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Papillary Glioneuronal Tumor

Known as: Papillary Glioneuronal Tumor (WHO Grade I) 
A WHO grade I, indolent and relatively circumscribed brain tumor. Morphologically it is characterized by the presence of astrocytes that line… 
National Institutes of Health

Papers overview

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Review
2009
Review
2009
CONTEXT Several distinctive mixed glioneuronal tumors that warrant recognition as clinicopathologic entities have been recently… 
Review
2009
Review
2009
OBJECTIVE Papillary glioneuronal tumors (PGNT) is well-recognized in the literature, although reports usually have not attempted… 
2007
2007
We describe a 34-year-old man who presented with headaches for about 3 months. Magnetic Resonance Imaging (MRI) revealed a large… 
2006
2006
The papillary glioneuronal tumor (PGNT) was first reported by Komori et al. as a type of mixed neuronalglial tumor. It is… 
2006
2006
Papillary glioneuronal tumor (PGNT) has recently been identified as a new variant of mixed neuronal‐glial tumors. We report the… 
Review
2005
Review
2005
Abstract Papillary glioneuronal tumors are rare, typically low-grade brain tumors that usually present with seizure activity… 
2004
2004
We report a case of a young female patient with a rare and recently described form of brain tumor. This patient had a history of… 
2003
2003
We report a case of a 14-year-old girl with papillary glioneuronal tumor (PGNT) in right parietal lobe. On MRI the tumor… 
2000
2000
Abstract Focal cortical dysplasia (FCD) is a pathological entity first described in 1971. Other more subtle cortical…