C. Dohlemann et al., PULMONARY SLING - MORPHOLOGICAL FINDINGS - PREOPERATIVE AND POSTOPERATIVE COURSE, European journal of pediatrics, 154(1), 1995, pp. 2-14
Pulmonary sling (PS) is a congenital condition in which the left pulmo
nary artery (LPA) arises from the right pulmonary artery (RPA), formin
g a sling around the trachea causing tracheal compression. The inciden
ce is not so rare as initially thought. Symptoms of severe airway obst
ruction often begin in the newborn or young infant. Echo-colour-Dopple
r may reveal the PS but emphysema can mask the typical findings. Devia
tion of fluid-filled lungs may be detected prenatally. Chest radiograp
hs show unusual air distribution, deviation of heart and mediastinum a
nd altered tracheobronchial angles. Bronchography and bronchoscopy dem
onstrate the high incidence of associated tracheal anomalies such as c
artilagenous rings and long tracheal stenosis. Anterior oesophageal in
dentation is not always seen in the oesophogram. Magnetic resonance im
aging (MRI) and computed tomography (CT) reveal the PS, but cautious i
nterpretation is necessary because of different levels of the anomalou
s LPA. PS and associated cardiovascular malformations can be clearly d
etected by angiography. Associated extrathoracic anomalies are common.
Early diagnosis and therapy of PS is mandatory and consists of reimpl
antation of the LPA into the pulmonary trunk and division of the ligam
entum arteriosum. The postoperative course may be cumbersome necessita
ting bronchological interventions. Tracheal resection may be necessary
but restenosis is frequent. A one-stage repair has been proposed in s
uch cases and was successfully done in a few reported cases. Relief of
respiratory obstruction is often complete when there are no associate
d tracheobronchial anomalies. Late postoperative course is favourable
but respiratory obstructive attacks may occur with decreasing incidenc
e over lime and tracheal growth.