Head and Neck Flashcards

1
Q

Helpful Videos

A

EUSTACHAIN TUBE DYSFUNCTION
https://www.youtube.com/watch?v=H29571Ex-kY

SALIVARY GLAND TUMOURS
https://www.youtube.com/watch?v=bQVlqTx18ds

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2
Q

Le Fort

A
LEFORT ONE (HORIZONTAL)
Anterolateral margin of nasal fossa. Palate separated from maxilla 'floating palate'
LEFORT TWO (PYRAMIDAL)
Inferior orbital rim and orbital floor. Maxilla separated from face 'pyramidal'
LEFORT THREE (TRANSVERSE)
Zygomatic arch and lateral orbital rim. Face separated from cranium 'floating face'

All three types have fractured pterygoid plates

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3
Q

Mucocoele

A

If fracture disrupts frontal sinus outflow tract (nasal-orbital-ethmoid types) you can develop adhesions with obstruct sinus and result in mucocoele development

‘airless expanded sinus’

T1 bright with thin rim enhancement. Frontal sinus most common due to trauma

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4
Q

CSF leak

A

Fractures of facial bones, sinus walls and anterior skull base can all lead to CSF leak. Anterior skull base most common. Recurent bacterial meningitis is association

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5
Q

Temporal bone fractures

A
LONGITUDINAL
Long axis of temporal bone (ear to apex)
More common.
More ossicular dislocation.
Less facial nerve damage 20%
More conductive hearing loss.
TRANSVERSE
Short axis tempral bone (perpendicular)
Less common.
More vascular injury (carotid/jugular)
More facial nerve damage >30%
More sensorineural hearing loss
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6
Q

Facial bone fractures

A

Nasal bone most common.
ZMC fracture is most common pattern and involves zygoma, inferior orbit and lateral orbit.
Le Fort high yield (1 floating palate, 2 pyramidal, 3 floating face)
Temporal bone fractures longitudinal and transverse. Otic capsule violation is better predictive factor.

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7
Q

Ear divisions

A

EXTERNAL
Everything superficial to tympanic membrane

MIDDLE
Tympanic membrane to medial wall tympanic cavity.
Epitympanum (attic) is everything above tip of scutum
Hypotympanum everything below tympanic membrane
Mesotympanum inbetween

INNER
Everything deep to medial wall of tympanic cavity.

Scutum is a shield like osseous spur formed via lateral wall of tympanic cavity. Involved with cholesteatomas

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8
Q

Cholesteatoma

A

Exfoliated/dead skin growing in wrong place. Creates inflammation ball that wrecks temporal bone and ossicles.

Restrict diffusion, can erode scutum.

PARS FLACCIDA
Flimsy part of tympanic membrane is superior.
Acquired more common, grow into Prussaks space.
Scutum eroded early.
Malleus head displaced medially
Long process of incus most common segment of ossicular chain to be eroded
Fistula to semicircular canal most commonly involves lateral segment

PARS TENSA
Inner ear structures involved earlier and more often.
Less common than pars flaccida type.

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9
Q

Prussaks space and scutum erosion

A

PRUSSAKS SPACE
Superior to scutum between lateral wall and ossicle (incus).
Most common location of pars flaccida choleseatoma (incus most commonly eroded)

SCUTUM
Shield like bony protuberance superomedial to tympanic membrane. Eroded first.

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10
Q

Labyrinthine/perilymphatic fistula

A

Potential complication of cholesteatoma (or iatrogenic/trauma).
Bony defect creating abnormal communication between fluid filled inner ear and air filled tympanic cavity.
Lateral semicircular canal most often involved.

‘sudden fluctuating sensorinerual hearing loss and vertigo’

Want to see soft tissue cholesteatoma eating through otic capsule into semicircular canal. Air in semicircular canal (pneumolabyrinth) is difinitive evidence of fistula, though uncommon.

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11
Q

Otitis media OM

A

Effusion and infection of middle ear. More common in children and Downs due to more horizontal Eustachian tube. Chronic if >6 weeks

COMPLICATIONS
Coalescent mastoiditis (erosion mastoid septae)
Facial nerve palsy (inflammation tympanic segment)
Dural sinus thrombosis (then venous infarct or otitic hydrocephalus)
Meningitis or labyrinthitis

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12
Q

Chronic OM vs cholesteatoma

A
CHRONIC OTITIS MEDIA
Poorly pneumatized mastoids
Middle ear can completely opacify
Thickened mucosa
Erosions of ossicles rare
No displacement ossicular chain
CHOLESTEATOMA
Poorly pneumatized mastoids
Middle ear can completely opacify
Non-dependent mass
Erosions of ossicles common
Can displace ossicular chain
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13
Q

Labyrinthitis ossificans

A

History of childhood meningitis, kids 2-18months.
Classic on CT with ossification of membranous labyrinth.
Sensorineural hearing loss
Calcification of cochlea is often considered contraindication to cochlear implant.

LABYRINTH
Vestibule, cochlea and semicircular canals
Bony is the series of canals tunneled out of bone and membranous is soft tissue lining them. Membranous can then be divided into cochlear or vestibular labyrinths.

