ENT Flashcards

1
Q

CN I: Olfactory nerve

A

Nerve type: sensory

Function: smell

exits skull via cribriform plate

palsy most commonly due to trauma to lateral/occipital regions, intracranial space occupying lesions

clinical features: anosmia

testing: identifying certain smells e.g. mint

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2
Q

CN II: Optic nerve

A

Nerve type: sensory

Function:
vision & afferent leg of pupillary light reflex

exits skull via optic canal

Causes of palsy: infection, tumours, ischaemic optic neuropathy, inflammation (MS), drugs (e.g. amiodarone, ethambutol)

clinical features:
impaired vision, ipsilateral blindness & absent direct pupillary light reflex

testing: visual fields, visual acuity, fundoscopy

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3
Q

CN III: Oculomotor nerve

A

Nerve type: somatic & parasympathetic motor

Function:

  • eye movements (superior rectus (elevation/intorsion/adduction), inferior rectus (depression/extorsion),medial rectus (adduction), inferior oblique (extorsion/elevation/abduction)
  • eyelid opening, pupillary constriction (efferent limb of pupillary light reflex), accommodation

exits skull via superior orbital fissure

Causes of palsy: strokes, MS, myasthenia gravis, aneurysms

clinical features:
down & out gaze, ptosis, weak adduction, horizontal diplopia, absent pupillary light reflex (both direct & indirect)

testing: ocular/extraoccular movements, pupillary response

NB parasympathetic fibres are on the outside so compression causes pupillary dilation before motor dysfunction

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4
Q

CN IV: Abducens nerve

A

Nerve type: motor

Function: 
eye movements (superior oblique (intorsion, depression, abduction))

exits skull via SOF

Causes of palsy: cavernous sinus thrombosis, microvascular damage

clinical features:
extortion of eye (inability to depress & adduct simultaneously) & diplopia (exacerbated on downward age e.g. going down stairs, reading)

testing: eye movements

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5
Q

CN V: Trigeminal nerve

A

Nerve type: sensory (V1/V2/V3) & motor (V3)

Function: 
facial sensation (V1 = ophthalmic, V2 = maxillary, V3 = mandibular), afferent limb of corneal reflex & jaw jerk reflex, muscle of mastication (V3)

exits skull via SOF (V1), foramen rotundum (V2), foramen ovale (V3)

Causes of palsy: cavernous sinus thrombosis, vascular compression

clinical features:
V1 = absent corneal reflex, loss of sensation to ipsilateral forehead
V2 = loss of sensation to ipsilateral midface
V3 = anaesthesia of lower 1/3 of face, anterior 2/3 of tongue, paresis of ipsilateral muscles of mastication & diminished jaw jerk reflex

testing: facial sensation, corneal reflex, jaw jerk, muscle of mastication

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6
Q

CN VI: Trochlear nerve

A

Nerve type: motor

Function: 
eye movements (lateral rectus = abduction)

exits skull via SOF

Causes of palsy: cavernous sinus thrombosis, diabetic neuropathy

clinical features:
horizontal diplopia worse when looking at far objects, esotropia (medial deviation of eye on neutral gaze), inability to abduct eye

testing: eye movements

NB most common ocular nerve plays

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7
Q

CN VII: Facial nerve

A

Nerve type: sensory, somatic & parasympathetic motor

Function:
taste (anterior 2/3 of tongue), sensation to tympanic membrane
muscles of facial expression, efferent limb of corneal reflex
salivation & lacrimation (submandibular/sublingual/lacrimal glands)

exits skull via internal acoustic meatus

clinical features:
flaccid paralysis of face, loss of taste, hyperacusis, loss of corneal reflex

testing: facial expression

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8
Q

CN VIII: Vestibulocochlear nerve

A

Nerve type: sensory

Function:
balance & equilibrium (vestibular)
hearing (cochlear)

exits skull via internal acoustic meatus

Causes of palsy:bacterial meningitis, lyme disease, acoustic neuroma, neurofibromatosis 2, basilar skull fracture

clinical features:
sensorineural hearing loss, vertigo, motion sickness, horizontal nystagmus

testing: audiometry (hearing test, Weber’s & Rhinnes)

