Pediatric Airway Flashcards
Causes of upper airway obstruction above trachea
choanal atresia, rhabdomyosarcoma, infectious (peritonsillar abscess)
Congenital occlusion of posterior nasal aperture(s)
choanal atresia; right side > left; bilateral cases have other anomalies; no communication between nasal cavity and nasopharynx
Types of choanal atresia
osseous, membranous, mixed; most are mixed (70%)
Choanal atresia findings
thickening of vomer, bowing of posterior maxilla/lateral nasal wall, air fluid level in nasal cavity; make sure to evaluate for associated head and neck anomalies (CHARGE)
Ddx for choanal atresia
chonal stenosis (more common than atresia), pyriform aperture stenosis, nasolacrimal duct mucosele
Chonal atresia presentation
respiratory distress in newborn if bilateral; chronic purulent unilateral rhinorrhea in older child
Associations with bilateral choanal atresia
CHARGE syndrome: coloboma (gap in iris/retina), heart defects, atresia of choanae, retardation of development, GU anomalies, and ear anomalies
Benign hamartomatous vascular lesion in adolescent males in the nasal cavity
JNA, juvenile nasopharyngeal angiofibroma
Where does JNA originate?
posterior wall of nasal cavity off midline at margin of sphenopalatine foramen –> PPF
Ddx for JNA
nasal rhabdomyosarcoma, nasopharyngeal carcinoma, antrochoanal polyp, esthesioneuroblastoma
CT imaging findings of JNA
heterogenous vs diffuse, avid enhancement; bone remodeling and destruction (posterior wall of maxillary sinus is bowed anteriorly),
MR findings of JNA
flow voids, intense enhancement, diffuse/heterogenous
Angio findings of JNA
tumor blush during preop embolization; usually the internal maxillary branch of ECA
JNA presentation
unilateral nasal obstruction with epistaxis
What is the antral sign?
anterior bowing of the posterior wall of maxillary antrum; nonspecific sign from a slowly growing mass seen in JNA; erosion of pterygoid lamina may be pathognomic for JNA
Most common childhood soft tissue sarcoma
rhabdomyosarcoma
Ddx rhabdomyosarcoma
JNA, LCH, plexiform neurofibroma, infantile hemangioma, nasopharyngeal carcinoma, lymphoma, leukemia
Pathology of rhabdomyosarcoma, tissue of origin
primitive mesenchymal cells (rhabdomyoblasts) commited to muscle differentiation
Presentation for rhabdomyosarcoma
most under 12 years old; 40% in head and neck (orbit; best prognosis, parameningeal site); increase with p53 tumor suppressor gene mutation and in Noonan syndrome or secondary to radiation therapy
Rhabdomyosarcoma CT findings
invasive soft tissue mass with variable enhancement, osseous erosion common
Best to evaluate for osseous erosion
Rhabdomyosarcoma MR findings
T1 isointense, T2 hyperintense to muscle; variable enhancement, intracranial
Best for evaluating intracranila and perineural spread; distinguish between sinonasal tumor and inflammatory disease
Pts who get epiglottitis
kids prior to H influenza immunization, immunocompromised (HIV, transplant)
Imaging findings epiglottitis
thickening of epilottis on lateral view (thumprint sign); thickening of aryepiglottic folds
Insipratory stridor and barking cough
Laryngotracheobronchitis (croup) ; exudative tracheitis can also present similarly