The diagnosis of laryngotracheal stenosis should be suspected in child
ren with recurrent, prolonged, or atypical croup; a history of endotra
cheal intubation; or a history of strider, feeding difficulties, and f
ailure to thrive. Only half of children with congenital laryngotrachea
l stenosis require tracheotomy, and many of these children are eventua
lly decannulated without the need for surgical therapy. Ln contrast, t
racheotomy-dependent patients with acquired laryngotracheal stenosis s
hould be referred for surgical evaluation to provide them with the ear
liest opportunity to develop normal oral communication.