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9
Q

CN IX: Glossopharyngeal nerve

A

Nerve type: sensory & somatic/parasympathetic motor

Function:
taste (posterior 1/3 of tongue), afferent limb of gag reflex
carotid sinus/body (chemo & baroreceptors)
swallowing, innervates stylopharyngeus
salivation (parotid gland), sensation to posterior 1/3 of tongue/soft palate/upper pharynx

exits skull via jugular foramen

clinical features:
absent gag reflex, loss of carotid sinus reflex, sensory loss of back of mouth & upper throat, mild dysphagia

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10
Q

CN X: Vagus nerve

A

Nerve type: somatic/visceral sensory & somatic/parasympathetic motor

Function:
sensation (supraglottic region, larynx, trachea), couch reflex , efferent limb of gag reflex, swallowing (pharyngeal muscles) speech (laryngeal muscles via recurrent laryngeal nerve), SA & AV node innervation

exits skull via jugular foramen

Causes of palsy: trauma, diabetes inflammation

clinical features:
flaccid paralysis & ipsilateral lowing of soft palate, dysphagia, loss of gaga & cough reflex, uvuala deviation away from lesion, dysphonia (unilateral recurrent laryngeal) or aphonia (bilateral)

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11
Q

CN XI: Accessory nerve

A

Nerve type: motor

Function: head turn via sternocleidomastoid, shoulder elevation via trapezius

exits skull via jugular foramen

clinical features:
paresis, atrophy, asymmetry of sternocleidomastoid & trapezius, ipsilateral shoulder drooping & lateral winging of scapula

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12
Q

CN XII: Hypoglossal nerve

A

Nerve type: motor

Function: tongue protrusion (intrinsic & extrinsic muscled of tongue)

exits skull via hypoglossal canal

clinical features:
fasciculations & atrophy of tongue, tongue deviated towards lesion

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13
Q

Tonsillitis

A

an infection of the parenchyma of the palatine tonsils, frequently occurring i combination with inflammation of the pharynx = tonsilopharyngitis

common in children & young adults

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14
Q

Aetiology of tonsillitis

A

Viral (50-80%)
adenovirus, EBV, CMV,

Bacterial (15-30%)
strep progenes (Group A strep)

NB viral = cough, bacterial = no cough

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15
Q

Presentation of tonsillitis

A
pain in throat/sore throat
dysphagia
fever
lymphadenopathy
headache
tonsillar exudates
tonsillar erythema
tonsillar enlargement
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16
Q

Investigations for tonsillitis

A

throat culture

rapid streptococcal antigen test

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17
Q

Management of tonsillitis

A

Viral:
self limiting, supportive (antipyretics, analgesia)

Bacterial:
if confirmed on swab/antigen test or CENTOR score >3
5-10 day course of phenoxymethylpenicillin (erythromycin/clarithromycin if penicillin allergy)

Surgical:
tonsillectomy, if recurrent (≥5x in previous year) / chronic episodes

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18
Q

CENTOR criteria

A

The Centor criteria are: score 1 point for each

  • presence of tonsillar exudate
  • tender anterior cervical lymphadenopathy/lymphadenitis
  • history of fever
  • absence of cough
  • age (<15 yrs = +1 point, >44 yrs = -1 point)

Abx indicated if CENTOR score >3

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19
Q

Peritonsillar abscess (Quinsy)

A

ENT emergency

usually in bacterial tonsillitis, seen in young adults & adolescents

presentation includes features of tonsillitis, drooling, severe throat pain, trismus, halitosis, ‘hot potato’ voice, contralateral uvula devotion, ↓ neck mobility

management:
1st line: needle aspiration or incision & drainage + Abx
2nd line: tonsillectomy, considered 6 weeks after

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20
Q

Acute otitis media (AOM)

A

a painful infection of the middle ear, generally secondary to a viral URTI as a bacterial superinfection e.g. due to strep pneumonia/H. influenzae/moraxella catarrhalis

very common in children (~80% experience AOM by age 3)

