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Published on: December 9, 2016
Primary Ewing sarcoma/primitive neuroectodermal tumor of the lung.
Devika Gupta1, Tathagata Chatterjee1, Rohit Tewari1
1Army Hospital, Department of Laboratory Science & Molecular Medicine, New Delhi, India.
This case report details a rare instance of primary Ewing sarcoma of the lung in a 42-year-old male. Autopsy revealed the tumor had replaced the right lung, a diagnosis made post-mortem due to rapid disease progression.
Area of Science:
- Oncology
- Pulmonology
- Pathology
Background:
- Ewing sarcoma is a rare bone and soft tissue cancer.
- Primary lung Ewing sarcoma is exceptionally rare, often presenting with aggressive symptoms.
Observation:
- A 42-year-old male presented with acute respiratory distress, fever, and chest pain.
- Imaging revealed a large unilateral lung mass causing tracheal deviation and superior vena cava obstruction.
- Despite two biopsy attempts suggesting malignancy, the patient experienced rapid deterioration.
Findings:
- Autopsy demonstrated complete replacement of the right lung by a necrotic tumor.
- Histopathology confirmed primary Ewing sarcoma of the lung.
- Other visceral organs were grossly unremarkable.
Implications:
- Highlights the importance of considering rare diagnoses in aggressive respiratory conditions.
- Underscores the diagnostic challenges and poor prognosis of primary lung Ewing sarcoma.
- Emphasizes the role of autopsy in diagnosing rare and rapidly fatal conditions.
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