| Descriptor English: | Paraganglioma, Extra-Adrenal | ||||||
| Descriptor Spanish: |
Paraganglioma Extraadrenal
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| Descriptor Portuguese: | Paraganglioma Extrassuprarrenal | ||||||
| Descriptor French: | Paragangliome extrasurrénalien | ||||||
| Entry term(s): |
Chemodectoma Chemodectomas Extra-Adrenal Paraganglioma Extra-Adrenal Paragangliomas Non-Chromaffin Paraganglioma Non-Chromaffin Paragangliomas Nonchromaffin Paraganglioma Nonchromaffin Paragangliomas Paraganglioma, Extra Adrenal Paraganglioma, Non Chromaffin Paraganglioma, Non-Chromaffin Paraganglioma, Nonchromaffin Paragangliomas, Extra-Adrenal Paragangliomas, Familial Nonchromaffin, 1 Paragangliomas, Non-Chromaffin Paragangliomas, Nonchromaffin |
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| Tree number(s): |
C04.557.465.625.650.700.705 C04.557.580.625.650.700.705 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D010236 | ||||||
| Scope note: | A relatively rare, usually benign neoplasm originating in the chemoreceptor tissue of the CAROTID BODY; GLOMUS JUGULARE; GLOMUS TYMPANICUM; AORTIC BODIES; and the female genital tract. It consists histologically of rounded or ovoid hyperchromatic cells that tend to be grouped in an alveolus-like pattern within a scant to moderate amount of fibrous stroma and a few large thin-walled vascular channels. (From Stedman, 27th ed) |
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| Annotation: | coordinate IM with precoordinated organ/neoplasm term (IM) |
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| Allowable Qualifiers: |
BL blood BS blood supply CF cerebrospinal fluid CH chemistry CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SC secondary SU surgery TH therapy UL ultrastructure UR urine VE veterinary VI virology |
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| Public MeSH Note: | 94; was PARAGANGLIOMA, NONCHROMAFFIN 1963-93 |
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| Online Note: | use PARAGANGLIOMA, EXTRA-ADRENAL to search PARAGANGLIOMA, NONCHROMAFFIN 1966-93 |
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| History Note: | 94; was PARAGANGLIOMA, NONCHROMAFFIN 1963-93 |
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| Related: |
Glomus Tumor
MeSH | ||||||
| DeCS ID: | 31884 | ||||||
| Unique ID: | D010236 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1994/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms
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Paraganglioma, Extra-Adrenal
- Preferred
| Concept UI |
M0015870 |
| Scope note | A relatively rare, usually benign neoplasm originating in the chemoreceptor tissue of the CAROTID BODY; GLOMUS JUGULARE; GLOMUS TYMPANICUM; AORTIC BODIES; and the female genital tract. It consists histologically of rounded or ovoid hyperchromatic cells that tend to be grouped in an alveolus-like pattern within a scant to moderate amount of fibrous stroma and a few large thin-walled vascular channels. (From Stedman, 27th ed) |
| Preferred term | Paraganglioma, Extra-Adrenal |
| Entry term(s) |
Chemodectoma Chemodectomas Extra-Adrenal Paraganglioma Extra-Adrenal Paragangliomas Non-Chromaffin Paraganglioma Non-Chromaffin Paragangliomas Nonchromaffin Paraganglioma Nonchromaffin Paragangliomas Paraganglioma, Extra Adrenal Paraganglioma, Non Chromaffin Paraganglioma, Non-Chromaffin Paraganglioma, Nonchromaffin Paragangliomas, Extra-Adrenal Paragangliomas, Familial Nonchromaffin, 1 Paragangliomas, Non-Chromaffin Paragangliomas, Nonchromaffin |
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