Ewing: Difference between revisions
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Latest revision as of 11:30, 17 March 2025
A type of cancerous tumor
| Ewing sarcoma | |
|---|---|
| [[File:|250px|alt=|]] | |
| Synonyms | |
| Pronounce | N/A |
| Field | Oncology |
| Symptoms | Pain, swelling, fever |
| Complications | Metastasis |
| Onset | |
| Duration | |
| Types | |
| Causes | Genetic mutation |
| Risks | |
| Diagnosis | Biopsy, imaging studies |
| Differential diagnosis | |
| Prevention | |
| Treatment | Chemotherapy, radiation therapy, surgery |
| Medication | |
| Prognosis | |
| Frequency | |
| Deaths | |
Ewing sarcoma is a rare type of cancer that occurs in bones or in the soft tissue around the bones. It primarily affects children and young adults. The tumor is named after James Ewing, the American pathologist who first described it in 1921.
Symptoms[edit]
The most common symptoms of Ewing sarcoma include:
Causes[edit]
Ewing sarcoma is caused by a genetic mutation that occurs after birth. This mutation involves a translocation between chromosomes 11 and 22, which leads to the formation of an abnormal fusion gene.
Diagnosis[edit]
Diagnosis of Ewing sarcoma typically involves:
- Biopsy: A sample of the tumor is taken and examined under a microscope.
- Imaging studies: Techniques such as X-ray, MRI, and CT scan are used to determine the size and location of the tumor.
Treatment[edit]
Treatment for Ewing sarcoma usually involves a combination of:
- Chemotherapy: The use of drugs to kill cancer cells.
- Radiation therapy: The use of high-energy rays to destroy cancer cells.
- Surgery: The removal of the tumor and some surrounding healthy tissue.
Prognosis[edit]
The prognosis for Ewing sarcoma depends on several factors, including the size and location of the tumor, whether the cancer has spread, and the patient's overall health. Early diagnosis and treatment improve the chances of a favorable outcome.
Related Pages[edit]
