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 |
|---|
| 2005 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Neuroectodermal Tumors, Primitive, Peripheral" by people in Profiles.
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Clinical features and outcomes in patients with Ewing sarcoma and regional lymph node involvement. Pediatr Blood Cancer. 2012 Oct; 59(4):617-20.
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Ewing's sarcoma/primitive neuroectodermal tumour in a possible primary testicular location. Pathology. 2007 Dec; 39(6):599-601.
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Protocol for the examination of specimens from pediatric and adult patients with osseous and extraosseous ewing sarcoma family of tumors, including peripheral primitive neuroectodermal tumor and ewing sarcoma. Arch Pathol Lab Med. 2005 Jul; 129(7):866-73.
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Cervical primitive neuroectodermal tumor. Gynecol Oncol. 2001 Oct; 83(1):138-42.
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Beam's-eye-view aided treatment planning for a nasopharyngeal lesion: a case report. Med Dosim. 1989 Dec; 14(4):231-5.
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Sinonasal undifferentiated carcinoma. An aggressive neoplasm derived from schneiderian epithelium and distinct from olfactory neuroblastoma. Am J Surg Pathol. 1986 Nov; 10(11):771-9.
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Olfactory neuroblastoma: an ultrastructural study. Cancer. 1977 Jan; 39(1):131-8.