Otolaryngology: Head and Neck Surgery, C70 P586-620 Flashcards

(344 cards)

1
Q

Define:
Anosmia
P586

A

Inability to smell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Define:
Otorrhea
P586

A

Fluid discharge from ear

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Define:
Dysphagia
P586

A

Difficulty swallowing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Define:
Odynophagia
P586

A

Painful swallowing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Define:
Globus
P586

A

Sensation of a “lump in the throat”

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Define:
Otalgia
P586

A

Ear pain (often referred from throat)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Define:
Trismus
P586

A

Difficulty opening mouth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

ANATOMY
Define the cranial nerves:
I
P586

A

Olfactory nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

ANATOMY
Define the cranial nerves:
II
P586

A

Optic nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

ANATOMY
Define the cranial nerves:
III
P586

A

Oculomotor nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

ANATOMY
Define the cranial nerves:
IV
P586

A

Trochlear nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

ANATOMY
Define the cranial nerves:
V
P586

A

Trigeminal nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

ANATOMY
Define the cranial nerves:
VI
P586

A

Abducens nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

ANATOMY
Define the cranial nerves:
VII
P586

A

Facial nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

ANATOMY
Define the cranial nerves:
VIII
P586

A

Vestibulocochlear nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

ANATOMY
Define the cranial nerves:
IX
P586

A

Glossopharyngeal nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

ANATOMY
Define the cranial nerves:
X
P586

A

Vagus nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

ANATOMY
Define the cranial nerves:
XI
P587

A

Accessory nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

ANATOMY
Define the cranial nerves:
XII
P587

A

Hypoglossal nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q
ANATOMY
Define motor/sensory
actions of the following
cranial nerves:
I
P567
A

Smell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q
ANATOMY
Define motor/sensory
actions of the following
cranial nerves:
II
P567
A

Sight (sensory pupil reaction)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q
ANATOMY
Define motor/sensory
actions of the following
cranial nerves:
III
P567
A
Eyeball movement, pupil sphincter,
ciliary muscle (motor pupil reaction)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q
ANATOMY
Define motor/sensory
actions of the following
cranial nerves:
IV
P567
A

Superior oblique muscle movement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q
ANATOMY
Define motor/sensory
actions of the following
cranial nerves:
V
P567
A

