Rare aggressive sarcoma cancer is a rare type of cancer that primarily affects the body's soft tissue and is most commonly found in the arms, legs, chest, abdomen, and head. Sarcoma cancer is often referred to as soft tissue sarcoma (STS) and is classified as either a low-grade or high-grade sarcoma, depending on its aggressiveness.
Symptoms of Rare Aggressive Sarcoma Cancer
The most common symptom of rare aggressive sarcoma cancer is a lump or mass that can be felt under the skin. Other symptoms may include pain, swelling, redness, or tenderness in the affected area. In some cases, the cancer may cause other symptoms such as weight loss, fever, or fatigue.
Diagnosis of Rare Aggressive Sarcoma Cancer
If a lump or mass is suspected of being a sarcoma, it is important to seek medical help right away. A doctor will typically order imaging tests such as an MRI or CT scan to get a better look at the tumor and determine its nature. A biopsy may also be ordered to confirm the diagnosis.
Treatment of Rare Aggressive Sarcoma Cancer
The treatment of rare aggressive sarcoma cancer will depend on the type of sarcoma and its stage. Generally, treatment involves surgery to remove the tumor, followed by radiation and/or chemotherapy to kill any remaining cancer cells. If the cancer has spread to other parts of the body, more aggressive treatments such as immunotherapy or targeted therapy may be recommended.