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Published on: March 12, 2020
Endobronchial inflammatory pseudotumor: a rare cause of a pneumothorax in children
Tarek El-Desoky1, Nehad Nasef, Engy Osman
1Department of Paediatrics, Mansoura University Children's Hospital, Mansoura, Dakahlia, Egypt.
Insights
This case study details an inflammatory pseudotumor in a child, a rare non-neoplastic lung condition. It highlights the first reported instance of this condition presenting as tension pneumothorax.
Area of Science:
- Pulmonology
- Pediatric Oncology
- Thoracic Surgery
Background:
- Inflammatory pseudotumors (IPTs) are rare, non-neoplastic lung lesions, typically originating in the lung parenchyma.
- Endobronchial IPTs are exceptionally uncommon, posing diagnostic challenges.
- Early diagnosis and management are crucial for favorable outcomes in pediatric lung conditions.
Observation:
- A 9-year-old girl presented with acute left-sided tension pneumothorax and subcutaneous emphysema.
- Imaging revealed an ill-defined left lung mass causing left main bronchus obstruction.
- Recurrent symptoms despite initial bronchoscopic intervention prompted further investigation.
Findings:
- Histological examination confirmed the mass as an inflammatory pseudotumor.
- The patient underwent a left upper lobectomy for definitive treatment.
- Complete symptom resolution was achieved post-surgery.
Implications:
- This case represents the first documented instance of inflammatory pseudotumor presenting with tension pneumothorax.
- Highlights the importance of considering IPTs in pediatric patients with obstructive lung masses and respiratory distress.
- Emphasizes the need for thorough histopathological evaluation for accurate diagnosis and appropriate surgical management.
Abstract:
Inflammatory pseudotumors of the lung are a group of non-neoplastic tumors, which are mainly of parenchymal origin and rarely endobronchial. We report a case of a 9-year-old girl who presented with left-sided tension pneumothorax and subcutaneous emphysema. After emergency management, chest computed tomography revealed an ill-defined left lung mass. Rigid bronchoscopy revealed a mass occluding the left main bronchus at the origin of the left upper lobe bronchus. Initially, the mass was thought to be a foreign body granuloma. Few weeks later, the child presented with recurrence of the same clinical, radiologic, and bronchoscopic outcomes. Histologic examination after the repeat bronchoscopic excision revealed the lesion to be consistent with inflammatory pseudotumor. Left upper lobectomy was performed with a complete resolution of symptoms and no recurrence was observed during the 2 years of follow-up. To the best of our knowledge, this is the first reported case of inflammatory pseudotumor presenting with tension pneumothorax.
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