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14
Q

Labyrinthitis

A

Inflammation of membranous labyrinth, usually viral infection. Acute otomastoiditis can also spread directly to inner ear. Bacterial meningitis can cause bilateral labyrinthitis

Cochlea and semicircular canals will be enhancing

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15
Q

Facial nerve

A

Intracranial (cisternal)
Meatal (canalicular in IAC)
Labyrinthine (from IAC to geniculate ganglion)
Tympanic (from geniculate ganglion to pyramidal eminence)
Mastoid (from pyramidal eminence to stylomastoid foramen)
Extratemporal (SMF onwards)

NORMAL ENHANCEMENT
Tympanic and mastoid segments, sometimes labyrinthine

NO ENHANCEMENT
Cisternal, canalicular or extratemporal

ABNORMAL ENHANCEMENT
Bells Palsy (viral) in canalicular segment
Ramsay Hunt (reactivation zoster)
Think cancer if nodular enhancement

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16
Q

Otosclerosis/otospongiosis

A

Classic conductive hearing loss in adult female. Bone becomes more lytic

FENESTRAL
Bony resorption anterior to oval window at fissula antefenestrum. If not addressed, footplate will fuse to window.

RETROFENESTRAL
More severe form progressed to demineralization around cochlea. Usually has sensorineural component and is bilateral and symmetric nearly 100%

May treat with flouride. Later may need stapedectomy with implantation of prosthetic device, or a cochlear implant.

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17
Q

Superior semicircular canal dehiscence

A

Longstanding elevated ICP. Noise induce vertigo “Tullios phenomenon”.

See on CORONAL, absence of bony roof over superior semicircular canal.Goes through into middle cranial fossa

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18
Q

Large vestibular aqueduct syndrome

A

Vestibular aqueduct is a bony canal that connects inner ear to endolymphatic sac. Enlargement >1.5mm is aunt minnie. Progressive sensorineural hearing loss. Apparently failure of endolymphatic sac to resorb endolymph

Most common cause of congenital sensorineural hearing loss. Usually bilateral. Associated with cochlear deformity nearly 100%. Not born deaf, get progressive sensorineural hearing loss.

See AXIAL, should be same diameter as adjacent (lateral) posterior semicircular canal.

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19
Q

Congenital malformations of inner ear

A

Earlier things go wrong, more severe malformation.

MICHELS APLASIA
Earliest and most severe.
Complete labyrinthine aplasia (CLA). Absence of cochlea, vestibule and vestibular aqueduct. Completely deaf. Association with anencephaly and thalidomide exposure.

MONDINI MALFORMATION
Cochlear hypoplasia where basal turn is normal but middle and apical turns fuse into cystic apex. 1.5 turns instead of 2.5. Association with enlarged vestibule and enlarged vestibular aqueduct. Sensorineural hearing loss but high pitch is preserved.

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20
Q

Mondini vs Michels

A
MONDINI
Happens later, 7th week.
Preserved high frequency
Cochlea shows cystic apex
Vestibule enlarged
Vestibular aqueduct enlarged
Frequency common
MICHELS
Early, 3rd week.
Total deafness
Cochlea, vestibule and VA absent.
Very rare
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21
Q

Endolymphatic sac tumour

A

Rare. Most are sporadic, first think VHL.

Almost all have internal amorphous calcification. T2 bright and intensely enhance. Very vascular with flow voids and tumour blush on angiography.

Next to aperture of vestibular aqueduct.

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22
Q

Paraganglioma

A

Can invade occipital bone and adjacent petrous apex.

40% time hereditary and multiple.
Most common presenting symptom is hoarseness from vagal nerve compression.
Salt and pepper appearance. Enhance avidly.
FDG avid

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23
Q

Petrous apex anatomical variation

A

ASYMMETRIC MARROW
Typically contains fat. When asymmetric can trick into thinking there is a mass, or overlook a cholesteatoma. Use STIR or fat sat imaging.

CEPHALOCOELES
Herniation of CNS content through defect. In petrous apex this can be cystic expansion and herniation of posterolateral portion of Meckels cave into superomedial petros apex. Unilateral or bilateral (more common)

ABERRANT INTERNAL CAROTID
Pulsatile tinnatus. Cervical segment ICA has underdeveloped and middle ear collaterals develop (enlarged caroticotympanic artery). Runs through tympanic cavity and joins horizontal carotid canal. Vascular mass pulsating behind eardrum.

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24
Q

Petrous apex anatomical variation

A

APICAL PETROSITIS
Rare complication of infectious otomastoiditis. Can progress to osteomyelitis of skull base, vasospasm of ICA, subdural empyema, venous sinus thrombosis, temporal lobe stroke, and meningitis. Children it can be primary process, adults in setting of chronic otomastoiditis or recent mastoid surgery.

