WHO classification of soft tissue tumours: an update based on the 2013 (4th) edition

VY Jo, CDM Fletcher - Pathology-Journal of the RCPA, 2014 - journals.lww.com
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 …

[HTML][HTML] Epithelioid hemangioendothelioma, an ultra-rare cancer: a consensus paper from the community of experts

S Stacchiotti, AB Miah, AM Frezza, C Messiou… - ESMO open, 2021 - Elsevier
Highlights•This consensus paper provides key recommendations on the management of
epithelioid hemangioendothelioma (EHE).•Recommendations followed a consensus …

Tazemetostat, an EZH2 inhibitor, in relapsed or refractory B-cell non-Hodgkin lymphoma and advanced solid tumours: a first-in-human, open-label, phase 1 study

A Italiano, JC Soria, M Toulmonde, JM Michot… - The Lancet …, 2018 - thelancet.com
Background Activating enhancer of zeste homolog 2 (EZH2) mutations or aberrations of the
switch/sucrose non-fermentable (SWI/SNF) complex (eg, mutations or deletions of the …

Loss of H3K27 trimethylation distinguishes malignant peripheral nerve sheath tumors from histologic mimics

IM Schaefer, CDM Fletcher, JL Hornick - Modern Pathology, 2016 - nature.com
The diagnosis of malignant peripheral nerve sheath tumor is challenging, particularly in the
sporadic setting. Inactivation of the polycomb repressive complex 2 (PRC2), resulting from …

SMARCB1 (INI-1)-deficient sinonasal carcinoma: a series of 39 cases expanding the morphologic and clinicopathologic spectrum of a recently described entity

A Agaimy, A Hartmann, CR Antonescu… - The American journal …, 2017 - journals.lww.com
To more fully characterize the clinical and pathologic spectrum of a recently described tumor
entity of the sinonasal tract characterized by loss of nuclear expression of SMARCB1 (INI1) …

The epigenomics of sarcoma

BA Nacev, KB Jones, AM Intlekofer, JSE Yu… - Nature Reviews …, 2020 - nature.com
Epigenetic regulation is critical to physiological control of development, cell fate, cell
proliferation, genomic integrity and, fundamentally, transcriptional regulation. This …

Synovial sarcoma: defining features and diagnostic evolution

K Thway, C Fisher - Annals of diagnostic pathology, 2014 - Elsevier
Synovial sarcoma (SS) is a malignant mesenchymal neoplasm with variable epithelial
differentiation, with a propensity to occur in young adults and which can arise at almost any …

SWI/SNF chromatin remodeling and human malignancies

J Masliah-Planchon, I Bièche… - Annual Review of …, 2015 - annualreviews.org
The SWI/SNF complexes, initially identified in yeast 20 years ago, are a family of multi-
subunit complexes that use the energy of adenosine triphosphate (ATP) hydrolysis to …

[HTML][HTML] Clinicopathological and molecular characterization of SMARCA4-deficient thoracic sarcomas with comparison to potentially related entities

A Yoshida, E Kobayashi, T Kubo, M Kodaira, T Motoi… - Modern Pathology, 2017 - Elsevier
A growing number of studies suggest critical tumor suppressor roles of the SWI/SNF
chromatin remodeling complex in a variety of human cancers. The recent discovery of …

Nuclear expression of CAMTA1 distinguishes epithelioid hemangioendothelioma from histologic mimics

LA Doyle, CDM Fletcher, JL Hornick - The American Journal of …, 2016 - journals.lww.com
Epithelioid hemangioendothelioma (EHE) is a malignant endothelial neoplasm
characterized by recurrent translocations involving chromosomal regions 1p36. 3 and 3q25 …