Ewing family of tumors

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Ewing Family of Tumors

The Ewing Family of Tumors (pronounced: YOO-ing) is a group of cancers that primarily affect children and young adults. These tumors are named after the pathologist James Ewing, who first described the disease in 1921.

Etymology

The term "Ewing" is derived from the name of the pathologist James Ewing, who first identified the disease. The term "family of tumors" refers to the fact that these tumors are related in terms of their origin and behavior.

Definition

The Ewing Family of Tumors is a group of cancers that primarily affect the bone or soft tissue. These tumors are rare and are most commonly found in children and young adults. The most common types of Ewing Family of Tumors include Ewing's Sarcoma of bone and Peripheral Primitive Neuroectodermal Tumor (PNET).

Symptoms

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 may include fever, fatigue, and weight loss.

Diagnosis

Diagnosis of Ewing Family of Tumors typically involves a combination of physical examination, imaging tests such as MRI or CT scan, and biopsy. The diagnosis is confirmed by a pathologist who examines the biopsy under a microscope.

Treatment

Treatment for Ewing Family of Tumors typically involves a combination of surgery, radiation therapy, and chemotherapy. The specific treatment plan will depend on the size, location, and stage of the tumor, as well as the patient's overall health.

Prognosis

The prognosis for Ewing Family of Tumors can vary depending on a number of factors, including the size and location of the tumor, the patient's age and overall health, and how well the tumor responds to treatment.

See Also

External links

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