GRADENIGO SYNDROME
Complication of apical petrositis when Dorellos canal (CN6) is involved. Lateral rectus palsy. Dorellos canal is most medial point of petrous ridge between pontine cistern and cavernous sinus.
Otomastoiditis, trigeminal neuropathy and lateral rectus palsy

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25
Q

Petrous apex inflammatory lesions

A

CHOLESTEROL GRANULOMA
Most common primary petrous apex lesion. Obstruction of air cell with repeated cycles of haemorrhage and inflammation leading to expansion and bone remodelling. Symptom is hearing loss. CT margins sharply defined. T1 and T2 bright. T2 dark haemosiderin rim with faint peripheral enhancement.

CHOLESTEATOMA
Basically an epidermoid (ectopic epithelial tissue). Petrous apex ones are congenital. Slow growing and produce well smooth expansile bony change. T1 dark, T2 bright and restrict diffusion.

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26
Q

External ear

A

REGULAR AND NECROTIZING OTITIS EXTERNA
Usually bacterial of external auditory canal. Necrotizing/malignant form almost only in diabetics and is more aggressive. Swollen EAC soft tissues, bunch of small abscesses and adjacent bony destruction. Usually diabetics and infected with pseudomonas.

EXTERNAL AUDITORY CANAL EXOSTOSIS
‘Swimmers ear”. Overgrowth of soft tissue in ear canal, classically surfers with repeated bouts of ear infections. usually bilateral and when chronic looks like bone. These patients are immunocompetent and not diabetic,

EXTERNAL AUDITORY CANAL OSTEOMA
Overgrowth of normal bone. Usually incidental and unilateral occuring near junction of bone and cartilage in ear canal.

EXTERNAL AUDITORY CANAL ATRESIA
Developmental. External auditory canal doesnt form. May or may not be mashed up ossicular chain. Key is whether tissue covering the area normally open is soft tissue or bone (atretic plate). Also need to know if there is aberrant course of facial nerve.

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27
Q

Pagets

A

Can have osteolysis circumscripta which is well defined large radiolucent region favoring frontal and occipital bones. Both inner and outer table involved.

Pagets skull related complications:
Deafness
Cranial nerve paralysis
Basilar invagination to hydrocephalus to brainstem compression
Secondary osteosarcoma
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28
Q

Chordoma and Chondrosarcoma

A

Midline and off midline - discussed in MSK

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29
Q

Fibrous Dysplasia

A

Ground glass. Can look similiar to Pagets but FD is young <30 and Pagets older.

Fibrous dysplasia spares otic capsule classically
McCune Albright syndrome is multifocal FD, cafe au lait spots and precocious puberty
Outer table favoured

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30
Q

Sinus disease strategy

A

CT for anterior 2/3 orbit. MRI for posterior 1/3 and cavernous sinus.

CT useful for characterization of anatomical variation, MRI for tumour progression/extension/PNI/marrow involvement

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31
Q

Fungal sinusitis

A

ALLERGIC FUNGAL SINUSITIS
Opacification of multiple sinuses, usually bilateral favouring ethmoid/maxillary.
Normal immune system (asthma common)
CT hyperdense centrally or with layers. Can erode and remodel sinus walls when chronic.
MRI T1 and T2 dark, high protein and heavy metals. Can mimic aerated sinus. Inflammed enhancing mucosa.

ACUTE INVASIVE FUNGAL SINUSITIS
Opacificaiton of multiple sinuses.
Stranding/extension into fat around sinuses is key.
Immunocompromised. Apergillus or Zygomycetes
CT opacified sinus not hyperdense. Fat stranding in orbit, masticator fat, pre antral fat or PPF suggests invasion. Does not require bone destruction
MRIT1 and T2 dark, mucosa doesnt enhance. Extension of disease out of sinus will be bright on STIR and enhance

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32
Q

Chronic inflammatory sinonasal disease

A

Inflammation of paranasal sinuses lasting at least 12 weeks. Issue is primarily anatomical patency of sinus ostia

See p254 vol 2 yellow book

INFUNDIBULAR PATTERN
Most common. Disease limited to maxillary sinus and occurs from obstruction at ipsilateral ostium/infundibulum

OSTIOMEATAL UNIT PATTERN
Second most common. Centred at middle meatus with disease involving ipsilateral maxillary, frontal and ethmoid sinuses. Contributors are: hypertrophied turbinates, anatomic variants, concha bullosa, middle turbinates curling wrong way, septal deviation.

SINONASAL POLYPOSIS PATTERN
Combination of soft tissue nasal polyps and variable degrees of sinus opacification. Fluids levels can be present. Bony remodelling and erosion are key. Widening of infundibula. Need to differentiate between erosion/remodelling and expansion (mucocoele). Associations are CF and aspirin sensitivity.

MUCOCOELE
Obstructed sinus. May have had prior trauma. May have CF with secretions clogging things up. Mucus accumulates, sinus becomes completely filled and starts to expand. buzzword is expanded airless sinus. Frontal sinus most common. Periphery may enhance.

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33
Q

Antrochoanal polyp

A

Young adults 30-40. Presents with congestion/obstruction. Arises within maxillary sinuses and passes through and enlarges sinus ostium.

