Myxofibrosarcoma of the extremity and trunk

Author:

Ghazala C. G.1,Agni N. R.1,Ragbir M.1,Dildey P.1,Lee D.1,Rankin K. S.2,Beckingsale T. B.1,Gerrand C. H.1

Affiliation:

1. Newcastle Upon Tyne Hospitals NHS Foundation Trust, Freeman Hospital, Newcastle Upon Tyne NE7 7DN, UK.

2. Newcastle University, Newcastle Upon Tyne NE1 7RU, UK.

Abstract

Aims Myxofibrosarcomas (MFSs) are malignant soft-tissue sarcomas characteristically presenting as painless slowly growing masses in the extremities. Locally infiltrative growth means that the risk of local recurrence is high. We reviewed our experience to make recommendations about resection strategies and the role of the multidisciplinary team in the management of these tumours. Patients and Methods Patients with a primary or recurrent MFS who were treated surgically in our unit between 1997 and 2012 were included in the study. Clinical records and imaging were reviewed. A total of 50 patients with a median age of 68.4 years (interquartile range 61.6 to 81.8) were included. There were 35 men; 49 underwent surgery in our unit. Results The lower limb was the most common site (32/50, 64%). The mean size of the tumours was 8.95 cm (1.5 to 27.0); 26 (52%) were French Fédération Nationale des Centres de Lutte Contre le Cancer grade III. A total of 21 (43%) had positive margins after the initial excision; 11 underwent further excision. Histology showed microscopic spread of up to 29 mm beyond macroscopic tumour. Local recurrence occurred in seven patients (14%) at a mean of 21 months (3 to 33) and 15 (30%) developed metastases at a mean of 17 months (3 to 30) post-operatively. Conclusion High rates of positive margins and the need for further excision makes this tumour particularly suited to management by multidisciplinary surgical teams. Microscopic tumour can be present up to 29 mm from the macroscopic tumour in fascially-based tumours. Cite this article: Bone Joint J 2016;98-B:1682–8.

Publisher

British Editorial Society of Bone & Joint Surgery

Subject

Orthopedics and Sports Medicine,Surgery

Reference26 articles.

1. Mentzel T, Hogendoorn PCW, Huang HY. Myxofibrosarcoma In: Fletcher CDM, Bridge JA, Hogendoorn PCW, Mertens F, eds. WHO Classification of Tumours of Soft Tissue and Bone . Fourth ed. Lyon: World Health Organization, 2013:93–94.

2. Fletcher CDM, Unni KK, Mertens F World Health Organization Classification of Tumours. Pathology and genetics of tumours of soft tissue and bone . Lyon: IARC Press, 2002.

3. No authors listed. National Institute for Health and Clinical Excellence. Improving Outcomes for People with Sarcoma. https://www.nice.org.uk/guidance/csg9 (date last accessed 12 July 2016).

4. Primary Cerebral Myxofibrosarcoma

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