EWING SARCOMA
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ALTERNATE NAMES
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Ewing Tumor; Ewing Sarcoma of Bone, Ewing Sarcoma of Soft Tissue; Primitive Neuroectodermal
Tumor; Askin Tumor; Askin's Tumor; Diffuse Bone Endothelioma; Endothelial Myeloma;
Bone Endothelioma; Endothelial Sarcoma of Bone; Extraosseous Ewing Sarcoma; Extraskeletal
Ewing Sarcoma
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DESCRIPTION
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Ewing Sarcoma is a malignant, vascular, solid, round-cell tumor in which cancer cells are found
in the bone or in soft tissue. The most common areas in which it occurs are the pelvis,
the femur, the humerus, and the ribs. It is an aggressive cancer and multimodal (therapy
that combines more than one method of treatment) therapy is virtually always required.
Ewing Sarcoma is part of a group of four different types of cancer, known collectively
as the Ewing Family of Tumors (EFT):
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Ewing Sarcoma of Bone, which accounts for about 85% of all cases, is usually found
in the long bones in the arm or leg, although it sometimes occurs in the pelvis or
ribcage;
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Extraosseous Ewing Sarcomas are tumors that occur in soft tissue;
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Primitive Neuroectodermal Tumor , also known as peripheral neuroepithelioma, can occur
in bone and/or soft tissue; and
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Askin tumor, a Primitive Neuroectodermal Tumor that occurs in the marrow cavities
of the chest wall.
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DIAGNOSTIC TESTING, PHYSICAL FINDINGS, AND
ICD-9-CM/ICD-10-CM
CODING
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Diagnostic testing: Diagnostic testing for Ewing Sarcoma includes:
The definitive diagnosis is based on histologic findings, immunohistochemistry, and
cytogenetic and molecular studies.
Physical findings: Physical findings for individuals with Ewing Sarcoma may include:
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Swelling and warmth at site of the tumor;
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Visible blood vessels on skin over the tumor.
ICD-9: 170.9
ICD-10: C41.9
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PROGRESSION
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Onset for Ewing Sarcoma can occur any time during childhood, with peak incidence in
the teen years. The prognosis depends on the location of the tumor and whether or
not the cancer has spread. Approximately 30% are metastatic at presentation. Diagnostic
staging procedures attempt to distinguish individuals with localized disease from
those with metastatic disease. Most commonly, metastases occur in the chest, bone,
and/or bone marrow. Less common sites of metastes include the central nervous system
and lymph nodes.
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TREATMENT
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All types of the EFTs are treated similarly based on clinical presentation of local
versus metastatic disease. The main treatments for Ewing Sarcoma are chemotherapy,
surgery, and radiation, almost always used in combination.
In the past, surgery on tumors in the arm or leg bones usually required amputation.
However, new techniques such as limb-sparing surgery, bone grafts, and artificial
bones, can help certain patients avoid losing an arm or leg and maintain some degree
of function.
Side effects associated with radiation treatment may include skin damage, muscle scarring
and loss of joint flexibility, damage to nearby organs, loss of bone growth in growing
children, secondary cancers caused by radiation, chronic swelling of an extremity,
and slow wound healing.
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SUGGESTED PROGRAMMATIC ASSESSMENT*
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Suggested MER for Evaluation:
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Report that specifies the type, extent, and site of the primary, recurrent, or metastatic
lesion;
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Biopsy or needle aspiration information found in operative notes, pathology reports,
summaries of hospitalization or other medical reports that include details of the
surgical and pathological findings;
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Clinical history and examination that describes the diagnostic features of the impairment;
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Treatment records including surgical procedures, and up-to-date progress notes.
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Suggested Listings for Evaluation:
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DETERMINATION
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LISTING
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REMARKS
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Meets
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13.04
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Extraosseous Ewing Sarcoma and other Ewing Sarcoma tumors that occur outside of the
bone in adults should be evaluated under listing 13.04.
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13.11
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Ewing Sarcoma of Bone in adults treated with multimodal therapy meets 13.11 D without
regard to effectiveness of treatment.
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113.03
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Pediatric Ewing Sarcoma meets 113.03. |
Equals
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* Adjudicators may, at their discretion, use the Medical Evidence of Record or the
listings suggested to evaluate the claim. However, the decision to allow or deny the
claim rests with the adjudicator.
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