Extraskeletal myxoid chondrosarcoma
Extraskeletal Myxoid Chondrosarcoma is a rare type of cancer that typically develops in the soft tissues of the body, such as the muscles, tendons, and fat. It is characterized by the presence of chondrosarcoma cells that are not attached to the bone (extraskeletal) and have a jelly-like (myxoid) appearance.
Symptoms[edit | edit source]
The symptoms of Extraskeletal Myxoid Chondrosarcoma can vary depending on the location and size of the tumor. Common symptoms may include a painless lump or swelling, pain or discomfort in the affected area, and limited range of motion.
Causes[edit | edit source]
The exact cause of Extraskeletal Myxoid Chondrosarcoma is unknown. However, it is believed to be associated with certain genetic changes.
Diagnosis[edit | edit source]
Diagnosis of Extraskeletal Myxoid Chondrosarcoma typically involves a physical examination, imaging tests such as MRI or CT scan, and a biopsy of the tumor.
Treatment[edit | edit source]
Treatment for Extraskeletal Myxoid Chondrosarcoma often involves surgery to remove the tumor. Other treatments may include radiation therapy, chemotherapy, and targeted therapy.
Prognosis[edit | edit source]
The prognosis for Extraskeletal Myxoid Chondrosarcoma varies depending on the size and location of the tumor, the patient's overall health, and the response to treatment.
See also[edit | edit source]
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Contributors: Prab R. Tumpati, MD
