Results 51 to 60 of about 2,340 (196)

Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA):a molecularly distinct brain tumor type with recurrent NTRK gene fusions [PDF]

, 2023
Glioneuronal tumors are a heterogenous group of CNS neoplasms that can be challenging to accurately diagnose. Molecular methods are highly useful in classifying these tumors—distinguishing precise classes from their histological mimics and identifying ...
Abdullaev, Zied, Aldape, Kenneth, Alexandrescu, Sanda, Banan, Rouzbeh, Blume, Christina, Bogumil, Henri, Boldt, Henning B., Boué, Daniel R., Brandner, Sebastian, Cherkezov, Asan, Deckert, Martina, Ecker, Jonas, Frank, Stephan, Friedel, Dennis, Goldbrunner, Roland, Haberler, Christine, Hench, Jürgen, Herold-Mende, Christel, Hinz, Felix, Ismer, Britta, Jones, David T.W., Korshunov, Andrey, Kristensen, Bjarne Winther, Kurth, Ina, Melchior, Linea C., Milde, Till, Ng, Ho Keung, Olesen, Viola, Pajtler, Kristian W., Pfister, Stefan M., Rahmanzade, Ramin, Reuss, David E., Sahm, Felix, Satgunaseelan, Laveniya, Scheie, David, Schittenhelm, Jens, Schrimpf, Daniel, Sehested, Astrid, Seidlitz, Annekatrin, Selt, Florian, Shi, Zhi Feng, Sievers, Philipp, Sill, Martin, Snuderl, Matija, Tauziède-Espariat, Arnault, Timmer, Marco, Unterberg, Andreas, Varlet, Pascale, von Deimling, Andreas, White, Christine L., Wick, Wolfgang, Witt, Olaf   +51 more
core   +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

Roles and Impacts of Integrative Medical Interventions in Central Nervous System Tumor Treatment: Multi‐Technology Convergence and the Paradigm Shift Toward Functional Reconstruction

CNS Neuroscience &Therapeutics, Volume 31, Issue 7, July 2025.
Multi‐technology interventions (non‐invasive neuromodulation, AI, 3D organoids) for CNS tumor treatment shift from monotherapy to functional reconstruction. They address BBB restriction, tumor heterogeneity, and immune suppression via biological–psychological–technological convergence, enabling precision oncology through dynamic monitoring and ...
Junda Lai, Ketao Liu, Yuhua Lin, Zhonglin Chen, Xianglun Ji, Junkai Wen   +5 more
wiley   +1 more source

Clinical course and MRI lesion progression over 4 years in a dog with final diagnosis of high‐grade oligodendroglioma

Veterinary Record Case Reports, Volume 13, Issue 1, March 2025.
Abstract A 9‐month‐old Cavalier King Charles Spaniel with 3‐month history of paroxysmal episodes of cervical pain and scratching had a magnetic resonance imaging revealing a large intra‐axial cystic lesion in the left frontal lobe, caudal transtentorial and foraminal brain herniation, and cervical syringomyelia.
Fabiana Graciolli Tomazi, Veronika M. Stein, Anna Oevermann, Felix Meneses, Arianna Maiolini   +4 more
wiley   +1 more source

Posterior pituitary tumors and other rare entities involving the pituitary gland

Brain Pathology, Volume 35, Issue 1, January 2025.
Abstract Non‐neuroendocrine tumors account for around 10% of all primary neoplasms of the sella. If meningiomas, craniopharyngiomas, and germ cell tumors are excluded, the remaining lesions include a broad spectrum of uncommon, benign, and aggressive, often diagnostically challenging lesions.
Federico Roncaroli, Caterina Giannini
wiley   +1 more source

Intraventricular Tumor: An Analysis of 18 Cases

Nepal Journal of Neuroscience, 2016
The main objective of this article is to describe transcallosal and transcortical approach to deal with intraventricular tumors. Details of the transcallosal and transcortical approach to intraventricular tumors of the lateral and third ventricles ...
Shamsul Alam , Abu NW Uddin , Mashiur R Majumder , Md M Hasan, Anis Ahmed   +4 more
doaj   +1 more source

Histological pattern of central nervous system neoplasms [PDF]

, 2001
Objective: To see in a large series of patients the histological pattern of CNS neoplasms and to provide a comprehensive data about the frequency of CNS neoplasms in Pakistani patients and to give a clearer idea about their prevalence.
Ahmed, Z., Hasan, S. H., Husainy, A. S., Kayani, Naila, Muzaffar, S., Pervez, Shahid   +5 more
core   +1 more source

MRI findings in six dogs with ependymoma of the brain and spinal cord

Veterinary Radiology &Ultrasound, Volume 66, Issue 1, January 2025.
Abstract There are few published descriptions of the MRI appearance of canine intracranial or spinal cord ependymoma. In this multicenter, retrospective, secondary analysis, case series study, three veterinary radiologists independently reviewed and recorded imaging characteristics of MRI studies in six dogs with histopathologically confirmed ...
John F Griffin IV, William S Stevenson, Nathan C Nelson, Annie V Chen, Silke Hecht, Brian F Porter, C Elizabeth Boudreau, Swan Specchi, Marco Bernardini, Wilfried Mai   +9 more
wiley   +1 more source

A patológus szerepe a központi idegrendszer tumorainak diagnosztikájában, a terápiatervezésben. Prognosztikus és prediktív markerek vizsgálata [PDF]

, 2015
Despite advances in imaging methods, the standard of diagnosis and treatment of the tumours of the nervous system remains the histological report issued by a neuropathologist.
Bálint, Katalin, Hanzely Z, Reiniger, Lilla, Turányi, Eszter   +3 more
core  

Bilateral Cerebral Calcifications in Secondary Fahr’s Syndrome

Case Reports in Neurological Medicine, Volume 2025, Issue 1, 2025.
Fahr’s syndrome is a rare, slowly progressive neurodegenerative disorder characterised by bilateral cerebral calcifications, mostly in the basal ganglia. These cerebral calcifications are composed of calcium and phosphate and are the result of disturbances in calcium‐phosphate homeostasis.
Andreas Posa, Stefan Schob, Walter A. Wohlgemuth, Malte E. Kornhuber, Matthias Reinhard   +4 more
wiley   +1 more source