Abstract
Congenital nasal pyriform aperture stenosis (CNPAS) is a rare cause of upper airway obstruction in the newborn. This affliction is due to bony overgrowth of the nasal process of the maxilla. CNPAS is diagnosed clinically and confirmed with CT scan. Patients can be managed conservatively or surgically. In this report, a male neonate had respiratory distress, cyclic cyanosis, and apnea after delivery. The patient underwent surgical correction of pyriform stenosis with a transnasal approach. During follow up, the patient showed recurred respiratory distress and cyanosis. Revision operation was necessary to reduce the bony inferior turbinate and pyriform aperture. CNPAS should be suspected in newborns with clinical signs of severe nasal obstruction associ-ated with difficulty passing a small catheter through the anterior nares.
References
1. Syed KA, Raja K, Kolethekkat AA, Varghese AM, Al Abri R, Ku-rine M. Congenital midnasal stenosis–A novel technique for management. Int J Pediatr Otorhinolaryngol. 2016; 87:117–20.
2. Douglas B. The relief of vestibular nasal obstruction by partial resection of the nasal process of the superior maxilla. Plast Reconstr Surg. 1952; 9(1):42–51.
3. Brown OE, Myer CM 3rd, Manning SC. Congenital nasal pyriform aperture stenosis. Layrngoscope. 1989; 99(1):86–91.
4. Levison J, Neas K, Wilson M, Cooper P, Wojtulewicz J. Neonatal nasal obstruction and a single maxillary central incisor. J Paediatr Child Health. 2005; 41(7):308–1.
5. Visvanathan V, Wynne DM. Congenital nasal pyriform aperture stenosis: a report of 10 cases and literature review. Int J Pediatr Otorhinolaryngology. 2012; 76(1):28–30.
6. Moreddu E, Le Treut-Gay C, Triglia JM, Nicollas R. Congenital nasal pyriform aperture stenosis: Elaboration of a management algorithm from 25 years of experience. Int J Pediatr Otorhinolaryngolo-gy. 2016; 83:7–11.
7. Moreddu E, Pereira J, Vaz R, Lena G, Triglia JM, Nicollas R. Combined endonasal and neurosurgical resection of a congenital teratoma with pharyngeal, intracranial and orbital extension: Case report, surgical technique and review of the literature. Int J Pediatr Otorhinolaryngol. 2015; 79(12):1991–4.
8. Bachelard-Serra M, Chau C, Farinetti A, Roman S, Triglia JM, Nicollas R. Prenatal diagnosis of congenital dacryocystocle, Int J Pediatr Otorhinolaryngol. 2013; 77(5):847–9.
9. Wormald R, Hinton-Bayre A, Bumbak P, Vijayasekaran S. Congenital nasal pyriform aperture stenosis 5.7 mm or less is associated with surgical intervention: A pooled case series, Int J Pediatr Otorhinolaryngology. 2015; 79(11):1802–5.
10. Belden CJ, Mancuso AA, Schmalfuss IM. CT features of congenital nasal pyriform aperture stenosis: initial experience. Radiology. 1999; 213(2):495–501.