Subscribe to RSS

DOI: 10.1055/s-0045-1809908
Percutaneous Image-Guided Cryoablation of Recurrent Myxofibrosarcoma in the Forearm: A Case Report and Review of Literature
Funding None.
Abstract
Myxofibrosarcoma (MFS) is a rare, aggressive soft tissue sarcoma with high recurrence rates. Conventional treatment involves wide surgical resection and radiotherapy, but the infiltrative nature of MFS often complicates complete resection. This case highlights an 81-year-old patient with recurrent MFS in the left forearm, initially treated with surgery and radiation therapy. Due to surgical limitations and desire for a minimally invasive approach after recurrence, cryoablation was performed. The patient underwent the procedure successfully, and postoperative imaging indicated effective ablation. This case demonstrates cryoablation as a feasible, minimally invasive alternative for managing recurrent MFS, particularly in anatomically challenging cases.
#
Introduction
Myxofibrosarcoma (MFS) is a soft tissue sarcoma that commonly presents in the extremities of adults.[1] MFS tends to be superficially located, however, can exhibit infiltrative growth leading to greater recurrence. Clinically, MFS manifests as slowly enlarging and painless mass and is often mistaken for a benign tumor. Due to the challenging growth pattern, it becomes difficult to evaluate the true extent of the tumor, ultimately preventing adequate surgical resection.[2] The invasive nature of MFS is associated with a higher tumor grade, increased risk of multiple recurrences, and other comorbidities such as cardiovascular diseases.[1] [2] [3]
Conventional treatment of MFS is surgical excision along with the use of radiotherapy.[4] However, the wide surgical margins and anatomical presentation of the tumor can pose great challenges. Cryoablation is a minimally invasive technique that uses cryoprobes to deliver compressed gas (argon) to cool tumor tissue for purposes of necrosis to less than −20°C.[5] Using cryoablation for the management of MFS allows for a minimally invasive procedure with potential for greater accuracy to target the tumor.
In this case report, we highlight the use of percutaneous image-guided cryoablation in a patient with MFS of the forearm.
#
Case Report
An 81-year-old male with a history of MFS in the left forearm, initially treated with surgical resection and subsequent radiation therapy in 2013, presented with local recurrence in 2017, necessitating repeat surgical resection. The postoperative course was complicated by infection. After multiple negative yearly surveillance MRIs of the left forearm, the patient unfortunately presented in June 2020 demonstrating a collection at the previous site of the surgical bed. Ultrasound-guided biopsy was performed and pathological results indicated low- to intermediate-grade, recurrent, MFS.
On physical examination, the patient presented with a well-healed free flap over the dorsal aspect of the forearm, accompanied by noticeable radiation changes indicative of previous treatment. There were no signs of open wounds, and the forearm and elbow were free of palpable masses or tenderness. Mobility in the elbow was preserved, allowing full range of motion without any pain. However, the patient exhibited a chronic contracture at the left wrist, significantly limiting the ability to fully extend the wrist and digits. Notably, there was observed weakness in the extensor pollicis longus and the flexor digitorum muscles, both deep and superficial.
For diagnostic assessment, a magnetic resonance imaging (MRI) with IV contrast was performed. The results of the MRI showed a heterogeneous T2 hyperintense mass lesion within the supinator muscle belly, which showed heterogeneous enhancement on the postcontrast imaging. This structure measured up to 2.6 cm in craniocaudal dimension and 1.3 × 1.1 cm in axial dimension (previously 2.1 × 1.0 × 0.8 cm). Axial T1 fat-saturated pre- and postcontrast images demonstrated avid heterogeneous enhancement of the mass within the supinator muscle belly ([Fig. 1]).


