Ewing Sarcoma is a rare type of cancer that primarily affects children and young adults. It is a form of bone cancer that usually starts in the long bones of the body such as the arms, legs, and pelvis, but can also occur in soft tissues like the lungs, kidneys or nerves. Ewing Sarcoma develops in the cells that for…
Ewing Sarcoma is a rare type of cancer that primarily affects children and young adults. It is a form of bone cancer that usually starts in the long bones of the body such as the arms, legs, and pelvis, but can also occur in soft tissues like the lungs, kidneys or nerves. Ewing Sarcoma develops in the cells that form the bone or the soft tissues, and it is classified as a type of bone cancer because it often spreads to adjacent bone. The cause of Ewing Sarcoma is not known, but certain genetic mutations are believed to play a role in its development. Symptoms of Ewing Sarcoma include pain, swelling, and tenderness in the affected area. Other symptoms may include fatigue, fever, weight loss or anemia. Ewing Sarcoma is usually diagnosed with imaging tests like X-rays, MRI, CT scans or PET scans, which can detect tumors and areas of metastasis. Treatment often involves a combination of chemotherapy, radiation therapy, and surgery to remove the tumor. Research into Ewing Sarcoma is ongoing, with the aim of finding safer and more effective treatments for this aggressive cancer. Hematology and Oncology researchers have developed new approaches that target specific genetic mutations that drive the growth of Ewing Sarcoma. With this research, there is hope for a cure and better outcomes for those affected by Ewing Sarcoma.
2 peer-reviewed articles, ranked by relevance. Each links to its DOI.
The 2 articles above have been cited 2 times in the scholarly literature. Citation data via OpenAlex and Crossref, updated Jun 2026.
A sample of recent works citing this journal's research on Ewing Sarcoma, linking to each citing work.