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Sarcoma, Synovial MeSH Descriptor Data 2022


MeSH Heading
Sarcoma, Synovial
Tree Number(s)
C04.557.450.565.835
C04.557.450.795.875
Unique ID
D013584
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D013584
Annotation
coordinate with precoordinated organ/neoplasm term
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)
Entry Term(s)
Synovioma
Public MeSH Note
94; was SYNOVIOMA 1963-93
Online Note
use SARCOMA, SYNOVIAL to search SYNOVIOMA 1966-93
History Note
94; was SYNOVIOMA 1963-93
Date Established
1994/01/01
Date of Entry
1999/01/01
Revision Date
2012/07/03
Sarcoma, Synovial Preferred
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