The patient ultimately refused a third surgical resection and opted for a cryoablation procedure using ultrasound and computed tomography (CT) guidance. A positron emission tomography-CT was performed to exclude any distant metastasis. The cryoablation procedure was performed under general anesthesia. The patient was placed on the CT table and axial CT images were obtained. An isodense lesion was identified within the proximal forearm. Initially, the tumor was targeted with real-time ultrasound guidance ([Fig. 2A]). Subsequently, two cryoablation probes were advanced under real-time ultrasound guidance into the tumor ([Fig. 2B]). The planned intralesional points of insertions were along the long axis of the lesion to maximize coverage and symmetry of the ice ball. Given the lesion's orientation within the forearm, the probe insertion was performed to achieve the shallowest possible trajectory while maintaining safe distance from critical structures. The position was verified by limited CT ([Fig. 3]). An ablation margin of 5 mm beyond the visible tumor boundary was planned to ensure adequate coverage. Two cycles of freeze–thaw–freeze–thaw ablation was performed at this location for a total of 8-minute freeze, 10-minute passive thaw, 8-minute freeze, and active thaw. CT was performed at approximately 2-minute intervals during the freeze–thaw cycles to ensure appropriate coverage of the ice ball surrounding the left forearm mass ([Fig. 4]). Additionally, the CT demonstrated no significant hemorrhage or other complications. Patient tolerated the procedure well and was transferred to the recovery unit.






Postoperative T1 pre- and post-gadolinium magnetic resonance images at 3 months following ablation demonstrated no significant enhancement ([Fig. 5]). The lesion appeared similar in size but was likely necrotic, indicating treatment-related effects.
#
Discussion
This case demonstrates the use of cryoablation for the treatment of MFS in the forearm. Due to the recurrent nature of MFS, the condition poses challenges in adequate treatment. Our patient presented with a history of recurrent MFS, despite management with surgical resection and radiation therapy twice. Cryoablation offers an alternative therapeutic method to precisely target the tumor while ensuring preservation of local tissues.
Cryoablation techniques use the precision of imaging modalities such as ultrasound and CT for real-time guidance of probe placement and monitoring of the ablation zone. This allows for preservation of healthy tissue and decreased morbidity. As seen in our patient, the use of intra-procedural imaging indicated no significant hemorrhage or other adverse events during the procedure while achieving an adequate zone of ablation for complete tumor necrosis. In addition, the postprocedural MRI findings showed no internal enhancement of the mass and no continued growth, further supporting the efficacy of cryoablation in controlling the tumor.
There is generally a low complication rate in patients who undergo percutaneous cryoablation (2–5%).[6] [7] [8] However, in superficial tumors such as those in the forearm, complications can arise. Skin necrosis is a serious complication that can occur as a result of cryotherapy due to freezing of the superficial surface.[9] In addition, damage to adjacent structures such as nerves is a well-documented risk of cryoablation in musculoskeletal interventions.[10] To mitigate these adverse risks, precautionary measures can be taken. In our case, we used warm saline gloves to prevent skin necrosis. Thermal protection of the skin reduces the risk of skin necrosis from the cryoprobe. Furthermore, maintaining a safe distance from neurovascular structures also further prevents complications. A study by Lippa et al documented a distance to skin >5 mm and a distance to neurovascular structures >3 mm as precautionary measures for cryoablation in their patients with recurrence of soft tissue sarcomas.[11] Techniques such as hydrodissection and CO2 pneumodissection have also been described in the literature.[12] [13] This offers enhanced protection of the skin due to the decreased thermal conductivity in comparison to saline. While our patient tolerated the procedure well without complications, it is important to recognize precautionary measures such as thermal protection, adequate intraprocedural monitoring, and close follow-up to prevent long-term complications with cryoablation.