Motor: chewing (masseter muscle)
Sensory: face, teeth, sinuses, cornea

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
``` ANATOMY Define motor/sensory actions of the following cranial nerves: VI P567 ```
Lateral rectus muscle (lateral gaze)
26
``` ANATOMY Define motor/sensory actions of the following cranial nerves: VII P567 ```
Motor: facial muscles, lacrimal/ sublingual/submandibular glands Sensory: anterior tongue/soft palate, taste
27
``` ANATOMY Define motor/sensory actions of the following cranial nerves: VIII P567 ```
Hearing, positioning
28
``` ANATOMY Define motor/sensory actions of the following cranial nerves: IX P567 ```
Motor: stylopharyngeus, parotid, pharynx Sensory: posterior tongue, pharynx, middle ear
29
``` ANATOMY Define motor/sensory actions of the following cranial nerves: X P567 ```
Motor: vocal cords, heart, bronchus, GI tract Sensory: bronchus, heart, GI tract, larynx, ear
30
``` ANATOMY Define motor/sensory actions of the following cranial nerves: XI P567 ```
Motor: trapezius muscle, | sternocleidomastoid muscle
31
``` ANATOMY Define motor/sensory actions of the following cranial nerves: XI P567 ```
Motor: tongue, strap muscles (ansa | cervicalis branch)
32
``` ANATOMY What are the three divisions of the trigeminal nerve (cranial nerve V)? P587 ```
1. Ophthalmic 2. Maxillary 3. Mandibular
33
``` ANATOMY What happens when the hypoglossal nerve (cranial nerve XII) is cut? P588 ```
When the patient sticks out the tongue, it deviates to the same side as the injury (wheelbarrow effect)
34
ANATOMY Name the duct of the submandibular gland. P588
Wharton’s duct
35
ANATOMY Name the duct of the parotid gland. P588
Stensen’s duct
36
ANATOMY What is the source of blood supply to the nose? P588
``` 1. Internal carotid artery: anterior and posterior ethmoidal arteries via ophthalmic artery 2. External carotid artery: superior labial artery (via facial artery) and sphenopalatine artery (via internal maxillary artery) ```
37
``` ANATOMY Name the three bones that make up the posterior nasal septum. P588 ```
1. Ethmoid (perpendicular plate) 2. Vomer (Latin for “plow”) 3. Palatine (some also include maxillary crest)
38
ANATOMY Name the seven bones of the bony eyeball orbit. P588
1. Frontal 2. Zygoma 3. Maxillary 4. Lacrimal 5. Ethmoid 6. Palatine 7. Sphenoid
39
ANATOMY Name the four strap muscles. P588
“TOSS”: 1. Thyrohyoid 2. Omohyoid 3. Sternothyroid 4. Sternohyoid
40
``` ANATOMY Which muscle crosses the external and internal carotid arteries? P588 ```
Digastric muscle
41
ANATOMY In a neck incision, what is the first muscle incised? P588
Platysma
42
ANATOMY Which nerve supplies the strap muscles? P588
Ansa cervicalis (XII)
43
ANATOMY What are the anterior and posterior neck triangles? P589 (picture)
Two regions of the neck, divided by the | sternocleidomastoid muscle
44
ANATOMY Which nerve runs with the carotid in the carotid sheath? P589
Vagus
45
``` ANATOMY Which nerve crosses the internal carotid artery at approximately 1 to 2 cm above the bifurcation? P589 ```
Hypoglossal nerve
46
ANATOMY Name the three auditory ossicle bones. P589
1. Malleus (hammer) 2. Incus (anvil) 3. Stapes (stirrup)
47
ANATOMY What comprises the middle ear? P589
Eustachian tube, ossicle bones, tympanic | membrane (“ear drum”), mastoid air cell
48
ANATOMY What comprises the inner ear? P589
Cochlea, semicircular canals, internal | auditory canal
49
EAR OTITIS EXTERNA (SWIMMER’S EAR) What is it? P589
Generalized infection involving the external ear canal and often the tympanic membrane
50
EAR OTITIS EXTERNA (SWIMMER’S EAR) What is the usual cause? P590
Prolonged water exposure and damaged squamous epithelium of the ear canal (e.g., swimming, hearing aid use)
51
``` EAR OTITIS EXTERNA (SWIMMER’S EAR) What are the typical pathogens? P590 ```
``` Most frequently Pseudomonas, may be Proteus, Staphylococcus, occasionally Escherichia coli, fungi (Aspergillus, Candida), or virus (herpes zoster or herpes simplex) ```
52
``` EAR OTITIS EXTERNA (SWIMMER’S EAR) What are the signs/ symptoms? P590 ```
Ear pain (otalgia); swelling of external ear, ear canal, or both; erythema; pain on manipulation of the auricle; debris in canal; otorrhea
53
EAR OTITIS EXTERNA (SWIMMER’S EAR) What is the treatment? P590
Keep the ear dry; mild infections respond to cleaning and dilute acetic acid drops; most infections require complete removal of all debris and topical antibiotics with or without hydrocortisone (anti-inflammatory)
54
EAR MALIGNANT OTITIS EXTERNA (MOE) What is it? P590
Fulminant bacterial otitis externa
55
EAR MALIGNANT OTITIS EXTERNA (MOE) Who is affected? P590
Most common scenario: elderly patient with poorly controlled diabetes (other forms of immunosuppression do not appear to predispose patients to MOE)
56
``` EAR MALIGNANT OTITIS EXTERNA (MOE) What are the causative organisms? P590 ```
Usually Pseudomonas aeruginosa
57
EAR MALIGNANT OTITIS EXTERNA (MOE) What is the classic feature? P590
Nub of granulation tissue on the floor of the external ear canal at the bony–cartilaginous junction
58
``` EAR MALIGNANT OTITIS EXTERNA (MOE) What are the other signs/ symptoms? P590 ```
Severe ear pain, excessive purulent | discharge, and usually exposed bone
59
``` EAR MALIGNANT OTITIS EXTERNA (MOE) What are the diagnostic tests? P591 ```
``` 1. CT scan: shows erosion of bone, inflammation 2. Technetium-99 scan: temporal bone inflammatory process 3. Gallium-tagged white blood cell scan: to follow and document resolution ```
60
EAR MALIGNANT OTITIS EXTERNA (MOE) What are the complications? P591
Invasion of surrounding structures to produce a cellulitis, osteomyelitis of temporal bone, mastoiditis; later, a facial nerve palsy, meningitis, or brain abscess
61
EAR MALIGNANT OTITIS EXTERNA (MOE) What is the treatment? P591
``` Control of diabetes, meticulous local care with extensive debridement, hospitalization and IV antibiotics (anti- Pseudomonas: usually an aminoglycoside plus a penicillin) ```
62
``` EAR TUMORS OF THE EXTERNAL EAR What are the most common types? P591 ```
Squamous cell most common; occasionally, | basal cell carcinoma or melanoma
63
``` EAR TUMORS OF THE EXTERNAL EAR From what location do they usually arise? P591 ```
Auricle, but occasionally from the | external canal
64
``` EAR TUMORS OF THE EXTERNAL EAR What is the associated risk factor? P591 ```
Excessive sun exposure
65
``` EAR TUMORS OF THE EXTERNAL EAR What is the treatment of the following conditions: Cancers of the auricle? P591 ```
Usually wedge excision
66
``` EAR TUMORS OF THE EXTERNAL EAR What is the treatment of the following conditions: Extension to the canal? P591 ```
May require excision of the external ear | canal or partial temporal bone excision
67
``` EAR TUMORS OF THE EXTERNAL EAR What is the treatment of the following conditions: Middle ear involvement? P591 ```
Best treated by en bloc temporal bone | resection and lymph node dissection
68
EAR TYMPANIC MEMBRANE (TM) PERFORATION What is the etiology? P591
``` Usually the result of trauma (direct or indirect) or secondary to middle ear infection; often occurs secondary to slap to the side of the head (compression injury), explosions ```
69
EAR TYMPANIC MEMBRANE (TM) PERFORATION What are the symptoms? P592
Pain, bleeding from the ear, conductive | hearing loss, tinnitus
70
EAR TYMPANIC MEMBRANE (TM) PERFORATION What are the signs? P592
Clot in the meatus, visible tear in the TM
71
EAR TYMPANIC MEMBRANE (TM) PERFORATION What is the treatment? P592
Keep dry; use systemic antibiotics if there | is evidence of infection or contamination
72
EAR TYMPANIC MEMBRANE (TM) PERFORATION What is the prognosis? P592
Most (90%) heal spontaneously, though larger perforations may require surgery (e.g., fat plug, temporalis fascia tympanoplasty)
73
EAR CHOLESTEATOMA What is it? P592
Epidermal inclusion cyst of the middle ear or mastoid, containing desquamated keratin debris; may be acquired or congenital
74
EAR CHOLESTEATOMA What are the causes? P592
``` Negative middle ear pressure from eustachian tube dysfunction (primary acquired) or direct growth of epithelium through a TM perforation (secondary acquired) ```
75
``` EAR CHOLESTEATOMA What other condition is it often associated with? P592 ```
