Primary mediastinal small round cell tumor suggestive of Ewing’s sarcoma associated with pneumothorax: a case report
Peter O. Adeoye1,2,Hassan I. Abubakar2,Akolo A. Dominic3,Robert Udo2
Current Thoracic Surgery
2026;11(2):214-219.
1Department of Surgery, Division of Thoracic and Cardiovascular Surgery, University of Ilorin and University of Ilorin Teaching Hospital, Kwara, Nigeria
2Department of Surgery, Division of Cardiothoracic Surgery, Federal Medical Centre Keffi, Nasarawa, Nigeria
3Department of Anatomic Pathology and Forensic Medicine, Federal Medical Centre Keffi, Nasarawa, Nigeria
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Ewing’s sarcoma (ES) is a rare form of malignancy that commonly affects the bone. Extraskeletal ES (EES) accounts for 20% of ES cases. The mediastinum is an exceedingly rare primary site of EES and presents with non-specific symptoms that may mimic several other thoracic pathologies. We describe a suspected case of primary mediastinal ES presenting with pneumothorax in a 17-year-old female who presented with chronic cough, dyspnea, and chest pain. The patient had been commenced on empirical treatment for tuberculosis (a common diagnosis in our sub-region) for six weeks before presentation to our facility, due to a lack of improvement in symptoms. Chest computed tomography scan revealed a huge anterior mediastinal mass extending into the left hemithorax with pneumothorax on the right. She underwent a transthoracic percutaneous biopsy, and histological analysis revealed a monomorphic small-round-cell morphology, suggestive of primary mediastinal Ewing’s sarcoma.
Keywords :
mediastinal neoplasms, Ewing’s sarcoma, pneumothorax, neuroectodermal tumors, extraskeletal