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21
Q

Presentation of Acute otitis media (AOM)

A

throbbing otalgia/earache
young children may be irritable & repeatedly touching/tugging at ear
hearing loss in affected ear
fever
otrohoea (if tympanic membrane perforated)

preceding URTI (coryza, rhinorrhoae etc)

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22
Q

Investigations of Acute otitis media (AOM)

A

Otoscopy (bulging tympanic membrane, opacification/erythema of tympanic membrane, visible perforation, purulent discharge from ear canal)

Weber’s/Rhinne’s test (conductive hearing loss)

consider culturing discharge

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23
Q

Management of Acute otitis media (AOM)

A

generally self limiting (~80%)
=pain relief & observation

Abx
1st line: amoxicillin (erythromycin if penicillin allergy)

indications for Abx
if >4 days of symptoms/no improvement, systemically unwell, bilateral AOM in <2y/o, perforation/discharge, immunocompromise

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24
Q

Indications for giving Abx in Acute otitis media (AOM)

A

Symptoms lasting more than 4 days or not improving
Systemically unwell but not requiring admission
Immunocompromise or high risk of complications secondary to significant heart, lung, kidney, liver, or neuromuscular disease
Younger than 2 years with bilateral otitis media
Otitis media with perforation and/or discharge in the canal

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25
Otitis media with effusion (OME) or glue ear
chronic mucoid/serous effusion in the tympanic cavity in the absence of infection lasting >3 months, though to be due to eustachian tube dysfunction causing fluid to accumulate most common cause of hearing impairment in childhood, where it usually follow and episode of AOM usually seen age 1-6 yrs
26
Risk factors for Otitis media with effusion (OME)
craniofacial malformations e.g. cleft palate Down's syndrome allergic rhinitis impaired ciliary motility e.g. cystic fibrosis
27
Presentation of Otitis media with effusion (OME)
hearing loss* presents as mishearing, difficulty communicating in a group, needing thing to be repeated, excessively high TV volume painless sensation of pressure school progress may be impaired easily missed in young children
28
Otitis media with effusion (OME) in adults
acute unilateral presentation in adults should trigger thoughts of nasopharyngeal carcinoma
29
Investigating Otitis media with effusion (OME)
hearing test (mild conductive hearing loss i.e. ↓20-40 dB)
30
Otitis media with effusion (OME) management
generally self limiting 1st line: active observation 2nd line surgery e.g. tympanovstomy tubes (grommets) indications for surgery: bilateral OME ≥3 months, hearing loss >30dB, developmental/educational difficulties
31
Chronic suppurative otitis media (CSOM)
chronic inflammation of the middle ear & mastoid cavity with persistent drainage from the middle ear through a perforated tympanic membrane lasting >6-12 weeks generally caused by bacterial infection following perforated tympanic membrane e.g. due to recurrent AOM, trauma, tympanostomy most common seen in those <15 y/o
32
Presentation of Chronic suppurative otitis media (CSOM)
``` painless recurrent otorrhoea conductive hearing loss no pain no fever perforated tympanic membrane on otoscopy ```
33
Complications of Chronic suppurative otitis media (CSOM)
cholesteatoma (keratinising epithelium growing into middle ear) hearing loss may improve but may not fully recover
34
Management of Chronic suppurative otitis media (CSOM)
specialist (ENT) referral topical Abx rinsing/cleaning of ear topical steroids
35
Infective labyrinthitis
inflammation/infection of the inner ear frequently secondary to AOM, where it spreads through the road window presents with severe vertigo, nausea, sensorineural hearing loss, nystagmus towards healthy ear management with IV Abx, tympanostomy, glucocorticoids
36
Otitis externa
acute otitis external (AOE) is a diffuse inflammation of the external ear canal which may involve the pinna or tympanic membrane, also known as swimmers ear