Chronic middle ear infection
76
EAR CHOLESTEATOMA What is the usual history? P592
Chronic ear infection with chronic, | malodorous drainage
77
EAR CHOLESTEATOMA What is the appearance? P592
Grayish-white, shiny keratinous mass behind or involving the TM; often described as a “pearly” lesion
78
``` EAR CHOLESTEATOMA What are the associated problems? P592 ```
``` Ossicular erosion, producing conductive hearing loss; also, local invasion resulting in: Vertigo/sensorineural hearing loss Facial paresis/paralysis CNS dysfunction/infection ```
79
EAR CHOLESTEATOMA What is the treatment? P592
Surgery (tympanoplasty/mastoidectomy) aimed at eradication of disease and reconstruction of the ossicular chain
80
EAR BULLOUS MYRINGITIS What is it? P593
Vesicular infection of the TM and | adjacent deep canal
81
``` EAR BULLOUS MYRINGITIS What are the causative agents? P593 ```
Unknown; viral should be suspected because of frequent association with viral URI (in some instances, Mycoplasma pneumoniae has been cultured)
82
EAR BULLOUS MYRINGITIS What are the symptoms? P593
Acute, severe ear pain; low-grade fever; | and bloody drainage
83
``` EAR BULLOUS MYRINGITIS What are the findings on otoscopic examination? P593 ```
Large, reddish blebs on the TM, wall of | the meatus, or both
84
EAR BULLOUS MYRINGITIS Is hearing affected? P593
Rarely; occasional reversible sensorineural | loss
85
EAR BULLOUS MYRINGITIS What is the treatment? P593
Oral antibiotics (erythromycin if Mycoplasma is suspected); topical analgesics may be used, with resolution of symptoms usually occurring in 36 hours
86
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is it? P593
Bacterial infection of the middle ear, often following a viral URI; may be associated with a middle ear effusion
87
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is the cause? P593
Dysfunction of the eustachian tube that allows bacterial entry from nasopharynx; often associated with an occluded eustachian tube, although it is uncertain whether this is a cause or a result of the infection
88
``` EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What are the predisposing factors? P593 ```
Young age, male gender, bottle feeding, crowded living conditions (e.g., day care), cleft palate, Down’s syndrome, cystic fibrosis
89
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is the etiology? P593
``` 1. Streptococcus pneumoniae (33% of cases) 2. Haemophilus influenzae 3. Moraxella catarrhalis 4. Staphylococcus 5. -hemolytic strep 6. Pseudomonas aeruginosa 7. Viral/no culture ```
90
``` EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is the etiology in infants younger than 6 months? P594 ```
1. Staphylococcus aureus 2. E. coli 3. Klebsiella
91
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What are the symptoms? P594
Otalgia, fever, decreased hearing, infant pulls on ear, increased irritability; as many as 25% of patients are asymptomatic
92
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What are the signs? P594
Early, redness of the TM; later, TM bulging with loss of the normal landmarks; finally, impaired TM mobility on pneumatic otoscopy
93
``` EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) If pain disappears instantly, what may have happened? P594 ```
TM perforation!
94
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What are the complications? P594
``` TM perforation, acute mastoiditis, meningitis, brain abscess, extradural abscess, labyrinthitis; if recurrent or chronic, OM may have adverse effects on speech and cognitive development as a result of decreased hearing ```
95
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is the treatment? P594
10-day course of antibiotics; amoxicillin is the first-line agent; if the patient is allergic to PCN, trimethoprim-sulfamethoxazole or erythromycin should be administered
96
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is the usual course? P594
Symptoms usually resolve in 24 to 36 hours
97
``` EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What are the indications for myringotomy and PE tube placement? P594 ```
``` 1. Persistent middle ear effusion over 3 months 2. Debilitated or immunocompromised patient 3. More than three episodes over 6 months (especially if bilateral) ```
98
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is a PE tube? P594
Pneumatic Equalization tube (tube placed | across tympanic membrane)
99
EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What is a Bezold’s abscess? P594
Abscess behind the superior attachment of the sternocleidomastoid muscle resulting from extension of a mastoid infection
100
``` EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What are causes of chronic otitis media? P594 ```
Mixed, S. aureus, P. aeruginosa
101
``` EAR ACUTE SUPPURATIVE OTITIS MEDIA (OM) What are the signs/symptoms of chronic otitis media? P595 ```
Otorrhea and hearing loss
102
EAR OTOSCLEROSIS What is it? P595
Genetic disease characterized by abnormal spongy and sclerotic bone formation in the temporal bone around the footplate of the stapes, thus preventing its normal movement
103
``` EAR OTOSCLEROSIS What is the inheritance pattern? P595 ```
Autosomal dominant with incomplete | one-third penetrance
104
EAR OTOSCLEROSIS What are the symptoms? P595
Painless, progressive hearing loss (may be | unilateral or bilateral), tinnitus
105
``` EAR OTOSCLEROSIS What is the usual age of onset? P595 ```
Second through fourth decade
106
EAR OTOSCLEROSIS How is the diagnosis made? P595
Normal TM with conductive hearing loss and no middle-ear effusion (though may be mixed or even sensorineural if bone of cochlea is affected)
107
EAR OTOSCLEROSIS What is Schwartze’s sign? P595
Erythema around the stapes from | hypervascularity of new bone formation
108
EAR OTOSCLEROSIS What is the treatment? P595
``` Frequently surgical (stapedectomy with placement of prosthesis), hearing aids, or observation; sodium fluoride may be used if a sensorineural component is present or for preoperative stabilization ```
109
MISCELLANEOUS FACIAL NERVE PARALYSIS How is the defect localized? P595
``` Supranuclear—paralysis of lower face only, forehead muscles are spared because of bilateral corticobulbar supply Intratemporal bone—paralysis of upper and lower face, decreased tearing, altered taste, absent stapedius reflex Distal to stylomastoid foramen—paralysis of facial muscles only ```
110
MISCELLANEOUS FACIAL NERVE PARALYSIS What are the causes? P596
``` Bell’s palsy Trauma Cholesteatoma Tumor (carcinoma, glomus jugulare) Herpes zoster inflammation of geniculate ganglion (Ramsay-Hunt syndrome) Peripheral lesions are usually parotid gland tumors ```
111
``` MISCELLANEOUS FACIAL NERVE PARALYSIS What is the most common cause of bilateral facial nerve palsy? P596 ```
Lyme disease (Borrelia burgdorferi)
112
MISCELLANEOUS BELL’S PALSY What is it? P596
Sudden onset, unilateral facial weakness or paralysis in absence of CNS, ear, or cerebellopontine angle disease (i.e., no identifiable cause)
113
MISCELLANEOUS BELL’S PALSY What is the clinical course? P596
Acute onset, with greatest muscle | weakness reached within 3 weeks
114
MISCELLANEOUS BELL’S PALSY What is the incidence? P596
Most common cause of unilateral facial | weakness/paralysis
115
MISCELLANEOUS BELL’S PALSY What is the pathogenesis? P596
Unknown; most widely accepted hypothesis is viral etiology (herpes virus); ischemic and immunologic factors are also implicated
116
``` MISCELLANEOUS BELL’S PALSY What is the common preceding event? P596 ```
URI
117
``` MISCELLANEOUS BELL’S PALSY What are the signs/ symptoms? P596 ```
Pathology is related to swelling of the facial nerve; may present with total facial paralysis, altered lacrimation, increased tearing on affected side, change in taste if region above chorda tympani is affected, dry mouth, and hyperacusis
118
MISCELLANEOUS BELL’S PALSY What is the treatment? P596
``` Usually none is required, as most cases resolve spontaneously in 1 month; protect eye with drops and tape closed as needed; most otolaryngologists advocate steroids and acyclovir Surgical decompression of CN VII is indicated if paralysis progresses or tests indicate deterioration ```
119
