ArticleBrain & spine2026
Post-therapy neuronal maturation in adult medulloblastoma: a case report with literature integration.
Article in Brain & spine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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5 authors.
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Abstract
Introduction: Post-therapy neuronal maturation (PTNM) is a rare phenomenon in medulloblastoma, in which a tumor that initially exhibits embryonal morphology acquires differentiated neuronal features after multimodal treatment. While several pediatric cases have been documented, reports in adults remain exceptional. Case presentation: We describe a 21-year-old woman who presented with headache, dizziness, and gait unsteadiness. MRI demonstrated a right cerebellar mass, and gross total resection revealed desmoplastic/nodular medulloblastoma (WHO grade 4) with high proliferative activity (Ki-67 ∼45% in internodular areas). She subsequently underwent craniospinal irradiation with a posterior fossa boost and multi-agent chemotherapy. Fourteen months later, surveillance MRI identified a recurrent posterior fossa lesion. Repeat resection showed a hypocellular nodular architecture within gliotic stroma, with diffuse synaptophysin and NeuN expression, strong neurofilament reactivity, partial GFAP positivity, and a markedly reduced Ki-67 index (1-2%). These findings were consistent with therapy-related neuronal maturation rather than true recurrence. No further adjuvant therapy was administered, and the patient remains alive and disease-free 40 months after initial diagnosis. Conclusions: This case provides additional evidence that post-therapy neuronal maturation can occur in adult medulloblastoma and may dominate the histological picture at recurrence. Accurate recognition of this endpoint preserves diagnostic continuity, prevents misclassification as a glioneuronal tumor, and emphasizes the need for larger adult series to clarify its prognostic significance and implications for long-term management.
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