Literature comparing cryoablation to radiofrequency ablation in the treatment of renal masses suggests cryoablation results in lower retreatments, and improved local tumor control.[14] The greater precision in cryoablation may be attributed to the visible ice-ball formation, allowing for real-time monitoring and adjustment intraoperatively. Using real-time guidance of ultrasound and CT, we were accurately able to position the probe and maximize the localization of the tumor while minimizing any complications to adjacent critical structures. In our case, CT guidance was used for intraprocedural ice-ball monitoring to ensure precise visualization and confirmation of ablation margins. CT imaging provides high-resolution images that clearly delineate the margins of the ice ball, allowing for assessment of tumor coverage and proximity to adjacent structures.[5] While ultrasound offers the advantage of real-time imaging without radiation exposure, its utility remains limited due to its limited tissue penetration, operator dependence, and significant acoustic shadowing.[15] Ultrasound has been used in the literature for intraprocedural monitoring of ice-ball formation in cryoablation; however, CT provides greater reliability for comprehensive ice-ball evaluation.[15] [16] [17] [18]
Our case supports the integration of cryoablation in the treatment for recurrent and anatomically complex MFS cases. For patients with recurrent disease or patients who are not suitable for surgery, cryoablation guided by radiologic imaging provides a safe, effective alternative.
Recent literature has demonstrated the expanding role of cryoablation in the management of both benign and malignant soft tissue tumors. A recent study by Pal et al highlighted the effectiveness of cryoablation in patients with recurrent or metastatic soft tissue sarcomas, indicating a progression-free survival rate of 86% at 1 year and 80% at 2 years.[6] To expand on this, a recent review reported an overall disease control rate of 85% in cryoablation of soft tissue tumors.[7] These positive outcomes of cryoablation are only paralleled in the treatment of desmoid fibromatosis, which shares similar infiltrative behavior and recurrence risk with MFS. Patients who underwent cryoablation for extra-abdominal desmoid-type fibromatosis demonstrated a 2-year disease control of 85% upon therapy.[19] [20] Clinical evidence from studies in recent years has demonstrated enhanced patient outcomes upon cryoablation for soft tissue tumors. As the field of interventional radiology continues to advance, minimally invasive therapeutic techniques such as cryoablation will only expand in its applications.
#
Conclusion
This case underscores the technically successful utility of cryoablation for the clinical management of a soft tissue MFS. Cryoablation offers a potential minimally invasive intervention for adequate localization of the tumor while preserving adjacent critical anatomical structures. This case further emphasizes the potential of cryoablation to be used for soft tissue sarcomas over conventional surgical methods in surgical beds with recurrent disease.


#
#
Conflict of Interest
None declared.
Ethical Approval
Research Ethics Board approval was waived per standard policy for case reports and/or series.
-
References
- 1 Willems SM, Debiec-Rychter M, Szuhai K, Hogendoorn PCW, Sciot R. Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model. Mod Pathol 2006; 19 (03) 407-416
- 2 Kang S, Kim HS, Kim W, Kim JH, Kang SH, Han I. Comorbidity is independently associated with poor outcome in extremity soft tissue sarcoma. Clin Orthop Surg 2015; 7 (01) 120-130
- 3 van Herk-Sukel MPP, Shantakumar S, Overbeek LIH, van Boven H, Penning-van Beest FJA, Herings RMC. Occurrence of comorbidities before and after soft tissue sarcoma diagnosis. Sarcoma 2012; 2012: 402109
