Clinical anatomy of the larynx Respiratory, protective, and vocal functions of the larynx. Muscles of the larynx. Blood supply of the larynx. Peculiarities of the innervation of the la of the larynx. Methods of examination of the larynx. Technique of direct and indirect laryngoscopy. Causes of acute stenosis of the larynx. Acute stenosis of the larynx - clinic, diagnosis and treatment. Acute laryngeal oedema, cause, clinic and diagnosis. Treatment of acute laryngeal stenosis Stages of acute laryngeal stenosis. False croup, etiology, clinic and diagnosis. True croup - etiology, clinic and diagnosis. Differential diagnosis of false and true croup. Indications and technique of tracheostomy and conicotomy? Indications and technique of tracheal intubation. Treatment of laryngeal oedema. Acute laryngitis (clinic, diagnosis and treatment). Chronic laryngitis (clinic, diagnosis and treatment). Foreign body of the bronchi and trachea (clinic, diagnosis and treatment). Laryngeal diphtheria (true croup) clinic, diagnosis and treatment. Clinical picture of chronic hyperplastic laryngitis. Clinical picture of atrophic laryngitis (laryngitis sicca). Acute epiglottitis (Supraglottic Laryngitis) Clinical features of tuberculosis of larynx. Oedema of larynx. Aetiology, symptoms, treatment Foreign bodies of the esophagus (clinic, diagnosis and treatment) Laryngomalacia (laryngeal stridor) aetiology, clinic, diagnosis and treatment Classification of laryngeal paralysis. Types and technique of tracheostomy. Complications of tracheotomy. Reinke s Oedema (polypoid degeneration of vocal cords) pathogenesis, clinic and treatment.

Reading File
Finding Sources
Finding Sources
Finding Sources
Finding Sources
Reading File
Reading File
Reading File
Reading File
Finding Sources
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Reading File
Here is a comprehensive, organized reference covering all topics:

The Larynx — Complete Clinical Reference


1. Clinical Anatomy of the Larynx

The larynx extends from the tip of the epiglottis (level of C3) to the inferior border of the cricoid cartilage (level of C6). It is intimately related to the hypopharynx, which lies posteriorly.
Three anatomic regions:
  • Supraglottis — includes the epiglottis (suprahyoid and infrahyoid), aryepiglottic folds, arytenoids, false vocal cords (vestibular folds), and ventricles
  • Glottis — true vocal cords plus anterior and posterior commissures; lower boundary is 5 mm below the free margin of the cords
  • Subglottis — from the lower glottic boundary to the inferior margin of the cricoid cartilage
Cartilages:
  • Thyroid cartilage — two quadrilateral hyaline cartilage laminae fused anteriorly; the laryngeal prominence ("Adam's apple") is the superior projection; superior and inferior horns project from posterior borders
  • Cricoid cartilage — signet-ring shaped hyaline cartilage; the only complete cartilaginous ring in the airway; arch anteriorly, lamina posteriorly; the arytenoid articular surfaces sit on the superior laminar border
  • Arytenoid cartilages — paired pyramids of hyaline cartilage; each has a muscular process (for muscle attachment) and a vocal process (for attachment of the vocal ligament)
  • Epiglottis — leaf-shaped elastic cartilage; attached to the thyroid cartilage by its stalk; elastic cartilage does not ossify
  • Corniculate and cuneiform cartilages — small elastic cartilages within the aryepiglottic folds
The thyroid, cricoid, and most of the arytenoid cartilages are hyaline and begin to ossify around age 20. Elastic cartilages (epiglottis, corniculates, cuneiforms, and the vocal processes) do not ossify.
Joints:
  • Cricothyroid joint — between inferior horn of thyroid and the arch of cricoid; permits rotation that tenses the vocal ligament (cricothyroid muscle action)
  • Cricoarytenoid joint — between arytenoid base and superior lamina of cricoid; permits rotation + gliding, opening/closing the rima glottidis
Ligaments and membranes:
  • Conus elasticus (cricovocal membrane) — spans the inner surface of the cricoid to the vocal ligaments; its anterior midline thickening is the median cricothyroid ligament, the surgical target for emergency cricothyrotomy (conicotomy)
  • Quadrangular membrane — upper portion of fibroelastic membrane; free inferior margin = vestibular ligament (core of the false vocal cord)
  • Thyrohyoid membrane — connects thyroid cartilage to hyoid; the superior laryngeal vessels and nerve pierce it
Color Atlas of Human Anatomy, Vol. 2, p. 190–195; Cummings Otolaryngology, p. 2124

2. Functions of the Larynx

Respiratory Function

The larynx maintains a patent airway. The rima glottidis widens progressively with deeper inspiration. The cricoid cartilage forms an absolute complete ring — it cannot expand, making subglottic oedema particularly dangerous (especially in children).

Protective Function

  • During swallowing, the epiglottis deflects food laterally into the pyriform sinuses; the laryngeal inlet narrows via aryepiglottic fold approximation; the true and false vocal cords adduct; the larynx is elevated under the base of the tongue
  • The glottic closure reflex (bilateral superior laryngeal nerves) guards against aspiration — sustained spasm = laryngospasm
  • The cough reflex opens the rima glottidis explosively to expel foreign material

Vocal (Phonatory) Function

Phonation requires:
  1. Adduction and tensioning of the vocal ligaments (closing the rima)
  2. Expiratory airflow forces the cords apart — they vibrate, producing sound
  3. Pitch depends on vibration frequency (determined by cord length, thickness, and tension — regulated by cricothyroid and vocalis muscles)
  4. Volume depends on the force of the airstream
  5. Resonance and articulation are provided by supraglottic structures, oral cavity, and nasal sinuses
Color Atlas of Human Anatomy, Vol. 2, p. 202; Miller's Anesthesia, p. 9789

3. Muscles of the Larynx

Extrinsic Laryngeal Muscles (move larynx as a whole)

Infrahyoid muscles (sternothyroid, thyrohyoid) and suprahyoid muscles depress and elevate the larynx during swallowing and phonation.

