Head and neck rhabdomyosarcoma in pediatric patients : an international collaborative study

dc.contributor.authorGallagher, Karen Patricia Dominguez
dc.contributor.authorHunter, Keith D.
dc.contributor.authorArboleda, Lady Paola Aristizabal
dc.contributor.authorPedroso, Caique Mariano
dc.contributor.authorMariz, Bruno Augusto Linhares Almeida
dc.contributor.authorPenafort, Paulo Victor Mendes
dc.contributor.authorDe Souza, Lucas Lacerda
dc.contributor.authorRodrigues-Fernandes, Carla Isabelly
dc.contributor.authorTager, Elena Maria Jose Roman
dc.contributor.authorCarlos, Roman
dc.contributor.authorRobinson, Liam
dc.contributor.authorSchouwstra, Ciska-Mari
dc.contributor.authorVillanueva-Sanchez, Francisco German
dc.contributor.authorGomez, Francisco Jose Paz
dc.contributor.authorGonzalez-Galvan, Maria del Carmen
dc.contributor.authorMartins-de-Barros, Allan Vinicius
dc.contributor.authorDe Vasconcelos Carvalho, Marianne
dc.contributor.authorCavalcante, Roberta Barroso
dc.contributor.authorTuratti, Eveline
dc.contributor.authorPontes, Helder Antonio Rebelo
dc.contributor.authorSiqueira, Sheila Aparecida Coelho
dc.contributor.authorDe Mendonca, Regina Maria Holanda
dc.contributor.authorInnocentini, Lara Maria Alencar Ramos
dc.contributor.authorDe Macedo, Leandro Dorigan
dc.contributor.authorRibeiro-Silva, Alfredo
dc.contributor.authorAbrahao, Aline Correa
dc.contributor.authorRomanach, Mario Jose
dc.contributor.authorVan Heerden, W.F.P. (Willem Francois Petrus)
dc.contributor.authorVargas, Pablo Agustin
dc.contributor.authorSantos-Silva, Alan Roger
dc.date.accessioned2025-04-10T05:19:48Z
dc.date.issued2025-02
dc.descriptionDATA 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.en_US
dc.description.abstractBACKGROUND : 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.en_US
dc.description.departmentOral Pathology and Oral Biologyen_US
dc.description.embargo2026-01-06
dc.description.librarianhj2024en_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.sponsorshipPathological Society of Great Britain and Ireland.en_US
dc.description.urihttp://wileyonlinelibrary.com/journal/jopen_US
dc.identifier.citationGallagher, 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.en_US
dc.identifier.issn0904-2512 (print)
dc.identifier.issn1600-0714 (online)
dc.identifier.other10.1111/jop.13600
dc.identifier.urihttp://hdl.handle.net/2263/101985
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rights© 2025 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. This is the pre-peer reviewed version of the following article : 'Head and neck rhabdomyosarcoma in pediatric patients: an international collaborative study', Journal of Oral Pathology and Medicine, vol. 54, no. 2, pp. 81-90, 2025, doi : 10.1111/jop.13600. The definite version is available at : http://wileyonlinelibrary.com/journal/jop.en_US
dc.subjectRhabdomyosarcoma (RMS)en_US
dc.subjectHead and necken_US
dc.subjectMolecularen_US
dc.subjectOral cavityen_US
dc.subjectPediatric patientsen_US
dc.subjectSDG-03: Good health and well-beingen_US
dc.titleHead and neck rhabdomyosarcoma in pediatric patients : an international collaborative studyen_US
dc.typePostprint Articleen_US

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