Summary
Cerebral primitive neuro-ectodermal tumour (PNET) occurring as a second primary malignancy in childhood is exceedingly rare. We present a 7-year-old boy who developed a proven supratentorial PNET five years after enucleation and radio-/chemotherapy for a sporadic, unilateral retinoblastoma with optic nerve invasion. The association with this malignant eye disease as well as the effect of irradiation and multi-agent chemotherapy on second tumour induction are evaluated.
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Dorfmüller, G., Würtz, F.G., Kleinert, R. et al. Cerebral primitive neuro-ectodermal tumour following treatment of a unilateral retinoblastoma. Acta neurochir 139, 749–755 (1997). https://doi.org/10.1007/BF01420048
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DOI: https://doi.org/10.1007/BF01420048