Intrinsic Laryngeal Muscles

MuscleActionInnervation
CricothyroidTilts cricoid posteriorly → tenses vocal ligament → raises pitchExternal branch of SLN
Posterior cricoarytenoid (PCA)Rotates arytenoid → abducts vocal cord → ONLY ABDUCTOR of glottisRLN
Lateral cricoarytenoid (LCA)Rotates arytenoid → adducts vocal cordRLN
Transverse arytenoidDraws arytenoids together → closes intercartilaginous rimaRLN
Oblique arytenoidNarrows laryngeal inlet; continues into aryepiglottic foldRLN
Thyroarytenoid (+ vocalis)Shortens/relaxes vocal fold; adjusts tension isometrically; adductsRLN
Thyroepiglottic partNarrows laryngeal inletRLN
The posterior cricoarytenoid is the sole abductor of the glottis — bilateral RLN palsy causes complete glottic closure and asphyxia.
Color Atlas of Human Anatomy, Vol. 2, p. 197–202

4. Blood Supply of the Larynx

  • Superior laryngeal artery — branch of the superior thyroid artery (from external carotid); passes with the internal branch of the superior laryngeal nerve through the thyrohyoid membrane; supplies supraglottic and most of the larynx
  • Inferior laryngeal artery — branch of the inferior thyroid artery (from thyrocervical trunk); supplies subglottis and lower larynx
Venous drainage: superior and inferior laryngeal veins drain into the internal jugular vein.
Lymphatics: The larynx has dual lymphatic drainage — supraglottic structures drain superiorly through the thyrohyoid membrane to upper deep cervical nodes (levels II–III); subglottic structures drain to pretracheal and paratracheal nodes (level VI). The true vocal cords have a sparse lymphatic supply, explaining the lower rate of nodal metastasis in glottic cancers.
Color Atlas of Human Anatomy, Vol. 2, p. 202

5. Peculiarities of Laryngeal Innervation

Both motor and sensory supply derive from the vagus nerve (CN X) via two branches:

Superior Laryngeal Nerve (SLN)

Arises from the vagus below the inferior ganglion; passes medial to the internal carotid artery; divides at the level of the hyoid into:
  • Internal branch (sensory) — pierces the thyrohyoid membrane with the superior laryngeal artery; provides sensory innervation to the laryngeal mucosa down to and including the level of the vocal cords; mediates the glottic closure reflex
  • External branch (motor) — supplies the cricothyroid muscle and the inferior pharyngeal constrictor

Recurrent Laryngeal Nerve (RLN)

Branches from the vagus in the thorax:
  • Right RLN — loops around the right subclavian artery, then ascends in the tracheo-oesophageal groove
  • Left RLN — loops around the aortic arch (longer, more vulnerable), then ascends
The RLN (as the inferior laryngeal nerve) provides:
  • Motor — all intrinsic laryngeal muscles except the cricothyroid
  • Sensory — laryngeal mucosa below the vocal cords and upper trachea
Clinical pearls on innervation:
  • Unilateral RLN injury → ipsilateral vocal cord paralysis in paramedian position → hoarseness, aspiration
  • Bilateral RLN injury → complete adduction of both cords → stridor, acute respiratory distress
  • SLN injury (e.g., thyroid surgery, neck dissection) → loss of pitch and projection (cricothyroid paralysis) + loss of protective glottic reflex → silent aspiration
  • Risk of RLN injury: thyroid/parathyroid surgery, oesophageal surgery, aortic arch procedures (left)
  • The sensory supply above the cords = SLN; below the cords = RLN — this is exploited in awake fiberoptic intubation with nerve blocks
Color Atlas of Human Anatomy, Vol. 2, p. 209; Miller's Anesthesia, p. 9789; Morgan & Mikhail's Clinical Anesthesiology, p. 931

6. Methods of Examination of the Larynx

  1. Indirect laryngoscopy — angled mirror placed in oropharynx; reflected light illuminates larynx; classic office technique
  2. Direct laryngoscopy — rigid laryngoscope; used under anaesthesia; gold standard for operative procedures
  3. Flexible nasopharyngolaryngoscopy (nasendoscopy) — fibre-optic or video endoscope passed transnasally; excellent for dynamic assessment of vocal cord movement, office-based
  4. Video laryngoscopy — indirect video system for airway management; GlideScope, McGrath, Pentax-AWS
  5. Microlaryngoscopy — operating microscope through direct laryngoscope for phonomicrosurgery
  6. Stroboscopy — flashing light synchronised to vocal cord vibration; evaluates mucosal wave
  7. Imaging — lateral neck X-ray (thumb-print sign of epiglottitis, "steeple sign" of croup), CT neck, MRI
  8. Panendoscopy (triple endoscopy) — laryngoscopy + bronchoscopy + oesophagoscopy; for head and neck malignancy staging
Miller's Anesthesia, p. 9796; Color Atlas of Human Anatomy, Vol. 2, p. 202

7. Technique of Indirect Laryngoscopy

Equipment: angled laryngeal mirror (no. 4–6), head mirror or fibre-optic headlight, spirit lamp.
Technique:
  1. Patient seated upright, neck slightly flexed, head extended ("sniffing position")
  2. Patient protrudes tongue; examiner grasps it gently with gauze
  3. Warm mirror briefly over flame; test temperature on examiner's hand
  4. Mirror inserted to posterior oropharynx, mirror face angled inferiorly, touching the soft palate/uvula (NOT the posterior pharyngeal wall to avoid gag)
  5. Patient breathes through mouth or says "eeee" (Valsalva) to elevate soft palate
  6. Observe: epiglottis, aryepiglottic folds, arytenoids, false and true vocal cords, subglottis, pyriform fossae
  7. Assess cord mobility: ask patient to say "eee" (adduction) and breathe deeply (abduction)
  8. Note: the image is inverted — anterior structures appear at the top of the mirror image
Contraindications/difficulties: gag reflex (topical lignocaine spray), trismus, obesity, short neck.

