Ewing sarcoma is the second most frequent bone tumour of childhood and adolescence that
can also arise in soft tissue. Ewing sarcoma is a highly aggressive cancer, with a survival of …

Ewing's sarcoma is a highly aggressive bone and soft tissue tumor of children and young
adults. At the molecular genetic level Ewing's sarcoma is characterized by a balanced …

PURPOSE: Alveolar rhabdomyosarcoma (ARMS) is an aggressive soft tissue malignancy of
children and adolescents. Most ARMS patients express PAX3-FKHR or PAX7-FKHR gene …

ERG, an ETS family transcription factor, is known to be expressed in endothelial cells, and
oncogenic ERG gene fusions occur in subsets of prostatic carcinoma, acute myeloid …

Primary cardiac tumors are a rare entity whose incidence, according to surgery and autopsy
reports, is 0.3% to 0.7% of all cardiac tumors. 1 Metastasis to the heart from other primary …

Ewing sarcoma (ES) is rare in Japanese people, and only 30–40 patients develop the
disease annually. To diagnose ES, molecular techniques that aim to detect characteristic …

Primitive small blue round cell tumours (SBRCT) of childhood and young adults have been
problematic to diagnose and classify. Diagnosis is also complicated in cases with atypical …

Ewing's sarcoma is a small round-cell tumor typically arising in the bones, rarely in soft
tissues, of children and adolescents. Ewing's sarcoma has retained the most unfavorable …

Several recent advances have been made in the diagnosis and therapy of malignant small
round cell tumors that affect children, particularly in rhabdomyosarcoma, Ewing sarcoma …

Purpose EWS-ETS fusion genes are the driving force in Ewing's sarcoma pathogenesis.
Because of the variable breakpoint locations in the involved genes, there is heterogeneity in …