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European Journal of Cardio-Thoracic Surgery, Vol 4, 351-353, Copyright © 1990 by European Association for Cardio-thoracic Surgery
P Horvath, R Dinwiddie and J Stark
Two patients (aged 10 and 16 months) underwent right pneumonectomy: one for
an oesophageal bronchus, the other for a hypoplastic right lung with
sequestration. Both patients subsequently developed severe stridor. The
heart rotated to the right and the aortic arch compressed the trachea. This
unusual vascular compression was treated by a bypass graft between the
ascending and descending aorta and division of the aortic arch between the
left carotid and left subclavian artery at the age of 5 years and 4 months,
and 20 months respectively. The postoperative recovery was uneventful in
the first patient. The second patient required 7 weeks of ventilatory
support. Both patients are well (14 and 7 years after surgery). Cardiac
catheterisation and angiography in the first patient and Doppler
echocardiography in the second demonstrated unrestricted flow through the
graft into the descending aorta. Pulmonary function studies showed a
restrictive defect with some obstruction in both children. Despite this
finding, both patients enjoy a normal life with some sporting activities.
The long-term results suggest the effectiveness of this procedure in the
treatment of this rare but severe complication of pneumonectomy in infancy.
ARTICLES
Successful surgical treatment of tracheal compression following right pneumonectomy in infancy. Long-term follow-up
Thoracic Unit, Hospital for Sick Children, London, UK.
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