What does STS mean in ONCOLOGY
Soft Tissue Sarcoma (STS) is a type of cancer of the body's soft tissues, such as muscles, fat, blood vessels, deep skin tissues, and connective tissues. Soft tissue sarcomas are rare forms of cancer that can occur anywhere in the body. STS can affect any age group but are much more common in adults. As a malignant (cancerous) tumor it has the potential to spread to other parts of the body if not treated early or correctly
STS meaning in Oncology in Medical
STS mostly used in an acronym Oncology in Category Medical that means Soft Tissue Sarcom
Shorthand: STS,
Full Form: Soft Tissue Sarcom
For more information of "Soft Tissue Sarcom", see the section below.
Essential Questions and Answers on Soft Tissue Sarcom in "MEDICAL»ONCOLOGY"
What is Soft Tissue Sarcoma?
Soft tissue sarcoma (STS) is a type of cancerous tumor that develops in soft tissues like muscle, fat, blood vessels, deep skin tissues, and connective tissues. It is a rare form of cancer that affects about 12,000 adults in the United States each year.
What are the common symptoms of Soft Tissue Sarcoma?
Common symptoms of STS include lumps or bumps on the body that may be tender to the touch and can increase in size over time; pain in the area near the lump; fatigue; and unexplained weight loss.
How does Soft Tissue Sarcoma metastasize?
Soft tissue sarcoma can spread to other parts of the body through the bloodstream and lymphatic system. This process is known as metastasis. Metastases can occur anywhere but most commonly occur in the lungs, liver, bones, and/or lymph nodes.
What are risk factors for developing Soft Tissue Sarcoma?
Risk factors for developing STS include previous radiation therapy, certain genetic conditions such as neurofibromatosis or Li-Fraumeni syndrome, exposure to certain pest chemicals or dioxin-containing herbicides such as Agent Orange, and immunosuppressive medications used after organ transplantation.
How is Soft Tissue Sarcoma diagnosed?
The diagnosis of STS typically begins with physical exam by a doctor. Imaging tests such as X-rays, MRI scans, and CT scans may also be used to confirm a potential diagnosis. Finally a biopsy may be performed where a sample of cells from the tumor are examined under a microscope to confirm whether it is cancerous or benign.
What treatments are available for people with Soft Tissue Sarcoma?
Treatment options for STS depend on several factors such as type and stage of tumor, location of tumor within body (e.g., near vital organs), age and general health of patient etc.. Common treatment options include surgery to remove tumor completely; chemotherapy and/or radiation therapy to shrink tumors; cryotherapy which uses extreme cold temperatures to freeze tumors away; immunotherapy which uses drugs or substances to boost patient’s immune systems so it can fight off cancer cells more effectively; targeted therapy which involves using drugs specifically designed to target cancer cells while leaving healthy cells unaffected.
Is there an increased risk associated with being diagnosed with Soft Tissue Sarcomas?
Yes, people diagnosed with this type of cancer have an increased risk for developing another sarcoma in future. Additionally those diagnosed with STS may also experience greater difficulty when trying to find life insurance due to their higher mortality risk.
Are there any lifestyle changes I should make if I'm diagnosed with Soft Tissue Cancer?
Yes! It is important for you to follow your doctor’s recommendations following diagnosis including gaining any needed supportive care services (e.g., dietician); reducing stress levels; making sure you're getting enough sleep; eating healthy foods (low fat/low sugar); exercising regularly; limiting alcohol consumption; quitting smoking if applicable etc..
Can my family members also get tested for the genetic mutations linked to Soft Tissue Sarcomas?
Yes! Genetic testing may be recommended for first degree relatives (e.g., parents, siblings) who show evidence or display signs similar symptoms linked with STS since they have increased risk compared to general population due family history.
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