Knowledge (XXG)

Nerve sheath tumor

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The primary Schwann cell differentiation and neoplastic proliferations are characteristics of peripheral nerve sheath tumors. For instance, the Schwann cell, which is the major neoplastic cell component of neurofibroma, is cytologically distinguished by the expression of S-100 protein and wavy
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nuclear outlines. A variety of peripheral nerve cells, including axons, perineurial cells, fibroblasts, and varying inflammatory components such as mast cells and lymphocytes, are also present in neurofibromas. A population of CD34-positive cells with an unknown histogenesis is also found.
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Slomiany MG, Dai L, Bomar PA, Knackstedt TJ, Kranc DA, Tolliver L, Maria BL, Toole BP. Abrogating drug resistance in malignant peripheral nerve sheath tumors by disrupting hyaluronan-CD44 interactions with small hyaluronan oligosaccharides. Cancer Res. 2009; 69:4992–4998.
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Perry A, Roth KA, Banerjee R, Fuller CE, Gutmann DH. NF1 deletions in S-100 protein-positive and negative cells of sporadic and neurofibromatosis 1 (NF1)-associated plexiform neurofibromas and malignant peripheral nerve sheath tumors. Am J Pathol. 2001; 159:57–61.
64:. From benign tumors like schwannoma to high grade malignant neoplasms known as malignant peripheral nerve sheath tumors, peripheral nerve sheath tumors include a range of clearly characterized clinicopathologic entities. A 768: 668: 386: 327: 194:
Weiss SW, Langloss JM, Enzinger FM. Value of S-100 protein in the diagnosis of soft tissue tumors with particular reference to benign and malignant Schwann cell tumors. Lab Invest. 1983; 49:299–308.
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Weiss SW, Nickoloff BJ. CD-34 is expressed by a distinctive cell population in peripheral nerve, nerve sheath tumors, and related lesions. Am J Surg Pathol. 1993; 17:1039–1045. [PubMed: 7690524]
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Louis, DN.; Ohgaki, H.; Wiestler, OD.; Cavenee, WK., editors. WHO Classification of Tumours of the Central Nervous System. International Agency for Research on Cancer; Lyon: 2007.
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Chaubal A, Paetau A, Zoltick P, Miettinen M. CD34 immunoreactivity in nervous system tumors. Acta Neuropathol. 1994; 88:454–458.
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Carroll S. Molecular mechanisms promoting the pathogenesis of Schwann cell neoplasms. Acta Neuropathol. 2012
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Note: Not all brain tumors are of nervous tissue, and not all nervous tissue tumors are in the brain (see
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peripheral nerve sheath tumor, which are frequently resistant to conventional treatments.
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WHO classification of the tumors of the central nervous system
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Retrieved 144: 135: 126: 112: 98: 92: 90: 69: 65: 60:surrounding 41: 39: 596:Neurocytoma 558:Gliosarcoma 424:Astrocytoma 344:Pituicytoma 245:: 9540-9570 146:Mayo Clinic 82:schwannomas 741:Schwannoma 654:Meningioma 497:Ependymoma 152:2007-08-06 118:References 416:Astrocyte 364:Pinealoma 317:Endocrine 266:115242003 261:SNOMED CT 103:cancerous 28:Specialty 798:Category 646:Meninges 489:Ependyma 255:D018317 101:) is a 48:of the 574:neuron 571:Mature 407:Glioma 355:Other: 328:Sellar 78:Benign 62:nerves 58:myelin 762:Other 242:ICD-O 99:MPNST 46:tumor 250:MeSH 84:and 70:PNST 691:PNS 378:CNS 800:: 784:). 584:: 264:: 253:: 143:. 91:A 88:. 76:. 40:A 739:/ 693:: 399:) 394:, 390:( 330:: 301:e 294:t 287:v 234:D 155:. 97:( 68:( 52:(

Index

Specialty
Neuro-oncology
tumor
nervous system
nervous system neoplasm
myelin
nerves
peripheral nervous system
Benign
schwannomas
neurofibromas
malignant peripheral nerve sheath tumor
cancerous
"Spinal Cord Tumors -- Nerve Sheath Tumors (Schwannomas and Neurofibromas)"
Mayo Clinic
D
ICD-O
MeSH
D018317
SNOMED CT
115242003
v
t
e
Tumours of the nervous system
Endocrine
Sellar
Craniopharyngioma
Pituicytoma
Pinealoma

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