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Periosteal Ewing Sarcoma Family of Tumors of the Femur Confirmed by Molecular Detection of EWS-FLI1 Fusion Gene Transcripts

Authors :
Hakozaki, Michiyuki
Hojo, Hiroshi
Tajino, Takahiro
Yamada, Hitoshi
Kikuta, Atsushi
Ito, Masaki
Sano, Hideki
Mochizuki, Kazuhiro
Akaihata, Mitsuko
Kikuchi, Shinichi
Abe, Masafumi
Source :
Journal of Pediatric Hematology / Oncology; August 2007, Vol. 29 Issue: 8 p561-565, 5p
Publication Year :
2007

Abstract

Ewing sarcoma family of tumors (ESFT) comprise common sarcomas in children and young adults. Such tumors usually occur in the medullary cavity of long bones and directly invade cortical bone and circumferential soft tissue, including periosteum. Periosteal ESFT is extremely rare and only a small numbers of cases, including cases not confirmed by molecular detection of chimeric fusion gene, have been reported. We describe herein a case of periosteal ESFT of the femur in a 13-year-old boy harboring EWS-FLI1 chimeric fusion gene transcripts detected by reverse transcription-polymerase chain reaction analysis. This report may provide an opportunity for further evaluation of the EWS-FLI1 type 1 fusion gene and detection of prognostic significance in periosteal ESFT.

Details

Language :
English
ISSN :
10774114 and 15363678
Volume :
29
Issue :
8
Database :
Supplemental Index
Journal :
Journal of Pediatric Hematology / Oncology
Publication Type :
Periodical
Accession number :
ejs48736789
Full Text :
https://doi.org/10.1097/MPH.0b013e3180f61ba3