Neuroectodermal Tumors, Primitive, Peripheral
"Neuroectodermal Tumors, Primitive, Peripheral" 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 highly cellular primitive round cell neoplasms which occur extracranially in soft tissue and bone and are derived from embryonal neural crest cells. These tumors occur primarily in children and adolescents and share a number of characteristics with EWING SARCOMA.
| Descriptor ID |
D018241
|
| MeSH Number(s) |
C04.557.465.625.600.590.650 C04.557.470.670.590.650 C04.557.580.625.600.590.650
|
| Concept/Terms |
Neuroectodermal Tumors, Primitive, Peripheral- Neuroectodermal Tumors, Primitive, Peripheral
- Peripheral Primitive Neuroectodermal Tumors
- (pPNET) Peripheral Primitive Neuroectodermal Tumors
- Neuroepithelioma, Peripheral
- Neuroepitheliomas, Peripheral
- Peripheral Neuroepithelioma
- Peripheral Neuroepitheliomas
- Neuroectodermal Neoplasm, Peripheral Primitive
- Neuroectodermal Tumor, Peripheral Primitive
- Peripheral Primitive Neuroectodermal Neoplasm
- Primitive Neuroectodermal Tumor, Extracranial
- Neuroectodermal Tumor, Peripheral
- Neuroectodermal Tumors, Peripheral
- Peripheral Neuroectodermal Tumor
- Peripheral Neuroectodermal Tumors
- Tumor, Peripheral Neuroectodermal
- Tumors, Peripheral Neuroectodermal
- Extracranial Primitive Neuroectodermal Tumor
|
Below are MeSH descriptors whose meaning is more general than "Neuroectodermal Tumors, Primitive, Peripheral".
- Diseases [C]
- Neoplasms [C04]
- Neoplasms by Histologic Type [C04.557]
- Neoplasms, Germ Cell and Embryonal [C04.557.465]
- Neuroectodermal Tumors [C04.557.465.625]
- Neoplasms, Neuroepithelial [C04.557.465.625.600]
- Neuroectodermal Tumors, Primitive [C04.557.465.625.600.590]
- Neuroectodermal Tumors, Primitive, Peripheral [C04.557.465.625.600.590.650]
- Neoplasms, Glandular and Epithelial [C04.557.470]
- Neoplasms, Neuroepithelial [C04.557.470.670]
- Neuroectodermal Tumors, Primitive [C04.557.470.670.590]
- Neuroectodermal Tumors, Primitive, Peripheral [C04.557.470.670.590.650]
- Neoplasms, Nerve Tissue [C04.557.580]
- Neuroectodermal Tumors [C04.557.580.625]
- Neoplasms, Neuroepithelial [C04.557.580.625.600]
- Neuroectodermal Tumors, Primitive [C04.557.580.625.600.590]
- Neuroectodermal Tumors, Primitive, Peripheral [C04.557.580.625.600.590.650]
Below are MeSH descriptors whose meaning is more specific than "Neuroectodermal Tumors, Primitive, Peripheral".
This graph shows the total number of publications written about "Neuroectodermal Tumors, Primitive, Peripheral" by people in this website by year, and whether "Neuroectodermal Tumors, Primitive, Peripheral" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Neuroectodermal Tumors, Primitive, Peripheral" by people in Profiles.
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Magers MJ, Perrino CM, Ulbright TM, Idrees MT. Immunophenotypic Characterization of Germ Cell Tumor-Derived Primitive Neuroectodermal Tumors: Evidence for Frequent Neuronal and/or Glial Differentiation. Arch Pathol Lab Med. 2021 08 01; 145(8):953-959.
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Janz TA, Camilon PR, Cheung AY, Nguyen SA, White DR, Weber PC. A review of pediatric middle ear tumors and analysis of the demographics, management, and survival of pediatric rhabdomyosarcomas of the middle ear. Int J Pediatr Otorhinolaryngol. 2018 Sep; 112:109-112.
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O'Sullivan M, Budhraja V, Sadovsky Y, Pfeifer JD. Tumor heterogeneity affects the precision of microarray analysis. Diagn Mol Pathol. 2005 Jun; 14(2):65-71.
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Kadish S, Goodman M, Wang CC. Olfactory neuroblastoma. A clinical analysis of 17 cases. Cancer. 1976 Mar; 37(3):1571-6.