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Recurrent croup in a young child: look beyond airways disease
Saurav Jain1, Taruna Yadav2, Prawin Kumar3
1Pediatrics, All India Institute of Medical Sciences, Jodhpur, India.
Insights
A rare case of unilateral absent pulmonary artery (PA) in a child presenting with recurrent croup was identified. This condition, causing lung hypoplasia, requires clinical suspicion in pediatric patients with similar symptoms.
Area of Science:
- Pediatric Pulmonology
- Cardiovascular Imaging
- Congenital Thoracic Abnormalities
Background:
- Recurrent croup in infancy can indicate underlying structural abnormalities.
- Unilateral lung hypoplasia may be associated with vascular anomalies.
Purpose of the Study:
- To report a rare case of unilateral absent pulmonary artery (PA) in a pediatric patient.
- To highlight the diagnostic approach and conservative management of this condition.
Main Methods:
- Clinical examination, chest radiography, flexible bronchoscopy, CT angiography, and echocardiography were utilized.
- Diagnostic imaging focused on evaluating lung development and pulmonary vasculature.
Main Results:
- A 5-year-old boy presented with recurrent croup, reduced breath sounds on the right, and mediastinal shift.
- Imaging revealed a hypoplastic right lung, absent right pulmonary artery, and dilated left pulmonary artery.
- Bronchoscopy showed tracheomalacia and left bronchomalacia due to external compression.
Conclusions:
- Unilateral absent pulmonary artery is a rare congenital anomaly.
- It should be suspected in children with unilateral hypoplastic lung and respiratory symptoms.
- Conservative management is appropriate in asymptomatic children without pulmonary arterial hypertension.
Abstract:
We reported here a boy aged 5 years who presented for the evaluation of recurrent croup since infancy. On chest examination, breath sounds were reduced throughout the right lung field with a shifting of the trachea and cardiac apex to the right side. The chest radiograph showed a small right lung with decreased vascularity, hyperinflated left lung and mediastinum shifted towards the right side. Flexible bronchoscopy revealed tracheomalacia with left bronchomalacia due to external pulsatile compression. In CT angiogram, the right pulmonary artery (PA) was absent with dilated left PA. Echocardiography did not show any features of pulmonary arterial hypertension (PAH). Since the child was growing well, and there was no limitation of activity and evidence of PAH, he was managed conservatively and kept on follow-up. Though unilateral absent PA is a rare condition, it should be suspected in children with unilateral hypoplastic lung.
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