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Spontaneous tracheal rupture: a case report
Loren R Gorosh1, Oscar Ingaramo2, David Nelson3
1Department of Emergency Medicine, University of Nevada Residency in Emergency Medicine, Las Vegas, Nevada.
Insights
Spontaneous tracheal rupture in children is rare and can mimic other conditions. Prompt diagnosis and surgical repair led to a full recovery in a 3-year-old boy with this life-threatening airway disruption.
Area of Science:
- Pediatric emergency medicine
- Thoracic surgery
- Diagnostic imaging
Background:
- Upper-airway disruption is a rare but serious condition.
- Pediatric cases of spontaneous tracheal rupture are exceptionally uncommon.
- Such events can arise spontaneously, from trauma, or iatrogenically.
Observation:
- A 3-year-old boy presented with respiratory distress, initially suspected as anaphylaxis.
- Despite interventions, the patient deteriorated, requiring intubation and chest tube placement.
- Computed tomography revealed a posterior tracheal defect, missed on initial bronchoscopy.
Findings:
- Spontaneous tracheal rupture in children can present with misleading symptoms.
- Early diagnosis is challenging due to non-specific initial presentations.
- Computed tomography is crucial for identifying tracheal defects.
Implications:
- Prompt diagnosis and management are vital for pediatric tracheal rupture.
- Surgical repair can be successful in treating tracheal defects.
- This case highlights the importance of advanced imaging in pediatric airway emergencies.
Background:
Upper-airway disruption is a rare but potentially life-threatening phenomenon. It can occur spontaneously, be due to trauma, or be iatrogenically induced. Even more rare are such events reported in the pediatric population.
Objective:
This article discusses the presentation, diagnostic difficulties, and management of spontaneous tracheal rupture in a child.
Case Report:
A 3-year-old boy was brought by emergency medical services to our emergency department with a presumptive diagnosis of anaphylaxis. With progressive swelling and respiratory distress, the patient quickly deteriorated. He received i.v. epinephrine, chest compressions, and bag-valve mask ventilation. He was intubated without difficulty and with no noted airway edema. Concomitant bilateral needle thoracostomies were performed and subsequent bilateral tube thoracostomies were placed. Immediately after intubation and chest tube placements, the patient's oxygen saturations and heart rate improved. Bronchoscopy failed to demonstrate any evident pathology. However, computed tomography scan revealed a defect in the posterior wall of the trachea proximal to the termination of the endotracheal tube. Cardiothoracic surgery was consulted and performed a primary repair of the tracheal defect. The patient was extubated soon after surgery, and he was discharged home neurologically intact.
Conclusions:
The initial presentation of spontaneous tracheal rupture can be misleading and difficult to diagnose. After resuscitation, stabilization, and diagnosis, both surgical repair and nonoperative management have been reported as successful treatment measures for tracheal disruption.
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