8. Technique of Direct Laryngoscopy

Indications: operative laryngoscopy, biopsy, foreign body removal, intubation, airway assessment.
Equipment: rigid laryngoscope (Macintosh or straight/Miller blade for intubation; Lindholm/suspension laryngoscope for microlaryngoscopy).
Technique:
  1. Patient supine; head in "sniffing position" (neck flexed, atlantooccipital joint extended)
  2. Open mouth with right hand; blade inserted on right side of tongue, sweeping it leftward
  3. Macintosh blade: tip placed in vallecula; upward lifting force (at 45°) elevates epiglottis indirectly
  4. Miller (straight) blade: tip placed posterior to epiglottis; lifts it directly
  5. Force directed along the blade handle axis (never lever against upper incisors)
  6. Glottis identified; procedure performed or ETT passed under vision
For suspension microlaryngoscopy: laryngoscope suspended from a chest support, freeing both hands; operating microscope used at 400 mm focal length.
Local anaesthesia for awake laryngoscopy: topical spray to oropharynx; superior laryngeal nerve block (inject 3 mL lidocaine 1 cm caudal to greater cornu of hyoid through thyrohyoid membrane); transtracheal block (25G needle through cricothyroid membrane midline, aspirate air, inject 4 mL lidocaine).
K.J. Lee's Essential Otolaryngology, p. 123; Miller's Anesthesia, p. 9796

9. Causes of Acute Laryngeal Stenosis

Inflammatory/Infectious:
  • Acute epiglottitis (H. influenzae)
  • Acute laryngotracheobronchitis (croup — parainfluenza virus)
  • Bacterial tracheitis (S. aureus)
  • Diphtheria (Corynebacterium diphtheriae — true croup)
  • Laryngeal abscess, Ludwig's angina extension
  • Measles laryngitis
Allergic/Oedematous:
  • Anaphylaxis
  • Angioedema (hereditary or allergic)
  • Drug reactions (ACE inhibitors — bradykinin-mediated)
Traumatic:
  • Foreign body aspiration
  • Post-intubation subglottic oedema/stenosis
  • Laryngeal fracture (blunt neck trauma)
  • Inhalation burns (smoke, steam, caustic agents)
  • Iatrogenic (post-operative, post-radiotherapy)
Neoplastic:
  • Rapidly growing laryngeal tumours
  • Bilateral vocal cord paralysis (thyroid/oesophageal surgery, mediastinal mass)
Neurological:
  • Laryngospasm (bilateral adductor muscle spasm, often from anaesthetic)

10. Acute Laryngeal Stenosis — Stages, Clinic, Diagnosis, Treatment

Stages (Classic Four-Stage Classification)

StageClinical Features
Stage I (Compensation)Inspiratory stridor only on exertion; mild retraction; no hypoxia; patient compensates by reducing activity
Stage II (Subcompensation)Stridor at rest; visible inspiratory retraction (suprasternal, supraclavicular, intercostal); tachypnoea; mild cyanosis; anxiety; patient is awake and fighting
Stage III (Decompensation)Severe stridor at rest; marked retractions; pronounced cyanosis; profuse sweating; restlessness turning to agitation/exhaustion; orthopnoea
Stage IV (Asphyxia)Loss of consciousness; cessation of struggle; paradoxical bradycardia then cardiac arrest; gasping; complete cyanosis

Diagnosis

  • Clinical: stridor, voice change, cough character, history
  • Lateral neck X-ray: epiglottitis (thumbprint sign, thickened aryepiglottic folds), croup (steeple sign)
  • Fibre-optic laryngoscopy (in cooperative patients without complete obstruction)
  • Pulse oximetry, ABG

Treatment by Stage

  • Stage I: Monitor, treat underlying cause (antibiotics, steroids, adrenaline)
  • Stage II: Nebulised adrenaline (epinephrine), systemic corticosteroids (IV dexamethasone), humidified oxygen, prepare for intubation
  • Stage III: Immediate tracheal intubation or tracheostomy; corticosteroids IV
  • Stage IV: Emergency cricothyrotomy (conicotomy) → secure airway → CPR → definitive airway

11. Acute Laryngeal Oedema — Cause, Clinic, Diagnosis, Treatment

Aetiology

  • Allergic: anaphylaxis (bee stings, drugs, foods, latex), angioedema
  • Hereditary angioedema (C1-esterase inhibitor deficiency — does NOT respond to adrenaline)
  • Iatrogenic: post-intubation, post-radiotherapy, post-operative
  • Inflammatory: acute epiglottitis, Ludwig's angina
  • Inhalation injury: steam, smoke, chemicals
  • Renal failure, cardiac failure (hypoproteinaemic states)

Clinical Features

  • Inspiratory stridor (± biphasic in severe cases)
  • Muffled or hoarse voice
  • Dysphagia, drooling (if supraglottic)
  • Progressive respiratory distress
  • Rapid onset (minutes in anaphylaxis; hours in hereditary angioedema/inflammatory)

Diagnosis

  • Clinical; direct/fibre-optic laryngoscopy shows pale, gelatinous supraglottic swelling
  • Lateral neck X-ray shows enlarged epiglottis
  • Lab: tryptase (anaphylaxis), C4/C1-inhibitor levels (hereditary angioedema)

