Results 51 to 60 of about 2,875 (210)

Malignant transformation of central neurocytoma with dissemination 17 years after initial treatment: illustrative case [PDF]

, 2022
BACKGROUND: Central neurocytomas usually have a favorable clinical course, and gross total resection (GTR) results in long-term survival. Recurrences of central neurocytomas are usually local, and dissemination is extremely rare.
Arakawa, Yoshiki, Haga, Hironori, Kojima, Kazuhiro, Mineharu, Yohei, Miyamoto, Susumu, Takeuchi, Yasuhide, Tanji, Masahiro, Terada, Yukinori   +7 more
core   +1 more source

Exploring the interdependencies of research funders in the UK [PDF]

, 2014
Investment in medical research is vital to the continuing improvement of the UK's health and wealth. It is through research that we expand our understanding of disease and develop new treatments for patients.
Crane, P, Farrell, C, Garau, M, Grassano, N, Hernandez-Villafuerte, K, Hopkins, M M, Hutton, J, Lang, F, Mawer, A, Pateman, C, Rotolo, D, Shah, K, Sharp, T, Sussex, J   +13 more
core   +1 more source

Molecular Landscape of Pediatric Low‐Grade Gliomas: Insights From RNA‐NGS and Bioinformatic Analysis

Genes, Chromosomes and Cancer, Volume 64, Issue 10, October 2025.
ABSTRACT Pediatric low‐grade gliomas (pLGG) are the most common group of childhood brain tumors. Genetic alterations in the RAS–RAF–mitogen‐activated protein kinase (MAPK) pathway are the molecular drivers in the vast majority of pLGG. A large proportion of pediatric pLGG are characterized by the presence of fusion genes.
Petr Brož, Martina Strnadová, Denisa Olejníková, Johana Kotiš, Tereza Pospíšilíková, Adéla Mišove, Miroslav Koblížek, Josef Zámečník, Michal Zápotocký, David Sumerauer, Aleš Vícha, Martin Kynčl, Petr Libý, Vladimír Beneš, Lenka Krsková   +14 more
wiley   +1 more source

Pan ventricular neurocytoma

Asian Journal of Neurosurgery, 2015
Central neurocytomas are intraventricular benign neoplasms located within the lateral ventricle adjacent to foramen of Monro. A rare case of a central neurocytoma extending throughout the entire ventricular system at the time of presentation is reported.
Jhawar, Sukhdeep Singh, Nadkarni, Trimurti   +1 more
openaire   +3 more sources

Tumor‐related epilepsy in glioma: A multidisciplinary overview

Epilepsia, Volume 66, Issue 10, Page 3621-3641, October 2025.
Abstract Seizures are a common and challenging symptom in brain tumors, affecting approximately 60% of patients. Tumor‐related epilepsy (TRE) in glioma patients requires personalized and dynamic management in a multidisciplinary environment, especially for its intricate pathophysiology and unpredictable disease evolution. This investigation provides an
Roberto Michelucci, Giada Pauletto, Antonio Silvani, Elena Pasini, Tamara Ius, Matteo Martinoni, Carlo Alberto Castioni, Andrea Salmaggi, Sofia Asioli, Marta Maschio, Giuseppe Minniti, Enrico Franceschi, Flavio Villani, Roberta Rudà, Eleonora Aronica, the Italian Multidisciplinary Group for Tumor Epilepsy, Paolo Vitali, Damiano Balestrini, Elisa D’Angelo, Lorenzo Bello, Marco Rossi, Marta Padovan, Anna Teresa Giallonardo, Carlo di Bonaventura, Francesco Toni, Angela La Neve, Simona Rizzato, Matteo Pugnaghi, Marco Vindigni, Carmelo Sturiale   +29 more
wiley   +1 more source

Atypical Extraventricular Neurocytoma

Journal of Korean Neurosurgical Society, 2011
The authors report a case of atypical extraventricular neurocytoma (EVN) transformed from EVN which had been initially diagnosed as an oligodendroglioma 15 years ago. An 8-year-old boy underwent a surgical resection for a right frontal mass which was initially diagnosed as oligodendroglioma. When the tumor recurred 15 years later, a secondary operation
Hyunho, Choi, Sung-Hye, Park, Dong Gyu, Kim, Sun Ha, Paek   +3 more
openaire   +2 more sources

Atypical central neurocytoma with leptomeningeal dissemination: a case report

Journal of the Egyptian National Cancer Institute, 2020
Background Central neurocytomas represent 0.25–0.5% of all intracranial tumors in adults. Leptomeningeal spread is uncommon, and the exact incidence of meningeal spread is unknown due to sparse literature.
Shikha Goyal, Tejinder Kataria, Deepak Gupta, Aruj Dhyani, Ishani Mohapatra, Karanjit Singh Narang   +5 more
doaj   +1 more source

Use of DNA Methylation Profiling as a Molecular Classification Tool for Paediatric Central Nervous System Tumours: A Middle‐Income Country Population–Based Study

Neuropathology and Applied Neurobiology, Volume 51, Issue 5, October 2025.
ABSTRACT Paediatric central nervous system (CNS) tumours are the second most common childhood malignancy and the leading cause of cancer‐related mortality in this age group. Histopathological diagnosis can be challenging, particularly for rare or ambiguous tumours, and may result in misclassification.
Mayara F. Euzébio, Felipe L. T. Silva, Iva L. Hoffmann, Juliana S. Ruas, Larissa Akemi Kido, Dieila G. de Lima, Luciano Queiroz, Izilda A. Cardinalli, Ana Luiza Seidinger, Suelen Nascimento, Helder Tedeschi, Renato D. Puga, Priscila Pini Zenatti Sales, Patricia Y. Jotta, Mariana Maschietto   +14 more
wiley   +1 more source

Rosette-forming glioneuronal tumor: a pineal region case with IDH1 and IDH2 mutation analyses and literature review of 43 cases [PDF]

, 2010
Rosette-forming glioneuronal tumor (RGNT) of the fourth ventricle is a mixed glio-neuronal neoplasm recently codified by the World Health Organization WHO Classification of Central Nervous System (CNS) Tumors (2007). To date, 43 cases have been described
Orestes E. Solis, Rupal I. Mehta, Albert Lai, Rashi I. Mehta, Lama O. Farchoukh, Richard M. Green, Jerry C. Cheng, Sathima Natarajan, Harry V. Vinters, Timothy Cloughesy, William H. Yong   +10 more
core   +2 more sources

Primary Gamma Knife Radiosurgery for pineal region tumors: A systematic review and pooled analysis of available literature with histological stratification [PDF]

, 2023
Pineal region tumors (PTs) represent extremely rare pathologies, characterized by highly heterogeneous histological patterns. Most of the available evidence for Gamma Knife radiosurgical (GKSR) treatment of PTs arises from multimodal regimens, including ...
De Domenico P., Gagliardi F., Garbin E., Mortini P., Snider S.   +4 more
core   +1 more source