- 4 Manoso MW, Pratt J, Healey JH, Boland PJ, Athanasian EA. Infiltrative MRI pattern and incomplete initial surgery compromise local control of myxofibrosarcoma. Clin Orthop Relat Res 2006; 450 (450) 89-94
- 5 Erinjeri JP, Clark TWI. Cryoablation: mechanism of action and devices. J Vasc Interv Radiol 2010; 21 (8, Suppl): S187-S191
- 6 Pal K, Awad A, Yevich S. et al. Safety and efficacy of percutaneous cryoablation for recurrent or metastatic soft-tissue sarcoma in adult patients. AJR Am J Roentgenol 2024; 223 (04) e2431490
- 7 Bodard S, Geevarghese R, Razakamanantsoa L. et al. Percutaneous cryoablation in soft tissue tumor management: an educational review. Insights Imaging 2024; 15 (01) 278
- 8 Auloge P, Cazzato RL, Rousseau C. et al. Complications of percutaneous bone tumor cryoablation: a 10-year experience. Radiology 2019; 291 (02) 521-528
- 9 Chen C, Garlich J, Vincent K, Brien E. Postoperative complications with cryotherapy in bone tumors. J Bone Oncol 2017; 7: 13-17
- 10 Papalexis N, Savarese LG, Peta G. et al. The new ice age of musculoskeletal intervention: role of percutaneous cryoablation in bone and soft tissue tumors. Curr Oncol 2023; 30 (07) 6744-6770
- 11 Lippa N, Sargos P, Italiano A. et al. Standardization of selection criteria for percutaneous image-guided cryoablation of recurrent soft-tissue sarcomas. Diagn Interv Imaging 2014; 95 (11) 1071-1077
- 12 Maybody M, Tang PQ, Moskowitz CS, Hsu M, Yarmohammadi H, Boas FE. Pneumodissection for skin protection in image-guided cryoablation of superficial musculoskeletal tumours. Eur Radiol 2017; 27 (03) 1202-1210
- 13 Sag AA, Riedel RF, Eward WC, Visgauss JD, Brigman BE. Hydropneumodissection-assisted cryoablation of recurrent sarcoma adjacent to the sciatic nerve as a limb-sparing alternative to hindquarter amputation. J Vasc Interv Radiol 2023; 34 (05) 923-926.e1
- 14 Cazzato RL, Gantzer J, de Marini P. et al. Sporadic desmoid tumours: systematic review with reflection on the role of cryoablation. Cardiovasc Intervent Radiol 2022; 45 (05) 613-621
- 15 Kwak K, Yu B, Lewandowski RJ, Kim DH. Recent progress in cryoablation cancer therapy and nanoparticles mediated cryoablation. Theranostics 2022; 12 (05) 2175-2204
- 16 Kim DK, Won JY, Park SY. Percutaneous cryoablation for renal cell carcinoma using ultrasound-guided targeting and computed tomography-guided ice-ball monitoring: radiation dose and short-term outcomes. Acta Radiol 2019; 60 (06) 798-804
- 17 Won JY, Kim DK, Park SY. Renal mass cryoablation: melting time analysis of radiographic ice-ball after 5-minute active thawing by using serial ultrasound. Eur J Radiol 2021; 134: 109409
- 18 Al-Assam H, Botchu R, Azzopardi C, Stevenson JD, James SL, Patel A. Measurement analysis of ice ball size during CT-guided cryoablation procedures for better prediction of final ice ball size and avoidance of complications. Indian J Radiol Imaging 2023; 33 (03) 321-326
- 19 Havez M, Lippa N, Al-Ammari S. et al. Percutaneous image-guided cryoablation in inoperable extra-abdominal desmoid tumors: a study of tolerability and efficacy. Cardiovasc Intervent Radiol 2014; 37 (06) 1500-1506
- 20 Mandel JE, Kim D, Yarmohammadi H. et al. Percutaneous cryoablation provides disease control for extra-abdominal desmoid-type fibromatosis comparable with surgical resection. Ann Surg Oncol 2022; 29 (01) 640-648
Address for correspondence
Publication History
Article published online:
03 July 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India
-
References
- 1 Willems SM, Debiec-Rychter M, Szuhai K, Hogendoorn PCW, Sciot R. Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model. Mod Pathol 2006; 19 (03) 407-416
