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Cell Culture Ontology
| Preferred Name | schwannoma | |
| Synonyms |
neurolemmoma SCHW benign neurilemmoma Neurilemmoma, NOS Benign Schwannoma Neurilemoma (morphologic abnormality) Ancient neurilemoma Psammomatous schwannoma Degenerated Neurilemmoma Ancient schwannoma Pigmented Schawnnoma Ancient neurilemmoma Acoustic neuroma Benign Neurilemmoma Schwannomas Melanotic schwannoma Neurilemoma, Malignant Cellular schwannoma Schwannomatosis, Plexiform Neurilemmomas Neurilemmoma Malignant Neurilemoma benign schwannoma Neurilemmosarcoma Pigmented schwannoma Degenerated Schwannoma Plexiform schwannoma Schwannoma (WHO Grade I) Plexiform Schwannomatoses Neurilemmoma (disorder) Malignant Neurilemomas Neurilemomas, Malignant Neurilemmosarcomas Ancient neurilemmoma (disorder) Schwannoma, NOS Neurilemomas Neurilemoma peripheral fibroblastoma Ancient schwannoma (morphologic abnormality) neurilemmoma Melanocytic Schwannoma schwannoma, benign psammomatous schwannoma schwannoma (WHO grade I) Plexiform Schwannomatosis Schwannomatoses, Plexiform Neurinoma Neurinomas neurinoma schwannoma |
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| Definitions |
A benign, usually encapsulated slow growing tumor composed of Schwann cells. It affects peripheral and cranial nerves. It recurs infrequently and only rare cases associated with malignant transformation have been reported. 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) A benign, usually encapsulated slow growing tumor of the peripheral nervous system composed of well differentiated Schwann cells. It recurs infrequently and only rare cases associated with malignant transformation have been reported. 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 (MeSH). A tumor of the peripheral nervous system composed of neoplastic Schwann cells. The vast majority of schwannomas follow a benign clinical course. Only rare cases associated with a malignant clinical course have been reported. |
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| ID |
http://www.ebi.ac.uk/efo/EFO_0000693 |
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| database_cross_reference |
SNOMEDCT:404022001 SNOMEDCT:985004 NIFSTD:birnlex_12603 SNOMEDCT:253086004 MedDRA:10039667 UMLS:C0027809 MONDO:0002546 SNOMEDCT:404023006 NANDO:2200103 MedDRA:10029235 MedDRA:10029234 SNOMEDCT:409704009 MeSH:D009442 Orphanet:252164 MEDGEN:45053 SCTID:404022001 OMIM:162091 ONCOTREE:SCHW SNOMEDCT:253087008 SNOMEDCT:253088003 ICDO:9560/0 SNOMEDCT:126949007 SNOMEDCT:77418004 DOID:12689 DOID:3192 DOID:3196 DOID:3206 DOID:955 GARD:4767 ICD9:215.9 NCIT:C3269 NCIt:C3269
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| definition |
A benign, usually encapsulated slow growing tumor composed of Schwann cells. It affects peripheral and cranial nerves. It recurs infrequently and only rare cases associated with malignant transformation have been reported. 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) A benign, usually encapsulated slow growing tumor of the peripheral nervous system composed of well differentiated Schwann cells. It recurs infrequently and only rare cases associated with malignant transformation have been reported. 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 (MeSH). A tumor of the peripheral nervous system composed of neoplastic Schwann cells. The vast majority of schwannomas follow a benign clinical course. Only rare cases associated with a malignant clinical course have been reported.
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| has_exact_synonym |
benign neurilemmoma Neurilemmoma, NOS Benign Schwannoma Neurilemoma (morphologic abnormality) Ancient neurilemoma Psammomatous schwannoma Degenerated Neurilemmoma Ancient schwannoma Pigmented Schawnnoma Ancient neurilemmoma Acoustic neuroma Benign Neurilemmoma Schwannomas Melanotic schwannoma Neurilemoma, Malignant Cellular schwannoma Schwannomatosis, Plexiform Neurilemmomas Neurilemmoma Malignant Neurilemoma benign schwannoma Neurilemmosarcoma Pigmented schwannoma Degenerated Schwannoma Plexiform schwannoma Schwannoma (WHO Grade I) Plexiform Schwannomatoses Neurilemmoma (disorder) Malignant Neurilemomas Neurilemomas, Malignant Neurilemmosarcomas Ancient neurilemmoma (disorder) Schwannoma, NOS Neurilemomas Neurilemoma peripheral fibroblastoma Ancient schwannoma (morphologic abnormality) neurilemmoma Melanocytic Schwannoma schwannoma, benign psammomatous schwannoma schwannoma (WHO grade I) Plexiform Schwannomatosis Schwannomatoses, Plexiform Neurinoma Neurinomas neurinoma schwannoma
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| has_related_synonym |
neurolemmoma SCHW
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| id |
EFO:0000693
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| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-base#orphanet_rare http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_disorder |
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| label |
schwannoma
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| notation |
EFO:0000693
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| preferred label |
schwannoma
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| prefLabel |
schwannoma
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| see also | ||
| skos_closeMatch | ||
| skos_exactMatch |
http://purl.obolibrary.org/obo/NCIT_C3269 http://purl.obolibrary.org/obo/DOID_3192 http://purl.obolibrary.org/obo/Orphanet_252164 http://purl.obolibrary.org/obo/DOID_955 http://purl.obolibrary.org/obo/EFO_0000693 http://linkedlifedata.com/resource/umls/id/C0027809 |
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| term editor |
Tomasz Adamusiak James Malone
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| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0021637 |
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