of the limb. He underwent amputation.
Conclusion: Major neurovascular involvement in extremity sarcoma is not considered a contraindication for limb salvage surgery. Review of literature also supports our view. Post-operative wound related complications are more in this group of patients. However, long term functional outcome is good. Literature suggests a good long term local control after vascular resection and reconstruction.

Keywords: Limb salvage surgery, major vascular infiltration in sarcomas, vessel reconstruction

How to cite this article:
Ramamurthy R, Soundrarajan JC, Mettupalayam V, Shanmugham S, Arumugam B, Periasamy S. Limb conservation in extremity soft tissue sarcomas with vascular involvement. Indian J Orthop 2009;43:403-7

How to cite this URL:
Ramamurthy R, Soundrarajan JC, Mettupalayam V, Shanmugham S, Arumugam B, Periasamy S. Limb conservation in extremity soft tissue sarcomas with vascular involvement. Indian J Orthop [serial online] 2009 [cited 2013 May 20];43:403-7. Available from: http://www.ijoonline.com/text.asp?2009/43/4/403/54969

   Introduction Top


Limb salvage surgery has become the standard of care in managing extremity sarcomas. [1],[2],[3],[4],[5] With recent advances in radiotherapy and chemotherapy, 95% of patients with extremity sarcomas will have limb conservation surgery but five per cent of these patients will still require amputation. Common indications for amputation are major neurovascular involvement and large primary tumor where resection would leave a functionally useless limb.

We offered limb salvage to four patients who had major vascular involvement. In this article we share our experience of extremity soft tissue sarcoma in patients, with major vascular involvement, who were successfully treated with limb conservative surgery along with vascular reconstruction.


   Materials and Methods Top


A retrospective review of all cases of limb salvage surgery on extremity soft tissue sarcomas cases, in our department, from 2004 to 2008, was done. Four patients who had major vascular involvement diagnosed pre-operatively and offered limb salvage surgery were taken up for analysis. All the four patients presented with complaints of painless swelling in the thigh. Average duration of presenting symptom was four months ranging from three to six months. In three of them vascular involvement was suspected on clinical examination because of weak peripheral pulses. All these patients were subjected to MRI and MR angiogram which confirmed the involvement of major vessel [Figure 1] and [Figure 2]. More than 50% circumferential encasement of major vessel in MRI is highly predictive of vascular infiltration by sarcomas. All these patients were subjected to Doppler study which showed loss of triphasic flow and reduced velocity in the involved vessel.

Our routine pre-operative staging workup included chest X-ray, CT scan of the chest and MRI of the involved local part. Histological diagnosis was made by trucut biopsy of the lesion. Biopsy site was chosen along the line of incision. After ruling out distant metastasis all of them were offered limb salvage surgery with curative intent for which they consented.

Surgery was planned according to the imaging extent of the tumor. Along with the muscle group involved a two cm clear margin all around the tumor was marked out in the pre-operative surgical planning sessions. Since vascular involvement was made out pre-operatively, resection and reconstruction of the involved vessel was planned pre-operatively. A wide monobloc excision, along with resection of the involved vessel, was done. Reconstruction of the vessel was done with saphenous vein harvested from opposite leg. All patients were heparinized during the surgery and in the immediate postoperative period. Oral anticoagulation with warfarin was started after five days and heparinization was stopped once the INR reached therapeutic levels. Warfarin was continued for six months.

Follow-up protocol for sarcomas includes clinical examination every month for two years, once in three months for next year, six-monthly up to five years and once yearly after that. Radiological examination with chest X-ray and local part MRI is done once in a year. Follow up protocol for vascular reconstruction group included hand held Doppler study on every visit and color Doppler study once in a year. If patients complain about any symptoms it is evaluated with imaging at any time during the follow-up.

Oncological and functional outcomes of this subset of patients were analyzed. Functional assessment was done with Musculoskeletal Tumor Society rating scale (Enneking score).


   Results Top


Over a period of four years, between 2005 and 2008, four patients presented to us with extremity soft tissue sarcoma involving the femoral vessels. Demographic details of these patients are given in [Table 1]. Mean size of the tumor was 13.5 cms. In three of these cases both adductor and anterior compartments of thigh were involved and in one patient only the anterior compartment was involved. Pre-operative diagnosis of vascular involvement was made with MRI and Color Doppler study. In two patients the superficial femoral artery alone was involved. In one patient common femoral vein alone was involved and in one both superficial femoral artery and common femoral vein were involved. Histologies were one each of synovial sarcoma, rhabadomyosarcoma, MPNST and MFH. There were three Grade III sarcomas and one Grade II sarcoma.

Limb salvage surgery in the form of wide monobloc excision was performed on all these patients adhering to oncological principles [Figure 3]. A two cm margin was given all around the tumor and it was excised enbloc with the involved vessel. Two of these patients underwent wide monobloc excision of tumor along with resection of a segment of superficial femoral artery. One underwent wide monobloc excision of tumor along with resection of a segment of superficial femoral artery, common femoral vein and anterior branch of femoral nerve; one had excision of common femoral vein alone with the tumor. Reconstruction was done in all cases with reversed saphanous vein graft harvested from opposite thigh [Figure 4]. An end-to-end anastamosis was done with 6-O prolene. Two patients had only arterial reconstruction while one had both arterial and venous reconstruction. One had venous reconstruction alone [Table 2]. After the vascular reconstruction adjacent muscles were transposed over the reconstructed vessels for protection [Figure 5].

