Head and neck rhabdomyosarcoma in pediatric patients : an international collaborative study
Loading...
Date
Authors
Gallagher, Karen Patricia Dominguez
Hunter, Keith D.
Arboleda, Lady Paola Aristizabal
Pedroso, Caique Mariano
Mariz, Bruno Augusto Linhares Almeida
Penafort, Paulo Victor Mendes
De Souza, Lucas Lacerda
Rodrigues-Fernandes, Carla Isabelly
Tager, Elena Maria Jose Roman
Carlos, Roman
Journal Title
Journal ISSN
Volume Title
Publisher
Wiley
Abstract
BACKGROUND : Rhabdomyosarcoma (RMS), a rare malignant tumor, frequently affects pediatric patients, with 35%–40% occurring in the head and neck. This study analyzes the clinicopathologic profile of pediatric head and neck rhabdomyosarcomas from Brazil, Guatemala, Mexico, and South Africa.
METHODS : We reviewed 44 cases from 10 Oral and Maxillofacial Pathology services, conducting immunohistochemical analyses of desmin, myogenin, Myo-D1, and Ki67, with quantification via QuPath software. Cases with ≥ 50% myogenin expression were tested for fusion status using AP2β, NOS-1, and HMGA2. Statistical analyses included the Kruskal–Wallis test for age and marker expression comparisons, Fisher's exact test for categorical variables, Spearman's rank correlation for marker relationships, and multinomial logistic regression to assess fusion status likelihood.
RESULTS : Cases were predominantly from Brazil (40.9%), followed by South Africa (27.3%), Guatemala (22.7%), and Mexico (9.1%). Two-thirds of patients were diagnosed in their first decade with no gender predilection. Nonparameningeal sites (45.5%) were more affected than parameningeal (40.9%) and orbital sites. Microscopically, embryonal RMS (77.3%) was most common, followed by alveolar (18.2%) and spindle cell (2.3%) tumors. Immunohistochemistry revealed positivity for myogenic markers, with significant differences in myogenin expression between embryonal and alveolar RMS variants (p < 0.05). Fusion status prediction identified two potential fusion-positive alveolar RMS cases, while all embryonal RMS and one alveolar RMS case appeared fusion-negative. Significant correlation with positive fusion status was found only between AP2β and NOS1 (p < 0.05).
CONCLUSION : Although there are slight clinical-demographic variations among pediatric head and neck rhabdomyosarcomas in these regions, identifying fusion status through immunohistochemistry remains a diagnostic challenge.
Description
DATA AVAILABILITY STATEMENT : The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions.
Keywords
Rhabdomyosarcoma (RMS), Head and neck, Molecular, Oral cavity, Pediatric patients, SDG-03: Good health and well-being
Sustainable Development Goals
SDG-03:Good heatlh and well-being
Citation
Gallagher, K.P.D., Hunter, K.D., Arboleda, L.P.A. et al. 2025, 'Head and neck rhabdomyosarcoma in pediatric patients: an international collaborative study', Journal of Oral Pathology and Medicine, vol. 54, no. 2, pp. 81-90, doi : 10.1111/jop.13600.