"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
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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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2001 | 1 | 0 | 1 |
2003 | 1 | 0 | 1 |
2005 | 1 | 0 | 1 |
2006 | 1 | 1 | 2 |
2007 | 0 | 1 | 1 |
2008 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
2011 | 2 | 0 | 2 |
2012 | 2 | 0 | 2 |
2014 | 2 | 0 | 2 |
2015 | 3 | 0 | 3 |
2016 | 1 | 0 | 1 |
2017 | 2 | 0 | 2 |
2018 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Neurilemmoma" by people in Profiles.
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Plexiform Schwannoma of the Oral Cavity: Report of Eight Cases and a Review of the Literature. Head Neck Pathol. 2021 Mar; 15(1):288-297.
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Recent Advances in the Diagnosis and Pathogenesis of Neurofibromatosis Type 1 (NF1)-associated Peripheral Nervous System Neoplasms. Adv Anat Pathol. 2018 Sep; 25(5):353-368.
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Asymptomatic Soft Erythematous Dome-Shaped Papule on the Chest: Answer. Am J Dermatopathol. 2017 Nov; 39(11):867-869.
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BH3 mimetics suppress CXCL12 expression in human malignant peripheral nerve sheath tumor cells. Oncotarget. 2017 Jan 31; 8(5):8670-8678.
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Current status and recommendations for biomarkers and biobanking in neurofibromatosis. Neurology. 2016 Aug 16; 87(7 Suppl 1):S40-8.
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The Challenge of Cancer Genomics in Rare Nervous System Neoplasms: Malignant Peripheral Nerve Sheath Tumors as a Paradigm for Cross-Species Comparative Oncogenomics. Am J Pathol. 2016 Mar; 186(3):464-77.
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Primary tumors of the facial nerve. Otolaryngol Clin North Am. 2015 Jun; 48(3):491-500.
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Stereotactic radiosurgery for facial nerve schwannomas: meta-analysis and clinical review. Otol Neurotol. 2015 Mar; 36(3):393-8.
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Combinatorial therapy with tamoxifen and trifluoperazine effectively inhibits malignant peripheral nerve sheath tumor growth by targeting complementary signaling cascades. J Neuropathol Exp Neurol. 2014 Nov; 73(11):1078-90.
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BNIP3 regulates AT101 [(-)-gossypol] induced death in malignant peripheral nerve sheath tumor cells. PLoS One. 2014; 9(5):e96733.