The 5th edition of the WHO Classification of Tumors of the Central Nervous System now classifies gliomas, glioneuronal tumors and neuronal tumors into 6 families, among which are six newly pediatric low‐grade gliomas and glioneuronal tumors: “diffuse astrocytoma, MYB or MYBL1‐altered”; “polymorphous low grade neuroepithelial tumor of the young (PLNTY)”;
Tejus A. Bale, Marc K. Rosenblum
wiley +1 more source
Personalized fMRI Delineates Functional Regions Preserved within Brain Tumors
Objective Accumulating evidence from invasive cortical stimulation mapping and noninvasive neuroimaging studies indicates that brain function may be preserved within brain tumors. However, a noninvasive approach to accurately and comprehensively delineate individual‐specific functional networks in the whole brain, especially in brain tissues within and
Weigang Cui +11 more
wiley +1 more source
Central Neurocytoma: A Review of Clinical Management and Histopathologic Features. [PDF]
Central neurocytoma (CN) is a rare, benign brain tumor often located in the lateral ventricles. CN may cause obstructive hydrocephalus and manifest as signs of increased intracranial pressure. The goal of treatment for CN is a gross total resection (GTR),
Bui, Timothy T +10 more
core +2 more sources
Central Neurocytoma with Hemorrhagic Presentation Case Report and Review of the Literature
Central neurocytoma (CN) is slow‐growing rare intraventricular tumor that represents 0.25‐0.5% of all intracranial tumors in adults. Typically, it is seen in young adults, yet with surgical resection, it has excellent prognosis. Due to CN rarity and its feature similarities with other common tumors, misdiagnosis can be an issue.
Mohammad Nasser Alsadiq +4 more
wiley +1 more source
A case of recurrent epilepsy-associated rosette-forming glioneuronal tumor with anaplastic transformation in the absence of therapy. [PDF]
Rosette-forming glioneuronal tumor (RGNT) most commonly occurs adjacent to the fourth ventricle and therefore rarely presents with epilepsy. Recent reports describe RGNT occurrence in other anatomical locations with considerable morphologic and genetic ...
Corless, Christopher L +14 more
core +1 more source
MR Finding of Extraventricular Neurocytoma
To determine the MR (magnetic resonance), pathologic, and clinical findings of extraventricular neurocytoma (EVN).Descriptive study.Department of Radiology, Affiliated Hospital of Jining Medical University, Jining, Shandong, China, from January 2020 to March 2022.The MR radiological and pathological data of 11 patients with EVNs proved by ...
Shuran, Huang +5 more
openaire +2 more sources
Molecular diagnostics in drug‐resistant focal epilepsy define new disease entities
The identification of lesion‐specific somatic variants, gene fusion, and epigenetic profiles has helped to rationalize disease classification in cancer and more recently also in epilepsy. Many structural brain lesions which are commonly associated with epilepsy including low‐grade epilepsy‐associated tumors (LEAT) and the broad spectrum of ...
Katja Kobow +3 more
wiley +1 more source
Systematic Analysis of Clinical Outcomes Following Stereotactic Radiosurgery for Central Neurocytoma. [PDF]
Central neurocytoma (CN) typically presents as an intraventricular mass causing obstructive hydrocephalus. The first line of treatment is surgical resection with adjuvant conventional radiotherapy.
Bui, Timothy T +7 more
core +1 more source
Central Neurocytoma with Extensive Intratumoral Hemorrhage : A Case Report [PDF]
Publisher Copyright: © Am J Case Rep,.Objective: Background: Case Report: Conclusions: Rare disease Central neurocytoma (CN) is a rare neuronal tumor of neuroepithelial origin.
Bicāns, Kārlis +3 more
core +1 more source
Spinal Neurocytoma: A Case Report and Review of Literature
Extraventricular locations of neurocytoma are extremely rare, especially in the spinal cord, which has been reported in only sporadic cases. In this article, we report a new pediatric case of a spinal neurocytoma in a 12-year-old girl and briefly review ...
Khalil Guedira +4 more
doaj +1 more source

