Neoplasms, Neuroepithelial
"Neoplasms, Neuroepithelial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Neoplasms composed of neuroepithelial cells, which have the capacity to differentiate into NEURONS, oligodendrocytes, and ASTROCYTES. The majority of craniospinal tumors are of neuroepithelial origin. (From Dev Biol 1998 Aug 1;200(1):1-5)
| Descriptor ID |
D018302
|
| MeSH Number(s) |
C04.557.465.625.600 C04.557.470.670 C04.557.580.625.600
|
| Concept/Terms |
Neoplasms, Neuroepithelial- Neoplasms, Neuroepithelial
- Neuroepithelial Tumors
- Neuroepithelial Tumor
- Tumor, Neuroepithelial
- Tumors, Neuroepithelial
- Neuroepithelial Neoplasms
- Neoplasm, Neuroepithelial
- Neuroepithelial Neoplasm
Spongioblastoma, Polar- Spongioblastoma, Polar
- Polar Spongioblastoma
- Polar Spongioblastomas
- Spongioblastomas, Polar
|
Below are MeSH descriptors whose meaning is more general than "Neoplasms, Neuroepithelial".
Below are MeSH descriptors whose meaning is more specific than "Neoplasms, Neuroepithelial".
This graph shows the total number of publications written about "Neoplasms, Neuroepithelial" by people in this website by year, and whether "Neoplasms, Neuroepithelial" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2003 | 2 | 0 | 2 |
| 2008 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2016 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Neoplasms, Neuroepithelial" by people in Profiles.
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Early ependymal tumor with MN1-BEND2 fusion: a mostly cerebral tumor of female children with a good prognosis that is distinct from classical astroblastoma. J Neurooncol. 2023 Feb; 161(3):425-439.
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Astroblastomas exhibit radial glia stem cell lineages and differential expression of imprinted and X-inactivation escape genes. Nat Commun. 2022 04 19; 13(1):2083.
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Desmoplastic Infantile Ganglioglioma: A MAPK Pathway-Driven and Microglia/Macrophage-Rich Neuroepithelial Tumor. J Neuropathol Exp Neurol. 2019 11 01; 78(11):1011-1021.
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Genomic analysis demonstrates that histologically-defined astroblastomas are molecularly heterogeneous and that tumors with MN1 rearrangement exhibit the most favorable prognosis. Acta Neuropathol Commun. 2019 03 15; 7(1):42.
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RBM10 truncation in astroblastoma in a patient with history of mandibular ameloblastoma: A case report. Cancer Genet. 2019 02; 231-232:41-45.
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Pediatric Solid Tumors of Infancy: An Overview. Pediatr Rev. 2018 Feb; 39(2):57-67.
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Perioperative Risk Assessment of Patients with Gliomatosis Cerebri. World Neurosurg. 2017 Feb; 98:334-338.
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Polymorphous low-grade neuroepithelial tumor of the young (PLNTY): an epileptogenic neoplasm with oligodendroglioma-like components, aberrant CD34 expression, and genetic alterations involving the MAP kinase pathway. Acta Neuropathol. 2017 03; 133(3):417-429.
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Morphological and molecular features of astroblastoma, including BRAFV600E mutations, suggest an ontological relationship to other cortical-based gliomas of children and young adults. Neuro Oncol. 2017 01; 19(1):31-42.
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Synchronous rosette-forming glioneuronal tumor and diffuse astrocytoma with molecular characterization: a case report. Clin Neuropathol. 2014 Nov-Dec; 33(6):407-11.