Buzzword widening of maxillary ostium. Smooth enlargement of the sinus with no bony destruction.Polyp will extend into nasopharynx. Monster inflammatory polyp

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34
Q

Juvenile Nasal Angiofibroma JNA

A

Male teenager with nose bleeds.

Centred in sphenopalatine foramen. Bony remodelling (not destruction). Very vascular and enhancing with intratumoral flow voids on MRI.
Presugical embolization common via internal maxillary and ascending pharyngeal artery.
Maxillary sinus in front smaller due to bony remodelling.

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35
Q

Inverted papilloma

A

Uncommon tumour. Lateral wall of nasal cavity most frequently related to middle turbinate. Impaired maxillary drainage expected.

Focal hyperostosis occurs at tumour origin. 10% harbour a squamous cell Ca.
Cerebriform pattern.

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36
Q

Enthesioneuroblastoma

A

Neuroblastoma of olfactory cells, starts at cribriform plate. Dumbbell appearance with growth up into skull and down into sinuses with a waist at the plate. Often cysts in mass. Bimodal age distribution.

Dumbbell shape
Intracranial posterior cyst classic
octreotide scan positive - neural crest origin

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37
Q

Squamous cell/SNUC (sinonasal undifferentiated carcinoma)

A

Squamous cell is most common tumour head and neck. Maxillary antrum is most common location. Highly cellular, low T2. Relative to other sinus masses it enhances less. SNUC is monster version of regular squamous cell.

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38
Q

Epistaxis

A

Usually idiopathic though can be iatrogenic. Could be in setting of HHT (hereditary haemorrhagic telangiectasia). also called osler weber rendu).

Anterior septal area (Kiesselbach plexus) is most common and can be compressed manually. Posterior ones are less common but bleed more. Main supply posterior nose is sphenopalatine artery (terminal internal maxillary artery) and tends to be first target. Watch out for variant anatomy between ECA and ophthalmic artery.

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39
Q

Nasal septal perforation

A

Typically involves anterior septal cartilagenous area.

Surgery (Killian submucous resection)
Cocaine use
Too much nose picking
Granulomatosis with polyangitis (Wegeners) which is renal masses, sinus mucosal thickening and nasal septal erosion and cavitatory lung nodules/fibrosis. cANCA positive.
Syphillis
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40
Q

Sialolithiasis

A

Stones in salivary duct, most commonly submandibular gland duct (Whartons). Can lead to infected gland “sialoadenitis” and chronic obstruction which can lead to fatty atrophy.

Submandibular - Whartons duct
Parotid - Stensons duct
Sublingual - Rivinus duct

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41
Q

Odontogenic infection

A

Can be dental or periodontal in origin. More common from an extracted tooth than an abscess involving an intact tooth.

Attachment of mylohyoid muscle to mylohyoid ridge dictates spread of infection to sublingual and submandibular spaces. Above mylohyoid line (anterior mandibular teeth) goes to sublingual space. Below mylohyoid line (posterior mandibular teeth) goes to submandibular space.

Odontogenic abscess is most common masticator space mass in adult.

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42
Q

Ludwigs angina

A

Aggressive cellulitis in floor of mouth, will be shown with gas in tissues. Most cases start with odontogenic infection

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43
Q

Torus palatinus

A

Normal variant. Bony exostosis arising from hard palate in midline.

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44
Q

Osteonecrosis of Mandible

A

Related to prior radiation or bisphophanate treatment.

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45
Q

Ranula

A

Mucous retention cyst, typically lateral. Arise from sublingual space and are termed plunging if under mylohyoid muscle

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46
Q

Thyroglossal duct cyst

A

Anywhere between foramen cecum and thyroid gland. Usually in midline. Thin walled cyst.

47
Q

Floor of mouth dermoid/epidermoid

A

Buzzword is ‘sack of marbles’ fluid sack with globules of fat. Typically midline

48
Q

Cancer in mouth

A

Squamous cell most common in mouth. think drinker/smoker. In young person think HPV, usually with large necrotic level 2 node.

49
Q

Periapical (radicular) cyst

A

Most common type. Result of inflammation of dental caries. Cystic degeneration around periodontal ligament.

Apex of non vital tooth.
Round with well corticated border.
Usually <2cm.

50
Q

Dentigerous (follicular) cyst

A

Cyst around crown of unerupted tooth. Developmental cyst. Displaces and absorbs adjacent teeth. Can displace tooth into condylar regions or into floor of orbit

51
Q

Keratogenic odontogenic tumour (odontogenic keratocyst)

A

Occur at mandibular ramus or body. Classic is multilocular.

Body/ramus
Grow along length of bone
No significant cortical expansion
May have daughter cysts
When multiple think Gorlin syndrome
52
Q

Ameloblastoma (adamantinoma of jaw)

A
Locally aggressive.
Multicystic with solid components and expansion of the mandible.
"soap bubbles"
Extensive tooth resorption.
Mandibular expansion
Solid component
5% arise from dentigerous cysts
53
Q

Odontoma

A

Start out lucent. Most common odontogenic tumour of mandible. Tooth hamartoma.
Radiodense with lucent rim.
Can be large with fluffy calcifications.

