Results 11 to 20 of about 1,185,879 (186)

Complex Form Variant of Dysembryoplastic Neuroepithelial Tumor of the Cerebellum [PDF]

open access: yesCase Reports in Pathology, 2012
Dysembryoplastic neuroepithelial tumor (DNT) is a benign neoplasm with typical supratentorial location, but the possibility of these rare tumors can also be located in the posterior fossa must be taken into account.
Jesús Vaquero   +3 more
doaj   +3 more sources

Atypical Presentation of Dysembryoplastic Neuroepithelial Tumor [PDF]

open access: yesАнналы клинической и экспериментальной неврологии
Dysembryoplastic neuroepithelial tumor (DNET) is a benign glioneuronal neoplasm, usually found in children and adolescents, in the vast majority of cases associated with drug-resistant epilepsy.
Varis S. Khalilov   +3 more
doaj   +3 more sources

Dysembryoplastic neuroepithelial tumor and probable sudden unexplained death in epilepsy: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2011
Introduction This is the first report of the case of a patient with a natural history of dysembryoplastic neuroepithelial tumor associated with probable sudden unexplained death in epilepsy.
Sîrbu Carmen-Adella
doaj   +3 more sources

Dysembryoplastic neuroepithelial tumor originally diagnosed as astrocytoma and oligodendroglioma [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 2012
Dysembryoplastic neuroepithelial tumor (DNT), described in 1988 and introduced in the WHO classification in 1993, affects predominantly children or young adults causing intractable complex partial seizures.
Diego Cassol Dozza   +2 more
doaj   +2 more sources

Dysembryoplastic Neuroepithelial Tumor with Atypical Presentation: MRI and Diffusion Tensor Characteristics [PDF]

open access: yesJournal of Radiology Case Reports, 2013
We report the neuroimaging findings of a 26-year-old female patient with a biopsy-proven dysembryoplastic neuroepithelial tumor (DNET). DNETs are an uncommon, usually benign, glial-neural cortical neoplasm of children and young adults who typically ...
Samuel Borofsky, Robert V Jones
exaly   +4 more sources

Diffuse Multifocal Bilateral Dysembryoplastic Neuroepithelial Tumor: A Very Unusual Case Report [PDF]

open access: yesInternational Clinical Neuroscience Journal, 2020
Dysembryoplastic neuroepithelial tumor (DNT) considered as a benign cortical glioneuronal neoplasm of children or young adults, typically present with drug-resistant focal epilepsy.
Hassan Reza Mohammadi   +4 more
doaj   +2 more sources

MRI-based radiomics model for differentiating focal cortical dysplasia from dysembryoplastic neuroepithelial tumor in epileptic children [PDF]

open access: yesFrontiers in Neurology
ObjectiveFocal cortical dysplasia (FCD) and dysembryoplastic neuroepithelial tumor (DNET) are two major causes of intractable epilepsy, often with confusing imaging findings.
Xinyi Yang   +4 more
doaj   +2 more sources

A rare case of dysembryoplastic neuroepithelial tumor combined with encephalocraniocutaneous lipomatosis and intractable seizures [PDF]

open access: yesKorean Journal of Pediatrics, 2016
Encephalocraniocutaneous lipomatosis (ECCL) is a rare neurocutaneous syndrome that affects ectomesodermal tissues (skin, eyes, adipose tissue, and brain). The neurologic manifestations associated with ECCL are various including seizures.
Jee-Yeon Han   +4 more
doaj   +2 more sources

Dysembryoplastic Neuroepithelial Tumor: A Benign but Complex Tumor of the Cerebral Cortex. [PDF]

open access: yesBrain Tumor Res Treat, 2022
Dysembryoplastic neuroepithelial tumor (DNET) is a distinct type of low-grade glioneuronal tumor. Clinically, DNET is highly associated with intractable epilepsy in young children and adolescents.
Phi JH, Kim SH.
europepmc   +2 more sources

Dysembryoplastic Neuroepithelial Tumor: A Rare Brain Tumor with Excellent Seizure Control after Surgical Resection

open access: yesIndian Journal of Neurosurgery, 2022
Introduction Dysembryoplastic neuroepithelial tumor (DNET) is a rare cause of intractable epilepsy, which has excellent results in terms of seizure control after surgical resection. We present one such case, because of its rarity, to highlight the effect
Rajnish Kumar Arora   +5 more
doaj   +2 more sources

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