Two patients received adjuvant radiation. Adjuvant chemotherapy and radiation was given to one patient.

All the four cases had negative margins on histopathological examination and Vessel infiltration was proved histologically. Three cases were Gr III sarcomas and 1 was Gr II sarcoma. Preoperative histology was confirmed in all cases.

One patient developed in-operable local recurrence and one developed distant recurrence. No patient has developed vascular insufficiency in the follow-up. Three patients reported lower limb edema which was amenable to conservative management (stocking and exercise). Functional assessment was done with Enneking score. Two patients scored 86% (26/30) and 80% (24/30) respectively. One patient scored 70% (21/30) and one patient 40% (12/30).

In the postoperative period one patient developed major flap necrosis and 2 developed minor wound infection. All three patients were managed conservatively. One patient developed vascular blow-out in the immediate post-operative period for which ligation of common femoral artery was done. Later he developed gangrene and underwent amputation [Table 3].


   Discussion Top


Vascular involvement by soft tissue sarcomas are diagnosed preoperatively with MRI and MR angiogram. MRI is considered the gold standard in diagnosing vascular involvement by soft tissue sarcomas. [6],[7] Vascular infiltration by sarcomas necessitating vessel resection is suspected preoperatively if more than 50% of the circumference of the vessel is encased by the tumor. If the tumor is found abutting the neurovascular bundle excision of the tumor along with the peri-advential tissues is sufficient.

Immediate goals in this kind of resection are to achieve a clear histological negative margin and postoperative wound healing with acceptable morbidity. Literature review suggests a high probability of achieving negative surgical margin even in the presence of vascular involvement requiring resection and reconstruction of the involved vessel. Autologus reversed saphenous vein graft is the most commonly used for reconstructing the vessel. In cases where the vein is not available artificial grafts made of poly tetra fluoro ethylene (PTFE) or Dacron can be used. [8] The incidence of graft related complications are more with artificial grafts.

Frequency of amputation following vascular reconstruction in literature is 15 to 25% which is much higher than limb salvage surgeries without reconstruction (five per cent). Literature reports a higher incidence of wound related complications, as high as 68% after vascular reconstruction. [9] Explanations given for higher incidence of complications are preoperative radiotherapy and extensive skeletonization of the vessels which lead to de-vascularization of the flaps. Other reported complications are DVT and pulmonary embolism.

Long term goals are to achieve good oncological and functional outcome. Review of the literature reveals a local recurrence rate of 0 to 20 % [10],[11],[12],[13],[14],[15],[16],[17],[18] in most large series of limb salvage surgery requiring vascular reconstruction which is similar to the recurrence rate following limb salvage surgery without vascular reconstruction. [9] Unlike carcinomas, where an increased incidence of distant metastasis is markedly seen with vascular involvement, sarcomas have modest increased incidence of distant metastasis when vessels are involved, 30 vs 10%. [19]

Limb salvage surgery in the presence of neurovascular bundle infiltration necessitating vascular reconstruction is a well established procedure in western literature. Many major centers in India, even today, continue to offer potentially morbid amputations to these patients. Post operative morbidity, fear of oncological outcome and complexity of the procedure associated with vascular reconstruction has deterred many to undertake limb salvage in this subset of patients in India despite being reported in western literature.

In our experience soft tissue sarcomas with vascular involvement are inherently very aggressive tumors which at presentation have large size and high grade. Resection usually involves large amount of tissue resulting in much higher incidence of wound related complication. Reconstruction of the resected vessels is prone to blow outs in the immediate postoperative period and vascular insufficiency in long term. Because of these factors functional outcome can be unpredictable.

Oncologically, sound resection is possible despite the aggressive presentation of these tumors. With addition of radiotherapy good local control can be achieved in good number of these patients. Literature also reports high local control. Although we could not salvage local recurrence in one of our patients, we expect this would not be the case in most local recurrences. These recurrences, in most cases, should be salvageable with amputation. However, distant recurrences would still be a major problem. This should not deter surgeons from performing limb salvage in this subset as these patients still would have a useful limb during their lifetime.


   Conclusion Top


In our experience limb salvage surgery in the presence of major vascular infiltration necessitating vascular reconstruction can be safely performed. Post-operative wound related complications are more in this group of patients. However, long term functional outcome is acceptable. Multi-modality treatment approach is needed in this group of patients to achieve optimal oncological outcome. These aggressive tumors may have poorer outcome but this should not deter surgeons from performing limb salvage in this subset as these patients still would have a useful limb during their lifetime.