54
Q

Parotid space

A

Parotid gland
Portions of facial nerve
Retromandibular vein

Parotid gland only salivary gland to have lymph nodes

55
Q

Parotid space pathology

A

PLEOMORPHIC ADENOMA
Most common salivary gland tumour. Usually in parotid and usually in superficial lobe. T2 bright. Small malignant potential. Superficial vs deep lobe is important for surgical approach. Benign mixed tumour.

WARTHINS
Second most common benign tumour. ONLY occurs in parotid. Cystic, male smoker, bilateral (15%). Takes up pertechnate.

MUCOEPIDERMOID CARCINOMA
Most common malignant tumour of minor salivary glands. Smaller the gland, more common the malignant tumour. Association with radiation

ADENOID CYSTIC CARCINOMA
Malignant salivary gland tumour that favours small but can be in large glands. Perineural spread.

56
Q

Parotid space pathology continued

A

LYMPHOMA
Parotid is only salivary gland with lymph nodes, therefore can get lymphoma. If bilateral, think Sjogrens. Bilateral homogenous masses.

SJOGRENS
Autoimmune lymphocyte induced destruction of gland. Dry eyes and dry mouth. Typically women in 60s. Raised risk of Non-Hodgkins MALT lymphoma. Honeycombed appearance to gland

BENIGN LYMPHOEPITHELIAL DISEASE
Bilateral mixed solid and cystic lesions with diffusely enlarged parotids. Seen in HIV. Painless

ACUTE PAROTITIS
Obstruction of flow of secretions most common. Stone in Stensens duct which will be dilated. Stones are calcium phosphate. Post infectious parotitis usually bacterial. Mumps most common viral.

57
Q

Parapharyngeal space

A

Mostly just fat with some branches of trigeminal nerve and pterygoid veins

Primary utility is when its displaced. Mets and infection can spread through in vertical direction (squamous from tonsils, tongue and larynx). Cystic mass could be branchial cleft cyst but more likely necrotic level 2 lymph node.

Posterior is carotid space
Lateral is parotid space
Superficial mucosal space is medial

58
Q

Carotid space

A

Carotid artery
Jugular vein
Portions of CN9, 10 and 11
Internal jugular chain LNs

paragangliomas, schwannomas, neurofibromas, secondary spread of aggressive multispatial disease or malignant spread.

59
Q

Paragangliomas

A

Hypervascular (intense tumour blush).
Salt and pepper on MRI - flow voids
Can be multiple and bilateral in familial conditions
In-Octreotide accumulates in these tumours

CAROTID BODY TUMOUR
Splaying ICA and ECA at carotid bifurcation

GLOMUS JUGULARE
Skull base often with destruction of jugular foramen.

GLOMUS VAGALE
Above carotid bifurcation but below jugular foramen.

GLOMUS TYMPANICUM
Confined to middle ear overlying cochlear promontory.

60
Q

Schwannoma

A

Most commonly vagal nerve CN10 but if lesion is high up near skull base it could be involving 9, 11 or 12. Oval mass with heterogenous bright T2.

Enhance a lot. NF2 association

61
Q

Neurofibroma

A

Less common than schwannoma. 10% of time related to NF1 in which case they may be multiple and bilateral.

62
Q

Neck infection syndromes

A

LEMIERRES SYNDROME
Thrombophlebitis of jugular veins with septic emboli in lung. In setting of oropharyngeal infection or recent ENT surgery. Fusobacterium necrophorum

GRISELS SYNDROME
Torticollis with atlantoaxial joint inflammation seen in ENT surgery or retropharyngeal abscess

63
Q

Masticator space

A

Muscles of mastication (masticator, temporalis, medial and lateral pterygoids)
Ramus of mandible and inferior alveolar nerve.
Extends superiorly along side of skull via temporalis muscle so infection can go right up there.

64
Q

Masticator space pathology

A

ODONTOGENIC INFECTION
Most common cause of masticator space mass. Look at mandible on bone windows. Look out for spread via pterygopalatine fossa to orbital apex and cavernous sinus

SARCOMAS
Rhabdomyosarcomas in kids. Can get sarcoma from mandible or chondrosarcoma which favors the TMJ.

CAVERNOUS HEMANGIOMA
Given away by presence of phleboliths. Venous or lymphatic malformations may involve multiple compartments/spaces. Congenital/aggressive infection/cancer tend to be multispatial

PERINEURAL SPREAD
Can have spread along V3 of trigeminal. Should think either adenoid cystic or melanoma.

NERVE SHEATH TUMOUR
Can have schwannoma or neurofibroma of V3.

65
Q

Retropharyngeal and Danger spaces

A

Midline space deep to oro and nasopharynx. Retropharyngeal space is anterior and true space which extends to C6/7. Posterior danger space extends to mediastinum. The two are separated by alar fascia.