37
Aetiology of otitis externa
most common bacterial infection e.g staph aureus, pseudomonas aeruginosa fungal is less common, but usually aspergillum non infectious e.g. seborrhoeic dermatitis or contact dermatitis
38
Risk factors for otitis externa
``` hot/humid climates swimming local trauma diabetes external auditory canal obstruction ```
39
Presentation of otitis externa
``` intense itching of external ear canal ear pain tender tragus ear canal swelling & erythema otorrhoea aural fullness conductive hearing loss ```
40
Management of otitis externa
1st line: topical Abx e.g. neomycin ± steroids 2nd line: ENT referral + systemic flucloxacillin + swab for culture
41
Perichondritis
infection of the tissue covering the cartilage of the pinna, usually after trauma e.g. piercing
42
Malignant otits externa (necrotising otitis externa)
a necrotising inflammation of the external ear canal, i.e. an infection extending into the bony ear canal & deep soft tissue 95% of cases are due to pseudomonas aeruginosa risk factors include poorly controlled diabetes, immunosuppression, elderly
43
Malignant otits externa (necrotising otitis externa)
a necrotising inflammation of the external ear canal, i.e. an infection extending into the bony ear canal & deep soft tissue 95% of cases are due to pseudomonas aeruginosa risk factors include poorly controlled diabetes, immunosuppression, elderly
44
Malignant otitis externa presentation
typically elderly pt with poorly controlled diabetes severe ear pain, erythematous/swollen periauricular soft tissue, otorrhoea, may have facial nerve palsy
45
Complication of Malignant otitis externa
osteomyelitis of the skull base, which may cause intracranial expansion of the infection
46
Investigations for Malignant otitis externa
CT/MRI (identify bone destruction & intracranial expansion e.g. cranial abscess or venous sinus thrombosis) biopsy (to distinguish from a tumour)
47
Treatment of Malignant otitis externa
IV Abx e.g. ciprofloxacin high mortality even with treatment
48
Epistaxis
Nosebleeds types: Anterior (~90%), bleeding usually from Kiesselbach plexus located on anterioinferioir nasal septum (Little's area) and anastomoses of the anterior ethmoidal/sphenopalatine/greater palatine/superioir labial arteries Posterior (~10%), more dangerous, generally seen in older individuals, ↑ risk of airway compromise & aspiration, usually bleeding from both nostrils & blood running own throat
49
Causes of epistaxis
``` trauma including picking nose vascular malformations nasal septum defect (e.g. deviated septum) tumours bleeding disorders ```
50
Management of epistaxis
1) ABCDE assessment 2) sit upright with torso forward, squeeze cartilaginous part of nose for 20 minutes ``` 3) Cautery with silver nitrate = 1st line if source of bleeding is visible use packing (nasal tampons, rapid rhino) if cautery not tolerated or source of bleeding not visible ``` 4) if persistent epistaxis then artery embolisation/ligation
51
Sinusitis
inflammation of the mucous membranes of the paranasal sinuses, rarely occurring without concurrent inflammation of the nasal mucous (rhinitis) = rhinosinusitis
52
Type of sinusitis
Acute <4 weeks subacute 4-12 weeks chronic > 12 weeks
53
Aetiology of sinusitis
viral: very common e.g. rhinovirus, influenza, parainfluenza, adenovirus bacterial: strep pneumonia, H. Influenzae
54
Risk factors for sinusitis
URTI smoking nasal obstruction e.g. septal deviation or nasal polyps nasal foreign body
55
Presentation of sinusitis
``` facial pain (frontal pressure pain, worse on bending forward) nasal discharge (thick & purulent) nasal obstruction ```
56
Management of sinusitis
intranasal decongestants/nasal saline intranasal corticosteroids (>10 days of symptoms) if severe = oral Abx if chronic consider intranasal saline washout
57
complications of sinusitis
``` preseptal/orbital cellulitis orbital abscess cavernous sinus thrombosis brain abscess subdural abscess (most common) osteomyelitis (especially of frontal bone = Pott's puffy tumour) ```
58
Rhinitis