Treatment

  • Anaphylaxis: IM adrenaline (0.5 mg, 1:1000), IV hydrocortisone, IV chlorphenamine, IV fluid; early endotracheal intubation; may need surgical airway
  • Hereditary angioedema: C1-inhibitor concentrate, icatibant, or tranexamic acid; NOT adrenaline/antihistamines
  • Inflammatory: treat underlying infection; corticosteroids; airway protection
  • All severe cases: oxygen, IV dexamethasone, nebulised adrenaline, early consideration of intubation or tracheostomy
  • If airway lost: emergency cricothyrotomy → tracheostomy
Miller's Anesthesia, p. 9799

12. False Croup vs True Croup — Differential Diagnosis

False Croup (Viral Laryngotracheobronchitis)

Aetiology: Parainfluenza virus type 1 (50–75% of cases); also RSV, influenza A & B, rhinovirus, measles.
Pathophysiology: Viral inflammation → oedema of the subglottic space (BELOW the cords) → the non-expandable cricoid ring concentrates the oedema → airway narrowed to 1–2 mm in severe cases.
Epidemiology: Most common cause of stridor in children; peak age 6–36 months.
Clinical Features:
  • 1–3 day prodrome of mild fever and URI symptoms
  • Barky ("seal-like") cough — pathognomonic
  • Hoarse voice
  • High-pitched inspiratory stridor
  • Worse at night; aggravated by crying/agitation
  • Duration 4–7 days; self-limiting
Severity Assessment:
  • Mild: barky cough, stridor only with agitation, minimal distress
  • Moderate: stridor at rest, retractions, tachypnoea, fussy
  • Severe: stridor at rest + severe retractions + agitation/lethargy/cyanosis
Diagnosis:
  • Clinical; radiography if diagnosis uncertain
  • CXR/neck X-ray: steeple sign (symmetric subglottic narrowing on AP view)
Treatment:
  • Mild: single oral dose of dexamethasone (0.15–0.6 mg/kg); supportive, humidified air
  • Moderate/severe: nebulised epinephrine (racemic or L-epinephrine) + dexamethasone
  • Severe: intubation (use a smaller tube than expected), heliox as temporising measure
  • Observation period of 2–4 hours after nebulised epinephrine before discharge

True Croup (Laryngeal Diphtheria)

Aetiology: Corynebacterium diphtheriae (gram-positive rod, toxin-producing). Spread by respiratory droplets.
Pathophysiology: Exotoxin causes coagulative necrosis of the laryngeal and tracheal mucosa → formation of a tough grey pseudomembrane → progressive mechanical obstruction; exotoxin absorbed systemically → myocarditis, polyneuritis.
Clinical Features:
  • Insidious onset; child appears toxic, pale
  • Low-grade fever; sore throat → hoarseness → aphonia
  • Barky cough
  • Progressive stridor (subglottic membrane extension)
  • Membranous exudate: tough grey/white membrane on tonsils, pharynx, larynx — bleeds on removal (pathognomonic)
  • "Bull neck" — cervical lymphadenopathy + soft tissue oedema
  • Systemic: myocarditis (arrhythmias, heart failure), late peripheral neuropathy
Diagnosis:
  • Clinical; throat swab with Loeffler's medium culture; Gram stain
  • Albert stain shows metachromatic granules
  • Elek test for toxin production
Treatment:
  • Diphtheria antitoxin (DAT) — IV, URGENT (neutralises free toxin)
  • Antibiotics: benzylpenicillin or erythromycin (eradicate organism)
  • Airway management: gentle removal of membrane, intubation or tracheostomy if needed
  • Isolation; cardiac monitoring for myocarditis
  • Quarantine + contact tracing

Differential Diagnosis: False vs True Croup

FeatureFalse Croup (Viral)True Croup (Diphtheria)
CauseParainfluenza virusC. diphtheriae
OnsetAcute; URI prodromeInsidious
FeverLow–moderateLow-grade
MembraneAbsentPresent — grey, adherent, bleeds
ToxicityMild–moderateSevere ("toxic" appearance)
Location of obstructionSubglotticGlottis + trachea
Vaccination historyUsually vaccinatedUnvaccinated / incomplete
Steeple signYes (AP X-ray)No
TreatmentSteroids + epinephrineAntitoxin + antibiotics
Systemic complicationsRareMyocarditis, neuropathy

13. Acute Epiglottitis (Supraglottic Laryngitis)

Aetiology: H. influenzae type b (Hib) — historically; post-Hib vaccine era: Hib remains most common, also other H. influenzae types, streptococci, S. aureus (incl. MRSA), N. meningitidis. Noninfectious: thermal injury, caustic ingestion, allergic reaction, foreign body.
Pathophysiology: Invasive bacterial inflammation of epiglottis, aryepiglottic folds, arytenoids → oedema → supraglottic structures prolapse over the glottic opening → ball-valve effect on inspiration.
Clinical Features (Classic):
  • Acute onset; high fever, intense sore throat, toxicity
  • "3 Ds" — Drooling, Dysphagia, Distress
  • Tripod/sniffing position: jaw forward, neck extended, leaning forward on hands
  • Muffled "hot-potato" voice (but hoarseness typically absent — differentiates from croup)
  • Cough absent or minimal
  • Stridor — usually inspiratory; may be absent in very severe obstruction
  • Rapid progression to complete airway obstruction (esp. in infants/young children)
  • Older patients: sore throat out of proportion to pharyngeal findings; anterior neck tenderness
Diagnosis:
  • Lateral neck X-ray: thumbprint sign — rounded, enlarged epiglottis; thickened aryepiglottic folds; lack of air in vallecula; hypopharyngeal overdistension
  • Up to 70% may have normal X-ray
  • Do NOT perform oropharyngeal examination in a child with suspected epiglottitis — may precipitate complete obstruction; examine only in OR with intubation equipment ready
  • Blood cultures (positive in <10% of cases)
Management:
  • Paediatric (≤12 yrs): immediate controlled intubation in OR under inhalation anaesthesia; surgeon scrubbed for emergency tracheostomy
  • Adult: flexible nasendoscopy + fiberoptic intubation if needed; may manage conservatively with IV antibiotics + close monitoring
  • IV antibiotics: 3rd-generation cephalosporin (ceftriaxone) ± MRSA cover
  • IV dexamethasone
  • Extubation after 24–48 hours when oedema resolved (confirm with direct laryngoscopy)
ROSEN's Emergency Medicine, p. 3723–3745; Miller's Anesthesia, p. 9799