Behind both is the prevetebral space where thinks like discitis/osteomyelitis go

66
Q

Retropharyngeal and Danger spaces

A

INFECTION
Usually spread from tonsillar tissue. Central low density tissue and stranding in the space. Evaluate for spread into mediastinum. Delays critical to distinguish phlegmon from abscess.

NECROTIC NODES
Nodes of Rouviere. Located in lateral retropharyngeal region. Kids get suppurative infection in these but start to regress around age 4 with adults much less likely to get infection here. Can get mets or lymphoma here

67
Q

Lymph node anatomy

A

Anterior belly digastric separates 1A from 1B.
Stylohyoid muscle separates 1B from 2A
Jugular vein separates 2A from 2B

VERTICAL BORDERS
2-3 is lower hyoid
3-4 lower cricoid
5A-5B lower cricoid, both posterior to SCM
6 is anterior and inferior to lower border cricoid
7 is upper mediastinal

68
Q

Floor of mouth SCC

A

Smoker/drinker in old person, HPV in young person.

Necrotic level 2 nodes.

69
Q

Nasopharyngeal SCC

A

Fossa of Rosenmuller is most common location
More common in Asians
Bimodal distribution (15-30 and >40)
Involvement of the parapharyngeal space results in worse prognosis

Unilateral mastoid effusion or pathological retropharyngeal LN check Fossa of Rosunmuller

Pathological retropharyngeal LN or supraclavicular LN chek clivus as 30% patients with nasopharyngeal tumours may have skull base erosion

70
Q

Laryngocoele

A

When laryngeal saccule dilates with air you call it a laryngocoele. If filled with fluid it may still be laryngocoele but can now call it a saccular cyst. Saccule is appendix of laryngeal ventricle. Typically closed and not seen in adults.

Can dilate if obstructed (ball valve mechanics) and testable point is 15% time obstruction is a tumour. Can see in forceful blowers like trumptet players and glass blowers.

Internal and external version based on containment of violation of thyrohyoid membrane

71
Q

Vocal cord paralysis

A

involved side will have expanded ventricle. If seen on left, look into chest for recurrent laryngeal nerve compression at AP window. Hoarseness is buzzword.

72
Q

Laryngeal cancer

A

85% squamous cell.

RISK FACTORS
Smoking, alcohol, radiation, laryngeal keratosis, HPV, GORD.

SUPRAGLOTTIC
More aggressive, early LN mets, dont get hoarseness.
Epiglottic centered - anterior, likes to invade pre-epiglottic space/fat
False cord centered - posterolateral, likes to invade paraglottic space
Aryepiglottic fold mass

GLOTTIC
Most common, best outcome, grows slowly, late metastatic disease.
Usually involve anterior cord and spread to anterior commisure
Progressive and continuous hoarseness

SUBGLOTTIC
Least common, often small compared to nodal burden. Bilateral nodal disease and mediastinal extension.

73
Q

Retinoblastoma

A

Most common primary malignancy of globe. Calcification in globe of child.

RB suppressor gene c13. Same chromosome osteosarcoma patients get so at risk of these after radiation.

Globe should be normal in size or slightly bigger (Coats disease its smaller). Usually seen before age 3.

Bilateral both eyes
Trilateral both eyes and pineal gland
Quadrilateral both eyes, pineal gland and suprasellar

74
Q

Coats disease

A

Retinal telengiectasia resulting in leaky blood and subretinal exudate. Can lead to retinal detachment. Young boys, typically unilateral. NOT CALCIFIED

75
Q

Persistent Hyperplastic Primary Vitreous (PHPV)

A

Failure of embryonic occular blood supply to regress. Can lead to retinal detachment. Small eye (microphthalmia) with increased density of vitreous. No calcification

76
Q

Retinal detachment

A

Can be secondary to PHPV or Coats. Can also be just from trauma, sickle cell or old age. See V or Y shape due to uplifted retinal leaves.

77
Q

Globe size comparison

A
Retinoblastoma - normal
Toxocariasis - normal
PHPV - small size (normal birth age)
Coats - small
Retinopathy of prematurity - bilaterally small
78
Q

Melonoma

A

Most common intra-occular lesion in an adult. Enhancing soft tissue mass in back of an adults eye. “collar button shaped”. Strong predilection for liver mets.

79
Q

Optic nerve glioma

A

90% under age 20. Expansion/enlargement of entire nerve. If bilateral think NF1. Usually pilocytic astrocytoma WHO1

80
Q

Optic nerve sheath meningioma

A

Tram track calcifications. Doughnut appearance on coronal. Circumferential enhancement around nerve

81
Q

Dermoid

A

Most common benign congenital orbital mass. Superior and lateral usually, arising from frontozygomatic suture and presenting <10yo. Has fat in it

82
Q

Rhabdomyosarcoma

A

Most common extraoccular malignancy in children.Superior medial orbit and classicaly has bone destruction. Bulky orbital mass in a 7 year old. Rare

83
Q

Lymphoma

A

Association with chlamydia psittaci (bird fever). and MALT lymphoma of orbit. usually involves upper outer orbit closely associated with lacrimal gland. Enhance homogenously and restrict diffusion.

