Ewing sarcoma

Tumor and
tumorlike conditions of the pleura and juxtapleural region: review of imaging findings. Diagnosis: Ewing sarcoma. Technique: standard chest radiography and contrast-enhanced chest CT. Description: A 23-year-old man was referred for a chest radiograph due to pain at the right hemithorax. The postero-anterior chest radiographs (a, b) show an opacity (arrow) projecting at the level of the 7th right rib. An external radio-opaque marker was placed on the painful area. The additional contrast-enhanced CT further characterizes the mass encasing the 7th right rib with a locoregional aggressive periosteal sunburst type reaction and a surrounding soft tissue component (c, d). On the axial T1-weighted MR image (e) the lesion has an isointense signal to muscle and a high signal intensity on the axial FS T2-WI (f) with invasion of the muscles of the chest wall (arrows). After intravenous contrast administration, the lesions show a heterogeneous enhancement (g), predominantly at the periphery of the lesion. The coronal T2-weighted MR image (h) shows the extrinsic impression of the lesion on the liver
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Ewing sarcoma
of rib. Note the heterogeneous enhancement of the mass with mediastinal extension.
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Ewing sarcoma
of rib. Lytic bone destruction of right third rib (yellow arrow) with large heterogenous intrathoracic mass causing mediastinal shift to lthe eft (red arrow).
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Ewing sarcoma
of rib. Note the calcific focus (arrow) within the mass.
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Tumor and
tumorlike conditions of the pleura and juxtapleural region: review of imaging findings. Diagnosis: extraskeletal Ewing sarcoma. Technique: standard chest radiography and contrast-enhanced chest CT. Description: A 17-year-old man presented with localized right-sided chest pain. Postero-anterior and lateral chest radiographs (a, b) show a well-delineated mass located posterior in the right lung. Axial contrast-enhanced CT (c) in the mediastinal window setting shows a heterogeneous mass with intralesional necrosis and focal bony destruction of the corpus of the vertebra, pedicle, and the posterior side of the rib (arrows), best seen in the bone window (d). The young age of the patient, locoregional bone destruction, and extensive soft tissue component is suggestive of an extraskeletal Ewing sarcoma
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Ewing sarcoma
of rib. Coronal image showing a large heterogenously enhancing mass occupying almost the whole right hemithorax.
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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.

Epidemiology

Ewing sarcoma 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) .

The Ewing sarcoma family of tumors primarily occurs in white patients. In the United States, the incidence in Asians/Pacific Islanders is about one-half that in Caucasians, while the incidence among African Americans is one-ninth that in Caucasians .

Clinical presentation

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.

Pathology

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

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

Alternatively :

  • 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 :

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

Radiographic features

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.

Plain radiograph and CT

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

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 .

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

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

Treatment and prognosis

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 . The overall 5 year survival is in the order of 50-75% of patients with local disease only at the time of presentation .

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%) .

Metastases most frequently go to lungs and bones in equal proportions. The spine is the most commonly affected bone .

History and etymology

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

Differential diagnosis

  • other Ewing sarcoma family of tumors
    • pPNET: large soft tissue component with extension into bone
    • Askin tumor: chest wall
  • osteosarcoma:
    • more often has amorphous calcified matrix
    • classically perimetaphyseal, Ewing sarcoma also occurs in other locations
    • more prevalent around the knee and in the proximal humerus, in other locations Ewing sarcoma is the more frequent of the two
  • osteomyelitis
  • metastatic disease
  • hematological malignancy
  • eosinophilic granuloma 
  • neuroblastoma (<age 5) 
Siehe auch:
und weiter:
Assoziationen und Differentialdiagnosen zu Ewing-Sarkom:
sekundärer
Knochenbefall bei Lymphom
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extraskelettales
Ewingsarkom
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Knochenmetastasen
 
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