"Spinal Cord Neoplasms" 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.
Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA.
Descriptor ID |
D013120
|
MeSH Number(s) |
C04.588.614.250.803 C10.228.854.765 C10.551.240.750
|
Concept/Terms |
Spinal Cord Neoplasms- Spinal Cord Neoplasms
- Tumors, Spinal Cord
- Spinal Cord Tumor
- Spinal Cord Tumors
- Tumor, Spinal Cord
- Neoplasms, Spinal Cord
- Neoplasm, Spinal Cord
- Spinal Cord Neoplasm
Intradural-Extramedullary Spinal Cord Neoplasms- Intradural-Extramedullary Spinal Cord Neoplasms
- Intradural Extramedullary Spinal Cord Neoplasms
- Spinal Cord Neoplasms, Intradural-Extramedullary
- Spinal Cord Neoplasms, Intradural Extramedullary
|
Below are MeSH descriptors whose meaning is more general than "Spinal Cord Neoplasms".
Below are MeSH descriptors whose meaning is more specific than "Spinal Cord Neoplasms".
This graph shows the total number of publications written about "Spinal Cord Neoplasms" by people in this website by year, and whether "Spinal Cord Neoplasms" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1995 | 1 | 0 | 1 |
1996 | 1 | 1 | 2 |
1997 | 1 | 0 | 1 |
2000 | 2 | 0 | 2 |
2003 | 3 | 1 | 4 |
2004 | 1 | 0 | 1 |
2005 | 1 | 0 | 1 |
2006 | 1 | 0 | 1 |
2007 | 1 | 0 | 1 |
2008 | 1 | 0 | 1 |
2009 | 3 | 0 | 3 |
2010 | 1 | 0 | 1 |
2011 | 3 | 0 | 3 |
2012 | 6 | 1 | 7 |
2013 | 3 | 0 | 3 |
2014 | 1 | 0 | 1 |
2015 | 2 | 0 | 2 |
2016 | 3 | 0 | 3 |
2019 | 2 | 0 | 2 |
2022 | 2 | 0 | 2 |
2023 | 2 | 0 | 2 |
2024 | 1 | 1 | 2 |
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Below are the most recent publications written about "Spinal Cord Neoplasms" by people in Profiles.
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Outcomes of patients with intermediate-risk neuroblastoma presenting with motor deficits relating to intraspinal tumor extension: A report from the Children's Oncology Group study ANBL0531. Pediatr Blood Cancer. 2025 Jan; 72(1):e31407.
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Intramedullary spinal cord tumors in pediatric patients presenting later with brain lesions: case series and systematic review of the literature. Childs Nerv Syst. 2024 Apr; 40(4):1079-1089.
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Advances in Imaging Modalities for Pediatric Brain and Spinal Cord Tumors. Pediatr Neurosurg. 2023; 58(5):240-258.
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Multi-institutional Characterization of Outcomes for Pediatric and Young Adult Patients With High-Risk Myxopapillary Ependymoma After Radiation Therapy. Int J Radiat Oncol Biol Phys. 2023 Dec 01; 117(5):1174-1180.
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Systemic considerations for the surgical treatment of spinal metastatic disease: a scoping literature review. Lancet Oncol. 2022 07; 23(7):e321-e333.
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Papilledema From Froin Syndrome due to a Myxopapillary Ependymoma. J Neuroophthalmol. 2023 Dec 01; 43(4):e161-e163.
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Leptomeningeal Metastases of the Spine: A Systematic Review. Anticancer Res. 2022 02; 42(2):619-628.
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Pediatric spinal cord diffuse midline glioma, H3 K27-altered with intracranial and spinal leptomeningeal spread: A case report. Neuroradiol J. 2022 Oct; 35(5):634-639.
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A phase II study of dose-dense temozolomide and lapatinib for recurrent low-grade and anaplastic supratentorial, infratentorial, and spinal cord ependymoma. Neuro Oncol. 2021 03 25; 23(3):468-477.
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Primary Spinal Cord Melanoma - An Uncommon Entity. Can J Neurol Sci. 2019 05; 46(3):348-350.