Extraskeletal myxoid chondrosarcoma
MONDO:0012825A rare malignant soft tissue neoplasm of uncertain differentiation, characterized by the presence of chondroblast-like cells in a myxoid stroma and a multinodular growth pattern. The most common sites of involvement are the deep soft tissues of the extremities, particularly the thigh. It usually presents as an enlarging soft tissue mass. Patients may have long survivals, but local recurrences and metastases occur in approximately half of the cases. The most common site of metastasis is the lungs.
Also known as: extraosseous chondrosarcoma, extraskeletal chondrosarcoma, myxoid extraosseous chondrosarcoma, myxoid extraskeletal chondrosarcoma, EMC, chondrosarcoma, extraskeletal myxoid
2828 clinical trials for this condition and its sub-types, 7 tagged with Extraskeletal myxoid chondrosarcoma itself.
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Browse by category →Sub-types of Extraskeletal myxoid chondrosarcoma
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New drug cocktail shows promise against rare sarcomas
Disease control OngoingThis study tests whether adding the targeted drug cabozantinib to immunotherapy (ipilimumab and nivolumab) works better than immunotherapy alone for people with advanced soft tissue sarcoma that has spread. About 66 adults with specific sarcoma types will take part. The goal is t…
Phase 2 • Sponsor: National Cancer Institute LAO • Aim: Disease control
Last updated Jun 27, 2026 12:23 UTC
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Ultrasound, CT, and MRI put to the test for identifying childhood neck lumps
Diagnosis OngoingThis study investigates how well different imaging methods—ultrasound, CT, and MRI—can identify the cause of neck swellings in children. Researchers will compare imaging results with the final diagnosis from biopsy, lab tests, or follow-up. The goal is to see if imaging can relia…
Sponsor: Sohag University • Aim: Diagnosis
Last updated Aug 01, 2026 00:00 UTC