84
Q

Metastatic neuroblastoma

A

Raccoon eyes o/e. Periorbital tumour infiltration with proptosis. Bony involvement of greater wing of sphenoid. Usually bilateral.

85
Q

Metastatic scirrhous breast cancer

A

Breast cancer met has desmoplastic reaction and enophthalmos

86
Q

IgG4 in orbit

A

ORBITAL PSEUDOTUMOUR
Idiopathic inflammatory conditions involving extraoccular muscles. Looks like expanded muscle. Painful and unilateral, most commonly involves lateral rectus and does not spare myotendinous junctions. Give steroids

TOLOSA HUNT
Same thing as orbital pseudotumour but in cavernous sinus. Painful and presents with multiple cranial nerve palsies. Give steroids.

LYMPHOCYTIC HYPOPHYSITIS
Same as above but in pituitary. Enlarged pituitary stalk in postpartum/3rd trimester woman.

87
Q

Thyroid orbitopathy

A

Seen in 1/4 of graves disease, most common cause of exophthalmos. Antibodies hat activate TSH receptors also activate orbital fibroblasts and adipocytes.

Risk of compressive optic neuropathy. Enlargement of only muscle belly (spares tendon). NOT painful. Order of involvement IMSLO

88
Q

Orbital vascular malformations

A

LYMPHANGIOMA
Mix of venous and lymphatic malformations. Ill defined, lack a capsule. Multispatial and infiltrative. Preseptal, postseptal, extraconal and intraconal.
Fluid-Fluid levels. Do NOT distend with provocative maneuvers.

VARIX
Secondary to weakness in post capillary venous wall. Massive dilatation of valveless orbital vein. Disetent with provocative maneuvers. Most common cause of spontaneous orbital haemorrhage. Can thrombose and present with pain

CCAROTID CAVERNOUS FISTULA
Direct is from trauma and indirect occurs randomly in postmenopausal women.
Direct is a communication between intracavernous ICA and cavernous sinus. Indirect kind usually dural shunt between meningeal branches of ECA and cavernous sinus.
Pulsatile exophthalmos (this can also be for NF1 with sphenoid wing dysplasia though)
89
Q

Pre-septal/post-septal cellulitis

A

Orbital cellulitis is post septal
Periorbital cellulitis is preseptal

Orbital septum originates from periosteum of the orbit and inserts in the palpebral tissue along tarsal plate. Preseptal infections start in adjacent structures. Post septal infections usually from paranasal sinusitis. preseptal infections treated medically, post septal is surgical

Periorbital abscess can cause thrombosis of ophthalmic veins or cavernous sinus. In extreme cases, usualy aspergillosus, can cause carotid/cavernous fistula

90
Q

Dacrocystitis

A

Inflammation and dilatation of lacrimal sac. Well circumscribed round rim enhancing lesion centered in lacrimal fossa. Typically from obstruction followed by bacterial infection (staph or strep). Usually diagnosed clinically unless there is an associated periorbital cellulitis in which case CT needed to exclude postseptal infection from simple dacrocystitis.

91
Q

Orbital subperiosteal abscess.

A

Inflammation under periosteum which can progress to abscess formation. Usually associated with ethmoid sinusitis. Classic look.

92
Q

Optic neuritis

A

Will be enhancement of the optic nerve without enlargement of the nerve/sheath complex. Usually 70% unilateral and painful. Often see intracrnial or spinal cord demyelination in setting of Devics (neuomyelitis optica). 50% patients with acute optic neuritis will develop MS

93
Q

Papilledema

A

Can see dilatation/swelling of optic nerve sheath.

DRUSEN
Mineralization at optic disc. Association with age related maculopathy.

INTRAOCULAR LENS IMPLANT
Standard treatment for cataracts. Replaced lens has thin linear appearance.

ECTOPIA LENTIS (LENS DISLOCATION)
Causes include trauma, marfans and homocystenuria
94
Q

Coloboma

A

Focal discontinuity of globe (failure of choroid fissure to close). Usually posterior. If you see bilateral ones, think CHARGE syndrome

95
Q

Odontoid fracture classification

A

TYPE 1
Rare, upper part of odontoid as result of avulsion of alar ligament. May be stable

TYPE 2
Fracture at base. High non-union rate. Unstable

TYPE 3
Fracture through dens into the body of C2. Unstable

96
Q

Jefferson fracture

A

Axial loading injury. Anterior and posterior arches blow out laterally. 30% will also have a C2 fracture. Cord damage rare as all force directed into bones. Open mouth view will show slipping of lateral masses.

97
Q

Os odontoideum/Os terminale

A

These variants can mimc a type 1 dens fracture. Ossicle located at the position of the odontoid tip. With os odontoideum, base of dens is hypoplastic.

Prone to sublaxation and instability. Associate with Morquios syndrome. Orthotopic position atop dens. Dystopic when fused to clivus.

