Intracranial Myxoid Mesenchymal Tumor With EWSR1-ATF1 Fusion

Author:

Ballester Leomar Y123,Meis Jeanne M4,Lazar Alexander J45,Prabhu Sujit S6,Hoang Kimberly B6,Leeds Norman E7,Fuller Gregory N4

Affiliation:

1. From the Department of Pathology and Laboratory Medicine

2. Vivian L. Smith Department of Neurosurgery (LYB), University of Texas Health Science Center at Houston, Houston, Texas

3. Memorial Hermann Hospital-Texas Medical Center, Houston, Texas

4. Department of Pathology

5. Department of Genomic Medicine

6. Department of Neurosurgery

7. Department of Diagnostic Radiology (Section of Neuroradiology) (NEL), The University of Texas MD Anderson Cancer Center, Houston, Texas

Abstract

Abstract Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor that arises primarily in the extremities of young adults. Recurrent gene fusions involving EWSR1 with members of the cAMP response element binding protein (CREB) family have been reported in a diverse group of tumors, including AFH. AFH-like lesions have been reported to occur intracranially and the reported cases show low proliferation indices, frequently have a connection with the dura, and show recurrent EWSR1 rearrangements. These tumors have been termed intracranial myxoid mesenchymal tumor with EWSR1-CREB family gene fusions. A literature search identified 11 reported cases of intracranial AFH-like lesions with an EWSR1 rearrangement. Here, we report a case of intracranial myxoid mesenchymal tumor with an EWSR1-ATF1 fusion in an adult patient, and review the existing literature on this recently described entity.

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Neurology,General Medicine,Pathology and Forensic Medicine

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