Pediatric mortality from neurofibromatosis and malignant peripheral nerve sheath tumors in Brazil, 2008–2023: a 16-year nationwide analysis of persistent disparities
PURPOSE: Neurofibromatosis (NF) comprises genetic tumor predisposition syndromes with multisystem involvement, yet pediatric mortality data remain scarce in middle-income settings. Malignant peripheral nerve sheath tumors (MPNST) represent the leading cause of premature death in this population. This study analyzed 16-year temporal trends and regional disparities in pediatric NF/MPNST mortality and hospitalizations in Brazil. METHODS: We conducted a nationwide ecological study of individuals aged 0-19 years from 2008 to 2023. Mortality data were obtained from the Mortality Information System (SIM) and hospital admissions from the Hospital Information System (SIH/SUS), with temporal trends assessed using Prais-Winsten regression. We calculated Age-Specific Mortality Rates (ASMRs) and assessed excess mortality risk using Standardized Mortality Ratios (SMR) to identify regional disparities. RESULTS: A total of 177 pediatric deaths were identified, with MPNST accounting for 64.9% (N = 115) and NF for 35.1% (N = 62). SMR analysis revealed significant geographic inequalities. Children aged 0-9 in the South region faced a mortality risk double that of the reference population (SMR = 2.02; 95% CI 1.08-3.46; p = 0.010), whereas adolescents in the North region exhibited significantly lower-than-expected mortality. Despite global therapeutic advances, mortality rates in Brazil remained statistically stagnant across all age groups and conditions (p values were non-significant). Conversely, NF-related hospitalizations demonstrated an increasing trend (+ 2.98% annually for ages 0-9; + 1.94% for ages 10-19), while MPNST admissions remained stable. CONCLUSION: Pediatric mortality from NF and MPNST in Brazil has remained unchanged for 16 years, contrasting with the rising trend in NF-related hospitalizations. This discrepancy, coupled with marked regional disparities, suggests persistent structural challenges in early diagnosis and equitable access to specialized oncology care. These findings highlight a critical need for national notification systems and improved therapeutic strategies for affected children and adolescents.
Authors
- Gustavo Rassier Isolan (ORCID: https://orcid.org/0000-0002-7863-0112)
- Bruna Louise Silva (ORCID: https://orcid.org/0000-0001-9756-4846)
- Rafael Roesler (ORCID: https://orcid.org/0000-0001-6016-2261)
- Karina Munhoz de Paula Alves Coelho (ORCID: https://orcid.org/0000-0002-4743-8742)
- Marcelo Gerardin Poirot Land (ORCID: https://orcid.org/0000-0001-9792-3167)
- Paula Franczak (ORCID: https://orcid.org/0000-0002-7462-9085)
- C F Fronza
- Bárbara Sarni Sanches (ORCID: https://orcid.org/0000-0002-3164-2626)
- Francis Rossetti Pedack (ORCID: https://orcid.org/0009-0007-9382-5042)
- Raquel Francine Liermann Garcia (ORCID: https://orcid.org/0009-0005-2600-6640)
- Paulo Henrique Condeixa de França (ORCID: https://orcid.org/0000-0002-1750-9132)
- José Cândido Caldeira Xavier-Júnior
- José Guilherme Pickler
- Acir Alves Coelho Junior
Institutions
- Universidade Federal do Rio de Janeiro (BR)
- Universidade Federal do Rio Grande do Sul (BR)
- Committee for Economic Development (US)
- Universidade do Estado de Santa Catarina (BR)
- Universidade Presbiteriana Mackenzie (BR)
- Centro Universitário Católico Salesiano Auxilium (BR)
- Hospital de Clínicas de Porto Alegre (BR)
- Center for Children (US)
- Universidade da Região de Joinville (BR)
- Pathological Society (GB)
- Hospital Municipal São José (BR)
- Children's Cancer Therapy Development Institute (US)
- National Institute of Science and Technology (ID)
- Universidade Estadual Paulista (Unesp) (BR)
Publication Details
- Journal
- Child s Nervous System
- Published
- 2026-07-24
- DOI
- https://doi.org/10.1007/s00381-026-07415-5
- Primary Topic
- Neurofibromatosis and Schwannoma Cases
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Universidade Federal do Rio Grande do Sul