MISCELLANEOUS BELL’S PALSY What is the prognosis? P597
Overall, 90% of patients recover completely; if paralysis is incomplete, 95% to 100% will recover without sequelae
120
SENSORINEURAL HEARING LOSS What is it? P597
Hearing loss from a lesion occurring in the cochlea or acoustic nerve, rather than the external or middle ear
121
SENSORINEURAL HEARING LOSS What are the symptoms? P597
Distortion of hearing, impaired speech | discrimination, tinnitus
122
SENSORINEURAL HEARING LOSS What are the signs? P597
``` Air conduction is better than bone conduction (positive Rinne test), Weber lateralizes to the side without the defect; audiogram most commonly shows greatest loss in high-frequency tones ```
123
SENSORINEURAL HEARING LOSS What is the Weber vs. Rinne test? P597
Weber: tuning fork on middle of head (lateral louder = either ipsilateral conductive loss or contralateral sensorineural) Rinne: tuning fork on mastoid and then next to ear (conductive loss louder on mastoid)
124
SENSORINEURAL HEARING LOSS What are the causes? P597
``` Aging (presbycusis)—leading cause Acoustic injury from sudden or prolonged exposure to loud noises Perilymph fistula Congenital (TORCHES: maternal TOxoplasmosis, Rubella, CMV, HErpes, and Syphilis) Ménière’s disease Drug/toxin-induced Acoustic neuroma Pseudotumor cerebri CNS disease Endocrine disorders Sarcoidosis ```
125
SENSORINEURAL HEARING LOSS What is the most common cause in children? P597
Meningitis (bacterial)
126
SENSORINEURAL HEARING LOSS What is the treatment? P598
Treatment of underlying cause, hearing | aids, lip reading, cochlear implant
127
VERTIGO What is it? P598
Sensation of head/body movement, or movement of surroundings (usually rotational)
128
VERTIGO What is the cause? P598
Asymmetric neuronal activity between | right and left vestibular systems
129
VERTIGO What is the history of peripheral vertigo? P598
Severe vertigo, nausea, vomiting, always accompanied by horizontal or rotatory nystagmus (fast component almost always to side opposite disease), other evidence of inner ear disease (tinnitus, hearing loss)
130
VERTIGO What are the risk factors for peripheral vertigo? P598
Frequently associated with a previously operated ear, a chronic draining ear, barotrauma, or head trauma
131
VERTIGO What is the history of central vertigo? P598
Found in brainstem or cerebellum: insidious onset, less intense and more subtle sensation of vertigo; occasionally, vertical nystagmus
132
VERTIGO What are the steps in diagnostic evaluation? P598
``` Depends on probability of central versus peripheral; careful neurologic and otologic examinations are required May need FTA/VDRL (syphilis), temporal bone scans/CT scan/MRI, ENG, position testing, audiometric testing ```
133
VERTIGO What is the most common etiology? P598
Benign Paroxysmal Positional Vertigo (BPPV); history of brief spells of severe vertigo with specific head positions
134
VERTIGO What is the differential diagnosis? P598
``` Central: vertebral basilar insufficiency (often in older patients with DJD of spine), Wallenberg syndrome, MS, epilepsy, migraine Peripheral: BPPV, motion sickness, syphilis, Ménière’s disease, vestibular neuronitis, labyrinthitis, acoustic neuroma, syphilis, perilymph fistula ```
135
VERTIGO What is Tullio’s phenomenon? P599
Induction of vertigo by loud noises; | classically, result of otosyphilis
136
MÉNIÈRE’S DISEASE What is it? P599
Disorder of the membranous labyrinth, causing fluctuating sensorineural hearing loss, episodic vertigo, nystagmus, tinnitus, and aural fullness, N/V
137
MÉNIÈRE’S DISEASE What is the classic triad? P599
Hearing loss, Tinnitus, Vertigo (H, T, V)
138
MÉNIÈRE’S DISEASE What is the pathophysiology? P599
Obscure, but most experts believe excessive production/defective resorption of endolymph
139
MÉNIÈRE’S DISEASE What is the medical treatment? P599
Salt restriction, diuretics (thiazides), antinausea agents; occasionally diazepam is added; 80% of patients respond to medical management, antihistamines
140
MÉNIÈRE’S DISEASE What are the indications for surgery? P599
Surgery is offered to those who fail medical treatment or who have incapacitating vertigo (60%–80% effective)
141
MÉNIÈRE’S DISEASE What are the surgical options? P599
``` 1. Shunt from membranous labyrinth to subarachnoid space 2. Vestibular neurectomy 3. Severe cases with hearing loss: labyrinthectomy ```
142
GLOMUS TUMORS What are they? P599
``` Benign, slow-growing tumors arising in glomus bodies found in the adventitial layer of blood vessels; often associated with cranial nerves IX and X in the middle ear ```
143
GLOMUS TUMORS What is the usual location? P599
Middle ear, jugular bulb, course of CN | IX to XII
144
GLOMUS TUMORS How common are they? P599
Most common benign tumor of the | temporal bone
145
GLOMUS TUMORS What is the treatment? P600
Surgical resection, radiation therapy for poor operative candidates or for recurrences
146
NOSE AND PARANASAL SINUSES EPISTAXIS What is it? P600
Bleeding from the nose
147
``` NOSE AND PARANASAL SINUSES EPISTAXIS What are the predisposing factors? P600 ```
Trauma, “nose picking,” sinus infection, allergic or atrophic rhinitis, blood dyscrasias, tumor, environmental extremes (hot, dry climates; winters)
148
NOSE AND PARANASAL SINUSES EPISTAXIS What is the usual cause? P600
Rupture of superficial mucosal blood vessels (Kiesselbach’s plexus if anterior, sphenopalatine artery if posterior)
149
``` NOSE AND PARANASAL SINUSES EPISTAXIS What is the most common type? P600 ```
Anterior (90%); usually the result of | trauma
150
NOSE AND PARANASAL SINUSES EPISTAXIS Which type is more serious? P600
Posterior; usually occurs in the elderly or is associated with a systemic disorder (hypertension, tumor, arteriosclerosis)
151
NOSE AND PARANASAL SINUSES EPISTAXIS What is the treatment? P600
Direct pressure; if this fails, proceed to anterior nasal packing with gauze strips, followed if necessary by posterior packing with Foley catheter or lamb’s wool; packs must be removed in <5 days to prevent infectious complications
152
``` NOSE AND PARANASAL SINUSES EPISTAXIS What is the treatment of last resort? P600 ```
``` Ligation or embolization of the sphenopalatine artery (posterior) or ethmoidal artery (anterior) ```
153
``` NOSE AND PARANASAL SINUSES EPISTAXIS What infectious disease syndrome is seen with nasal packing? P600 ```
Toxic shock syndrome: fever, shock, rash caused by exotoxin from Staphylococcus aureus
154
``` NOSE AND PARANASAL SINUSES EPISTAXIS What is the treatment of this syndrome? P600 ```
Supportive with removal of nasal packing, IV hydration, oxygen, and antistaphylococcal antibiotics
155
NOSE AND PARANASAL SINUSES ACUTE RHINITIS What is it? P601
Inflammation of nasal mucous membrane
156
``` NOSE AND PARANASAL SINUSES ACUTE RHINITIS What is the most common cause? P601 ```
``` URI infection; rhinovirus is the most common agent in adults (other nonallergic causes: nasal deformities and tumors, polyps, atrophy, immune diseases, vasomotor problems) ```
157
NOSE AND PARANASAL SINUSES ALLERGIC RHINITIS What are the symptoms? P601
Nasal stuffiness; watery rhinorrhea; paroxysms of morning sneezing; and itching of nose, conjunctiva, or palate
158
``` NOSE AND PARANASAL SINUSES ALLERGIC RHINITIS How is the condition characterized? P601 ```
Early onset (before 20 years of age), familial tendency, other allergic disorders (eczema, asthma), elevated serum IgE, eosinophilia on nasal smear
159
``` NOSE AND PARANASAL SINUSES ALLERGIC RHINITIS What are the findings on physical examination? P601 ```
``` Pale, boggy, bluish nasal turbinates coated with thin, clear secretions; in children, a transverse nasal crease sometimes results from repeated “allergic salute” ```
160
NOSE AND PARANASAL SINUSES ALLERGIC RHINITIS What is the treatment? P601
``` Allergen avoidance, antihistamines, decongestants; steroids or sodium cromylate in severe cases; desensitization via allergen immunotherapy is the only “cure” ```
161
NOSE AND PARANASAL SINUSES ACUTE SINUSITIS What is the typical history? P601
Previously healthy patient with unrelenting progression of a viral URI or allergic rhinitis beyond the normal 5- to 7-day course
162
NOSE AND PARANASAL SINUSES ACUTE SINUSITIS What are the symptoms? P601
