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Summary
The fourth edition of the World Health Organization (WHO) Classification of Tumours
of Soft Tissue and Bone was published in February 2013, and serves to provide an updated
classification scheme and reproducible diagnostic criteria for pathologists. Given
the relative rarity of soft tissue tumours and the rapid rate of immunohistochemical
and genetic/molecular developments (not infrequently facilitating recognition of new
tumour entities), this updated text edited by a consensus group is important for both
practising pathologists and oncologists. The 2013 WHO classification includes several
changes in soft tissue tumour classification, including several new entities (e.g.,
pseudomyogenic haemangioendothe-lioma, haemosiderotic fibrolipomatous tumour, and
acral fibromyxoma), three newly included sections for gastrointestinal stromal tumours,
nerve sheath tumours, and undifferentiated/unclassified soft tissue tumours, respectively,
various ‘reclassified’ tumours, and a plethora of new genetic and molecular data for
established tumour types that facilitate better definition and are useful as diagnostic
tools. This article briefly outlines these updates based on the 2013 WHO classification
of soft tissue tumours.
Key words
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Article info
Publication history
Accepted:
November 13,
2013
Received:
October 28,
2013
Identification
Copyright
© 2014 Royal College of Pathologists of Australasia. Published by Elsevier Inc. All rights reserved.