Discussion
Diagnosis With Brief Discussion
- Diagnosis
- Extraskeletal ewing sarcoma
- Radiologic Findings
- Fig 1. Chest PA shows large amount of left pleural effusion.
Fig 2-5. CT scans reveal multiple pleural-based heterogeneous enhancing masses in the left hemithorax. The largest one of the masses is measured about 9.8 x 7.5 x 9.0 cm. There is no evidence of invasion of the adjacent chest wall or rib. Left pleural effusion with passive atelectasis of the left lower lobe is noted.
Fig 6. No metastatic nodules are noted in both lungs.
- Brief Review
- A percutaneous biopsy was performed under ultrasonographic guidance. The histology of the specimen showed diffuse proliferation of small round cells. Immunohistochemically, the tumor cells were diffusely positive for CD99+.
Thoracopulmonary extraskeletal Ewing sarcoma (EES) is a rare disease in the pediatric group, even rarer in adults, and is predominantly seen in White patients. It typically manifests as a painful chest wall mass with symptoms of cough, respiratory distress, weight loss, anorexia, Horner syndrome, or regional lymphadenopathy.
Radiologically, thoracopulmonary EES often manifests as an aggressive unilateral pleural-based mass. Direct invasion of the chest wall musculature or ribs, mediastinum, or lung is common. Pleural effusions are often large, with loculated fluid sometimes forming a pseudotumor. Ipsilateral mediastinal or hilar adenopathy manifests in about 25% of thoracopulmonary EES cases. As with other sites of EES, calcifications are infrequent and are seen in approximately 10% of cases. MRI may be particularly useful for helping determine the presence and extent of chest wall muscle invasion
- References
- 1. RadioGraphics 2022; 42:1145
- Keywords
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