Periorbital pressure/pain, nasal obstruction, nasal/postnasal mucopurulent discharge, fatigue, fever, headache
163
NOSE AND PARANASAL SINUSES ACUTE SINUSITIS What are the signs? P602
Tenderness over affected sinuses, pus in the nasal cavity; may also see reason for obstruction (septal deviation, spur, tight osteomeatal complex); transillumination is unreliable
164
NOSE AND PARANASAL SINUSES ACUTE SINUSITIS What is the pathophysiology? P602
``` Thought to be secondary to decreased ciliary action of the sinus mucosa and edema causing obstruction of the sinus ostia, lowering intrasinus oxygen tension and predisposing patients to bacterial infection ```
165
``` NOSE AND PARANASAL SINUSES ACUTE SINUSITIS What are the causative organisms? P602 ```
``` Up to 50% of patients have negative cultures and cause is presumably (initially) viral; pneumococcus, S. aureus, group A streptococci, and H. influenzae are the most common bacteria cultured ```
166
NOSE AND PARANASAL SINUSES ACUTE SINUSITIS What is the treatment? P602
14-day course of antibiotics (penicillin G, amoxicillin, Ceclor®, and Augmentin® are commonly used), topical and systemic decongestants, and saline nasal irrigation
167
``` NOSE AND PARANASAL SINUSES ACUTE SINUSITIS What is the treatment for fungal sinusitis? P602 ```
``` Fungal sinusitis is commonly caused by Mucor and seen in immunosuppressed patients; treatment is IV antifungals (e.g., amphotericin or caspofungin) and surgical débridement of all necrotic tissue ```
168
NOSE AND PARANASAL SINUSES CHRONIC SINUSITIS What is it? P602
Infection of nasal sinuses lasting longer than 4 weeks, or pattern of recurrent acute sinusitis punctuated by brief asymptomatic periods
169
NOSE AND PARANASAL SINUSES CHRONIC SINUSITIS What is the pathology? P602
``` Permanent mucosal changes secondary to inadequately treated acute sinusitis, consisting of mucosal fibrosis, polypoid growth, and inadequate ciliary action, hyperostosi ```
170
NOSE AND PARANASAL SINUSES CHRONIC SINUSITIS What are the symptoms? P603
Chronic nasal obstruction, postnasal drip, mucopurulent rhinorrhea, low-grade facial and periorbital pressure/pain
171
``` NOSE AND PARANASAL SINUSES CHRONIC SINUSITIS What are the causative organisms? P603 ```
``` Usually anaerobes (such as Bacteroides, Veillonella, Rhinobacterium); also H. influenzae, Streptococcus viridans, Staphylococcus aureus, Staphylococcus epidermidis ```
172
NOSE AND PARANASAL SINUSES CHRONIC SINUSITIS What is the treatment? P603
``` Medical management with decongestants, mucolytics, topical steroids, and antibiotics; if this approach fails, proceed to endoscopic or external surgical intervention ```
173
NOSE AND PARANASAL SINUSES CHRONIC SINUSITIS What is FESS? P603
Functional Endoscopic Sinus Surgery
174
``` NOSE AND PARANASAL SINUSES CHRONIC SINUSITIS What are the complications of sinusitis? P603 ```
Orbital cellulitis (if ethmoid sinusitis), meningitis, epidural or brain abscess (frontal sinus), cavernous sinus thrombosis (ethmoid or sphenoid), osteomyelitis (a.k.a. Pott’s puffy tumor if frontal)
175
``` NOSE AND PARANASAL SINUSES CANCER OF THE NASAL CAVITY AND PARANASAL SINUSES What are the usual locations? P603 ```
Maxillary sinus (66%) Nasal cavity Ethmoid sinus Rarely in frontal or sphenoid sinuses
176
``` NOSE AND PARANASAL SINUSES CANCER OF THE NASAL CAVITY AND PARANASAL SINUSES What are the associated cell types? P603 ```
Squamous cell (80%) Adenocellular (15%) Uncommon: sarcoma, melanoma
177
``` NOSE AND PARANASAL SINUSES CANCER OF THE NASAL CAVITY AND PARANASAL SINUSES What rare tumor arises from olfactory epithelium? P603 ```
Esthesioneuroblastoma; usually arises high in the nose (cribriform plate) and is locally invasive
178
``` NOSE AND PARANASAL SINUSES CANCER OF THE NASAL CAVITY AND PARANASAL SINUSES What are the signs/ symptoms? P603 ```
``` Early—nasal obstruction, blood-tinged mucus, epistaxis Late—localized pain, cranial nerve deficits, facial/palate asymmetry, loose teeth ```
179
NOSE AND PARANASAL SINUSES CANCER OF THE NASAL CAVITY AND PARANASAL SINUSES How is the diagnosis made? P604
CT scan can adequately identify extent of the disease and local invasion; MRI is often also used to evaluate soft-tissue disease
180
NOSE AND PARANASAL SINUSES CANCER OF THE NASAL CAVITY AND PARANASAL SINUSES What is the treatment? P604
Surgery with or without x-ray therapy
181
NOSE AND PARANASAL SINUSES CANCER OF THE NASAL CAVITY AND PARANASAL SINUSES What is the prognosis? P604
5-year survival for T1 or T2 lesions | approaches 70%
182
NOSE AND PARANASAL SINUSES JUVENILE NASOPHARYNGEAL ANGIOFIBROMA What is it? P604
Most commonly encountered vascular mass in the nasal cavity; locally aggressive but nonmetastasizing
183
NOSE AND PARANASAL SINUSES JUVENILE NASOPHARYNGEAL ANGIOFIBROMA What is the usual history? P604
Adolescent boys who present with nasal obstruction, recurrent massive epistaxis, possibly anosmia
184
NOSE AND PARANASAL SINUSES JUVENILE NASOPHARYNGEAL ANGIOFIBROMA What is the usual location? P604
Site of origin is the roof of the nasal cavity at the superior margin of sphenopalatine foramen
185
``` NOSE AND PARANASAL SINUSES JUVENILE NASOPHARYNGEAL ANGIOFIBROMA Into what can the mass transform? P604 ```
Fibrosarcoma (rare cases reported)
186
NOSE AND PARANASAL SINUSES JUVENILE NASOPHARYNGEAL ANGIOFIBROMA How is the diagnosis made? P604
Carotid arteriography, CT scan; biopsy is contraindicated secondary to risk of uncontrollable hemorrhage
187
``` NOSE AND PARANASAL SINUSES JUVENILE NASOPHARYNGEAL ANGIOFIBROMA What are indications for biopsy? P604 ```
None!
188
NOSE AND PARANASAL SINUSES JUVENILE NASOPHARYNGEAL ANGIOFIBROMA What is the treatment? P604
Surgery via lateral rhinotomy or sublabial maxillotomy with bleeding controlled by internal maxillary artery ligation or preoperative embolization, in the setting of hypotensive anesthesia; preoperative irradiation has also been used to shrink the tumor
189
``` ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What is the common site of referred throat pain P605 ```
EAR
190
ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What is it? P605
``` Acute or chronic infection of the nasopharynx or oropharynx and/or Waldeyer’s ring of lymphoid tissue (consisting of palatine, lingual, and pharyngeal tonsils and the adenoids) ```
191
ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What is the etiology? P605
Acute attacks can be viral (adenovirus, enterovirus, coxsackievirus, Epstein-Barr virus in infectious mononucleosis) or bacterial (group A -hemolytic streptococci are the leading bacterial agent); chronic tonsillitis often with mixed population, including streptococci, staphylococci, and M. catarrhalis
192
ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What are the symptoms? P605
``` Acute—Sore throat, fever, local lymphadenopathy, chills, headache, malaise Chronic—Noisy mouth breathing, speech and swallowing difficulties, apnea, halitosis ```
193
ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What are the signs? P605
Viral—Injected tonsils and pharyngeal mucosa; exudate may occur, but less often than with bacterial tonsillitis Bacterial—Swollen, inflamed tonsils with white-yellow exudate in crypts and on surface; cervical adenopathy
194
ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS How is the diagnosis made? P605
CBC, throat culture, Monospot test
195
``` ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What are the possible complications? P605 ```
``` Peritonsillar abscess (quinsy), retropharyngeal abscess (causing airway compromise), rheumatic fever, poststreptococcal glomerulonephritis (with -hemolytic streptococci) ```
196
ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What is the treatment? P606
``` Viral—Symptomatic → acetaminophen, warm saline gargles, anesthetic throat spray Bacterial—10 days PCN (erythromycin if PCN-allergic) ```
197
``` ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What are the indications for tonsillectomy? P606 ```
``` Sleep apnea/cor pulmonale secondary to airway obstruction, suspicion of malignancy, hypertrophy causing malocclusion, peritonsillar abscess, recurrent acute or chronic tonsillitis ```
198