 
   References Top

1.Karakousis CP, Emrich LJ, Rao U, Khalil M. Limb salvage in soft tissue sarcomas with selective combination of modalities. Eur J Surg Oncol 1991;17:71-80.  Back to cited text no. 1      
2.Kraybill WG, Emami B, Lyss AP. Management of soft tissue sarcomas of the extremities Surgery 1991;109:233-5.  Back to cited text no. 2      
3.Popov P, Tukiainen E, Asko-Seljaavaara S, Huuhtanen R, Virolainen M, Virkkunen P, et al . Soft tissue sarcomas of the lower extremity: surgical treatment and outcome. Eur J Surg Oncol 2000;26:679-85  Back to cited text no. 3      
4.Keus RB, Rutgers EJ, Ho GH, Gortzak E, Albus-Lutter CE, Hart AA. Limb-sparing therapy of extremity soft tissue sarcomas: treatment outcome and long-term functional results. Eur J Cancer 1994;30:1459-63  Back to cited text no. 4      
5.Fortner JG, Kim DK, Shiu MH. Limb-preserving vascular surgery for malignant tumors of the lower extremity. Arch Surg 1977;112:391-4.  Back to cited text no. 5      
6.Bland KI, McCoy DM, Kinard RE, Copeland EM 3rd. Application of magnetic resonance imaging and computerized tomography as an adjunct to the surgical management of soft tissue sarcomas. Ann Surg 1987;205:473-81.  Back to cited text no. 6      
7.Chang AE, Matory YL, Dwyer AJ, Hill SC, Girton ME, Steinberg SM, et al . Magnetic resonance imaging versus computed tomography in the evaluation of soft tissue tumors of the extremities. Ann Surg 1987;205:340-8.   Back to cited text no. 7      
8.Klinkert P, Post PN, Breslau PJ, van Bockel JH. Saphenous Vein Versus PTFE for above-knee femoropopliteal bypass: A review of the literature. Eur J Vasc Endovasc Surg 2004;27:357-62.  Back to cited text no. 8      
9.Ghert MA, Davis AM, Griffin AM, Alyami AH, White L, Kandel RA, et al . The surgical and functional outcome of limb-salvage surgery with vascular reconstruction for soft tissue sarcoma of the extremity E grafts in infrainguinal reconstruction. J Vasc Surg 1986;3:104-14.   Back to cited text no. 9      
10.Nishinari K, Wolosker N, Yazbek G, Malavolta LC, Zerati AE, Penna V, et al . Vascular reconstruction in limbs associated with resection of tumors. Ann Vasc Surg 2003;17:411-6.  Back to cited text no. 10      
11.Baxter BT, Mahoney C, Johnson PJ, Selmer KM, Pipinos II, Rose J, et al . Concomitant arterial and venous reconstruction with resection of lower extremity sarcomas. Ann Vasc Surg 2007;21:272-9.  Back to cited text no. 11      
12.Tsukushi S, Nishida Y, Sugiura H, Nakashima H, Ishiguro N. Results of limb-salvage surgery with vascular reconstruction for soft tissue sarcoma in the lower extremity: comparison between only arterial and arterovenous reconstruction. J Surg Oncol 2008;97:216-20.  Back to cited text no. 12      
13.Ghert MA, Davis AM, Griffin AM, Alyami AH, White L, Kandel RA, et al . The surgical and functional outcome of limb-salvage surgery with vascular reconstruction for soft tissue sarcoma of the extremity. Ann Surg Oncol 2005;12:1102-10.  Back to cited text no. 13      
14.Matsushita M, Kuzuya A, Mano N, Nishikimi N, Sakurai T, Nimura Y, et al . Sequelae after limb-sparing surgery with major vascular resection for tumor of the lower extremity. J Vasc Surg 2001;33:694-9.  Back to cited text no. 14      
15.Schwarzbach MH, Hormann Y, Hinz U, Bernd L, Willeke F, Mechtersheimer G, et al . Results of limb-sparing surgery with vascular replacement for soft tissue sarcoma in the lower extremity. J Vasc Surg 2005;42:88-97.  Back to cited text no. 15      
16.Karakousis CP, Karmpaliotis C, Driscoll DL. Major vessel resection during limb-preserving surgery for soft tissue sarcomas. World J Surg 1996;20:345-9.  Back to cited text no. 16      
17.Hohenberger P, Allenberg JR, Schlag PM, Reichardt P. Results of surgery and multimodal therapy for patients with soft tissue sarcoma invading to vascular structures. Cancer 1999;85:396-408.  Back to cited text no. 17      
18.McKay A, Motamedi M, Temple W, Mack L, Moore R. Vascular reconstruction with the superficial femoral vein following major oncologic resection. J Surg Oncol 2007;96:151-9.  Back to cited text no. 18      
19.Bianchi C, Ballard JL, Bergan JH, Killeen JD. Vascular reconstruction and major resection for malignancy. Arch Surg 1999:134:851-5.  Back to cited text no. 19      

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Correspondence Address:
Rajaraman Ramamurthy
"Rama Swathi", Old No.11, New No. 25, 7th Main Road, Raja Annamalaipuram, Chennai - 600 028, Tamil Nadu
India
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DOI: 10.4103/0019-5413.54969

PMID: 19838393

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    Figures

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