Pediatric thalamic incidentalomas: a retrospective analysis of their characteristics, evolution, management, and prognostic factors for progression
Jazyk angličtina Země Rakousko Médium electronic
Typ dokumentu časopisecké články
PubMed
40779174
PubMed Central
PMC12334495
DOI
10.1007/s00701-025-06632-2
PII: 10.1007/s00701-025-06632-2
Knihovny.cz E-zdroje
- Klíčová slova
- Follow-up, Incidentaloma, Pediatric tumor, Prognostic factors, Thalamus,
- MeSH
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- magnetická rezonanční tomografie MeSH
- mladiství MeSH
- nádory mozku * patologie diagnostické zobrazování chirurgie diagnóza MeSH
- náhodný nález * MeSH
- předškolní dítě MeSH
- prognóza MeSH
- progrese nemoci MeSH
- retrospektivní studie MeSH
- thalamus * patologie diagnostické zobrazování chirurgie MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
PURPOSE: The increasing availability of advanced neuroimaging has led to a rise in incidental findings among pediatric patients. Management strategies include immediate surgical intervention, observation or surgery upon progression. These are influenced by imaging characteristics, lesion behavior over time, patient/family preferences, and the lesion's surgical risks. The thalamus's eloquent location often warrants a more conservative approach. Identifying features predictive of growth could help inform clinical decisions regarding surveillance and potential intervention. METHODS: We retrospectively analyzed 44 pediatric patients with 46 thalamic incidentalomas, assessing radiological characteristics, temporal changes, and factors predictive of progression. Progression was defined as a change in size and/or new/increased contrast enhancement. Prognostic factors for progression (demographics, initial tumor volume, extension beyond thalamus, changes in enhancement, margin characteristics) were assessed for significance. RESULTS: Of 46 incidentalomas, 40 were followed longitudinally. Nine incidentalomas (22.5%) showed regression, while nine (22.5%) progressed. The average time to regression was 947 days, and to progression, 516 days. Three patients underwent biopsy due to progressive changes; each was diagnosed with low-grade glioma. Statistical analysis revealed that initial incidentaloma volume, extension beyond the thalamus, and contrast enhancement were significantly associated with progression (p = 0.025, p < 0.001, and p = 0.001, respectively). CONCLUSIONS: Most pediatric thalamic incidentalomas are small, stable, and likely low-grade. However, approximately one-fifth exhibit progressive features, warranting prolonged surveillance. Larger initial volume, extra-thalamic extension, and contrast enhancement are significant predictors of progression and may justify earlier intervention. Individualized management remains essential, balancing natural history with surgical risk.
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