``` ORAL CAVITY AND PHARYNX PHARYNGOTONSILLITIS What are the possible complications? P606 ```
Acute or delayed hemorrhage
199
ORAL CAVITY AND PHARYNX PERITONSILLAR ABSCESS What is the clinical setting? P606
Inadequately treated recurrent acute or | chronic tonsillitis
200
ORAL CAVITY AND PHARYNX PERITONSILLAR ABSCESS What is the assoc P606
Mixed aerobes and anaerobes (which | may be PCN resistant)
201
ORAL CAVITY AND PHARYNX PERITONSILLAR ABSCESS What is the site of formation? P606
Begins at the superior pole of the tonsil
202
ORAL CAVITY AND PHARYNX PERITONSILLAR ABSCESS What are the symptoms? P606
Severe throat pain, drooling dysphagia, odynophagia, trismus, cervical adenopathy, fever, chills, malaise
203
``` ORAL CAVITY AND PHARYNX PERITONSILLAR ABSCESS What is the classic description of voice? P606 ```
“Hot-potato voice”
204
ORAL CAVITY AND PHARYNX PERITONSILLAR ABSCESS What are the signs? P606
Bulging, erythematous, edematous tonsillar pillar; swelling of uvula and displacement to contralateral side
205
ORAL CAVITY AND PHARYNX PERITONSILLAR ABSCESS What is the treatment? P606
IV antibiotics and surgical evacuation by incision and drainage; most experts recommend tonsillectomy after resolution of inflammatory changes
206
ORAL CAVITY AND PHARYNX LUDWIG ANGINA What is it? P606
``` Infection and inflammation of the floor of the mouth (sublingual and submandibular) ```
207
ORAL CAVITY AND PHARYNX LUDWIG ANGINA What is the source? P607
Dental infection
208
ORAL CAVITY AND PHARYNX LUDWIG ANGINA What is the treatment? P607
Antibiotics, emergency airway, I & D
209
ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the usual cell type? P607
Squamous cell (90% of cases)
210
``` ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What are the most common sites? P607 ```
Lip, tongue, floor of mouth, gingiva, | cheek, and palate
211
ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the etiology? P607
Linked to smoking, alcohol, and smokeless tobacco products (alcohol and tobacco together greatly increase the risk)
212
``` ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the frequency of the following conditions: Regional metastasis? P607 ```
≈30%
213
``` ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the frequency of the following conditions: Second primary? P607 ```
≈25%
214
``` ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the frequency of the following conditions: Nodal metastasis? P607 ```
Depends on size of tumor and ranges from 10% to 60%, usually to jugular and jugulodigastric nodes, submandibular nodes
215
``` ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the frequency of the following conditions: Distant metastasis? P607 ```
Infrequent
216
ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY How is the diagnosis made? P607
``` Full history and physical examination, dental assessment, Panorex or bone scan if mandible is thought to be involved, CT scan/MRI for extent of tumor and nodal disease, FNA (often U/S guided) ```
217
ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the treatment? P607
``` Radiation, surgery, or both for small lesions; localized lesions can usually be treated surgically; larger lesions require combination therapy, possible mandibulectomy and neck dissection ```
218
ORAL CAVITY AND PHARYNX CANCER OF THE ORAL CAVITY What is the prognosis? P608
``` Depends on stage and site: Tongue: 20% to 70% survival Floor of mouth: 30% to 80% survival Most common cause of death in successfully treated head and neck cancer is development of a second primary (occurs in 20%–40% of cases) ```
219
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the frequency of gland involvement? P608 ```
``` Parotid gland (80%) Submandibular gland (15%) Minor salivary glands (5%) ```
220
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the potential for malignancy? P608 ```
``` Greatest in minor salivary gland tumors (80% are malignant) and least in parotid gland tumors (80% are benign); the smaller the gland, the greater the likelihood of malignancy ```
221
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS How do benign and malignant tumors differ in terms of history and physical examination? P608 ```
``` Benign—mobile, nontender, no node involvement or facial weakness Malignant—painful, fixed mass with evidence of local metastasis and facial paresis/paralysis ```
222
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the diagnostic procedure? P608 ```
FNA; never perform excisional biopsy of a parotid mass; superficial parotidectomy is the procedure of choice for benign lesions of the lateral lobe
223
ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the treatment? P608
Involves adequate surgical resection, sparing facial nerve if possible, neck dissection for node-positive necks
224
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What are the indications for postop XRT? P608 ```
Postoperative radiation therapy if highgrade cancer, recurrent cancer, residual disease, invasion of adjacent structures, any T3 or T4 parotid tumors
225
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the most common benign salivary tumor? P608 ```
``` Pleomorphic adenoma (benign mixed tumor) 66% Think: Pleomorphic = Popular ```
226
ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the usual location? P608
Parotid gland
227
ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the clinical course? P609
They are well delineated and slow | growing
228
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the second most common benign salivary gland tumor? P609 ```
Warthin’s tumor (1% of all salivary gland | tumors)
229
ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the usual location? P609
95% are found in parotid; 3% are | bilateral
230
ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS Describe the lesion. P609
Slow-growing, cystic mass is usually located in the tail of the superficial portion of the parotid; it rarely becomes malignant
231
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the most common malignant salivary tumor? P609 ```
``` Mucoepidermoid carcinoma (10% of all salivary gland neoplasms) Think: Mucoepidermoid = Malignant Most common parotid malignancy Second most common submandibular gland malignancy ```
232
``` ORAL CAVITY AND PHARYNX SALIVARY GLAND TUMORS What is the second most common malignant salivary tumor in adults? P609 ```
Adenoid cystic carcinoma; most common malignancy in submandibular and minor salivary glands
233
ORAL CAVITY AND PHARYNX LARYNX ANATOMY Define the three parts. P609
1. Glottis: begins halfway between the true and false cords (in the ventricle) and extends inferiorly 1.0 cm below the edge of the vocal folds 2. Supraglottis: extends from superior glottis to superior border of hyoid and tip of epiglottis 3. Subglottis: extends from lower border of glottis to inferior edge of cricoid cartilage
234
ORAL CAVITY AND PHARYNX LARYNX ANATOMY Innervation? P610
``` Vagus nerve: superior laryngeal and recurrent laryngeal nerves; superior laryngeal supplies sensory to supraglottis and motor to inferior constrictor and cricothyroid muscle; recurrent laryngeal supplies sensory to glottis and subglottis and motor to all remaining intrinsic laryngeal muscles ```
235
ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What is it? P610
Viral infection of the larynx and trachea, | generally affecting children (boys > girls)
236
ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What is the usual cause? P610
Parainfluenza virus | Think: crouP = Parainfluenza
237
``` ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What age group is affected most? P610 ```
6 months to 3 years of age
238
``` ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) Is the condition considered seasonal? P610 ```
Yes; outbreaks most often occur in | autumn
239
``` ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What are the precipitating events? P610 ```
Usually preceded by URI
240
ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What is the classic symptom? P610
Barking (seal-like), nonproductive cough
241
``` ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What are the other symptoms? P610 ```
Respiratory distress, low-grade fever
