| Descriptor English: | Sarcoma, Synovial | ||||||
| Descriptor Spanish: |
Sarcoma Sinovial
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| Descriptor Portuguese: | Sarcoma Sinovial | ||||||
| Descriptor French: | Sarcome synovial | ||||||
| Entry term(s): |
Sarcomas, Synovial Synovial Sarcoma Synovial Sarcomas Synovioma Synoviomas |
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| Tree number(s): |
C04.557.450.565.835 C04.557.450.795.875 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D013584 | ||||||
| Scope note: | A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) |
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| Annotation: | coordinate with precoordinated organ/neoplasm term |
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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 SYNOVIOMA 1963-93 |
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| Online Note: | use SARCOMA, SYNOVIAL to search SYNOVIOMA 1966-93 |
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| History Note: | 94; was SYNOVIOMA 1963-93 |
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| DeCS ID: | 31919 | ||||||
| Unique ID: | D013584 | ||||||
| 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: | 2012/07/03 |
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DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms
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Sarcoma, Synovial
- Preferred
| Concept UI |
M0020963 |
| Scope note | A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) |
| Preferred term | Sarcoma, Synovial |
| Entry term(s) |
Sarcomas, Synovial Synovial Sarcoma Synovial Sarcomas Synovioma Synoviomas |
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