1.
Ann Intern Med
; 167(5): 362-363, 2017 09 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28869979
2.
Cancer Genet Cytogenet
; 201(1): 1-5, 2010 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20633761
RESUMO
From a morphologic standpoint, Ewing sarcoma (EWS) is one of a number of pediatric malignancies that are characterized by sheets of small, round, blue cells. Ewing sarcoma can usually be differentiated from other small round blue cell tumors by the presence of a gene rearrangement having a consistent breakpoint within the Ewing sarcoma gene (EWSR1) at 22q12. Although the most common translocation partner is FLI1, located at 11q24, there is a growing list of alternate rearrangements involving different loci. We describe the first example of a soft-tissue sarcoma morphologically and immunohistochemically similar to Ewing sarcoma, but with a novel t(18;19)(q23;q13.2).