Results 31 to 40 of about 4,805 (157)

Spinal ependymoma in adults: from molecular advances to new treatment perspectives

open access: yesFrontiers in Oncology, 2023
Ependymomas are rare glial tumors with clinical and biological heterogeneity, categorized into supratentorial ependymoma, posterior fossa ependymoma, and spinal cord ependymoma, according to anatomical localization.
Giulia Cerretti   +20 more
doaj   +1 more source

Pediatric Extraspinal Sacrococcygeal Ependymoma: Report of Two Cases and Literature Review

open access: yesDiagnostics, 2021
Primary central nervous system (CNS) tumors represent the most common solid tumors in childhood. Ependymomas arise from ependymal cells lining the wall of ventricles or central canal of spinal cord and their occurrence outside the CNS is extremely rare ...
Francesco Fabozzi   +7 more
doaj   +1 more source

Surgical management of a rare myxopapillary ependymoma of the gluteal region: A case report. [PDF]

open access: yes, 2021
BackgroundEpendymomas are rare tumors originating from neuroepithelial cells lining the wall of the ventricles or central canal of the spinal cord. While these tumors mainly occur within the central nervous system (CNS), there are occasional reports in ...
Stitzlein, Russell N   +10 more
core   +1 more source

Outcome Analysis in Cases of Spinal Conus Cauda Ependymoma [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Introduction: One half of all central nervous system ependymomas, arise within the spinal canal and about 40% of these arise from filum terminale. The myxopapillary variant of spinal ependymoma almost exclusively occurs in the lumbosacral region and ...
Srikant Balasubramaniam   +3 more
doaj   +1 more source

Sacrococcygeal myxopapillary ependymoma with anaplastic ependymoma component in an infant

open access: yesJournal of Pediatric Neurosciences, 2012
Sacrococcygeal location of myxopapillary ependymoma (MPE) is uncommon. Local recurrence and metastases are on record inspite of its benign characteristics.
Shrijeet Chakraborti   +3 more
doaj   +1 more source

Reports of a conus cauda tumor with holocord syrinx in an adolescent girl

open access: yesJournal of Pediatric Neurosciences, 2020
Introduction: Spinal cord ependymoma seldom presents with holocord syringomyelia in pediatric age-group. Association of ependymoma with a lipoma is also rare.
Smriti Sinha   +3 more
doaj   +1 more source

Sporadic NF2 Mosaic: Multiple spinal schwannomas presenting with severe, intractable pain following pregnancy

open access: yesInterdisciplinary Neurosurgery, 2017
The aim of the present paper is to report undiagnosed sporadic neurofibromatosis type 2 presenting with symptomatic compressive spinal tumors following pregnancy.
Jeffrey H. Zimering   +5 more
doaj   +1 more source

Primary spinal primitive neuroectodermal tumor on MR imaging

open access: yesIndian Journal of Radiology and Imaging, 2015
Neoplasms in the region of filum terminale are not uncommon. Myxopapillary ependymoma is the commonest tumor at this location. The differentials reported for this entity are nerve sheath tumor, meningioma, paraganglioma, intradural metastases, lymphoma ...
Prashant J Thoriya   +3 more
doaj   +1 more source

Non-Hodgkin lymphoma of cauda equina: A diagnostic conundrum: Case report

open access: yesAdvanced Biomedical Research, 2023
Primary central nervous system lymphoma (PCNSL) is uncommon with scarce cases having involvement of the spinal cord. Cauda equina is unique in its location and shows very rare involvement by diseases pathologies.
Pranati Misra   +5 more
doaj   +1 more source

Sacral myxopapillary ependymoma with extensive osteolysis

open access: yes, 2006
Myxopapillary ependymoma rarely presents as a primary intra-sacral lesion and extensive bony destruction is unusual. Radiological features do not help in distinction from other commoner sacral tumors, like chordoma.
Gupta, Ruchika   +6 more
core   +1 more source

Home - About - Disclaimer - Privacy