Title of article
Ewing sarcoma–peripheral neuroectodermal tumor of the kidney with a FUS–ERG fusion transcript
Author/Authors
Berg، نويسنده , , Thomas and Kalsaas، نويسنده , , Ann-Hilde and Buechner، نويسنده , , Jochen and Busund، نويسنده , , Lill-Tove، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2009
Pages
5
From page
53
To page
57
Abstract
The Ewing family of tumors (EFTs) represents a neoplastic entity characterized by specific chromosomal rearrangements. The most commonly detected translocation involves fusion of EWSR1 to one of the genes encoding ETS family of transcription factors, usually FLI1 or ERG. In rare cases, FUS or FEV has been shown to substitute for EWSR1. The detection of specific translocations by fluorescence in situ hybridization (FISH), reverse transcription-polymerase chain reaction (RT-PCR), or both has become a diagnostic hallmark for the EFTs. We report here a case of small round blue cell tumor detected in the kidney of a 3-year-old girl. The use of FISH in combination with RT-PCR led to identification of a novel FUS–ERG fusion transcript in the tumor, with FUS exons 1–5 fused in-frame to ERG exons 6–9. The results from the molecular analyses were critical for reaching a final diagnostic conclusion of Ewing tumor–peripheral neuroectodermal tumor and hence had important therapeutic implications for the patient.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2009
Journal title
Cancer Genetics and Cytogenetics
Record number
1829917
Link To Document