| Literature DB >> 18561177 |
Susana Lisboa1, Nuno Cerveira, Joana Vieira, Lurdes Torres, Ana Maia Ferreira, Mariana Afonso, Lucília Norton, Rui Henrique, Manuel R Teixeira.
Abstract
Alveolar rhabdomyosarcoma (ARMS) is characterized by two pathognomonic translocations, both involving the FOXO1 gene. We describe a case of a 10-year-old child with multiple lytic lesions involving all the vertebral bodies, sternum and femur and a bone marrow biopsy compatible with a small round cell neoplasia, but no evidence of a primary tumor. Interphase FISH analysis with specific probes evidenced a rearrangement involving the FOXO1 gene and RT-PCR identified the PAX7-FOXO1 fusion transcript. These data show a case of ARMS with no evidence of primary tumor presenting the PAX7-FOXO1 fusion gene. (c) 2008 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2008 PMID: 18561177 DOI: 10.1002/pbc.21646
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167