inflammation & swelling of the nasal mucous membranes can be allergic or non allergic
59
allergic rhinitis
acute/chronic rhinitis due to inhaled allergens causing a type I hypersensitivity reaction (IgE mediated), may be seasonal, occupational or perennial (throughout year) most common form of rhinitis presents with sneezing, bilateral nasal congestion, clear nasal discharge, post nasal drip, nasal pruritis managed with allergen avoidance, oral/intranasal antihistamines, short course of decongestants e.g. oxyetazoline
60
Complications of intranasal decongestant use
prolonged use leads to tolerance meaning ↑ doses are needed to achieve the same affect & may cause rebound hypertrophy of the nasal mucosa when withdrawn
61
types of non allergic rhinitis
rhinitis medicamentosum: rebound nasal congestion when discontinuing nasal decongestant, pts often use ↑dose/frequency to treat leading to vicious cycle atrophic rhinitis: chronic rhinitis associated with atrophy & sclerosis of the nasal mucosa drug induced rhinitis: e.g. snorting cocaine or ketamine
62
Epiglottitis
progressive inflammation of the epiglottis & supra glottis with the potential to cause airway compromise caused by haemophilia infleuzae type B (Hib), has become rare since Hib vaccination usually seen ages 2-5 yrs
63
Presentation of epiglottitis
acute onset high fever, sore throat, dysphagia, odynophagia tripod position, stridor, respiratory distress muffled ('hot potato' voice) drooling
64
Investigating epiglottitis
direct visualisation via laryngoscopy (must be airway trained/senior doctor) lateral neck X-ray (thumb sign)
65
Management of epiglottitis
immediate senior & airway trained personnel involvement DO NOT examine throat (using tongue depressor may cause obstruction) IV/PO Abx supplemental O2 airway management if indicated
66
Nasal polyps
associated with asthma cystic fibrosis, Kartengers affect ~1% of adult population 2-4x more common in men features include nasal obstruction, rhinorrhoea, sneezing, poor sense of taste & smell NB unilateral nasal polyp should raise suspicion of cancer management with ENT referral, topical steroids (↓ polyp size)
67
Nasal septum deviation
most common cause of nasal obstruction, usually due to direct trauma to nose/face or due to Marfan's/Ehler-Danlos syndrome features include recurrent sinusitis, facial pain, mouth breathing, ↓ wens of smell, repetitive sneezing, noisy breathing managed with topical decongestants, steroid, antihistamines & surgery
68
Choanal atresia
congenital bony/membranous obstruction of the posterior nasal passage which can be unilateral/bilateral associated with other abnormalities e.g. CHARGE syndrome features: if bilateral = obligate mouth breathing, cyanosis worse on feeding, noisy breathing, struggling with food intake if unilateral: chronic rhinitis, congestion, rhinorrhoea management surgical perforation (urgently if bilateral, or at 1-2y/o if unilateral)
69
Thyroglossal cyst
a remnant of the thyroglossal duct formed during embryonic development of the thyroid gland & normally regress before birth 2nd most common neck abnormality (~7% of population) Presents as cyst present from birth, painless firm midline neck mass that elevates with swallowing & tongue protrusion USS neck (evaluate cyst & confirm location of thyroid) elctive surgical removal to treat
70
Brachial cyst
remand of the embryological 2nd brachial cleft/cervical sinus which normally regresses after birth ~20% of paediatric neck masses presents as cyst diagnosed in late childhood/adolescence usually when cyst becomes infected, painless firm mass located lateral to midline usually anterior to SCM and does not move on swallowing USS neck & CT/MRI (to plan surgery) managed with surgical excision
71
Head & neck cancers
90% are squamous cell carcinomas
72
Risk factors for head & neck cancer
``` smoking heavy alcohol consumption poor dentition poor diet GORD HPV 16 +ve male gender ```
73
Cancer of the oral cavity
cancers of oral mucosa, tonsils, salivary glands & tongue, usually seen in males aged 55-60 present as dysphagia, non healing ulcers, halitosis, unusual bleeding in mouth, facial swelling, lymphadenopathy biopsy & histopathology, panednoscopy (to assess extent of tumour), CT chest/abdo/pelvis (check for spread) treat with surgical resection if local, or resection +radio/chemotherapy
74
Pharyngeal cancer
cancer of the oro/naso/hypopharynx, less common than other head & neck cancers, generally seen in males aged >50yrs presents as enlarged lymph nodes, severe air pain, dysphagia, sore throat, foreign body sensation, recurrent otitis media & conductive hearing loss, epistaxis investigate with panendoscopy, biopsy, MRI/CT (to check infiltration into surrounding structure) Managed with surgery ± radio/chemo therapy NB nasopharyngeal cancer usually not SCC
75
Laryngeal cancer
cancers of supraglottis, glottis, subglottis, 2nd most common head & neck cancer, usually seen in males age 40-70 presents with hoarseness, change in voice, foreign body sensation, dyspnoea, dysphagia, stridor, aspiration investigate with direct laryngoscopy, CT/MRI or USS neck Management with radiotherapy/transednoscpopic laser resection if early, larynectomy if advanced
76
Reineke's oedema
benign build up of fluid in the lamina propria of the true vocal cords, looks like a sac-like fluid filled vocal cords due to irritation & inflammation secondary to smoking presents with deep/low pitched voice,rough voice, dysphonia, bilaterally swollen vocal cords on laryngoscopy managed with smoking cessation & voice therpay
77
Laryngeal papillomatosis/recurrent respiratory papillomatosis (RRP)
being tumour of the laryngeal epithelium caused by HPV infection (the 6&11) presents as white exophylic cauliflower like lesion located in the larynx/trachea/vocal cords which may cause dysphonia, hoarseness, stridor should be surgical removed but may reoccur
78
Laryngopharyngeal reflux (LPR)
inflammatory changes of the larynx/pharynx secondary to GORD, common presents with globes (felt in midline, worse on swallowing), hoarseness, chronic cough, dysphagia, heart burn managed with lifestyle changes, PPIs or alginates e.g. gaviscon
79
Laryngopharyngeal reflux (LPR)
inflammatory changes of the larynx/pharynx secondary to GORD, common presents with globus (felt in midline, worse on swallowing), hoarseness, chronic cough, dysphagia, heart burn managed with lifestyle changes, PPIs or alginates e.g. gaviscon
80
Laryngitis
inflammation of the larynx acute: <3 wks, usually viral ± bacterial superinfection chronic >3 wks, usually GORD related or smoking related
81
Presentation of laryngitis
hoarseness of voice, dysphonia, dry cough, stridor, fever, dysphagia, lymphadenopathy, globus, sore throat mainly clinical diagnosis, consider laryngoscopy (shows oedema, eryhtma, or cobble stoning (if GORD))
82
Management of laryngitis
``` vocal rest smoking cessation speech therapy humidification Abx for bacterial superinfection ```
83
Foreign nasal body
mostly young children (<2.5yrs) presents as unilateral nasal obstruction, epistaxis or mould smelling purulent rhinorrhoea nasal cavity inspection (otoscope) or flexible fiberoptic endoscopy removal via positive pressure, forceps or endoscopy
84
Foreign bodies in the ear
usually seen in children (older children/adults will know something is i their ear) may present as ear pain, deafness, ↓hearing or discharge visualise on otoscopy remove with forceps (if insect should kill insect first)
85
Swallowed foreign bodies
generally seen in children <5yrs coins = most common object to swallow, items like button batteries are very dangerous presents with vomiting, choking, refusal to eat, blood stained saliva, drooling, wheezing, respiratory distress investigate with plain CXR or endoscopy managed by endoscopic removal or if in stomach waiting for it to pass in stool
86
Obstructive sleep apnoea (OSA)
characterised by episodes of complete/partial upper airway obstruction during sleep most common breathing related sleep disorder, 2x more common in men
87
Risk factors for OSA
``` obesity adenotonsillar hypertrophy (in children) nasal septum deviation nasal polyps macroglossia family history Down's syndrome ```
88
Presentation of OSA
excessive snoring reports of apnoea (from sleep partner/parents) day time somnolence restless sleep frequent waking mouth breathing impaired cognitive function (poor concentration)
89
Investigating OSA
Polysomnography (1st line) | Epworth sleepiness scale
90
Management of OSA
weight loss, sleep hygiene, lateral sleeping position CPAP surgical removal of tonsils/adenoids in children
91
Vertigo
dizziness is a general, non specific term to indicate the sense of disorientation vertigo is a type of dizziness & refers to the false sensation that oneself or the surroundings are moving/spinning due to mismatch of vestibular, visual & somatosensory systems
92
Causes of vertigo
cerebral: CVD, migraine, MS, acoustic neuroma, alcohol intoxication Vestibular: vestibular neuritis, viral labyrinthitis, BPPV, Meniers, motion sickness, ototoxicity (e.g. gentamicin), HZV (ramsay hunt syndrome)
93
Benign paroxysmal positional vertigo (BPPV) presentation
gradual onset, triggers by change in head position, episodes lasts 10-20secs
94
Meniere's disease presentation
hearing loss, tinnitus & sensation of pressure/fullness in one/both ears nystagmus
95
Vertebrobasillar ischaemia
elderly pts, presents with dizziness on extension of neck
96
acoustic neuroma presentation
hearing loss, vertigo, tinnitus ± absent corneal reflex/facial nerve palsy if bilateral then neurofibromatosis 2
97
Investigating vertigo
``` Romberg's test Dix-Hallpike manoeuvre head impulse test CT/MRI audiometry vestibular function ```
98
Laryngeal nerve palsy/vocal cord paralysis
clinical features depend if one or 2 cords are affected & position of chords, due to injury of one/both recurrent laryngeal nerves unilateral: hoarseness bilateral: dysphonia, stridor, snoring, breathing problems treatment: voice therapy, surgery
99
Benign lesions of the vocal cords
present as hoarseness include: vocal cord nodules (bilateral), treated with voice therapy polyps of vocal folds (unilateral), treated with excision to exclude malignancy
100
Voice overuse/misuse
common in professions such as acting/singing/teaching may lead to being lesions such as nodules (singers nodules) or cysts treated with voice therapy or surgery
101
Labyrinthitis
inflammatory disorder of the membranes of the labyrinth affecting both vestibular & cochlear organs, usually preceded by URTI may be viral (most common), bacterial or associated with systemic disease usually seen age 40-70
102
Presentation of labyrinthitis
acute onset vertigo (not triggered by movement but exacerbated by movement) hearing loss* nausea&vomiting, tinnitus spontaneous unidirectional horizontal nystagmus towards unaffected side, sensorineural hearing loss
103
Vestibular neuritis
inflammation of the vestibular nerve, usually follows a viral illness
104
Presentation of vestibular neuritis
recurrent vertigo attacks lasting hours to days, nausea & vomiting, horizontal nystagmus NO hearing loss or tinnitus (unlike labyrinthitits)
105
Management of vestibular neuritis
vestibular rehabilitation exercises
106
Cholesteatoma
presence of keratinising squamous cell epithelium within the middle ear or in other pneumatised areas of the temporal bone, the epithelium exhibits independent growth leading to expansion & reabsorption of underlying bone risk ↑ 100x with cleft palate
107
presentation of cholesteatoma
painless otorhhoea (scant but foul smelling discharge from affected ear) conductive hearing loss (painless) retraction pocket/attic crust seen on otoscopy
108
Pleomorphic adenoma
commonest tumour of parotid glands Slow growing, lobular, and not well encapsulated
109
Normal Webers & Rhinnes test
Rhinnes: Air conduction > bone conduction bilaterally Webers: equal on both sides, no lateralisation, stays in midline
110
Conductive hearing loss Webers & Rhinnes test
Rhinnes: Bone conduction > air conduction in affected ear Air conduction > bone conduction in unaffected ear Webers: Lateralises to affected ear
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Sensorineural hearing loss Webers & Rhinnes test
Rhinnes: Air conduction > bone conduction bilaterally Webers: Lateralises to unaffected ear