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Papillary Glioneuronal Tumor

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Atlas of Pediatric Brain Tumors

Abstract

A benign (WHO grade I), relatively circumscribed, biphasic cerebral neoplasm occurring predominantly in the temporal lobe and most commonly affecting young adults. No population-based epidemiologic data are available to date. Papillary glioneuronal tumor (PGNT) was initially described as “pseudopapillary ganglioglioneurocytoma” or “pseudopapillary neurocytoma with glial differentiation.” Established as a distinct clinicopathologic entity in 1998 by Komori et al. Regarded as a variant of ganglioglioma in the 2000 WHO classification of central nervous system tumors. Recently added as a new entity in the 2007 WHO classification.

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Suggested Reading

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Rivera-Zengotita, M., Illner, A., Adesina, A.M. (2010). Papillary Glioneuronal Tumor. In: Adesina, A., Tihan, T., Fuller, C., Poussaint, T. (eds) Atlas of Pediatric Brain Tumors. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1062-2_20

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  • DOI: https://doi.org/10.1007/978-1-4419-1062-2_20

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  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4419-1061-5

  • Online ISBN: 978-1-4419-1062-2

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