Ewing sarcoma

Ewing sarcomas are the second most common malignant primary bone tumors of childhood after osteosarcoma, typically arising from medullary cavity with invasion of the Haversian system. They usually present as moth-eaten destructive permeative lucent lesions in the shaft of long bones with large soft tissue component without osteoid matrix and typical onion skin periostitis. It may also involve flat bones and appears sclerotic in up to 30% of cases.

Typically occurs in children and adolescents between 10 and 20 years of age (95% between 4 and 25 years of age), and has a slight male predilection (M:F 1.5:1) 1,2.

Presentation is non-specific with local pain being by far the most common symptom. Occasionally a soft tissue mass may be palpable. Pathological fractures also occur. Systemic symptoms including fever may be present. ESR is also elevated.

Ewing sarcoma is a small round blue cell tumor with regular sized primitive appearing cells. It is closely related to the soft tissue tumors pPNETAskin tumor and neuroepithelioma, which collectively are referred to as Ewing sarcoma family of tumors (ESFT) 1. They share not only microscopic appearances but also demonstrate a non-random t(11;22)(q24;q12) chromosome rearrangement. 

  • lower limb: 45%
    • femur most common
  • pelvis: 20%
  • upper limb: 13%
  • spine and ribs: 13% (see thoracic Ewings sarcoma)
    • sacrococcygeal region most common 4
  • skull/face: 2%

Alternatively 3:

  • long bones: 50-60%
    • femur: 25%
    • tibia: 11%
    • humerus: 10%
  • flat bones: 40%

As far as location within long bones, the tumor is almost always metadiaphyseal or diaphyseal 2-3:

  • mid-diaphysis: 33%
  • metadiaphysis: 44%
  • metaphysis: 15%
  • epiphysis: 1-2%

Ewing sarcomas tend to be large with poorly marginated tumors, with over 80% demonstrating extension into adjacent soft tissues. It should be noted that pPNET often extend into bone, making the distinction difficult.

The appearance of these tumors is very variable, but they usually have clearly aggressive appearance. Common findings include 2:

They occasionally demonstrate other appearances, including Codman triangles, spiculated (sunburst) or thick periosteal reaction and even bone expansion or cystic components.

Soft tissue calcification is uncommon, seen in less than 10% of cases 2.

  • T1: low to intermediate signal
  • T1 C+ (Gd): heterogeneous but prominent enhancement
  • T2: heterogeneously high signal, may see hair on end low signal striations

Ewing sarcomas demonstrate increased uptake on both Gallium67-citrate and all three phases of the Technetium99m methylene diphosphonate bone scans 6.

Systemic chemotherapy is the mainstay of treatment with surgery and/or radiotherapy playing a role depending on the location and size of the tumor.

What was once a uniformly fatal tumor now has respectable survival rates, although these vary with location. Spinal tumors for example have up to 86% long term survival compared to 25% of sacrococcygeal tumors 4. The overall 5 year survival is in the order of 50-75% of patients with local disease only at the time of presentation 5.

Prognosis is significantly impacted by the presence of distant metastases at the time of diagnosis, which is far more common for the pelvis (25-30%) compared to extremities (<10%) 5. Metastases most frequently go to bone or lungs.

It is named after James Stephen Ewing (1866-1943), an American pathologist, who first described his eponymous tumor in 1920 8,11.

Bone tumours

The differential diagnosis for bone tumors is dependent on the age of the patient, with a very different set of differentials for the pediatric patient.

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Article information

rID: 7852
Tag: sarcoma
Synonyms or Alternate Spellings:
  • Ewing sarcomas
  • Ewing's sarcoma

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Cases and figures

  • Distribution of E...
    Figure 1: distribution
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  • Case 1
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  • Case 2: femur : T1
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  • Case 3: acetabulum : T2
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  • Case 4: with onion skin appearence
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  • Case 5: pelvis: T1 FS gad
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  • Coronal femora
    Case 6: polyostotic
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  • Ewing/PNET
    Case 7
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  • EWING SARCOMA
    Case 8
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  • Case 9
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  • Case 10
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  • Case 12
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  • Case 11
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  • Case 14: involving the C1 lateral mass
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  • Case 13
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  • Case 15
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  •  Case 16
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  •  Case 17
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  • Case 18: spine
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  • STIR axl
    Case 19: extra-osseous
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  • Case 20: PET-CT
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  • Case 21: scapula
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  • Case 22: scapula
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