Abstract The Children's Oncology Group (COG) uses Clinical Group (CG) and modified
Tumor Node Metastasis (TNM) stage to classify rhabdomyosarcoma (RMS). CG is based on …

Simple Summary Pediatric testicular tumors are rare and represent 1% to 2% of all solid
tumors in children. Germ-cell tumors are the most frequent etiology; most are benign in the …

Rhabdomyosarcoma, although rare, is the most frequent soft tissue sarcoma in children and
adolescents. It can present as a mass at nearly any site in the body, with most common …

Background In certain rare undifferentiated small round cell sarcomas new specific
molecular CIC‐DUX4/other partner, BCOR‐CCNB3/other partner, YWHAE fusions, or BCOR …

Simple Summary Evidence-based medicine uses healthcare professional experience,
research evidence, and patient preferences to support the best decisions in healthcare …

Simple Summary Although survival after rhabdosarcoma treatment has improved over the
years, one third of patients still develop locoregional relapse. This review aims to highlight …

Nuclear medicine and molecular imaging have a small but growing role in the management
of paediatric and neonatal diseases. During the past decade, combined PET/MRI has …

The most common abdominal malignancies diagnosed in the pediatric population include
neuroblastoma, Wilms tumor, hepatoblastoma, lymphoma, germ cell tumor, and …

Background Cross-sectional imaging-based morphological characteristics of pediatric
rhabdomyosarcoma have failed to predict outcomes. Objective To evaluate the feasibility …

Abstract In the United States, more than 10 000 cancers occur annually in children aged 0–
14 years, and more than 5000 in adolescents aged 15–19. In the last 50 years, significant …