14. Acute Laryngitis — Clinic, Diagnosis, Treatment

Definition: Acute inflammation of the laryngeal mucosa, usually viral, lasting <3 weeks.
Aetiology: Viruses (rhinovirus, parainfluenza, adenovirus, influenza); secondary bacterial infection (H. influenzae, S. pneumoniae, M. catarrhalis); vocal overuse; irritants (smoke, chemicals, GORD).
Clinical Features:
  • Hoarseness or dysphonia (cardinal symptom)
  • Dry irritating cough
  • Throat discomfort/soreness
  • Low-grade fever
  • Mild dysphagia
  • Laryngoscopy: erythema and oedema of vocal cords; mucosal secretions
Diagnosis: Clinical; laryngoscopy to confirm and exclude other pathology.
Treatment:
  • Voice rest (avoid whispering — increases cord strain)
  • Humidification; adequate hydration
  • Analgesics/anti-inflammatories
  • Antibiotics only if bacterial secondary infection is confirmed
  • Treat GORD if present
  • Short-course systemic corticosteroids if rapid recovery needed (e.g., professional voice user)
  • Resolution within 1–2 weeks

15. Chronic Laryngitis — Clinic, Diagnosis, Treatment

Aetiology: Prolonged vocal abuse, smoking, GORD, alcohol, chronic nasal/sinus infection with postnasal drip, occupational exposure, persistent viral infection.

Chronic Hyperplastic Laryngitis (Laryngitis Chronica Hyperplastica)

  • Most common type
  • Persistent hoarseness, rough voice, chronic cough
  • Laryngoscopy: diffuse erythema; thickened, irregular vocal cord mucosa; surface leukoplakia (white patches) — must be biopsied to exclude dysplasia/carcinoma
  • Treatment: eliminate causative factors; voice therapy; microlaryngoscopy and biopsy/laser vaporisation for resistant lesions; cessation of smoking is mandatory

Atrophic Laryngitis (Laryngitis Sicca)

  • Often associated with atrophic rhinitis
  • Dry, crusted, thick secretions on the cords → persistent dry cough, hawking, sensation of foreign body
  • Laryngoscopy: dry, pale, thin mucosa; adherent brownish/greenish crusts
  • Voice may be roughened, weak
  • Treatment: humidification; alkaline saline sprays/irrigations; iodine-glycerine applications; mucophage agents; treat underlying atrophic rhinitis

16. Foreign Bodies of the Larynx, Trachea, and Bronchi

Epidemiology: More common in children 6 months–3 years; also elderly with dysphagia. Right main bronchus receives >60% of aspirated objects (departs at 20° from trachea; more vertical than the left).
Types: Organic (nuts, seeds — most dangerous; swell with moisture, release oils causing reactive bronchitis) and inorganic (coins, plastic, metal).
Clinical Features:
  • Laryngeal/tracheal foreign body: sudden choking; coughing/stridor; aphonia/dysphonia; cyanosis; may be life-threatening immediately
  • Bronchial foreign body: Initial choking attack followed by apparent improvement; chronic phase: wheeze, unilateral reduced air entry, recurrent pneumonia in same lobe
  • Classic triad: wheeze + unilateral reduced breath sounds + cough
Diagnosis:
  • Plain X-ray: radiopaque objects visible; radiolucent objects → unilateral hyperinflation (air trapping), mediastinal shift away from obstruction on expiratory film
  • CT chest: sensitive for non-opaque foreign bodies
  • Bronchoscopy: definitive — both diagnostic and therapeutic
Treatment:
  • Immediate choking (witnessed): Heimlich manoeuvre (abdominal thrusts); back blows in infants
  • Complete obstruction: emergency Heimlich; emergency cricothyrotomy
  • Bronchoscopy: rigid bronchoscopy under GA — procedure of choice for removal; flexible bronchoscopy has a role in adults
  • Antibiotics if post-obstructive pneumonia
Complications: Pneumonia, bronchiectasis, lung abscess, haemoptysis.

17. Foreign Bodies of the Oesophagus

Common sites of impaction:
  1. Upper oesophageal sphincter (cricopharyngeus) — most common (C5–6)
  2. Level of aortic arch (T4)
  3. Lower oesophageal sphincter
Common objects: Fish/chicken bones, coins, dentures, meat bolus.
Clinical Features:
  • Dysphagia (solids > liquids)
  • Drooling/hypersalivation
  • Retrosternal pain
  • Regurgitation
  • Neck pain; torticollis (vertebral penetration)
  • In children: refusal to feed, distress
Diagnosis:
  • Plain X-ray neck/chest: radiopaque objects; cervical soft tissue swelling
  • Coins in oesophagus = frontal (en face); coins in trachea = lateral (edge-on)
  • Barium swallow (if X-ray negative and high suspicion)
  • Oesophagoscopy: definitive
Treatment:
  • Rigid oesophagoscopy: gold standard for removal
  • Flexible endoscopy: option for soft food boluses, non-sharp objects in cooperative adults
  • Glucagon IV (relaxes LOS for food bolus)
  • Sharp objects, batteries: urgent removal (batteries cause liquefactive necrosis within hours)
  • Perforation: IV antibiotics, surgical drainage/repair