- 2 Kang S, Kim HS, Kim W, Kim JH, Kang SH, Han I. Comorbidity is independently associated with poor outcome in extremity soft tissue sarcoma. Clin Orthop Surg 2015; 7 (01) 120-130
- 3 van Herk-Sukel MPP, Shantakumar S, Overbeek LIH, van Boven H, Penning-van Beest FJA, Herings RMC. Occurrence of comorbidities before and after soft tissue sarcoma diagnosis. Sarcoma 2012; 2012: 402109
- 4 Manoso MW, Pratt J, Healey JH, Boland PJ, Athanasian EA. Infiltrative MRI pattern and incomplete initial surgery compromise local control of myxofibrosarcoma. Clin Orthop Relat Res 2006; 450 (450) 89-94
- 5 Erinjeri JP, Clark TWI. Cryoablation: mechanism of action and devices. J Vasc Interv Radiol 2010; 21 (8, Suppl): S187-S191
- 6 Pal K, Awad A, Yevich S. et al. Safety and efficacy of percutaneous cryoablation for recurrent or metastatic soft-tissue sarcoma in adult patients. AJR Am J Roentgenol 2024; 223 (04) e2431490
- 7 Bodard S, Geevarghese R, Razakamanantsoa L. et al. Percutaneous cryoablation in soft tissue tumor management: an educational review. Insights Imaging 2024; 15 (01) 278
- 8 Auloge P, Cazzato RL, Rousseau C. et al. Complications of percutaneous bone tumor cryoablation: a 10-year experience. Radiology 2019; 291 (02) 521-528
- 9 Chen C, Garlich J, Vincent K, Brien E. Postoperative complications with cryotherapy in bone tumors. J Bone Oncol 2017; 7: 13-17
- 10 Papalexis N, Savarese LG, Peta G. et al. The new ice age of musculoskeletal intervention: role of percutaneous cryoablation in bone and soft tissue tumors. Curr Oncol 2023; 30 (07) 6744-6770
- 11 Lippa N, Sargos P, Italiano A. et al. Standardization of selection criteria for percutaneous image-guided cryoablation of recurrent soft-tissue sarcomas. Diagn Interv Imaging 2014; 95 (11) 1071-1077
- 12 Maybody M, Tang PQ, Moskowitz CS, Hsu M, Yarmohammadi H, Boas FE. Pneumodissection for skin protection in image-guided cryoablation of superficial musculoskeletal tumours. Eur Radiol 2017; 27 (03) 1202-1210
- 13 Sag AA, Riedel RF, Eward WC, Visgauss JD, Brigman BE. Hydropneumodissection-assisted cryoablation of recurrent sarcoma adjacent to the sciatic nerve as a limb-sparing alternative to hindquarter amputation. J Vasc Interv Radiol 2023; 34 (05) 923-926.e1
- 14 Cazzato RL, Gantzer J, de Marini P. et al. Sporadic desmoid tumours: systematic review with reflection on the role of cryoablation. Cardiovasc Intervent Radiol 2022; 45 (05) 613-621
- 15 Kwak K, Yu B, Lewandowski RJ, Kim DH. Recent progress in cryoablation cancer therapy and nanoparticles mediated cryoablation. Theranostics 2022; 12 (05) 2175-2204
- 16 Kim DK, Won JY, Park SY. Percutaneous cryoablation for renal cell carcinoma using ultrasound-guided targeting and computed tomography-guided ice-ball monitoring: radiation dose and short-term outcomes. Acta Radiol 2019; 60 (06) 798-804
- 17 Won JY, Kim DK, Park SY. Renal mass cryoablation: melting time analysis of radiographic ice-ball after 5-minute active thawing by using serial ultrasound. Eur J Radiol 2021; 134: 109409
- 18 Al-Assam H, Botchu R, Azzopardi C, Stevenson JD, James SL, Patel A. Measurement analysis of ice ball size during CT-guided cryoablation procedures for better prediction of final ice ball size and avoidance of complications. Indian J Radiol Imaging 2023; 33 (03) 321-326
- 19 Havez M, Lippa N, Al-Ammari S. et al. Percutaneous image-guided cryoablation in inoperable extra-abdominal desmoid tumors: a study of tolerability and efficacy. Cardiovasc Intervent Radiol 2014; 37 (06) 1500-1506
- 20 Mandel JE, Kim D, Yarmohammadi H. et al. Percutaneous cryoablation provides disease control for extra-abdominal desmoid-type fibromatosis comparable with surgical resection. Ann Surg Oncol 2022; 29 (01) 640-648









