Results 11 to 20 of about 25,306 (190)

Single-cell RNA sequencing of anaplastic ependymoma and H3K27M-mutant diffuse midline glioma [PDF]

open access: yesBMC Neurology
Background Anaplastic ependymoma and H3K27M-mutant diffuse midline glioma are two common subtypes of brain tumors with poor long-term prognosis. The present study analyzed and compared the differences in cell types between two tumors by single-cell RNA ...
Dongdong Zang   +3 more
doaj   +3 more sources

Adult supratentorial extraventricular anaplastic ependymoma with cerebrospinal fluid dissemination metastases: a case report [PDF]

open access: yesFrontiers in Neurology
BackgroundEpendymomas mostly locate in the infratentorial region and often occur in children. Anaplastic ependymomas account for 45–47% of supratentorial and 15–17% of infratentorial ependymomas, also known as malignant ependymomas.
Daojin Zhang   +3 more
doaj   +3 more sources

Treatment outcome of anaplastic ependymoma under the age of 3 treated by intensity-modulated radiotherapy [PDF]

open access: yesRadiat Oncol J, 2020
Purpose: Intensity-modulated radiotherapy (IMRT) allows for more precise treatment, reducing unwanted radiation to nearby structures. We investigated the safety and feasibility of IMRT for anaplastic ependymoma patients below 3 years of age.
김동석   +3 more
core   +2 more sources

Multifocal intradural extramedullary anaplastic ependymoma of the spine [PDF]

open access: yesJ Spine Surg, 2017
Ependymomas are neuroectodermal tumours arising from the ependymal lining of the ventricles and central canal of the spinal cord. Intradural extramedullary (IDEM) ependymomas which are multifocal, and/or anaplastic (WHO grade III) at presentation are ...
Steel, TR   +11 more
core   +2 more sources

Anaplastic ependymoma metastases though a ventriculoperitoneal shunt [PDF]

open access: yesRadiology Case Reports, 2020
Ependymomas are rare glial tumors that comprise 10% of intracranial pediatric malignancies. Primary central nervous system malignancies can rarely metastasize extracranially.
Jeffery D. St Jeor   +3 more
doaj   +2 more sources

Primary spinal anaplastic ependymoma: A single-institute retrospective cohort and systematic review [PDF]

open access: yesFrontiers in Oncology, 2023
ObjectivePrimary spinal anaplastic ependymoma (PSAE) is an extremely rare disease. We aim to report the largest PSAE cohort, evaluate the treatments, and investigate the prognostic factors for progression-free survival (PFS).MethodsClinical data ...
Liang Wu   +5 more
doaj   +2 more sources

Extensive anaplastic multi-centric ependymoma in a young adult: case report and literature review

open access: yesThe Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2023
Background Ependymoma is a rare adult tumor that originates from ependymal cells of the ventricles and the spinal cord. The diagnosis and management can be very challenging.
Lamya Aballa   +3 more
doaj   +2 more sources

Intraparenchymal clear cell ependymoma

open access: yesJournal of Cytology, 2011
Clear cell ependymoma (CCE) is an uncommon variant of ependymoma having a predilection for the supratentorial region. Histologically, it bears an uncanny resemblance to oligodendroglioma, central neurocytoma, hemangioblastoma and metastasis from clear ...
Prabal Deb   +3 more
doaj   +2 more sources

Cortical Anaplastic Ependymoma with Significant Desmoplasia: A Case Report and Literature Review [PDF]

open access: yesCase Reports in Oncological Medicine, 2013
Ectopic brain anaplastic ependymomas with no connection to the ventricles are rare. We present a rare case of a 25-year-old male who presented with generalized convulsions.
Alaa Eldin Elsharkawy   +5 more
doaj   +2 more sources

Non-Ossifying Fibroma Mimicking Extra-Neural Metastasis in Pediatric Cerebral Anaplastic Ependymoma: A Case Report [PDF]

open access: yesCentral Asian Journal of Medical Sciences
Objective: This case report focuses on the differential diagnosis of non-ossifying fibroma and extra-neural metastasis in pediatric cerebral anaplastic ependymoma.
Munkhgerel Davaa   +5 more
doaj   +4 more sources

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