18. Indications and Technique of Tracheostomy

Indications

  1. Upper airway obstruction (unrelieved or anticipated) — laryngeal stenosis, bilateral cord palsy, tumour, trauma
  2. Prolonged mechanical ventilation (>7–14 days)
  3. Need to bypass upper airway (obstructive sleep apnoea; neuromuscular disease)
  4. Pulmonary toilet — facilitation of tracheal suctioning in patients with poor cough
  5. Prophylactic (pre-operatively before major head/neck surgery)

Types of Tracheostomy

  • Emergency (high) tracheostomy: above isthmus of thyroid — used in acute obstructive emergencies
  • Standard (low) tracheostomy: below isthmus (between 2nd and 4th tracheal rings) — standard elective procedure
  • Percutaneous dilational tracheostomy (PDT): bedside technique using Seldinger technique + serial dilators; increasingly used in ICU

Technique (Standard Surgical Tracheostomy)

  1. Patient supine; shoulder roll to extend neck; local anaesthesia ± GA
  2. Transverse or midline incision 2 cm below cricoid (2 finger-widths)
  3. Divide platysma; separate strap muscles in midline
  4. Thyroid isthmus: divide and suture-ligate if it overlies the trachea
  5. Identify trachea; confirm with needle aspiration of air
  6. Make incision into trachea between 2nd–4th rings (avoid 1st ring to prevent subglottic stenosis):
    • Window (H or U flap); or
    • Vertical midline incision (in emergency)
    • Stay sutures placed lateral to incision for emergency retrieval
  7. Insert appropriately-sized tracheostomy tube; confirm with capnography and chest auscultation
  8. Secure tube with ties around neck; suture flange to skin

Complications of Tracheostomy

Immediate:
  • Haemorrhage (anterior jugular veins, thyroid vessels)
  • False passage
  • Apnoea (loss of hypercapnic drive in chronic CO2 retainers)
  • Tube misplacement (subcutaneous/paratracheal)
  • Cardiorespiratory arrest
Early (Days 1–7):
  • Tube displacement/decannulation
  • Surgical emphysema
  • Wound infection
  • Obstruction of tube (secretions, crusting)
  • Pneumothorax, pneumomediastinum
Late (Weeks/Months):
  • Tracheomalacia (cartilage destruction)
  • Subglottic/tracheal stenosis (most important late complication)
  • Tracheo-innominate artery fistula (life-threatening haemorrhage ~day 7–10 — tube erodes into innominate artery)
  • Tracheo-oesophageal fistula
  • Persistent tracheocutaneous fistula after decannulation
  • Difficulty swallowing (reduced laryngeal elevation)
  • Cosmetic scarring

19. Technique of Conicotomy (Cricothyrotomy)

Definition: Emergency incision through the cricothyroid membrane (median cricothyroid ligament) to establish an airway.
Indication: Life-threatening airway obstruction when intubation has failed or is impossible — "cannot intubate, cannot oxygenate" scenario.
Anatomy of the cricothyroid membrane: Located between the lower border of the thyroid cartilage and the upper border of the cricoid arch; midline structure, covered only by skin and subcutaneous tissue; dimensions approximately 9 mm height × 30 mm width in adults; superior laryngeal vessels run along the upper margin (avoid).
Surgical Technique:
  1. Patient supine; neck extended
  2. Stabilise thyroid cartilage between thumb and middle finger of non-dominant hand
  3. Identify cricothyroid membrane with index finger (soft depression between two hard cartilages)
  4. Transverse stab incision through skin and membrane — 1.5 cm wide, in the LOWER half of the membrane to avoid the cricothyroid artery
  5. Hook the cricoid cartilage downward; insert tracheal dilator or curved haemostat; insert small cuffed tracheostomy tube (6.0 or 6.5 mm)
  6. Confirm: capnography, bilateral chest auscultation
Needle (Mini) Cricothyrotomy:
  • 14G IV cannula through membrane; attach oxygen via Y-connector or improvised Luer-lock; jet insufflation 15 L/min
  • Buys up to 30–45 minutes in adults; preferred in infants/small children (surgical cricothyrotomy challenging due to small membrane)

20. Tracheal Intubation — Indications and Technique

Indications

  • Protection of airway (aspiration risk, impaired consciousness)
  • Mechanical ventilation
  • Upper airway obstruction (stages III–IV laryngeal stenosis)
  • Facilitation of general anaesthesia
  • Pulmonary toilet

Technique (Direct Laryngoscopy)

  1. Pre-oxygenation — 100% O₂ × 3–5 min; allows denitrogenation
  2. Induction — IV anaesthetic ± muscle relaxant
  3. Sniffing position (neck flexed at C7, head extended at atlantooccipital joint)
  4. Blade inserted as above; glottis identified
  5. ETT passed through vocal cords under direct vision; cuff inflated
  6. Confirmation: capnography (gold standard); bilateral chest auscultation; CXR
  7. Cuff pressure maintained <25 mmHg to prevent tracheal mucosal ischaemia
Difficult airway: Video laryngoscopy; awake fiberoptic intubation (topical anaesthesia + nerve blocks); surgical airway backup.
Rapid Sequence Induction (RSI): Pre-oxygenation → cricoid pressure (Sellick's manoeuvre) → propofol/thiopentone + suxamethonium → intubate without bag-mask ventilation (reduces aspiration risk).

