Rarely metastasizing soft tissue tumours
Correction(s) for this article
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Erratum
- Volume 64Issue 4Histopathology
- pages: 608-608
- First Published online: February 4, 2014
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 authorCorresponding 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 authorD 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 authorCorresponding 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 authorAbstract
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).
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