DiseaseID 26064

滑膜肉瘤

Sarcoma, Synovial

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Disease: 1Symptom: 3Target: 12Links: 15

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Record Fields

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Disease Id: 26064
Core Entity Id: 118632
Source Entity Count: 1
Preferred Name: Sarcoma, Synovial
Name Cn: 滑膜肉瘤
Name Pinyin: Hua Mo Rou Liu
Name En: Sarcoma, Synovial
Name Latin
Bilingual Status: complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition: NCI2016_NCI-GLOSS_1602D:A malignant tumor that develops in the synovial membrane of the joints.|NCI2016_CDISC_1602D:A malignant neoplasm that usually arises in the synovial membranes of the joints and the synovial cells of the tendons and bursae.|NCI2016_02D:A malignant neoplasm characterized by the chromosomal translocation t(X;18)(p11;q11). It can occur at any age, but mainly affects young adults, more commonly males. Although any site can be affected, the vast majority of the cases arise in the deep soft tissues of extremities, especially around the knee. Microscopically, synovial sarcoma is classified as monophasic (with a spindle or epithelial cell component) or biphasic (with both spindle and epithelial cell components). Synovial sarcomas can recur or metastasize to the lungs, bones, and lymph nodes.|MSH2017_2016_08_12: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)|HPO2016_07_04:A type of mesenchymal tissue cell tumor that exhibits epithelial differentiation, which most frequently arises in the extremities. [HPO:probinson]
Version: v1,v2
Suppressed: No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name

Sarcoma, Synovial

Role

preferred

Source

SymMap_v2

Preferred

Yes

Cross References

Trusted external identifiers retained for this final record.

Umls

C0039101

Sym Map

SMDE01768

Attributes

Merged source attributes and domain-specific metadata.

Version

v1,v2

Suppress

Disease Definition

NCI2016_NCI-GLOSS_1602D:A malignant tumor that develops in the synovial membrane of the joints.|NCI2016_CDISC_1602D:A malignant neoplasm that usually arises in the synovial membranes of the joints and the synovial cells of the tendons and bursae.|NCI2016_02D:A malignant neoplasm characterized by the chromosomal translocation t(X;18)(p11;q11). It can occur at any age, but mainly affects young adults, more commonly males. Although any site can be affected, the vast majority of the cases arise in the deep soft tissues of extremities, especially around the knee. Microscopically, synovial sarcoma is classified as monophasic (with a spindle or epithelial cell component) or biphasic (with both spindle and epithelial cell components). Synovial sarcomas can recur or metastasize to the lungs, bones, and lymph nodes.|MSH2017_2016_08_12: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)|HPO2016_07_04:A type of mesenchymal tissue cell tumor that exhibits epithelial differentiation, which most frequently arises in the extremities. [HPO:probinson]