ALK rearrangement and overexpression in epithelioid fibrous histiocytoma. (Q53551480)

15 May 2018

title

ALK rearrangement and overexpression in epithelioid fibrous histiocytoma. (English)

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15 May 2018

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4

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15 May 2018

author name string

Leona A Doyle

series ordinal

1

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15 May 2018

Adrián Mariño-Enriquez

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2

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15 May 2018

Christopher D M Fletcher

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3

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15 May 2018

publication date

10 April 2015

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15 May 2018

published in

Modern Pathology

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15 May 2018

volume

28

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issue

7

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15 May 2018

page(s)

904-912

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https://scigraph.springernature.com/pub.10.1038/modpathol.2015.49

exact match

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cites work

Epithelioid benign fibrous histiocytoma of skin: clinico-pathological analysis of 20 cases of a poorly known variant.

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Epithelioid cell histiocytoma: a simulant of vascular and melanocytic neoplasms

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Metastasizing "benign" cutaneous fibrous histiocytoma: a clinicopathologic analysis of 16 cases

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Malignant dermatofibroma: clinicopathological, immunohistochemical, and molecular analysis of seven cases.

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Advances in understanding the pathogenesis of systemic anaplastic large cell lymphomas

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Epithelioid inflammatory myofibroblastic sarcoma: An aggressive intra-abdominal variant of inflammatory myofibroblastic tumor with nuclear membrane or perinuclear ALK.

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Crizotinib in ROS1-rearranged non-small-cell lung cancer.

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Inflammatory myofibroblastic tumors harbor multiple potentially actionable kinase fusions

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ALK rearrangement in sickle cell trait-associated renal medullary carcinoma

21 January 2018

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Renal cell carcinoma with novel VCL-ALK fusion: new representative of ALK-associated tumor spectrum

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VCL-ALK renal cell carcinoma in children with sickle-cell trait: the eighth sickle-cell nephropathy?

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Identification of a novel fusion, SQSTM1-ALK, in ALK-positive large B-cell lymphoma.

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STAT3 pathway is activated in ALK-positive large B-cell lymphoma carrying SQSTM1-ALK rearrangement and provides a possible therapeutic target

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ALK as a paradigm of oncogenic promiscuity: different mechanisms of activation and different fusion partners drive tumors of different lineages

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Cutaneous syncytial myoepithelioma: clinicopathologic characterization in a series of 38 cases

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Epithelioid sarcoma.A sarcoma simulating a granuloma or a carcinoma

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Epithelioid sarcoma of Enzinger

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Hybrid schwannoma/perineurioma: clinicopathologic analysis of 42 distinctive benign nerve sheath tumors

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Kinase fusions are frequent in Spitz tumours and spitzoid melanomas

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Clinical and pathologic findings of Spitz nevi and atypical Spitz tumors with ALK fusions.

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Metastasizing fibrous histiocytoma of the skin: a clinicopathologic and immunohistochemical analysis of three cases

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12 December 2020

Cell Differentiation in Benign Cutaneous Fibrous Histiocytomas An Immunohistochemical Study with Antibodies to Histiomonocytic Cells and Intermediate Filament Proteins

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Atypical fibrous histiocytoma of the skin with CD30 and p80/ALK1 positivity and ALK gene rearrangement

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Ultrastructural Aspects of the Dermatofibroma

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Desmin and CD34 positivity in cellular fibrous histiocytoma: an immunohistochemical analysis of 100 cases

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Epithelioid sarcoma: an immunohistochemical analysis of 112 classical and variant cases and a discussion of the differential diagnosis

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Loss of INI1 expression is characteristic of both conventional and proximal-type epithelioid sarcoma.

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Expression of ROS1 predicts ROS1 gene rearrangement in inflammatory myofibroblastic tumors.

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Epithelioid cell histiocytoma of the skin with clonal ALK gene rearrangement resulting in VCL-ALK and SQSTM1-ALK gene fusions.

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Epithelioid cell histiocytoma. A clinicopathologic and immunohistochemical study of eight cases

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Epithelioid cell histiocytoma. A report of 10 cases including a new cellular variant

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EMA positivity in epithelioid fibrous histiocytoma: a potential diagnostic pitfall

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Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma

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Typical, dysplastic, congenital, and Spitz nevi: a comparative immunohistochemical study

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10.1038/MODPATHOL.2015.49

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DOI

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15 May 2018

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15 May 2018