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)
|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
- Neoplasms, Primitive Neuroepithelial
- Neoplasm, Primitive Neuroepithelial
- Neuroepithelial Neoplasm, Primitive
- Primitive Neuroepithelial Neoplasm
- Neuroepithelial Neoplasms, Primitive
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".
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Below are the most recent publications written about "Neuroectodermal Tumors, Primitive" by people in Profiles.
Prognostic validity of the American joint committee on cancer eighth edition staging system for well-differentiated pancreatic neuroendocrine tumors. HPB (Oxford). 2022 05; 24(5):681-690.
Primary intracranial Ewing's sarcoma with unusual features. Int J Clin Exp Pathol. 2015; 8(1):260-74.
A novel translocation t(11;13) (q21;q14.2) in a child with suprasellar primitive neuroectodermal tumor and retinoblastoma. Ophthalmic Genet. 2013 Mar-Jun; 34(1-2):97-100.
Diagnosis and management of brain and spinal cord tumors in the neonate. Semin Fetal Neonatal Med. 2012 Aug; 17(4):202-206.
Glioblastoma with PNET-like components has a higher frequency of isocitrate dehydrogenase 1 (IDH1) mutation and likely a better prognosis than primary glioblastoma. Int J Clin Exp Pathol. 2011; 4(7):651-60.
Extraosseous Ewing's sarcoma of the pancreas. Int J Clin Oncol. 2012 Aug; 17(4):399-406.
A 15-year-old female with progressive myelopathy. Brain Pathol. 2005 Jul; 15(3):265-7.
Using a bioabsorbable copolymer plate for chest wall reconstruction. J Pediatr Surg. 2004 Apr; 39(4):626-8.
Expression of alpha-, beta-, and gamma-synuclein in glial tumors and medulloblastomas. Acta Neuropathol. 2003 Aug; 106(2):167-75.