242
ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What are the signs? P610
Tachypnea, inspiratory retractions, prolonged inspiration, inspiratory stridor, expiratory rhonchi/wheezes
243
``` ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What is the differential diagnosis? P610 ```
Epiglottitis, bacterial tracheitis, foreign body, diphtheria, retropharyngeal abscess, peritonsillar abscess, asthma
244
ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) How is the diagnosis made? P610
A-P neck x-ray shows classic “steeple sign,” indicating subglottic narrowing; ABG may show hypoxemia plus hypercapnia
245
ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What is the treatment? P611
Keep child calm (agitation only worsens obstruction); cool mist; steroids; aerosolized racemic EPI may be administered to reduce edema/airway obstruction
246
``` ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What are the indications for intubation? P611 ```
If airway obstruction is severe or child | becomes exhausted
247
ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What is the usual course? P611
Resolves in 3 to 4 days
248
``` ORAL CAVITY AND PHARYNX CROUP (LARYNGOTRACHEOBRONCHITIS) What type of secondary infection occurs? P611 ```
Secondary bacterial infection | streptococcal, staphylococcal
249
ORAL CAVITY AND PHARYNX EPIGLOTTITIS What is it? P611
Severe, rapidly progressive infection of | the epiglottis
250
``` ORAL CAVITY AND PHARYNX EPIGLOTTITIS What is the usual causative agent? P611 ```
Haemophilus influenzae type B
251
ORAL CAVITY AND PHARYNX EPIGLOTTITIS What age group is affected? P611
Children 2 to 5 years of age
252
``` ORAL CAVITY AND PHARYNX EPIGLOTTITIS What are the signs/ symptoms? P611 ```
``` Sudden onset, high fever (40C); “hot-potato” voice; dysphagia (Sudden onset, high fever (40C); “hot-potato” voice; dysphagia ( → drooling); no cough; patient prefers to sit upright, lean forward; patient appears toxic and stridulous ```
253
ORAL CAVITY AND PHARYNX EPIGLOTTITIS How is the diagnosis made? P611
Can usually be made clinically and does not involve direct observation of the epiglottis (which may worsen obstruction by causing laryngospasm)
254
ORAL CAVITY AND PHARYNX EPIGLOTTITIS What is the treatment? P611
Involves immediate airway support in the O.R.: intubation or possibly tracheostomy, medical treatment is comprised of steroids and IV antibiotics against H. influenzae
255
ORAL CAVITY AND PHARYNX MALIGNANT LESIONS OF THE LARYNX What is the incidence? P611
Accounts for ≈2% of all malignancies, | more often in males
256
``` ORAL CAVITY AND PHARYNX MALIGNANT LESIONS OF THE LARYNX What is the most common site? P611 ```
Glottis (66%)
257
``` ORAL CAVITY AND PHARYNX MALIGNANT LESIONS OF THE LARYNX What is the second most common type? P612 ```
Supraglottis (33%)
258
``` ORAL CAVITY AND PHARYNX MALIGNANT LESIONS OF THE LARYNX Which type has the worst prognosis? P612 ```
Subglottic tumors (infrequent)
259
ORAL CAVITY AND PHARYNX MALIGNANT LESIONS OF THE LARYNX What are the risk factors? P612
Tobacco, alcohol
260
ORAL CAVITY AND PHARYNX MALIGNANT LESIONS OF THE LARYNX What is the pathology? P612
90% are squamous cell carcinoma
261
ORAL CAVITY AND PHARYNX MALIGNANT LESIONS OF THE LARYNX What are the symptoms? P612
Hoarseness, throat pain, dysphagia, odynophagia, neck mass, (referred) ear pain
262
ORAL CAVITY AND PHARYNX SUPRAGLOTTIC LESIONS What is the usual location? P612
Laryngeal surface of epiglottis
263
ORAL CAVITY AND PHARYNX SUPRAGLOTTIC LESIONS What area is often involved? P612
Pre-epiglottic space
264
ORAL CAVITY AND PHARYNX SUPRAGLOTTIC LESIONS Extension? P612
Tend to remain confined to supraglottic region, though may extend to vallecula or base of tongue
265
``` ORAL CAVITY AND PHARYNX SUPRAGLOTTIC LESIONS What is the associated type of metastasis? P612 ```
High propensity for nodal metastasis
266
ORAL CAVITY AND PHARYNX SUPRAGLOTTIC LESIONS What is the treatment? P612
Early stage = XRT | Late stage = laryngectomy
267
ORAL CAVITY AND PHARYNX GLOTTIC LESIONS What is the usual location? P612
Anterior part of true cords
268
ORAL CAVITY AND PHARYNX GLOTTIC LESIONS Extension? P612
May invade thyroid cartilage, cross midline to invade contralateral cord, or invade paraglottic space
269
``` ORAL CAVITY AND PHARYNX GLOTTIC LESIONS What is the associated type of metastasis? P612 ```
Rare nodal metastasis
270
ORAL CAVITY AND PHARYNX GLOTTIC LESIONS What is the treatment? P612
Early stage = XRT | Late stage = laryngectomy
271
``` ORAL CAVITY AND PHARYNX NECK MASS What is the usual etiology in infants? P613 ```
Congenital (branchial cleft cysts, | thyroglossal duct cysts)
272
``` ORAL CAVITY AND PHARYNX NECK MASS What is the usual etiology in adolescents? P613 ```
Inflammatory (cervical adenitis is #1), | with congenital also possible
273
``` ORAL CAVITY AND PHARYNX NECK MASS What is the usual etiology in adults? P613 ```
Malignancy (squamous is #1), especially | if painless and immobile
274
ORAL CAVITY AND PHARYNX NECK MASS What is the “80% rule”? P613
In general, 80% of neck masses are benign in children; 80% are malignant in adults older than 40 years of age
275
``` ORAL CAVITY AND PHARYNX NECK MASS What are the seven cardinal symptoms of neck masses? P613 ```
Dysphagia, odynophagia, hoarseness, stridor (signifies upper airway obstruction), globus, speech disorder, referred ear pain (via CN V, IX, or X)
276
ORAL CAVITY AND PHARYNX NECK MASS What comprises the workup? P613
``` Full head and neck examination, indirect laryngoscopy, CT scan and MRI, FNA for tissue diagnosis; biopsy contraindicated because it may adversely affect survival if malignant ```
277
``` ORAL CAVITY AND PHARYNX NECK MASS What is the differential diagnosis? P613 ```
Inflammatory: cervical lymphadenitis, cat-scratch disease, infectious mononucleosis, infection in neck spaces Congenital: thyroglossal duct cyst (midline, elevates with tongue protrusion), branchial cleft cysts (lateral), dermoid cysts (midline submental), hemangioma, cystic hygroma Neoplastic: primary or metastatic
278
``` ORAL CAVITY AND PHARYNX NECK MASS What is the workup of node-positive squamous cell carcinoma and no primary site? P613 ```
Triple endoscopy (laryngoscopy, esophagoscopy, bronchoscopy) and blind biopsies
279
ORAL CAVITY AND PHARYNX NECK MASS What is the treatment? P613
Surgical excision for congenital or neoplastic; two most important procedures for cancer treatment are radical and modified neck dissection
280
``` ORAL CAVITY AND PHARYNX NECK MASS What is the role of adjuvant treatment in head and neck cancer? P614 ```
Postoperative chemotherapy/XRT
281
ORAL CAVITY AND PHARYNX RADICAL NECK DISSECTION What is involved? P614
``` Classically, removal of nodes from clavicle to mandible, sternocleidomastoid muscle, submandibular gland, tail of parotid, internal jugular vein, digastric muscles, stylohyoid and omohyoid muscles, fascia within the anterior and posterior triangles, CN XI, and cervical plexus sensory nerves ```
282
ORAL CAVITY AND PHARYNX RADICAL NECK DISSECTION What are the indications? P614
1. Clinically positive nodes that likely contain metastatic cancer 2. Clinically negative nodes in neck, but high probability of metastasis from a primary tumor elsewhere 3. Fixed cervical mass that is resectable
283
``` ORAL CAVITY AND PHARYNX RADICAL NECK DISSECTION What are the contraindications? P614 ```
1. Distant metastasis 2. Fixation to structure that cannot be removed (e.g., carotid artery) 3. Low neck masses
284
``` ORAL CAVITY AND PHARYNX MODIFIED NECK DISSECTION What are the types: Type I? P614 ```
Spinal accessory nerve preserved
285
``` ORAL CAVITY AND PHARYNX MODIFIED NECK DISSECTION What are the types: Type II? P614 ```
Spinal accessory and internal jugular vein | preserved
286
``` ORAL CAVITY AND PHARYNX MODIFIED NECK DISSECTION What are the types: Type III? P614 ```
Spinal accessory, IJ, and | sternocleidomastoid nerves preserved
287
ORAL CAVITY AND PHARYNX MODIFIED NECK DISSECTION What are the advantages? P614
``` Increased postoperative function and decreased morbidity (especially if bilateral), most often used in NO lesions; these modifications are usually intraoperative decisions based on the location and extent of tumor growth ```
