"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 |
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1994 | 2 | 1 | 3 |
1995 | 1 | 0 | 1 |
1997 | 5 | 0 | 5 |
1998 | 2 | 0 | 2 |
1999 | 3 | 1 | 4 |
2000 | 0 | 1 | 1 |
2001 | 1 | 0 | 1 |
2002 | 1 | 0 | 1 |
2003 | 3 | 2 | 5 |
2004 | 2 | 0 | 2 |
2005 | 2 | 1 | 3 |
2006 | 1 | 0 | 1 |
2007 | 1 | 1 | 2 |
2008 | 3 | 1 | 4 |
2009 | 3 | 0 | 3 |
2010 | 2 | 2 | 4 |
2011 | 1 | 1 | 2 |
2012 | 2 | 2 | 4 |
2013 | 3 | 1 | 4 |
2014 | 6 | 0 | 6 |
2015 | 2 | 0 | 2 |
2016 | 5 | 0 | 5 |
2017 | 5 | 1 | 6 |
2018 | 4 | 0 | 4 |
2019 | 0 | 1 | 1 |
2020 | 1 | 1 | 2 |
2022 | 1 | 0 | 1 |
2024 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Neurilemmoma" by people in Profiles.
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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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TRPS1 expression in MPNST is correlated with PRC2 inactivation and loss of H3K27me3. Hum Pathol. 2024 09; 151:105632.
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Loss of dimethylated H3K27 (H3K27me2) expression is not a specific marker of malignant peripheral nerve sheath tumor (MPNST): An immunohistochemical study of 137 cases, with emphasis on MPNST and melanocytic tumors. Ann Diagn Pathol. 2022 Aug; 59:151967.
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Radiation-associated sarcomas other than malignant peripheral nerve sheath tumours demonstrate loss of histone H3K27 trimethylation?. Histopathology. 2021 Jan; 78(2):321-326.
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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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Pigmented Melanotic Schwannoma of the Neck: Report of 2 Cases and Review of the Literature. Ear Nose Throat J. 2019 Feb; 98(2):102-106.
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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.