98
Q

Hangmans fracture

A

Seen usually when chin hits dashboard in MVA (direct blow to face). Fracture through bilateral pars at C2. ANterior subluxation of C2 on C3. Cord damage uncommon as acquired aprs defect allows for canal widening. Associated fracture at anterior/inferior corner of C2 from avulsion of ALL.

99
Q

Teardrop flexion vs extension

A
FLEXION
Teardrop shaped fracture fragment at inferior/anterior vertebral body. Bad as 85% will have anterior cord syndrome associated. Unstable fracture associated with posterior subluxtion of vertebral body
Impaction injury
Extremely unstable
hyperflexion
"ran into wall"

EXTENSION
Anterior inferior teardrop shaped fragment with avulsion of ALL. Less serious
Distraction injury
Stable in flexion (unstable in extension)
Hyperextension
“hit from behind”

100
Q

Clay shovellers fracture

A

Avulsion injury of lower cervical/upper thoracic spinous process (usually C7). Forceful hyperflexion.

101
Q

Chance fracture

A

Flexion distraction fractures classically associated with lap band seatbelt. These are3 column unstable fractures. Usually at upper lumbar and thoracolumbar junction. High association with solid organ trauma

102
Q

Facet dislocation

A

Spectrum: subluxed - perched - locked

UNILATERAL
Usually from hyperflexion and rotation. Superior facet slides over inferior facet and gets locked. Unilateral is stable injury. Inverted hamburger sign on axial.

BILATERAL
Severe hyperflexion. Disruption of PLL. Dislocated vertebra displaced forward half AP diameter. Highly unstable and strongly associated with cord injury

103
Q

Atlantoaxial instability

A

Transverse cruciform ligament straps dens to anterior arch of C1. Distance between anterior arch and dens shouldnt be >5mm. Association with Downs and JRA

Rotatory subluxation can occur in kids without fracture stuck in cock robin position. Looks like torticollis. Cannot happen in absence of fracture in adult.

104
Q

Pars Interarticularis defects

A

Spondylolysis or adult isthmic spondylolisthesis.
Caused by repetitive microtrauma related to hyperextension. Nearly always at L5/S1 90%. Typically pain is L5 radiculopathy caused by foraminal stenosis at L5S1.

105
Q

Occipitocervical instability

A

Can be traumatic or congenital (seen in Downs). two popular methods for evaluating this, Powers ration and Harris Lines rule of 12.

106
Q

Denis 3 spinal column concept

A

Vertebral column divided into 3 vertical parallel columns. Instability suggested when all 3 or 2 contiguous columns are disrupted.

Anterior column: ALL, ant 2/3 body
Middle column: post 1/3 body and PLL
Posterior column: posterior ligaments, pedicles, factes, lamina, spinous processes

107
Q

Canadian C spine rules

A
Age >65
Parasthesias in extremities
Dangerous mechanism
Fall >3ft or 5 stairs
Axial load to head
High speed MVA
Pedestrian vs car
108
Q

Nexus criteria

A
Focal neurological deficit
Midline spinal tenderness
Altered level of consciousness
Intoxication
Distracting injury
109
Q

Unstable

A
Vertebral overriding >3mm
Angulation >11 degrees
Flexion tear drop
Bilateral locked facets
Odontoid fracture types 2 and 3
Two contiguous column fractures or 3 column
Jeffersons
Hangmans
Atlanto-occipital and atlantoaxial dislocations
110
Q

Stable

A
Extension tear drop in flexion
Unilateral locked facet
Odontoid fracture type 1
Single column vertebral fracture
Clay shovelers
Transverse process fracture
111
Q

Spinal cord syndromes

A

CENTRAL CORD
Old lady with spondylosis or young person with bad extension injury
Upper extremity deficit worse than lower

ANTERIOR CORD
Flexion injury. Immediate paralysis. Anterior cord damaged. Motor function and anterior column sensation (pain and temperature) gone. Dorsal column (vibration and proprioception) still intact.

BROWN SEQUARD
Rotation injury or penetrating trauma
One side motor, other side sensory deficits

POSTERIOR CORD
Uncommon but can be seen in hyperextension.
Proprioception gone

112
Q

AVFs/AVMs

A

TYPE 1
By far most common 85%. Dural AVF
Resukt of fistula between dorsal radiculomedullary arteries and radiculomedullary vein/coronal sinus with the dural nerve sleeve. Acquired and seen in old patients with progressive radiculomyopathy. Most common location thoracic spine. Gold standard is angiography. Swollen cord with high T2 signalin central cord with serpentine perimedullary flow voids

TYPE 2
Intramedullary nidus from ant spinal artery or post spinal artery. Can have aneurysms and can bleed. Mos common rpesentation SAH. Associated with HHT and KTS

TYPE 3
Juvenile, very rare, complex, bad prognosis

TYPE 4
Intradural perimedullary with subtypes depending on arterial supply. Near conus

113
Q

Foix Alajouanine syndrome

A

Congestive mylopathy associated with dural AVF. 45m with lwoer extremity weakness and sensory deficits. Increased T2 signal conus or lower T spine with associated prominent vessels. Venous HTN due to vascular malformation