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 |
|---|
| 2004 | 2 | 0 | 2 |
| 2018 | 0 | 1 | 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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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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The Ews/Fli-1 fusion gene switches the differentiation program of neuroblastomas to Ewing sarcoma/peripheral primitive neuroectodermal tumors. Cancer Res. 2004 Feb 15; 64(4):1266-77.
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Constitutive activation of the neuregulin-1/erbB signaling pathway promotes the proliferation of a human peripheral neuroepithelioma cell line. J Neurooncol. 2004 Feb; 66(3):273-84.
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Malignant teratoid medulloepithelioma of the ciliary body. J Clin Neuroophthalmol. 1990 Dec; 10(4):291-2.