Ewing family of tumors
Ewing Family of Tumors is a group of cancers that primarily affect children and young adults. These tumors are typically found in the bone or soft tissue, and include Ewing's sarcoma, peripheral primitive neuroectodermal tumor (pPNET), and Askin's tumor.
Overview[edit | edit source]
The Ewing family of tumors is a group of cancers that primarily affect children and young adults. These tumors are typically found in the bone or soft tissue. The Ewing family of tumors includes Ewing's sarcoma, peripheral primitive neuroectodermal tumor (pPNET), and Askin's tumor.
Types[edit | edit source]
There are three main types of tumors in the Ewing family:
- Ewing's sarcoma: This is the most common type of Ewing tumor. It usually starts in the bones, but can also start in other tissues and organs.
- Peripheral Primitive Neuroectodermal Tumor (pPNET): This tumor is similar to Ewing's sarcoma, but it starts in nerve tissue. It can occur anywhere in the body, but is most commonly found in the chest, abdomen, or pelvis.
- Askin's tumor: This is a rare type of Ewing tumor that starts in the chest wall.
Symptoms[edit | edit source]
The symptoms of Ewing family of tumors can vary depending on the location and size of the tumor. Common symptoms include pain, swelling, and a lump in the affected area. Other symptoms can include fever, weight loss, and fatigue.
Diagnosis[edit | edit source]
Diagnosis of Ewing family of tumors typically involves a physical examination, imaging tests such as X-ray, CT scan, or MRI, and a biopsy of the tumor.
Treatment[edit | edit source]
Treatment for Ewing family of tumors typically involves a combination of surgery, radiation therapy, and chemotherapy. The specific treatment plan will depend on the type, location, and stage of the tumor, as well as the patient's overall health.
Prognosis[edit | edit source]
The prognosis for Ewing family of tumors can vary widely depending on a number of factors, including the type and stage of the tumor, the patient's age and overall health, and how well the tumor responds to treatment.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD
