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ENT OSCE Cases — Medical Student (Finals Level)

6 Full OSCE Cases covering Ear, Nose, and Throat topics. Each case follows the format: Scenario → History → Examination → Investigations → Management → Examiner Questions.

CASE 1 — Acute Otitis Media (Ear)

Scenario

A 2-year-old boy is brought to the GP by his mother. She says he has been pulling at his right ear for 2 days, is irritable, and has had a fever of 38.5°C. He had a runny nose last week.

History to Elicit

DomainKey Points
Presenting complaintRight ear pain (tugging), fever, irritability, poor feeding
HPCPreceded by viral URTI (1 week ago); bilateral vs unilateral; otorrhea?
Risk factorsDaycare attendance, parental smoking, bottle-fed in supine position, pacifier use, previous AOM episodes
PMH/FHRecurrent ear infections? Cleft palate or craniofacial abnormality?
ImmunisationUp to date? (Pneumococcal vaccine reduces AOM incidence)

Examination Findings

  • Otoscopy: Moderate-to-severe bulging, opaque, erythematous right tympanic membrane (TM) with loss of normal light reflex
  • Pneumatic otoscopy: Reduced TM mobility — confirms middle ear effusion (MEE)
  • Temperature: 38.5°C
  • No mastoid tenderness (rules out mastoiditis at this stage)
Diagnosis: Acute Otitis Media (AOM)
Key diagnostic criteria: acute onset otalgia + bulging TM + middle ear effusion.

Investigations

  • Usually a clinical diagnosis — no routine investigations needed
  • Tympanometry: flat type B curve (no TM movement) confirms MEE
  • If recurrent / treatment failure: culture if perforation with otorrhea

Management

SeverityTreatment
Severe (temp ≥39°C or moderate–severe otalgia, age <2 yr)Amoxicillin 80–90 mg/kg/day divided doses for 10 days
Mild–moderate, age ≥2 yrWatchful waiting for 48–72 hours first; analgesia (paracetamol/ibuprofen)
Treatment failure (no improvement at 3 days)Amoxicillin-clavulanate 80–90 mg/kg/day OR Ceftriaxone IM 50 mg/kg
Penicillin allergyCefuroxime or Cefpodoxime
Adjuncts: Analgesia, reassurance. Antibiotics should NOT be prescribed for viral URTI without AOM.
Referral for ENT / grommet insertion: If recurrent AOM (≥3 episodes in 6 months) or persistent otitis media with effusion (OME/"glue ear") >3 months with hearing loss.

Examiner Questions

  • Q: What are the 3 most common bacterial causes of AOM? S. pneumoniae (25–40%), H. influenzae (10–30%), M. catarrhalis (2–15%)
  • Q: What distinguishes AOM from OME? AOM has acute symptoms (fever, pain) + bulging TM; OME is painless with fluid behind the TM, no acute inflammation
  • Q: What is the most common cause of eustachian tube dysfunction? Abnormal tubal compliance + delayed tensor veli palatini innervation; commonly triggered by viral URTI

CASE 2 — Epistaxis (Nose)

Scenario

A 65-year-old man presents to the ED with a 20-minute history of bleeding from his right nostril. He is on warfarin for AF and takes aspirin. His BP is 170/100 mmHg.

History to Elicit

DomainKey Points
Onset & severityDuration, volume of blood, any airway compromise or swallowing blood?
LateralityUnilateral (anterior likely) vs bilateral
Prior episodesFirst episode? Recurrent? Any family history of bleeding disorder?
MedicationsWarfarin, aspirin, clopidogrel, NSAIDs, nasal sprays
PMHHypertension, liver disease, haematological disorders, hereditary haemorrhagic telangiectasia (HHT/Osler-Weber-Rendu), nasal tumour
Red flagsYoung male + recurrent epistaxis + unilateral nasal obstruction → juvenile nasopharyngeal angiofibroma

Examination Findings

  • Sit patient upright, leaning forward, pinching the soft part of the nose
  • Visualise with bright light + nasal speculum: bleeding from anterior septum (Kiesselbach's plexus in most cases)
  • Posterior epistaxis (>65 yr, hypertensive): bleeding not visible anteriorly, blood in oropharynx
  • Check BP (170/100 mmHg → needs treatment), HR, SpO₂
  • Examine for signs of coagulopathy: bruising, petechiae, hepatosplenomegaly
Most likely: Anterior epistaxis from Kiesselbach's (Little's) area

Kiesselbach's Plexus — Blood Supply

Anastomosis of five vessels at the anteroinferior nasal septum:
  1. Anterior ethmoidal artery
  2. Posterior ethmoidal artery
  3. Septal branch of sphenopalatine artery
  4. Greater palatine artery
  5. Branch from the superior labial artery

Investigations

  • FBC (anaemia, thrombocytopenia)
  • PT / INR (warfarin — check supratherapeutic?)
  • APTT, group & save if severe
  • IV access if haemodynamically compromised

Management

Stepwise (anterior epistaxis):
  1. Sit forward, pinch soft nose for 10–15 minutes — patient/carer can do this at home
  2. Topical vasoconstrictor + local anaesthetic (e.g. co-phenylcaine spray)
  3. Silver nitrate cautery to visible bleeding point (if identifiable)
  4. Anterior nasal packing (BIPP ribbon gauze or Merocel pack) — pack for 24–48 hrs
  5. Posterior epistaxis: Foley catheter or posterior pack; ENT admission
  6. Reverse anticoagulation if INR supratherapeutic; withhold antiplatelet if safe to do so
  7. Refractory cases: sphenopalatine artery ligation or embolisation
Analgesia during packing — risk of vasovagal response especially in hypovolaemic patients.

Examiner Questions

  • Q: What is Kiesselbach's plexus? Rich arterial anastomosis at the anteroinferior nasal septum; site of 90% of anterior nosebleeds
  • Q: What makes epistaxis posterior? Bleeding from posterior two-thirds of nasal cavity; often heavy, bilateral, blood visible in oropharynx; more common in elderly hypertensive patients
  • Q: What rare diagnosis must be excluded in a young male with recurrent epistaxis and nasal obstruction? Juvenile nasopharyngeal angiofibroma — benign but locally aggressive vascular tumour

CASE 3 — Peritonsillar Abscess (Quinsy) (Throat)

Scenario

An 18-year-old male presents with 5 days of worsening sore throat, now with difficulty swallowing and speaking. He sounds like he has a "hot potato voice."

History to Elicit

DomainKey Points
SymptomsSevere unilateral sore throat, dysphagia, odynophagia, drooling, trismus (jaw stiffness/difficulty opening mouth), "hot potato voice"
SystemicFever, rigors, poor oral intake, dehydration
Prior historyPrevious tonsillitis episodes? Previous quinsy?
MedicationsAny antibiotics already started?

Examination Findings

  • Trismus (difficulty opening mouth — spasm of pterygoid muscles)
  • Uvular deviation away from the affected side
  • Peritonsillar bulge: Unilateral soft palate swelling, displaced tonsil medially
  • Erythema, oedema of soft palate
  • Ipsilateral tender cervical lymphadenopathy
  • Check for airway patency — is the patient in respiratory distress?
Diagnosis: Peritonsillar Abscess (Quinsy)
Pus between the tonsil capsule and the superior constrictor muscle.

Investigations

  • Clinical diagnosis primarily
  • FBC (leukocytosis), CRP
  • Throat swab (Group A β-haemolytic Streptococcus most common)
  • Monospot / EBV serology if suspected glandular fever (can mimic quinsy)
  • Neck USS or CT if parapharyngeal/deep space extension suspected

Management

  1. Surgical drainage — needle aspiration (first line) or incision & drainage under LA
  2. IV antibiotics: Co-amoxiclav OR Benzylpenicillin + Metronidazole
  3. IV fluids + analgesia (IV paracetamol, NSAID)
  4. Steroids (IV dexamethasone) — reduce oedema, shorten hospital stay
  5. Admit for monitoring; ENT team management
Tonsillectomy indications (recurrent tonsillitis criteria):
  • ≥7 episodes in 1 year, or ≥5/year for 2 years, or ≥3/year for 3 years
  • Previous peritonsillar abscess
  • Airway obstruction / obstructive sleep apnoea

Potential Complications

ComplicationMechanism
Airway obstructionBilateral oedema
Parapharyngeal abscessRupture through superior constrictor
Mediastinitis / Lemierre syndromeJugular vein thrombophlebitis
Septic emboli / bacteraemiaVenous involvement
Aspiration pneumoniaSpontaneous rupture

Examiner Questions

  • Q: How does peritonsillar abscess differ clinically from severe tonsillitis? Quinsy has trismus, uvular deviation, peritonsillar bulge, and "hot potato" muffled voice — all absent in simple tonsillitis
  • Q: What organism most commonly causes quinsy? Group A β-haemolytic Streptococcus (GABHS)
  • Q: What life-threatening complication can occur if the abscess extends to the parapharyngeal space? Lemierre syndrome (septic thrombophlebitis of the internal jugular vein) → septic emboli to lungs; or mediastinitis (descending necrotising mediastinitis)

CASE 4 — Sudden Sensorineural Hearing Loss (SSNHL) (Ear)

Scenario

A 45-year-old woman wakes up one morning with sudden loss of hearing in her left ear, associated with tinnitus and mild left-sided vertigo. She has no ear pain or discharge.

History to Elicit

DomainKey Points
OnsetSudden (woke up with it)? Over hours? After loud noise exposure?
LateralityUnilateral (SSNHL typical) vs bilateral
Associated symptomsTinnitus, aural fullness, vertigo; neurological symptoms (facial palsy, diplopia, dysarthria → posterior fossa lesion)?
Preceding eventsViral illness (Ramsay Hunt, measles, mumps), barotrauma, head trauma, ototoxic drugs
PMHAutoimmune disease, syphilis, diabetes, MS, previous acoustic neuroma workup
MedicationsAminoglycosides, platinum chemotherapy, furosemide, quinine

Examination Findings

  • Rinne test (affected ear): AC > BC (sensorineural pattern — normal bone conduction still better reference but AC > BC maintained in SNHL)
  • Weber test: Lateralises to the normal (right) ear — away from the lesion
  • Otoscopy: Normal tympanic membrane (distinguishes from conductive loss)
  • Full cranial nerve exam — particularly VII, VIII
  • Cerebellar signs (rule out acoustic neuroma / posterior fossa lesion)
Diagnosis: Sudden Sensorineural Hearing Loss (SSNHL) — idiopathic until proven otherwise

Investigations

InvestigationRationale
Audiogram (urgent, same day)Confirms SNHL ≥30 dB in 3 consecutive frequencies; documents severity
MRI internal auditory meatiExclude acoustic neuroma (vestibular schwannoma)
FBC, ESR, CRPInfection/inflammation
Syphilis serology (RPR/VDRL)Treatable cause
Autoimmune screen (ANA, ANCA)Autoimmune SNHL
Blood glucoseDiabetes

Management

  • ENT emergency — refer same day
  • High-dose oral corticosteroids (prednisolone 1 mg/kg/day for 7–14 days) — mainstay treatment; improves recovery when given within 2 weeks of onset
  • Intratympanic steroid injection if systemic contraindicated or as salvage
  • Treat underlying cause if identified (antiviral for Ramsay Hunt; penicillin for syphilis)
  • Hearing aid if residual deficit
  • If acoustic neuroma found → MDT discussion (surveillance, radiosurgery, or surgery)

Examiner Questions

  • Q: What are the 4 types of hearing loss? Conductive (CHL), sensorineural (SNHL), mixed, and central hearing loss
  • Q: How do you differentiate CHL from SNHL on tuning fork tests? Rinne: CHL → BC > AC (abnormal); SNHL → AC > BC (normal Rinne, but reduced overall). Weber: CHL → lateralises to affected ear; SNHL → lateralises to unaffected ear
  • Q: What is the commonest cause of conductive hearing loss in an adult with no trauma or infection history? Otosclerosis — autosomal dominant, fixation of stapes footplate; treated with stapedectomy (>95% success)

CASE 5 — Benign Paroxysmal Positional Vertigo (BPPV) (Ear)

Scenario

A 55-year-old woman presents with brief episodes of intense spinning, each lasting <1 minute, triggered when she rolls over in bed or looks up. No hearing loss. No headache.

History to Elicit

DomainKey Points
CharacterTrue rotatory vertigo (spinning sensation) vs presyncope/lightheadedness
DurationSeconds to <1 minute (BPPV) vs minutes to hours (Ménière's) vs constant (central)
TriggersHead position change — rolling in bed, looking up (BPPV); Valsalva (perilymphatic fistula)
AssociatedHearing loss/tinnitus (absent in BPPV; present in Ménière's / acoustic neuroma)
NeurologicalDiplopia, dysarthria, dysphagia, ataxia → central cause (posterior fossa stroke/tumour)
MedicationsAminoglycosides, antihypertensives, antiepileptics

Examination — Dix-Hallpike Manoeuvre

Procedure: Patient sits on couch → lay back rapidly to 30° below horizontal with head turned 45° to affected side.
Positive result (BPPV): After a 2–5 second latency, brief (10–40 second) upbeat-torsional nystagmus occurs, fatigues on repetition.
Diagnosis: BPPV — posterior semicircular canal (most common type)
Red flags for central vertigo: vertical nystagmus, no latency, no fatigue, persistent nystagmus, neurological signs → urgent MRI brain.

Peripheral vs Central Vertigo

FeaturePeripheral (BPPV, Ménière's)Central (stroke, tumour)
OnsetEpisodicConstant
Nystagmus directionHorizontal / rotatoryVertical (pathognomonic of central)
FatigableYesNo
Neurological symptomsNonePresent
Hearing lossMay be presentUsually absent

Investigations

  • Clinical diagnosis — Dix-Hallpike is diagnostic
  • Audiogram if hearing loss present
  • MRI brain if central cause suspected
  • Electronystagmography (ENG) / vestibular function tests if diagnosis uncertain

Management

  1. Epley manoeuvre (canalith repositioning) — first-line; highly effective (>80%)
  2. Brandt-Daroff exercises — home vestibular rehabilitation
  3. Betahistine (limited evidence in BPPV; used for Ménière's)
  4. Short-term vestibular suppressants (prochlorperazine) for acute severe nausea — avoid long-term
  5. Refer to ENT / audiovestibular medicine if treatment fails or atypical features

Examiner Questions

  • Q: What is the anatomical mechanism of BPPV? Otoliths (calcium carbonate crystals) detach from the utricle and enter the posterior semicircular canal (canalolithiasis), causing abnormal endolymph movement with head position change
  • Q: What distinguishes Ménière's disease from BPPV? Ménière's: triad of episodic vertigo (>20 min), fluctuating sensorineural hearing loss, and tinnitus/aural fullness; attacks last hours, not seconds
  • Q: What is the Epley manoeuvre? Series of 4 head position changes to move the displaced otolith out of the posterior canal back into the utricle

CASE 6 — Acute Rhinosinusitis (Nose/Sinus)

Scenario

A 30-year-old woman presents with a 10-day history of nasal congestion, thick green nasal discharge, facial pain over her cheeks (worse on bending forward), and reduced smell. She had a cold 2 weeks ago. She is afebrile.

History to Elicit

DomainKey Points
SymptomsNasal blockage, purulent nasal discharge, facial pain/pressure (maxillary/frontal/periorbital), anosmia, post-nasal drip, headache
DurationAcute (<3 weeks), subacute (3–6 weeks), chronic (>6 weeks/12 weeks)
Preceding URTIMost common trigger — viral URI → bacterial secondary infection
Red flagsHigh fever, periorbital swelling/erythema/proptosis (orbital cellulitis), severe headache (intracranial extension), meningism
AllergiesAllergic rhinitis — predisposing factor
PMHNasal polyps, septal deviation, cystic fibrosis, immunodeficiency, dental infection

Examination Findings

  • Nasal endoscopy / anterior rhinoscopy: Mucosal oedema, purulent discharge from middle meatus
  • Facial tenderness: Maxillary sinuses (under eyes) ± frontal sinuses (above eyes, on brow)
  • Transillumination (limited use) — dullness of maxillary sinus
  • Check for orbital signs (lid swelling, proptosis, restricted eye movement, reduced vision) → orbital complication
Diagnosis: Acute bacterial rhinosinusitis (bacterial if ≥10 days duration + purulent discharge + facial pain)

Differentiating Bacterial vs Viral Sinusitis

FeatureViral URIBacterial Rhinosinusitis
Duration<10 days, improving≥10 days, or worsening after initial improvement
DischargeClear/wateryThick, purulent, unilateral
FeverLow-gradeModerate–high
Antibiotic neededNoYes

Investigations

  • Usually clinical diagnosis — no imaging for uncomplicated cases
  • CT sinuses: for chronic/recurrent sinusitis, surgical planning, or complications
  • CT with contrast if orbital or intracranial complication suspected (emergency)

Management

Uncomplicated acute bacterial rhinosinusitis:
  1. Intranasal saline irrigation (first line)
  2. Intranasal corticosteroids (mometasone, fluticasone) — reduce mucosal oedema
  3. Oral amoxicillin 500 mg TDS for 5–7 days (or amoxicillin-clavulanate if severe/failed amoxicillin)
  4. Analgesia (NSAIDs) for facial pain
  5. Nasal decongestants (oxymetazoline) short-term (≤3 days) — avoid rebound rhinitis
Complications requiring urgent referral:
  • Orbital cellulitis / abscess → IV antibiotics, CT, ophthalmology + ENT
  • Meningitis / intracranial abscess → neurosurgery + ENT emergency
  • Frontal osteomyelitis (Pott's puffy tumour) → neurosurgical emergency
Chronic sinusitis not responding to medical management → functional endoscopic sinus surgery (FESS)

Examiner Questions

  • Q: Which sinus is most commonly affected in sinusitis and why? Maxillary sinus — largest, most dependent (ostium drains superiorly making drainage against gravity), frequently obstructed at the ostiomeatal unit
  • Q: What is the ostiomeatal unit? Functional drainage pathway of the anterior ethmoid, maxillary, and frontal sinuses converging into the middle meatus; blockage here causes rhinosinusitis
  • Q: What are the intracranial complications of frontal sinusitis? Meningitis, epidural/subdural empyema, brain abscess, cavernous sinus thrombosis, Pott's puffy tumour (frontal bone osteomyelitis)

Quick-Reference Summary Table

CaseConditionKey Diagnosis ClueFirst-Line Rx
1Acute Otitis MediaBulging TM + fever + otalgia in childAmoxicillin 80–90 mg/kg/day
2EpistaxisKiesselbach's plexus, anterior septumPinch + cautery ± packing
3Peritonsillar AbscessTrismus + uvular deviation + hot potato voiceDrainage + IV co-amoxiclav
4Sudden SNHLUnilateral hearing loss on waking, normal TMUrgent steroids + MRI IAMs
5BPPVBrief positional vertigo, positive Dix-HallpikeEpley manoeuvre
6Acute Rhinosinusitis≥10 days purulent discharge + facial painAmoxicillin + intranasal steroid

Sources: Textbook of Family Medicine 9e; Cummings Otolaryngology Head and Neck Surgery; K.J. Lee's Essential Otolaryngology
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