"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 |
|---|
| 1994 | 1 | 0 | 1 |
| 1996 | 1 | 0 | 1 |
| 1999 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 1 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 2 | 0 | 2 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Neurilemmoma" by people in Profiles.
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Schwannomas Mimicking Leptomeningeal Spread in the Setting of Breast Cancer: A Case Report. In Vivo. 2023 Nov-Dec; 37(6):2835-2839.
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Beyond schwannomas and neurofibromas: a radiological and histopathological review of lesser-known benign lesions that arise in association with peripheral nerves. Skeletal Radiol. 2023 Apr; 52(4):649-669.
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Current Recommendations for Patient-Reported Outcome Measures Assessing Domains of Quality of Life in Neurofibromatosis Clinical Trials. Neurology. 2021 08 17; 97(7 Suppl 1):S50-S63.
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Novel response to neoadjuvant anti-PD1 therapy for a patient with retrocaval melanotic schwannoma. Melanoma Res. 2021 02 01; 31(1):92-97.
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Soft-Tissue Tumors of the Hand-Imaging Features. Can Assoc Radiol J. 2020 May; 71(2):161-173.
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Retroperitoneal schwannoma: an unusual cause of abdominal distention. BMJ Case Rep. 2017 May 12; 2017.
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Epigenetic regulation of SMARCB1 By miR-206, -381 and -671-5p is evident in a variety of SMARCB1 immunonegative soft tissue sarcomas, while miR-765 appears specific for epithelioid sarcoma. A miRNA study of 223 soft tissue sarcomas. Genes Chromosomes Cancer. 2016 10; 55(10):786-802.
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Patient-reported outcomes in neurofibromatosis and schwannomatosis clinical trials. Neurology. 2013 Nov 19; 81(21 Suppl 1):S6-14.
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Expression profiling of 519 kinase genes in matched malignant peripheral nerve sheath tumor/plexiform neurofibroma samples is discriminatory and identifies mitotic regulators BUB1B, PBK and NEK2 as overexpressed with transformation. Mod Pathol. 2013 Jul; 26(7):930-43.
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Giant neurilemmoma of the vagus nerve: a case report and review of literature. J Indian Med Assoc. 2012 Dec; 110(12):926-8.