| Literature DB >> 24896634 |
Jill C Rubinstein1, Arjun Visa, Lei Zhang, Cristina R Antonescu, Emily R Christison-Lagay, Raffaella Morotti.
Abstract
We present the case of a 6-year-old boy with a deceptively bland spindle cell renal neoplasm found to harbor the EWSR1-CREB3L1 gene fusion. This fusion has recently been described as a variant translocation in low-grade fibromyxoid sarcoma (LGFMS), a tumor more typically characterized by a recurrent t(7;16) chromosomal translocation, resulting in the fusion of FUS and CREB3L2 genes. LGFMS is an indolent tumor with late metastatic potential and a propensity for long-term disease recurrence. The tumor is rare in children, with only 33 published cases. In the pediatric population, it has not previously been reported arising in the kidney.Entities:
Keywords: EWSR1-CREB3L1 fusion; low-grade fibromyxoid sarcoma; pediatric; renal
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Year: 2014 PMID: 24896634 DOI: 10.2350/14-05-1487-CR.1
Source DB: PubMed Journal: Pediatr Dev Pathol ISSN: 1093-5266