A rare case of dysembryoplastic neuroepithelial tumor. [PDF]
We present a rare case of dysembryoplastic neuroepithelial tumor, a rare benign glioneuronal tumor of the central nervous system. It generally occurs in the supratentorial region and the temporal cerebral cortex in children and young adults. The most common presentation is epilepsy.
Guduru H, Shen JK, Lokannavar HS.
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A clinicopathological analysis of 6 cases with dysembryoplastic neuroepithelial tumor [PDF]
Background and purpose: Dysembryoplastic neuroepithelial tumor (DNT) is a rare and benign mixed neuronal-glial tumor. This paper was to study the clinicopathological features and the key points of differential diagnosis of DNT.
何晓顺 +5 more
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From a dysembryoplastic neuroepithelial tumor to a glioblastoma multiforme: Pitfalls of initial diagnosis on biopsy material, a case report. [PDF]
Background: Ganglioglioma (GG) and dysembryoplastic neuroepithelial tumor (DNET) belong to the group of low-grade epilepsy-associated tumors (LEAT) and are the most prevalent tumor types found in patients undergoing epilepsy surgery.
Slegers RJ +9 more
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Dysembryoplastic Neuroepithelial Tumor (Dnet) in a Young Female: A Rare Case Presentation
Dysembryoplastic neuroepithelial tumor (DNET) is a recently described, morphologically unique, and surgically curable low grade brain tumor which is included in the WHO CNS classification as neuronal and mixed neuronal glial tumor.
Sarah Irfan +3 more
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Association of CT and MRI Manifestations with Pathology in Dysembryoplastic Neuroepithelial Tumors
Objective: To investigate the CT, MRI and pathological features of dysembryoplastic neuroepithelial tumor (DNET). Methods: The CT and MRI features of six cases of pathologically confirmed DNET were retrospectively analyzed and compared with pathology ...
Da-wei Liao +3 more
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Dysembryoplastic neuroepithelial tumors (DNETs) are benign neoplasms classified in the category of glioneuronal tumors. The estimated incidence of DNETs is 0.03 per 100,000 person per year with the age peak in a range between 10 and 14 years, and ...
Tomislav Sajko +5 more
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PAPILLARY GLIONEURONAL TUMOR: A CASE REPORT & REVIEW OF LITERATURE [PDF]
BackgroundPapillary glioneuronal tumors (PGNT) are rare, with only around 140 cases being reported since this tumor was first described in the fourth edition of the WHO classification of tumors of the central nervous system.
Shankar Ayyappan Kutty +2 more
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Long-term epilepsy associated-tumors (LEATs): what is new?
Long-term epilepsy-associated tumors (LEATs) include a series of neoplasms that commonly occur in children, adolescents, or young adults, have an astrocytic or glioneuronal lineage, are histologically benign (WHO grade1) with a neocortical localization ...
Sergio Rosemberg
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SOX10 distinguishes oligodendrogliomas from low-grade glioneuronal tumors/low-grade gliomas with oligodendrocyte-like features. [PDF]
Abstract Oligodendrogliomas exhibit significant morphological overlap with low‐grade glioneuronal tumors/low‐grade gliomas with oligodendrocyte‐like features, posing challenges in histopathological diagnosis. SOX10, a transcription factor critical for oligodendrocyte maturation and central nervous system myelination, may serve as a diagnostic marker ...
Zhou D +5 more
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Brain tumors can always result in seizures when involving the cortical neurons or their circuits, and they were found to be one of the most common etiologies of intractable focal seizures.
Mingguo Xie +8 more
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