Overview
Sarcoma is an uncommon malignancy that arises in connective tissues, such as bones, muscles, adipose tissue, cartilage, blood vessels, and other supportive structures of the body. Sarcomas arise from mesenchymal cells, whereas carcinomas arise from epithelial cells. They can be put into two main groups: bone sarcomas and soft tissue sarcomas. Sarcomas can happen to anyone, but some types are more common in kids and young adults. Symptoms can be hard to spot at first because they can grow deep inside tissues. Early diagnosis and specialized treatment are important for getting better results.
Symptoms
The size and location of the tumor affect the symptoms. A painless lump or swelling is a common early sign of soft tissue sarcoma. The tumor may hurt, feel sore, or make it hard to move as it grows. Bone sarcomas often present as pain, swelling, or fractures in bones that don't resolve after a minor injury. In later stages, you may feel tired and lose weight.
Causes
We don't know what causes most sarcomas. Some risk factors are genetic syndromes that run in families, previous radiation therapy, chronic lymphedema, and being around certain chemicals. Some sarcomas are associated with viral infections or genetic mutations. But many cases occur without any known risk factors.
Diagnosis
To find the tumor, doctors perform a physical exam and imaging tests such as an MRI, CT scan, or X-ray. To confirm the diagnosis and find out what kind of sarcoma it is, a biopsy is necessary. More tests look at the stage of the cancer and whether it has spread.
Treatment
The kind, size, and stage of sarcoma determine how it is treated. The most common way to treat the tumor is to remove it with surgery. Radiation therapy and chemotherapy can be administered prior to or subsequent to surgery. Some subtypes may be eligible for targeted therapy. Multidisciplinary care leads to better treatment results and faster recovery.
The prognosis for sarcoma depends on the type and stage. Tumors that are still in their early stages have a better chance of survival. Long-term outcomes have gotten better because of new surgical techniques and therapies that work together. Regular follow-up is necessary to monitor recurrence.
