eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | soft tissue sarcoma |
| Comorbidity | C0029463|osteosarcoma |
| Sentences | 5 |
| PubMedID- 20604931 | Significantly better survival rates were found for chondrosarcoma compared with osteosarcoma (p = 0.001) and for osteosarcoma compared with ewing sarcoma (p = 0.001) (figure 1). |
| PubMedID- 25621678 | Regarding the histotypes of sarcoma associated with fd, osteosarcoma (7/10) was the most common type, followed by fibrosarcoma (2/10) and mfh (1/10). |
| PubMedID- 20224645 | This neoplasm is rare compared with bone osteosarcoma, accounting for 1-2% of all soft tissue sarcomas [5], and has a calculated annual incidence of 2 to 3 per million population [5]. |
| 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- 22829774 | Based on these criteria, alt is relatively common in many sarcomas (osteosarcoma and some types of soft tissue sarcomas), certain endocrine tumors (pancreatic neuroendocrine tumors, paraganglioma), a subset of nervous system tumors (e.g. |
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