288
ORAL CAVITY AND PHARYNX MODIFIED NECK DISSECTION What are the disadvantages? P615
May result in increased mortality from | local recurrence
289
FACIAL FRACTURES MANDIBLE FRACTURES What are the symptoms? P615
Gross disfigurement, pain, malocclusion, | drooling
290
FACIAL FRACTURES MANDIBLE FRACTURES What are the signs? P615
Trismus, fragment mobility and lacerations of gingiva, hematoma in floor of mouth
291
``` FACIAL FRACTURES MANDIBLE FRACTURES What are the possible complications? P615 ```
Malunion, nonunion, osteomyelitis, TMJ | ankylosis
292
FACIAL FRACTURES MANDIBLE FRACTURES What is the treatment? P615
Open or closed reduction MMF = MaxilloMandibular Fixation (wire jaw shut)
293
FACIAL FRACTURES MIDFACE FRACTURES How are they evaluated? P615
Careful physical examination and CT scan
294
``` FACIAL FRACTURES MIDFACE FRACTURES Classification Le Fort I? P615 (picture) ```
Transverse maxillary fracture above the dental apices, which also traverses the pterygoid plate; palate is mobile, but nasal complex is stable
295
``` FACIAL FRACTURES MIDFACE FRACTURES Classification Le Fort II? P616 (picture) ```
Fracture through the frontal process of the maxilla, through the orbital floor and pterygoid plate; midface is mobile
296
``` FACIAL FRACTURES MIDFACE FRACTURES Classification Le Fort III? P616 (picture) ```
Complete craniofacial separation; differs from II in that it extends through the nasofrontal suture and frontozygomatic sutures
297
``` FACIAL FRACTURES MIDFACE FRACTURES Classification What is a “tripod” fracture? P616 (picture) ```
``` Fracture of the zygomatic complex; involves four fractures: 1. Frontozygomatic suture 2. Inferior orbital rim 3. Zygomaticomaxillary suture 4. Zygomaticotemporal suture ```
298
FACIAL FRACTURES MIDFACE FRACTURES What is a “blowout” fracture? P617
Orbital fracture with “blowout” of supporting bony structural support of orbital floor; patient has enophthalmos (sunken-in eyeball)
299
FACIAL FRACTURES MIDFACE FRACTURES What is “entrapment”? P617
``` Orbital fracture with “entrapment” of periorbital tissues within the fracture opening, including entrapment of extraocular muscles; loss of extraocular muscle mobility (e.g., lateral tracking) and diplopia (double vision) ```
300
FACIAL FRACTURES MIDFACE FRACTURES What is a “step off”? P617
Fracture of the orbit with palpable “step off” of bony orbital rim (inferior or lateral)
301
``` FACIAL FRACTURES MIDFACE FRACTURES Are mandibular fractures usually a single fracture? P617 ```
No; because the mandible forms an anatomic ring, >95% of mandible fractures have more than one fracture site
302
``` FACIAL FRACTURES MIDFACE FRACTURES What is the best x-ray study for mandibular fractures? P617 ```
Panorex
303
``` FACIAL FRACTURES MIDFACE FRACTURES What must be ruled out and treated with a broken nose (nasal fracture)? P617 ```
Septal hematoma; must drain to remove | chance of pressure-induced septal necrosis
304
``` ENTWARD QUESTIONS How can otitis externa be distinguished from otitis media on examination? P617 ```
Otitis externa is characterized by severe | pain upon manipulation of the auricle
305
ENTWARD QUESTIONS What causes otitis media? P617
Most cases are caused by pneumococci | and H. influenzae
306
ENTWARD QUESTIONS What causes otitis externa? P617
Pseudomonas aeruginosa
307
ENTWARD QUESTIONS What must be considered in unilateral serous otitis? P617
Nasopharyngeal carcinoma
308
ENTWARD QUESTIONS What is the most common cause of facial paralysis? P617
Bell’s palsy, which has an unidentified | etiology
309
``` ENTWARD QUESTIONS What is the single most important prognostic factor in Bell’s palsy? P618 ```
Whether the affected muscles are completely paralyzed (if not, prognosis is >95% complete recovery)
310
ENTWARD QUESTIONS What is the most common cause of parotid swelling? P618
Mumps
311
ENTWARD QUESTIONS What is Heerfordt’s syndrome? P618
Sarcoidosis with parotid enlargement, | facial nerve paralysis, and uveitis
312
ENTWARD QUESTIONS Which systemic disease causes salivary gland stones? P618
Gout
313
``` ENTWARD QUESTIONS What is the most common salivary gland site of stone formation? P618 ```
Submandibular gland
314
ENTWARD QUESTIONS What is Mikulicz’s syndrome? P618
Any cause of bilateral enlargement of the | parotid, lacrimal, and submandibular glands
315
ENTWARD QUESTIONS What are the three major functions of the larynx? P618
1. Airway protection 2. Airway/respiration 3. Phonation
316
ENTWARD QUESTIONS What is a cricothyroidotomy? P618
Emergent surgical airway by incising the | cricothyroid membrane
317
``` ENTWARD QUESTIONS Name the four major indications for a tracheostomy. P618 ```
``` 1. Prolonged mechanical ventilation (usually 2 weeks) 2. Upper airway obstruction 3. Poor life-threatening pulmonary toilet 4. Severe obstructive sleep apnea ```
318
ENTWARD QUESTIONS What is a ranula? P618
Sublingual retention cyst arising from | sublingual salivary glands
319
ENTWARD QUESTIONS What is Frey’s syndrome? P618
Flushing, pain, and diaphoresis in the auriculotemporal nerve distribution initiated by chewing
320
ENTWARD QUESTIONS What causes Frey’s syndrome? P618
``` Cutting the auriculotemporal nerve causes abnormal regeneration of the sympathetic/parasympathetic nerves, which, once destined for the parotid gland, find new targets in skin sweat glands; thus, people sweat when eating ```
321
ENTWARD QUESTIONS What is the classic triad of Ménière’s disease? P619
Hearing loss, tinnitus, vertigo (HTV)
322
``` ENTWARD QUESTIONS What is the most common posterior fossa tumor and where is it located? P619 ```
Acoustic neuroma, usually occurring at | the cerebellopontine angle
323
ENTWARD QUESTIONS What is the most common site of sinus cancer? P619
Maxillary sinus
324
ENTWARD QUESTIONS What tumor arises from olfactory epithelium? P619
Esthesioneuroblastoma
325
``` ENTWARD QUESTIONS What cell type is most common in head and neck cancer? P619 ```
Squamous cell
326
``` ENTWARD QUESTIONS What are the most important predisposing factors to head and neck cancer? P619 ```
Excessive alcohol use and tobacco abuse | of any form
327
ENTWARD QUESTIONS What is the most frequent site of salivary gland tumor? P619
Parotid gland
328
``` ENTWARD QUESTIONS What is the most common salivary gland neoplasm: Benign? P619 ```
Pleomorphic adenoma
329
``` ENTWARD QUESTIONS What is the most common salivary gland neoplasm: Malignant? P619 ```
Mucoepidermoid carcinoma
330
ENTWARD QUESTIONS What is the classic feature of croup? P619
Barking, seal-like cough
331
ENTWARD QUESTIONS What are the classic features of epiglottitis? P619
“Hot-potato” voice, sitting up, drooling, toxic appearance, high fever, leaning forward
332
ENTWARD QUESTIONS What comprises the workup of neck mass? P619
Do not biopsy; obtain tissue via FNA | and complete head and neck examination
333
ENTWARD QUESTIONS What is Ramsay-Hunt syndrome? P620
Painful facial nerve paralysis from herpes | zoster of the ear
334
``` ENTWARD QUESTIONS What is the most common malignant neck mass in children, adolescents, and young adults? P620 ```
Lymphoma
335
``` ENTWARD QUESTIONS What is the most common primary malignant solid tumor of the head and neck in children? P620 ```
Rhabdomyosarcoma
336
ENTWARD QUESTIONS Throat pain is often referred to what body area? P620
Ear
337
``` ENTWARD QUESTIONS What ENT condition is described as “crocodile tears”? P620 ```
Frey’s syndrome!
338
ENTWARD QUESTIONS What is Brown’s sign? P620
Tympanic membrane pulsations that cease with positive pressure (from a “pneumatic” otoscope); seen with middle ear tumor mass
339
RAPID-FIRE REVIEW OF MOST COMMON CAUSES OF ENT INFECTIONS Croup? P620
Parainfluenza virus
340
RAPID-FIRE REVIEW OF MOST COMMON CAUSES OF ENT INFECTIONS Otitis externa? P620
Pseudomonas
341
RAPID-FIRE REVIEW OF MOST COMMON CAUSES OF ENT INFECTIONS Epiglottitis? P620
H. influenzae
342
RAPID-FIRE REVIEW OF MOST COMMON CAUSES OF ENT INFECTIONS Malignant otitis externa? P620
Pseudomonas
343
RAPID-FIRE REVIEW OF MOST COMMON CAUSES OF ENT INFECTIONS Parotitis? P620
Staphylococcus
344
``` RAPID-FIRE REVIEW OF MOST COMMON CAUSES OF ENT INFECTIONS Acute suppurative otitis media? P620 ```
S. pneumoniae (33%)