Choanal atresia
A choanal atresia refers to a lack of formation of the choanal openings. It can be unilateral or bilateral.
Epidemiology
It frequently presents in neonates where it is one of the commonest causes of nasal obstruction in this age group. There is a recognised female predilection. The incidence is estimated at ~ 1 : 5000 - 8000.
Clinical presentation
Depends on whether it is uni or bilateral. Unilateral choanal atresias present late and can be asymptomatic or present with rhinorrhoea while bilateral atresias can present with neonatal respiratory distress (infants are obligate nose breathers). Another finding is failure to pass a nasogastric tube.
Approximately two third of cases are unilateral 6-7.
Pathology
Structurally there are two main types
- osseous : ~ 90 % 2
- membraneous : ~ 10 %
Associations
Syndromic associations include
- CHARGE syndrome
- Crouzon syndrome
- DiGeorge syndrome
- amniotic band syndrome
- foetal alcohol syndrome
- Treacher Collins syndrome
Other associations include
Radiographic features
CT
Axial CT scans are best as assessment
- may a show a uni or bilateral posterior nasal narrowing with an obstruction
- airway less than 0.3 cm
- an air fluid level may be present above the obstruction point
- may show thickening of the vomer
- medial bowing of posterior maxillary sinus
Treatment
Options include
- endoscopic perforation (for membranous types)
- full choanal reconstruction
Differential diagnosis
On an axial CT consider

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