Pediatric Airway Flashcards

1
Q

Causes of upper airway obstruction above trachea

A

choanal atresia, rhabdomyosarcoma, infectious (peritonsillar abscess)

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2
Q

Congenital occlusion of posterior nasal aperture(s)

A

choanal atresia; right side > left; bilateral cases have other anomalies; no communication between nasal cavity and nasopharynx

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3
Q

Types of choanal atresia

A

osseous, membranous, mixed; most are mixed (70%)

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4
Q

Choanal atresia findings

A

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)

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5
Q

Ddx for choanal atresia

A

chonal stenosis (more common than atresia), pyriform aperture stenosis, nasolacrimal duct mucosele

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6
Q

Chonal atresia presentation

A

respiratory distress in newborn if bilateral; chronic purulent unilateral rhinorrhea in older child

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7
Q

Associations with bilateral choanal atresia

A

CHARGE syndrome: coloboma (gap in iris/retina), heart defects, atresia of choanae, retardation of development, GU anomalies, and ear anomalies

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8
Q

Benign hamartomatous vascular lesion in adolescent males in the nasal cavity

A

JNA, juvenile nasopharyngeal angiofibroma

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9
Q

Where does JNA originate?

A

posterior wall of nasal cavity off midline at margin of sphenopalatine foramen –> PPF

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10
Q

Ddx for JNA

A

nasal rhabdomyosarcoma, nasopharyngeal carcinoma, antrochoanal polyp, esthesioneuroblastoma

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11
Q

CT imaging findings of JNA

A

heterogenous vs diffuse, avid enhancement; bone remodeling and destruction (posterior wall of maxillary sinus is bowed anteriorly),

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12
Q

MR findings of JNA

A

flow voids, intense enhancement, diffuse/heterogenous

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13
Q

Angio findings of JNA

A

tumor blush during preop embolization; usually the internal maxillary branch of ECA

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14
Q

JNA presentation

A

unilateral nasal obstruction with epistaxis

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15
Q

What is the antral sign?

A

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

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16
Q

Most common childhood soft tissue sarcoma

A

rhabdomyosarcoma

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17
Q

Ddx rhabdomyosarcoma

A

JNA, LCH, plexiform neurofibroma, infantile hemangioma, nasopharyngeal carcinoma, lymphoma, leukemia

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18
Q

Pathology of rhabdomyosarcoma, tissue of origin

A

primitive mesenchymal cells (rhabdomyoblasts) commited to muscle differentiation

19
Q

Presentation for rhabdomyosarcoma

A

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

20
Q

Rhabdomyosarcoma CT findings

A

invasive soft tissue mass with variable enhancement, osseous erosion common

Best to evaluate for osseous erosion

21
Q

Rhabdomyosarcoma MR findings

A

T1 isointense, T2 hyperintense to muscle; variable enhancement, intracranial

Best for evaluating intracranila and perineural spread; distinguish between sinonasal tumor and inflammatory disease

22
Q

Pts who get epiglottitis

A

kids prior to H influenza immunization, immunocompromised (HIV, transplant)

23
Q

Imaging findings epiglottitis

A

thickening of epilottis on lateral view (thumprint sign); thickening of aryepiglottic folds

24
Q

Insipratory stridor and barking cough

A

Laryngotracheobronchitis (croup) ; exudative tracheitis can also present similarly

25
Steeple sign
Croup; shouldering of subglottic trachea, ballooning of hypopharynx
26
Aspirated foreign body, views
AP chest, decubitus views on obstructed side for persistent expansion/air trapping
27
Ddx prevertebral soft tissue swelling
retropharyngeal abscess/cellulitis, lymphoma, foregut duplication cyst, pseudothickening from neck flexion,
28
Exudative bacterial tracheitis presentation
fever, stridor, resiratory distress; older kids (S aureus) vs H influenza for epiglottitis
29
Imaging exudative tracheitis
filling defects/membranes in the subglottic and cervical trachea
30
Most common subglottic tracheal mass
subglottic hemangioma
31
Imaging findings subglottic hemangioma
asymmetric narrowing of subglottic trachea on frontal view
32
Laryngeal papillomatosis
HPV infection with multiple laryngeal nodules and thick/nodular vocal cords; increased risk for laryngeal SCC; can also cause multiple cavitary nodules
33
Tracheobronchomalacia
airway collapse from weak cartilage (congenital, intubation, infection, inflammation)
34
Vascular ring vs sling
ring: complete encircling of trachea and esophagus; sling: anomalous course of left pulmonary artery that traps trachea on 3 sides
35
Vascular anomaly that causes stridor
pulmonary artery sling with a normal left aortic arch or right sided aortic arch with aberrant L subclavian, double aortic arch
36
Most common vascular ring and symptoms
Double aortic arch; arches encircle both trachea and esophagus; cause stridor
37
4 artery sign
Double aortic arch
38
Second most common vascular ring
Right arch with aberrant left subclavan artery; arch indents trachea, left subclavian wraps around esophagus; ring completed by ligamentum arteriosum
39
Ddx lateral esophagram with posterior indentation
double aortic arch, aberrant left subclavian with R arch
40
Pulmonary sling
Anomalous L pulmonary artery from the right pulmoary artery; courses between trachea/esophagus; may also capture bronchus intermedius
41
Only vascular cause of strider with L arch
pulmonary artery sling
42
Associations with pulmonary artery sling
tracheal anomalies: tracheomalacia, bronchus suis or pig bronchus (RUL bronchus from trachea)
43
Dysphagia lursoria association
L aortic arch with aberrant right subclavian artery; not ring/sling. Not associated with stridor , just dysphagia; posterior indentation of esophagus
44
Innominate artery syndrome
large thymus pushes innominate artery against anterior trachea