 Nerve Sheath Neoplasms
"Nerve Sheath 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.
Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category.
| Descriptor ID |
D018317
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| MeSH Number(s) |
C04.557.580.600 C10.551.775.500 C10.668.829.725.500
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| Concept/Terms |
Nerve Sheath Neoplasms- Nerve Sheath Neoplasms
- Neoplasm, Nerve Sheath
- Nerve Sheath Neoplasm
- Nerve Sheath Tumors
- Tumors of the Nerve Sheath
- Neoplasms, Nerve Sheath
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Below are MeSH descriptors whose meaning is more general than "Nerve Sheath Neoplasms".
Below are MeSH descriptors whose meaning is more specific than "Nerve Sheath Neoplasms".
This graph shows the total number of publications written about "Nerve Sheath Neoplasms" by people in this website by year, and whether "Nerve Sheath 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 |
|---|
| 2007 | 1 | 0 | 1 | | 2012 | 0 | 1 | 1 | | 2013 | 1 | 0 | 1 | | 2019 | 2 | 0 | 2 | | 2020 | 0 | 1 | 1 | | 2021 | 1 | 0 | 1 | | 2023 | 1 | 0 | 1 | | 2024 | 0 | 2 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Nerve Sheath Neoplasms" by people in Profiles.
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Warmke LM, Davis JL, Al-Ibraheemi A, Arnold M, Tan S, Shenoy A, Surrey LF, Parham DM, Rudzinski ER. Loss of H3K27me3 Is Not Specific to Malignant Triton Tumor: Immunohistochemical Analysis of 23 Cases of Embryonal Rhabdomyosarcoma. Arch Pathol Lab Med. 2025 10 01; 149(10):944-949.
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Lingo JJ, Voigt E, Quelle DE. Linking FOXM1 and PD-L1 to CDK4/6-MEK targeted therapy resistance in malignant peripheral nerve sheath tumors. Oncotarget. 2024 09 30; 15:638-643.
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Brockman QR, Rytlewski JD, Milhem M, Monga V, Dodd RD. Integrated Epigenetic and Transcriptomic Analysis Identifies Interleukin 17 DNA Methylation Signature of Malignant Peripheral Nerve Sheath Tumor Progression and Metastasis. JCO Precis Oncol. 2024 05; 8:e2300325.
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Monárrez R, Chen Z, Dubin JA, Ingari JV. Rare peripheral nerve tumor of the median nerve. Hand Surg Rehabil. 2023 09; 42(4):374-377.
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Newman WC, Berry-Candelario J, Villavieja J, Reiner AS, Bilsky MH, Laufer I, Barzilai O. Improvement in Quality of Life Following Surgical Resection of Benign Intradural Extramedullary Tumors: A Prospective Evaluation of Patient-Reported Outcomes. Neurosurgery. 2021 04 15; 88(5):989-995.
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Banerjee J, Allaway RJ, Taroni JN, Baker A, Zhang X, Moon CI, Pratilas CA, Blakeley JO, Guinney J, Hirbe A, Greene CS, Gosline SJ. Integrative Analysis Identifies Candidate Tumor Microenvironment and Intracellular Signaling Pathways that Define Tumor Heterogeneity in NF1. Genes (Basel). 2020 02 21; 11(2).
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Graham DS, Russell TA, Eckardt MA, Motamedi K, Seeger LL, Singh AS, Bernthal NM, Kalbasi A, Dry SM, Nelson SD, Elashoff D, Levine BD, Eilber FC. Oncologic Accuracy of Image-guided Percutaneous Core-Needle Biopsy of Peripheral Nerve Sheath Tumors at a High-volume Sarcoma Center. Am J Clin Oncol. 2019 10; 42(10):739-743.
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Shurell-Linehan E, DiPardo BJ, Elliott IA, Graham DS, Eckardt MA, Dry SM, Nelson SD, Singh AS, Kalbasi A, Federman N, Bernthal NM, Eilber FC. Pathologic Response to Neoadjuvant Therapy is Associated With Improved Long-term Survival in High-risk Primary Localized Malignant Peripheral Nerve Sheath Tumors. Am J Clin Oncol. 2019 05; 42(5):426-431.
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Smith RE, Kebriaei MA, Gard AP, McComb RD, Bridge JA, Lennarson PJ. Intracranial malignant triton tumor in a patient with neurofibromatosis type 1: case report and review of the literature. Brain Tumor Pathol. 2014 Apr; 31(2):149-54.
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Rawal YB, Rosebush MS, Rawal SY, Anderson KM. Mandibular abnormalities in a patient with neurofibromatosis type 1. J Tenn Dent Assoc. 2012; 92(1):29-31; quiz 32-3.
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