Neuroectodermal Tumors, Primitive
"Neuroectodermal Tumors, Primitive" 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.
A group of malignant tumors of the nervous system that feature primitive cells with elements of neuronal and/or glial differentiation. Use of this term is limited by some authors to central nervous system tumors and others include neoplasms of similar origin which arise extracranially (i.e., NEUROECTODERMAL TUMORS, PRIMITIVE, PERIPHERAL). This term is also occasionally used as a synonym for MEDULLOBLASTOMA. In general, these tumors arise in the first decade of life and tend to be highly malignant. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2059)
| Descriptor ID |
D018242
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| MeSH Number(s) |
C04.557.465.625.600.590 C04.557.470.670.590 C04.557.580.625.600.590
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| Concept/Terms |
Neuroectodermal Tumors, Primitive- Neuroectodermal Tumors, Primitive
- Neuroectodermal Tumor, Primitive
- Primitive Neuroectodermal Tumor
- Primitive Neuroectodermal Tumors
- Tumor, Primitive Neuroectodermal
- Tumors, Primitive Neuroectodermal
- Primitive Neuroepithelial Neoplasms
- Neuroepithelial Tumors, Primitive
- Neuroepithelial Tumor, Primitive
- Primitive Neuroepithelial Tumor
- Primitive Neuroepithelial Tumors
- Tumor, Primitive Neuroepithelial
- Tumors, Primitive Neuroepithelial
- PNET
- PNETs
- Neoplasms, Primitive Neuroepithelial
- Neoplasm, Primitive Neuroepithelial
- Neuroepithelial Neoplasm, Primitive
- Primitive Neuroepithelial Neoplasm
- Neuroepithelial Neoplasms, Primitive
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Below are MeSH descriptors whose meaning is more general than "Neuroectodermal Tumors, Primitive".
Below are MeSH descriptors whose meaning is more specific than "Neuroectodermal Tumors, Primitive".
This graph shows the total number of publications written about "Neuroectodermal Tumors, Primitive" by people in this website by year, and whether "Neuroectodermal Tumors, Primitive" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 1 | 2 |
| 1998 | 1 | 0 | 1 |
| 2001 | 2 | 1 | 3 |
| 2004 | 2 | 0 | 2 |
| 2006 | 2 | 1 | 3 |
| 2008 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2012 | 1 | 2 | 3 |
| 2014 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
| 2016 | 1 | 0 | 1 |
| 2022 | 3 | 0 | 3 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Neuroectodermal Tumors, Primitive" by people in Profiles.
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Breastfeeding and risk of childhood brain tumors: a report from the Childhood Cancer and Leukemia International Consortium. Cancer Causes Control. 2023 Nov; 34(11):1005-1015.
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Malignant teratoid intraocular ciliary body medulloepithelioma in a 5-year-old male with corresponding somatic copy number alteration profile of aqueous humor cell-free DNA. Ophthalmic Genet. 2022 12; 43(6):855-861.
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Molecular classification and outcome of children with rare CNS embryonal tumors: results from St. Jude Children's Research Hospital including the multi-center SJYC07 and SJMB03 clinical trials. Acta Neuropathol. 2022 10; 144(4):733-746.
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Epigenetic age acceleration among survivors of pediatric medulloblastoma and primitive neuroectodermal tumor. Pediatr Hematol Oncol. 2023 May; 40(4):407-411.
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A Prospective Evaluation of Fatigue in Pediatric Brain Tumor Patients Treated With Radiation Therapy. J Pediatr Hematol Oncol Nurs. 2022 Nov-Dec; 39(6):358-365.
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DICER1 Syndrome: Characterization of the Ocular Phenotype in a Family-Based Cohort Study. Ophthalmology. 2019 02; 126(2):296-304.
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Suprasellar Primitive Neuroectodermal Tumor in an Adult. J Neuroophthalmol. 2016 09; 36(3):299-303.
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Traffic-related air pollution and the incidence of childhood central nervous system tumors: Texas, 2001-2009. Pediatr Blood Cancer. 2015 Sep; 62(9):1572-8.
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A patient tumor-derived orthotopic xenograft mouse model replicating the group 3 supratentorial primitive neuroectodermal tumor in children. Neuro Oncol. 2014 Jun; 16(6):787-99.
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Glutathione S-transferase P1 single nucleotide polymorphism predicts permanent ototoxicity in children with medulloblastoma. Pediatr Blood Cancer. 2013 Apr; 60(4):593-8.