Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Nerve Tissue » Neuroectodermal Tumors » Neoplasms, Neuroepithelial » Neuroectodermal Tumors, Primitive
Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Germ Cell and Embryonal » Neuroectodermal Tumors » Neoplasms, Neuroepithelial » Neuroectodermal Tumors, Primitive
Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Glandular and Epithelial » Neoplasms, Neuroepithelial » Neuroectodermal Tumors, Primitive
Description
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) MeSH
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Subtype Terms (2)
Medulloblastoma
152 drugs (86 approved, 66 experimental)
Neuroectodermal Tumors, Primitive, Peripheral
10 drugs (6 approved, 4 experimental)
Phase 1 Indicated Drugs (27)
Other Experimental Indicated Drugs (1)
Organization Involved with Phase 3 Indications (6)
Organization Involved with Phase 2 Indications (44)
Istituto Clinico Humanitas - Rozzano (MI), Italy
National Institute of Neurological Disorders and Stroke (NINDS)
Organization Involved with Phase 1 Indications (11)
Organization Involved with Other Experimental Indications (8)
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UMLS Data
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