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Surgical Treatment of Postpneumonectomy Syndrome with Tissue Expanders in Children
Hee Suk Jung1, Jee Won Suh1, Tae Hoon Kim1
1Department of Thoracic and Cardiovascular Surgery, Yonsei University College of Medicine.
Insights
Postpneumonectomy syndrome (PPS), a rare complication after lung removal, can cause respiratory failure due to mediastinal shift. Tissue expanders offer a novel treatment for PPS in patients with esophageal atresia.
Area of Science:
- Thoracic Surgery
- Pediatric Surgery
- Critical Care Medicine
Background:
- Postpneumonectomy syndrome (PPS) is a rare but serious complication following lung removal surgery.
- It is characterized by respiratory compromise due to bronchial compression from mediastinal shift, occurring more frequently in pediatric patients.
- Current treatments for PPS include aortopexy and various implantable devices.
Observation:
- This report details two pediatric cases of PPS following right pneumonectomy.
- Both patients had a history of esophageal atresia, a condition often associated with complex thoracic anomalies.
- The primary complication observed was severe mediastinal shift leading to bronchial compression and respiratory failure.
Findings:
- The study successfully utilized tissue expanders to correct PPS in both patients.
- Tissue expanders provided a method for gradual volume restoration in the hemithorax, counteracting mediastinal shift.
- This approach led to significant clinical improvement and resolution of respiratory distress.
Implications:
- Tissue expanders represent a promising and effective treatment modality for postpneumonectomy syndrome, particularly in pediatric patients with complex conditions like esophageal atresia.
- This technique may offer an alternative to existing surgical interventions, potentially improving outcomes and quality of life.
- Further research is warranted to evaluate the long-term efficacy and safety of tissue expanders in managing PPS.
Abstract:
Postpneumonectomy syndrome (PPS) is a rare late complication of pneumonectomy. It occurs more often in children than in adults, and is characterized by respiratory failure resulting from bronchial compression caused by severe mediastinal shift. Various methods have been used to treat PPS, including aortopexy and the insertion of plastic balls, silastic implants, and saline-filled breast prostheses. We describe two cases of PPS corrected with tissue expanders after right pneumonectomy in patients with esophageal atresia.
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