21. Chronic Hyperplastic Laryngitis — Clinical Picture

  • Persistent hoarseness; rough, low-pitched voice; vocal fatigue
  • Chronic nonproductive cough; throat clearing
  • Laryngoscopy: diffuse hyperaemia; mucosal thickening of cords; irregular surface; leukoplakia (white patches) on the cords — dysplastic potential
  • Pachydermia: warty thickening of interarytenoid mucosa
  • Risk factors: smoking, alcohol, GORD, vocal abuse, chronic sinusitis
  • Key concern: leukoplakia → mandatory microlaryngoscopy biopsy to exclude carcinoma in situ or SCC
  • Treatment: eliminate causative factors; CO₂ laser stripping/microlaryngoscopy; strict follow-up for leukoplakia

22. Atrophic Laryngitis (Laryngitis Sicca) — Clinical Picture

  • Usually co-exists with atrophic rhinitis and pharyngitis ("ozaena complex")
  • Dry, harsh, weak voice; persistent tickling cough
  • Sensation of foreign body in the throat; constant hawking
  • Laryngoscopy: pale, dry, thin mucosa; adherent yellowish-green or brownish crusts covering the vocal cords and subglottis; wide rima glottidis; atrophic-looking cords
  • Voice worsens with talking; improves after crust removal
  • Pathology: squamous metaplasia; gland atrophy; reduced mucus production
  • Treatment: humidification; alkaline-saline irrigations; iodine-glycerine; vitamin A; treat atrophic rhinitis; reassurance (not malignant)

23. Laryngeal Tuberculosis — Clinical Features

Epidemiology: Rare in developed countries; secondary to pulmonary TB in almost all cases; haematogenous or contact spread (infected sputum).
Pathology: Miliary mucosal tubercles → caseating granulomas → ulceration → fibrous healing → stenosis. Most commonly involves the posterior larynx (posterior commissure, arytenoids, epiglottis).
Clinical Features:
  • Persistent progressive hoarseness
  • Odynophagia (marked pain on swallowing — differentiates from carcinoma)
  • Chronic non-productive or productive cough (sputum may be acid-fast bacilli positive)
  • Stridor (late/stenosis)
  • Systemic TB: weight loss, night sweats, haemoptysis, fever
  • "Pale oedematous" appearance of laryngeal mucosa (vs red, irregular carcinoma)
  • May simulate carcinoma — biopsy essential
Diagnosis:
  • Laryngoscopy + biopsy: caseating granulomata with Langhans giant cells; ZN stain / culture for AFB
  • CXR / chest CT (primary pulmonary focus)
  • Sputum AFB; Mantoux/IGRA
Treatment:
  • Standard anti-TB regimen (RIPE): rifampicin + isoniazid + pyrazinamide + ethambutol × 2 months, then continuation phase
  • Corticosteroids for severe oedema/stenosis
  • Voice rest

24. Laryngomalacia (Laryngeal Stridor) — Aetiology, Clinic, Diagnosis, Treatment

Definition: The most common cause of chronic stridor in neonates and infants; caused by immaturity or hypotonia of supraglottic structures.
Aetiology: Immaturity of the cartilaginous and neuromuscular support of the supraglottis; floppy epiglottis collapses posteriorly, short aryepiglottic folds tether the epiglottis, bulky arytenoids prolapse into the airway on inspiration. Associated with GORD (in >75%), neurological conditions.
Clinical Features:
  • Onset: 1st–2nd week of life (may be present from birth)
  • Inspiratory stridor — high-pitched, fluctuating; worst when supine, feeding, crying; better prone or with neck extension
  • Stridor worsens 4–8 months (peak) then gradually resolves by 18–24 months in 90%
  • Feeding difficulties; prolonged feeding times; failure to thrive in severe cases
  • Cyanotic episodes (severe)
  • No voice change (unlike croup)
Diagnosis:
  • Flexible nasopharyngolaryngoscopy — shows dynamic supraglottic collapse on inspiration (omega-shaped, elongated epiglottis; short aryepiglottic folds; prolapsing arytenoid mucosa)
  • Also rules out other causes of neonatal stridor (vocal cord paralysis, subglottic stenosis, haemangioma)
Treatment:
  • Mild–moderate: reassurance; prone positioning; anti-reflux therapy (ranitidine/PPI + thickened feeds); parental education; spontaneous resolution expected
  • Severe (failure to thrive, severe desaturation, apnoea): supraglottoplasty — CO₂ laser or cold steel division of aryepiglottic folds ± excision of redundant arytenoid mucosa; success rate >90%
  • Tracheostomy rarely required for refractory cases

25. Classification of Laryngeal Paralysis

By Side

  • Unilateral (more common) — usually tolerated; hoarse, breathy voice; mild aspiration
  • Bilateral — potential life-threatening airway emergency; usually presents with stridor ± dyspnoea

By Level of Lesion (Anatomical)

  • Peripheral (RLN) — paralysis of all intrinsic laryngeal muscles except cricothyroid; cord in paramedian position; most common
  • Superior laryngeal nerve — cricothyroid paralysis only; pitch and projection affected; loss of protective reflex → silent aspiration
  • Combined (vagus nerve trunk) — paralysis of both RLN and SLN; cord in cadaveric (lateral) position
  • Central — upper motor neuron lesion; bilateral; cortical, brainstem, or skull base pathology

By Cord Position (Semon & Rosenbach)

  • Median position — complete adduction; both cords together (bilateral adductor paralysis — rare)
  • Paramedian position — just off midline; most common in RLN palsy; reasonable voice, impaired airway
  • Intermediate position — mid-abduction
  • Cadaveric position — full abduction; poor voice; good airway

By Cause

  • Surgical: thyroidectomy (most common cause), parathyroid, oesophageal, cardiac, aortic arch
  • Neoplastic: lung apex (left RLN), thyroid, oesophageal, mediastinal
  • Neurological: CVA, multiple sclerosis, syringomyelia, bulbar palsy
  • Idiopathic: post-viral
  • Traumatic: intubation injury, external laryngeal trauma
Management:
  • Unilateral: observe 6–12 months for recovery; voice therapy; medialization thyroplasty or injection augmentation if persistent
  • Bilateral (acute): intubation/tracheostomy for airway; later, arytenoidectomy or posterior cordotomy to widen the glottic aperture (sacrifices some voice)

26. Reinke's Oedema (Polypoid Degeneration of Vocal Cords)

Pathogenesis

Reinke's space is the superficial lamina propria of the vocal cord — a loose connective tissue layer between the epithelium and the vocal ligament. Chronic irritation (especially tobacco smoke) → increased vascular permeability → accumulation of oedematous fluid within Reinke's space bilaterally → gradual polypoid expansion of the entire cord length.
Pathological factors:
  • Smoking (most important — present in >90%)
  • GORD
  • Hypothyroidism
  • Vocal abuse
Histology: oedematous stroma; dilated tortuous vessels; myxoid stroma; epithelial hyperplasia without dysplasia.

Clinical Features

  • Predominantly in middle-aged women who smoke
  • Progressive deepening and roughening of the voice — characteristic low, "whisky voice"
  • Chronic hoarseness; vocal fatigue
  • Occasional mild stridor (if extensive)
  • Laryngoscopy: bilateral translucent, pale, gelatinous-appearing swellings occupying the entire cord; "water-bag" appearance; worse anteriorly
  • Endoscopy (Fig. 66.6B in Miller's Anesthesia) shows characteristic bilateral cord swelling

Treatment

  • Mandatory: cessation of smoking (treatment fails without it); treat GORD; voice therapy
  • Surgical (if voice or airway affected): microlaryngoscopy under GA — microsurgical cordotomy (longitudinal epithelial incision at the superior surface) → suck out gelatinous fluid → redraped epithelium; CO₂ laser can also be used
  • Staged bilateral procedures (never strip both cords simultaneously — risk of anterior commissure web)
  • Hypothyroidism: thyroid replacement alone may partially resolve oedema
Miller's Anesthesia, FIG. 66.6B; Color Atlas of Human Anatomy, Vol. 2

Summary Differential — Upper Airway Obstruction in Children

ConditionKey Distinguishing Feature
Viral croupURI prodrome; barky cough; stridor ± agitation; steeple sign
EpiglottitisToxic; drooling; no cough; thumb-print sign; tripod position
Bacterial tracheitisViral prodrome → acute decompensation; fails croup Rx; ragged trachea on X-ray
Diphtheria (true croup)Membrane; bull neck; systemic toxicity; unvaccinated
Foreign bodySudden choking; no fever/URI; unilateral wheeze
AnaphylaxisAbrupt; trigger identified; urticaria/angioedema
LaryngomalaciaNeonatal; worse supine; improves with neck extension; no fever

Sources: Color Atlas of Human Anatomy Vol. 2 (Thieme) — Internal Organs, pp. 190–209; Cummings Otolaryngology Head and Neck Surgery, pp. 1958–2124; Miller's Anesthesia 10e, pp. 9789–9802; ROSEN's Emergency Medicine, pp. 3523–3905; Morgan & Mikhail's Clinical Anesthesiology 7e, pp. 401–939; K.J. Lee's Essential Otolaryngology, pp. 123–124.

136 Physiology of hearing 137 Anatomy of the outer ear (blood supply, innervation). 138 Anatomy of the middle ear (blood supply, innervation). 139 Anatomy of the eustachian tube, functions and differences between the adult and infant ET 140 Anatomy of the auditory analyzer (cochlea) 141 Anatomy of the vestibular analyzer (vestibule, semicircular canals) 142 Auditory neural pathways and their nuclei 143 Physiology of hearing and vestibular system 144 Eustachian tube function tests 145 Tuning fork tests (Rinne, Weber,Bing) 146 Assesment of vestibular functions (Fistula, Romberg, Gait, Caloric, Rotation test) 147 Subjective methods of hearing research (Pure Tone audiometry, Speech audiometry) 148 Types of tympanogram 149 Objective methods of hearing research (OAE, BERA, ASSR, Tympanometry) 150 Anatomy of inner ear 151 Technique of otoscopy 152 Characteristics of types and degrees of hearing loss. 153 Structure of organ of corti 154 The technique of conducting the Rinne experience. 155 Technique of conducting Weber's experiment. 156 The technique of conducting the Schwabach experiment. 157 Anomalies of the development of the outer ear. 158 Trauma to the Auricle, causes, classification, first aid. 159 Traumatic rupture of tympanic membrane (causes and treatment). 160 Foreign bodies of the external auditory canal, tactics of treatment. 161 Haematoma of the auricle, diagnosis and treatment methods. 162 External otitis media, etiology, pathogenesis, classification and treatment. 163 Eczematous otitis externa (clinic, diagnosis and treatment) 164 Furuncle of the external auditory canal, diagnosis and treatment methods. 165 Otomycosis, diagnosis and treatment methods. 166 Perichondritis of the auricle, diagnosis and treatment. 167 Disorders of eustachian tube (tubal blockage) 168 Acute suppurative otitis media (etiology, diagnosis and treatment) 169 Otitis media with effusion (Glue Ear), diagnosis and treatment tactics. 170 Cholesteatoma (classification) 171 Paracentesis- Myringotomy (technique, indication). 172 Complications of acute otitis media 173 Mastoiditis, etiology, pathogenesis, classification. 174 Classification of chronic otitis media. 175 Chronic purulent otitis media, diagnosis and treatment methods.

Reading File
Your credits are exhausted. Your daily credits reset tomorrow, or you can purchase a top-up for more.
This is a shared conversation. Sign in to Orris to start your own chat.