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[Ewing sarcoma located in the mandible: A case report].

M Hernandez1, D Droz1, L Mansuy2

  • 1Département d'odontologie pédiatrique, CHU de Nancy, 2, rue du Docteur-Heydenreich, 54000 Nancy, France.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|April 22, 2015
PubMed
Summary

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Ewing sarcoma, a rare pediatric bone cancer, can present unusually without pain. This case highlights mandibular swelling as a key symptom in a child, emphasizing the need for vigilance in diagnosis.

Area of Science:

  • Pediatric Oncology
  • Skeletal Radiology
  • Maxillofacial Pathology

Background:

  • Ewing sarcoma is the second most frequent primary malignant bone tumor in pediatric populations.
  • Typical symptoms include localized pain and a palpable mass, often prompting initial radiographic evaluation.
  • Radiographic findings may show poorly defined osteolytic lesions with periosteal reactions, but these are not definitive.

Observation:

  • This report details a 7-year-old boy with mandibular Ewing sarcoma.
  • The child presented with progressive mandibular swelling but notably lacked pain.
  • The unusual presentation and location highlight potential diagnostic challenges.

Findings:

  • The case underscores that Ewing sarcoma can manifest without the hallmark symptom of pain.

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  • An unusual localization, such as the mandible, can complicate early recognition.
  • Diagnostic delays may occur if typical symptoms are absent.
  • Implications:

    • This case emphasizes the importance of considering Ewing sarcoma in pediatric patients with unexplained swelling, even in the absence of pain.
    • Radiologists and clinicians should be aware of atypical presentations of Ewing sarcoma in unusual locations like the mandible.
    • Prompt biopsy remains crucial for definitive diagnosis when suspicion is raised, regardless of initial imaging findings.