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Journal ArticleDOI

The evolving classification of soft tissue tumours – an update based on the new 2013 WHO classification

Christopher D.M. Fletcher
- 01 Jan 2006 - 
- Vol. 64, Iss: 1, pp 2-11
TLDR
A brief overview summarizes changes in the classification in each of the broad categories of soft tissue tumour (adipocytic, fibroblastic, etc.) and also provides a short summary of newer genetic data which have been incorporated in the WHO classification.
Abstract
The new World Health Organization (WHO) classification of soft tissue tumours was published in early 2013, almost 11 years after the previous edition. While the number of newly recognized entities included for the first time is fewer than that in 2002, there have instead been substantial steps forward in molecular genetic and cytogenetic characterization of this family of tumours, leading to more reproducible diagnosis, a more meaningful classification scheme and providing new insights regarding pathogenesis, which previously has been obscure in most of these lesions. This brief overview summarizes changes in the classification in each of the broad categories of soft tissue tumour (adipocytic, fibroblastic, etc.) and also provides a short summary of newer genetic data which have been incorporated in the WHO classification.

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Citations
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Journal ArticleDOI

Pericytes: developmental, physiological, and pathological perspectives, problems, and promises.

TL;DR: The history of investigations into pericytes, the mural cells of blood microvessels, are reviewed, emerging concepts are indicated, and problems and promise are pointed out.
Journal ArticleDOI

Survival and prognosis with osteosarcoma: outcomes in more than 2000 patients in the EURAMOS-1 (European and American Osteosarcoma Study) cohort

Sigbjørn Smeland, +51 more
TL;DR: Survival rates from >2000 patients registered to EURAMOS-1 demonstrated survival rates in concordance with institution- or group-level osteosarcoma trials, and known prognostic factors were reaffirmed.
Journal ArticleDOI

Side population cells isolated from mesenchymal neoplasms have tumor initiating potential.

TL;DR: A subpopulation of cells within a broad range of benign and malignant mesenchymal tumors with tumor-initiating capacity is identified and it is suggested that therapeutically targeting this sub population of cells could be used to improve patient outcome.
References
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Pathology and genetics of tumors of soft tissue and bone

C Fletcher
TL;DR: This list includes tumours of undefined neoplastic nature, which are of uncertain differentiation Bone Tumours, Ewing sarcoma/Primitive neuroedtodermal tumour, Myogenic, lipogenic, neural and epithelial tumours, and others.
Journal ArticleDOI

NCCN Task Force report: update on the management of patients with gastrointestinal stromal tumors

TL;DR: The standard of care for managing patients with gastrointestinal stromal tumors (GISTs) rapidly changed after the introduction of effective molecularly targeted therapies involving tyrosine kinase inhibitors (TKIs), such as imatinib mesylate and sunitinib malate.
Journal ArticleDOI

Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics

TL;DR: STAT6 is a highly sensitive and almost perfectly specific immunohistochemical marker for SFT and can be helpful to distinguish this tumor type from histologic mimics.
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