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Epithelioid fibrous histiocytoma: molecular characterization of ALK fusion partners in 23 cases

Epithelioid fibrous histiocytoma: molecular characterization of ALK fusion partners in 23 cases

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1989608452

Epithelioid fibrous histiocytoma: molecular characterization of ALK fusion partners in 23 cases

About this item

Full title

Epithelioid fibrous histiocytoma: molecular characterization of ALK fusion partners in 23 cases

Publisher

New York: Elsevier Inc

Journal title

Modern pathology, 2018-05, Vol.31 (5), p.753-762

Language

English

Formats

Publication information

Publisher

New York: Elsevier Inc

More information

Scope and Contents

Contents

Epithelioid fibrous histiocytoma is a rare and distinctive cutaneous neoplasm. Most cases harbor ALK rearrangement and show ALK overexpression, which distinguish this neoplasm from conventional cutaneous fibrous histiocytoma and variants. SQSTM1 and VCL have previously been shown to partner with ALK in one case each of epithelioid fibrous histiocyt...

Alternative Titles

Full title

Epithelioid fibrous histiocytoma: molecular characterization of ALK fusion partners in 23 cases

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1989608452

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1989608452

Other Identifiers

ISSN

0893-3952

E-ISSN

1530-0285

DOI

10.1038/modpathol.2017.191

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