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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease soft tissue sarcoma
Comorbidity C1261473|sarcoma
Sentences 16
PubMedID- 24085323 Synovial sarcoma, accounting for <5–10% of all soft tissue sarcomas, develops in the synovial membrane of the joints, mainly in the lower limbs, but can also occur in the trunk and head/neck (4).
PubMedID- 24707262 Synovial sarcoma is a subset of the soft tissue sarcomas with unknown histological origin.
PubMedID- 23664540 Although rare, synovial sarcoma (ss) is one of the most common soft tissue sarcomas affecting young adults.
PubMedID- 24661286 Synovial sarcoma is part of soft tissue sarcomas, an uncommon group of malignant tumors of mesenchymal origin.
PubMedID- 21921334 Results: osteosarcoma constituted half of the metastatic sarcomas (48 cases, 50.5%) followed by synovial sarcoma (16 cases, 16.8%) and high grade spindle cell sarcoma-nos (10 cases, 10.5%).
PubMedID- 25506014 We present a 46-year-old female patient who is diagnosed with synchronous postirradiation sarcoma, cutaneous relapse of a previous soft tissue sarcoma, and lung adenocarcinoma.
PubMedID- 24575008 Synovial sarcoma (svs) represents ∼10% of all soft-tissue sarcomas [1].
PubMedID- 21948137 Retroperitoneal sarcoma represents approximately 12-15% of all sarcomas and between 0.2 and 0.5% of all neoplasia.
PubMedID- 24206917 Synovial sarcoma is a type of soft tissue sarcoma that most commonly forms near the joints of the arm or leg but has been documented in various places in the body, including the heart, prostate, and brain.
PubMedID- 22173238 Background: alveolar soft part sarcoma accounts for 0.5-1.0% of soft tissue sarcomas in the united states.
PubMedID- 21092216 Results: vascular leiomyosarcomas accounted for 0.7% of all malignant soft tissue tumors treated at our soft tissue sarcoma reference center.
PubMedID- 20807625 Conclusions: magnetic resonance imaging does not reliably detect residual gross or microscopic soft tissue sarcoma after marginal excision of unsuspected soft tissue sarcomas of the hand, with residual tumor not readily distinguished from postoperative change.
PubMedID- 25621034 This can aid in differentiating synovial sarcoma from other types of soft-tissue sarcomas (13).
PubMedID- 20730885 Breast metastases in children and adolescents with rhabdomyosarcoma: experience of the italian soft tissue sarcoma committee.
PubMedID- 25624911 Körner et al (14) reported that the ewing’s sarcoma family of tumors and synovial sarcomas expressed the npy receptor subtype y1 at a high incidence rate (84 and 40%, respectively) and density (mean, 5,314 and 7,497 disintegrations/min/mg tissue).
PubMedID- 20165867 This sarcoma category includes most of spindle cell/pleomorphic sarcomas (myxofibrosarcoma, pleomorphic liposarcoma, etc.)

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