| Literature DB >> 27542645 |
Regan F Williams1, Israel Fernandez-Pineda2, Ankush Gosain3.
Abstract
Pediatric sarcomas are a heterogeneous group of tumors accounting for approximately 10% of childhood solid tumors. Treatment is focused on multimodality therapy, which has improved the prognosis over the past two decades. Current regimens focus on decreasing treatment for low-risk patients to decrease the long-term side effects while maximizing therapy for patients with metastatic disease to improve survival. Pediatric sarcomas can be divided into soft tissue sarcomas and osseous tumors. Soft tissue sarcomas are further delineated into rhabdomyosarcomas, which affect young children and nonrhabdomyosarcomas, which are most common in adolescents. The most common bone sarcomas are osteosarcomas and Ewing's sarcoma.Entities:
Keywords: Ewing’s sarcoma; Nonrhabdomyosarcoma soft tissue sarcoma; Osteosarcoma; Rhabdomyosarcoma
Mesh:
Year: 2016 PMID: 27542645 DOI: 10.1016/j.suc.2016.05.012
Source DB: PubMed Journal: Surg Clin North Am ISSN: 0039-6109 Impact factor: 2.741