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Letter to editor: comment on, "Imaging manifestations of papillary glioneuronal tumors".
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.
Chiasmal shift and differential radiological diagnosis of papillary glioneuronal tumors.
Neurosurg Rev
September 2024
Jinnah Postgraduate Medical Centre, Rafiqi H J Shaheed Road, Karachi, 75510, Pakistan.
Synchronous intracranial arteriovenous malformation and papillary glioneuronal tumour: hypothesis or reality?
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 PDFLow-grade glioma of the temporal lobe and tumor-related epilepsy in children.
Childs Nerv Syst
October 2024
Department of Neurosurgery, The Royal Children's Hospital, Melbourne, Australia.
Article Synopsis
- Low-grade gliomas are the most common brain tumors in children and adolescents, often leading to uncontrolled seizures when located in the temporal lobe.
- A review of literature highlights various tumor types, surgical treatment options, and outcomes, indicating that complete resection of tumors is crucial for achieving favorable seizure outcomes.
- Management of these conditions should involve a multidisciplinary team focused on epilepsy surgery, as early and effective intervention significantly improves patient survival and reduces seizure-related issues.
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