The recently described 'papillary glioneuronal tumour' is not currently included in the WHO classification of tumours of the CNS. We present the youngest recorded case to date, and only the 3rd documented in the paediatric population. The incorporation of this neoplasm into the WHO classification would facilitate its wider recognition, providing an opportunity to elucidate its natural history and determine an evidence-based approach to treatment.
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http://dx.doi.org/10.1159/000058431 | DOI Listing |
Neurosurg Rev
September 2024
Department of Cariology, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha Dental College and Hospitals, Saveetha University, Chennai, 600 077, India.
Neurosurg Rev
September 2024
Jinnah Postgraduate Medical Centre, Rafiqi H J Shaheed Road, Karachi, 75510, Pakistan.
Childs Nerv Syst
December 2024
Department of Neurosurgery, Queensland Children's Hospital, 501 Stanley St, South Brisbane, QLD, 4101, Australia.
Brain arteriovenous malformations (AVM) rarely occur with spatial and/or temporal co-localisation to intracranial neoplasms. Most prior reports describe this association with high-grade gliomas; however, reports of a co-occurrence with low grade gliomas are very rare. It is unclear whether such cases represent a true co-occurrence of separate pathologies or simply an unusually vascular phenotype of the neoplasm.
View Article and Find Full Text PDFPapillary glioneuronal tumors (PGNTs), classified as Grade I by the WHO in 2016, present diagnostic challenges due to their rarity and potential for malignancy. Xiaodan Du et al.'s recent study of 36 confirmed PGNT cases provides critical insights into their imaging characteristics, revealing frequent presentation with headaches, seizures, and mass effect symptoms, predominantly located in the supratentorial region near the lateral ventricles.
View Article and Find Full Text PDFChilds Nerv Syst
October 2024
Department of Neurosurgery, The Royal Children's Hospital, Melbourne, Australia.
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