"Neurilemmoma" 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 neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5)
| Descriptor ID |
D009442
|
| MeSH Number(s) |
C04.557.465.625.650.595 C04.557.580.600.610.595 C04.557.580.625.650.595
|
| Concept/Terms |
Neurilemmoma- Neurilemmoma
- Neurilemmomas
- Schwannoma
- Schwannomas
- Neurilemoma
- Neurilemomas
- Neurinoma
- Neurinomas
Malignant Peripheral Nerve Sheath Tumors- Malignant Peripheral Nerve Sheath Tumors
- Malignant Neurilemoma
- Malignant Neurilemomas
- Neurilemoma, Malignant
- Neurilemomas, Malignant
- Schwannoma, Malignant
- Malignant Schwannoma
- Malignant Schwannomas
- Schwannomas, Malignant
- Neurilemmosarcoma
- Neurilemmosarcomas
- Peripheral Nerve Sheath Tumors, Malignant
- Malignant Neurilemmoma
- Malignant Neurilemmomas
- Neurilemmoma, Malignant
- Neurilemmomas, Malignant
- MPNST
- MPNSTs
|
Below are MeSH descriptors whose meaning is more general than "Neurilemmoma".
Below are MeSH descriptors whose meaning is more specific than "Neurilemmoma".
This graph shows the total number of publications written about "Neurilemmoma" by people in this website by year, and whether "Neurilemmoma" 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 |
|---|
| 1997 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 1 | 2 |
| 2005 | 1 | 1 | 2 |
| 2007 | 2 | 0 | 2 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2014 | 4 | 0 | 4 |
| 2017 | 2 | 0 | 2 |
| 2018 | 3 | 0 | 3 |
| 2019 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
| 2025 | 3 | 1 | 4 |
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Below are the most recent publications written about "Neurilemmoma" by people in Profiles.
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Evaluating the consistency of SMARCB1 variant classification and assertions of genotype-phenotype relationships in ClinVar. Cancer Genet. 2025 Sep; 296-297:84-87.
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Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric NF2-, SMARCB1-, and LZTR1-Related Schwannomatosis. Clin Cancer Res. 2025 Apr 14; 31(8):1400-1406.
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Frontal lobe intra-axial schwannoma harboring a CHD7::VGLL3 fusion and heterozygous TSC2 p.F1510del mutation in a young child. Mol Biol Rep. 2025 Jan 10; 52(1):112.
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Cochlear Implantation With Sporadic Inner Ear Schwannomas: Outcomes in 106 Patients From an International Multi-Institutional Study. Otol Neurotol. 2025 Jan 01; 46(1):10-18.
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Progestin-associated meningiomatosis with unusual schwannoma-like morphology. J Neuropathol Exp Neurol. 2024 02 21; 83(3):214-216.
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Recurrent Schwannomatosis of the Hand. Hand (N Y). 2020 09; 15(5):732-738.
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Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1A. Ann Neurol. 2019 03; 85(3):316-330.
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Commentary in Response to Letter to the Editor: "T2-weighted MRI screening algorithm for patients with asymmetric sensorineural hearing loss". Am J Otolaryngol. 2018 Nov - Dec; 39(6):801.
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2016 Children's Tumor Foundation conference on neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. Am J Med Genet A. 2018 05; 176(5):1258-1269.
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Orbital cystic schwannoma masquerading as hydatid cyst. BMJ Case Rep. 2018 Apr 13; 2018.