Volume 64, Issue 1 pp. 88-100
Review

Rarely metastasizing soft tissue tumours

D Chas Mangham

D Chas Mangham

Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Trust, Robert Aitken Institute of Clinical Research and School of Cancer Sciences, Medical School, Birmingham University, Birmingham, UK

Department of Musculoskeletal Pathology, Robert Jones and Agnes Hunt Orthopaedic Hospital NHS Trust, Oswestry, UK

Search for more papers by this author
Lars-Gunnar Kindblom

Corresponding Author

Lars-Gunnar Kindblom

Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Trust, Robert Aitken Institute of Clinical Research and School of Cancer Sciences, Medical School, Birmingham University, Birmingham, UK

Address for correspondence: L-G Kindblom, Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Trust, Robert Aitken Institute of Clinical Research, Birmingham B15 2TT, UK. e-mail: [email protected]Search for more papers by this author
First published: 12 October 2013
Citations: 10
The copyright line for this paper has been changed since first published on 28 November 2013, due to removal of Open Access.

Abstract

Soft tissue tumours that rarely metastasize have been afforded their own subcategory in recent WHO classifications. This review discusses the nature of these tumours and the difficulty in constructing usefully simple classifications for heterogeneous and complex groups of tumours. We also highlight the specific rarely metastasizing soft tissue tumours that have been recently added to the WHO classification (phosphaturic mesenchymal tumour, pseudomyogenic haemangioendothelioma) and those entities where there have been recent important defining genetic discoveries (myxoinflammatory fibroblastic sarcoma, solitary fibrous tumour, myoepitheliomas).

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.