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10.1097/PAS.0000000000000788

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suck abstract from ncbi


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pmid28009602      Am+J+Surg+Pathol 2017 ; 41 (4): 482-490
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  • EWSR1 Fusions With CREB Family Transcription Factors Define a Novel Myxoid Mesenchymal Tumor With Predilection for Intracranial Location #MMPMID28009602
  • Kao YC; Sung YS; Zhang L; Chen CL; Vaiyapuri S; Rosenblum MK; Antonescu CR
  • Am J Surg Pathol 2017[Apr]; 41 (4): 482-490 PMID28009602show ga
  • Recurrent gene fusions involving EWSR1 with members of the cAMP response element binding protein (CREB) family (ATF1 and CREB1) have been reported in a diverse group of tumors including angiomatoid fibrous histiocytoma (AFH), soft tissue and gastrointestinal clear cell sarcoma, primary pulmonary myxoid sarcoma, and hyalinizing clear cell carcinoma of salivary gland. We have recently encountered a group of 5 myxoid mesenchymal tumors positive for EWSR1 fusions with one of the CREB family member (ATF1, CREB1, and CREM), with histologic features distinct from any of the previously described pathologic entities. Tumors occurred in children or young adults (12 to 23 y; mean, 18 y), with equal sex distribution. All except 1 were intracranial (intra-axial, 2; meningeal, 2), whereas 1 was perirectal. Histologically, the tumors were well circumscribed, often lobulated, composed of uniform ovoid to round cells, and arranged in cord-like or reticular structures in a myxoid background. All except 1 displayed unique sunburst amianthoid fibers. Immunohistochemically, tumors were positive for epithelial membrane antigen (5/5; 4 focal, 1 diffuse) and desmin (3/5). A novel EWSR1-CREM fusion was identified by RNA sequencing in the perirectal tumor, which was further confirmed by fluorescence in situ hybridization (FISH) and reverse transcription-polymerase chain reaction (RT-PCR). A second case with similar EWSR1-CREM fusion was identified by RT-PCR and FISH in a meningeal tumor. The remaining cases studied by FISH showed the presence of EWSR1-CREB1 fusion in 2 cases and EWSR1-ATF1 in 1. In conclusion, we report a distinct group of myxoid mesenchymal neoplasms occurring in children or young adults with a predilection for intracranial locations. Although the immunoprofile [epithelial membrane antigen (EMA), desmin] and the fusion type raise the possibility of a myxoid AFH, none of the typical histologic findings of AFH were present, suggesting a novel entity.
  • |*Gene Fusion[MESH]
  • |Adolescent[MESH]
  • |Biomarkers, Tumor/analysis/*genetics[MESH]
  • |Biopsy[MESH]
  • |Brain Neoplasms/chemistry/*genetics/pathology[MESH]
  • |Calmodulin-Binding Proteins/*genetics[MESH]
  • |Child[MESH]
  • |Cyclic AMP Response Element Modulator/*genetics[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunohistochemistry[MESH]
  • |In Situ Hybridization, Fluorescence[MESH]
  • |Male[MESH]
  • |Oncogene Proteins, Fusion/*genetics[MESH]
  • |RNA-Binding Protein EWS[MESH]
  • |RNA-Binding Proteins/*genetics[MESH]
  • |Rectal Neoplasms/chemistry/*genetics/pathology[MESH]
  • |Reverse Transcriptase Polymerase Chain Reaction[MESH]
  • |Sequence Analysis, RNA[MESH]
  • |Soft Tissue Neoplasms/chemistry/*genetics/pathology[MESH]
  • |Stromal Cells/chemistry/pathology[MESH]


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