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Ewing Sarcoma, Pediatric

Steven G. DuBois, MD, MS Reviewed 10/2018
 


BASICS

DESCRIPTION

  • Family of cancers with common biology and treatment:

    • Ewing sarcoma of bone

    • Extraskeletal Ewing sarcoma (arises in soft tissue adjacent to bone)

    • Peripheral neuroectodermal tumor (PNET) o...

DIAGNOSIS

HISTORY

  • Pain is most common symptom.

  • Pain is often attributed to minor injuries that are common in this age group.

  • Other presenting symptoms are as follows:

    • Palpable mass

    • Fever

    • Limp

  • Systemic sympto...

TREATMENT

GENERAL MEASURES

  • In addition to systemic treatment with chemotherapy, patients need local control treatment to the site of the primary tumor and metastases (if present) with surgery, radiatio...

ONGOING CARE

PROGNOSIS

  • 5-year overall survival rate for all patients is ~60%.

  • Presence of metastases is the most important prognostic factor.

    • Estimated overall survival in those with metastatic disease a...

ADDITIONAL READING

  • Grier HE, Krailo MD, Tarbell NJ, et al. Addition of ifosfamide and etoposide to standard chemotherapy for Ewing’s sarcoma and primitive neuroectodermal tumor of bone. N Engl J Med. ...

CODES

ICD9

  • 170.9 Malignant neoplasm of bone and articular cartilage, site unspecified

  • 170.6 Malignant neoplasm of pelvic bones, sacrum, and coccyx

  • 170.7 Malignant neoplasm of long bones of lower limb

  • 195....

FAQ

  • Q: At what time point is a child with Ewing sarcoma considered cured?

  • A: Most cases of recurrence in Ewing sarcoma occur within 2 years of initial diagnosis. However, late relapses beyond 5 years f...

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