Dr Manpreet Singh Nanda
Associate Professor ENT
MMMC&H Solan
Stridor
 Abnormal high pitched noisy respiration due to flow of air
through a partially obstructed narrowed lower airway
mainly larynx and tracheobronchial tree
 Types
 Inspiratory – supraglottis, glottis, hypopharynx
 Expiratory (wheeze) – thoracic trachea, bronchi,
bronchioles
 Biphasic – cervical trachea, subglottis
 Stertor – snoring low pitched noise due to obstruction in
nasopharynx and oropharynx
 Rales and crepitations – distal portion of bronchial tree
and alveoli
Etiology
 Neonates – laryngomalacia (mc), laryngeal webs, cysts,
subglottic stenosis, laryngeal paralysis
 Children – laryngotracheobronchitis (croup), acute
epiglottis, laryngeal FB
 Nose – choanal atresia
 Tongue – macroglossia, haemangioma, lymphangioma
 Mandible – micrognathia
 Pharynx – abscess
 Larynx – paralysis, trauma
 Trachea – tumours, FB, stenosis, TOF
 Oesophagus – FB
 Neck – tumours, abscess
 Children affected more – narrrow airway, softer
cartilage collapse easily
 Adults
 Malignancy of larynx, pharynx, tongue, neck, trachea
(mc)
 Infections – ludwigs angina
 Allergy – angioneurotic oedema
 Trauma – fractures, iatrogenic, radiotherapy, caustic
agents
 Neurogenic - paralysis
Assessment
 Mc physical sign of larynx
 History
 Age – at birth (congenital), after few weeks (laryngomalacia)
 Onset – sudden (FB)
 Progress – rapid (acute epiglottitis), gradual (subglottic haemangioma,
malignancy)
 h/o fever – infective
 h/o cough – aspiration, TOF
 h/o hoarseness – vc
 h/o apnoea and cyanosis – tracheobronchomalacia
 h/o trauma, intubation
 h/o FB
 Improves in prone position – laryngomalacia, macroglossia, micrognathia
 Improves during crying – B/L chonal atresia
 Worsens during crying - laryngomalacia
Examination
 Note the type of stridor
 Note the sound of stridor
 - musical quality – laryngomalacia
 - breathy – vc paralysis
 - aspiration – vc paralysis
 - barking cough – tracheomalacia
 Note associated symptoms
 - hoarseness – larynx
 - wheeze – bronchi
 - dysphagia – hypopharynx
 Note the severity
 - subcostal, intercostal, suprasternal recession
 - cyanosis
 Detailed examination of oral cavity, nasal cavity,
pharynx and larynx (IDL)
 INVESTIGATIONS
 Oxygen saturation monitoring
 - arterial blood gas estimation, pulse oxymetry
 Radiographs
 - x ray chest, neck
 - CT, MRI
 pH monitoring
 Endoscopy –
 - Bronchoscopy
 - Oesophagoscopy
 - Laryngoscopy
 Along with intubation in OT
 Flexible endoscopy
 Videofluoroscopy – chest movements
 USG Neck
Treatment
 Acute condition
 Admit
 Conservative
 - oxygen and humidification
 - antibiotics
 - IV steroids
 - Nebulized epinephrine
 - mucolytics
 - IV fluids
 - CPAP (Continued Positive Airway Pressure)
 Intubation
 Endotracheal intubation – nasal (secure)
 Preferred
 Ventilatory bronchoscopy
 Endoscopy and FB removal
 Not done in acute epiglottitis, impacted FB, trismus,
severe subglottic stenosis, mandible fracture,
supraglottic tumours
 Tracheostomy
 Cricothyroidotomy
 Chronic
 - Anti reflux treatment
 - Systemic steroids
 - Prophylactic antibiotics
 - Treat the cause
Congenital lesions of larynx
 Laryngomalacia
 Subglottic stenosis
 Laryngeal web/atresia/cyst
 Vocal cord paralysis
 Subglottic haemangioma
 Laryngocele
 Laryngo oesophageal cleft
Laryngomalacia
 Congenital laryngeal stridor
 Excessive flaccidity of supraglottic larynx which gets
sucked in during inspiration producing stridor and
sometimes cyanosis
 Pathology
 Excessive softening of laryngeal skeletal framework ->
indrawing of aryepiglottic folds -> narrowing -> stridor
Clinical features
 M:F 2:1
 Low socio economic group
 Intermittent low pitched inspiratory stridor develops
during first two weeks of life (rare at birth)
 Aggravates on crying, feeding, exertion
 Relieved in prone position, rest and sleep
 Seen maximum at 9-12 months of age
 Completely disappears after 2 years of age (5 years)
 Normal cry and voice
 In severe cases – feeding difficulty, failure to thrive and
cyanosis
Signs
 Awake flexible laryngoscopy
 Anterior collapse of arytenoid
 Posterior collapse of epiglottis
 Inward collapse of aryepiglottic folds
 Omega shaped/tubular epiglottis
 Prominent arytenoids
 Normal vocal cords
 Complications – GERD, recurrent URTI, OSA
 D/D – laryngeal webs, cysts
 Treatment
 Conservative (90%)
 - Reassurance
 - Observation
 - Treat the URTI
 Tracheostomy
 Surgery (10%) – when failure to thrive or cyanosis
 - Supraglottoplasty (Aryepiglottoplasty)
Congenital laryngeal haemangioma
 Subglottic haemangioma
 Benign vascular malformation involving subglottis
 C/F
 Females mc
 Asymptomatic for 3 to 6 months of age
 With increase size progressive disease
 Inspiratory or mostly biphasic stridor which is progressive
 Appears with URTI
 Aggravated by crying or agitation
 Dyspnoea and cyanosis
 Associated with cutaneous haemangioma or mediatinal
haemangioma
 Rapid growth till 1 year of age then regress
 Diagnosis
 X Ray Neck – soft tissue seen
 CT Scan/MRI with contrast – mass in larynx
 DL Scopy – Reddish blue mass in subglottis
 Biopsy
 Treatment
 Observation
 Antibiotics and anti inflammatory
 Steroids –IV dexamethasone, intra lesional
 Intubation/tracheostomy
 Resection – Co2 and KTP lasers/laryngofissure
Congenital subglottic stenosis
 Abnormal thickening of cricoid cartilage or fibrous tissue
below the vc
 Here subglottic diameter in full term <3.5 – 4 mm (normal
4.5 – 5.5 mm) and in preterm 3 mm (normal 3.5mm)
 C/F
 Evident after 1st week of life with URTI
 Biphasic stridor
 Dyspnoea
 Normal cry
 Grading I - <50% obstruction, II – 51-70% obstruction, III
– 71-99% obstruction, IV – no detectable lumen..
 Diagnosis
 X Ray Neck, CT/MRI
 Bronchoscopy/MLS/DL Scopy
 Treatment
 Observation – improves as larynx grows
 II/III/IV – tracheostomy
 Excision – laser (Co2/KTP), Laryngotracheoplasty
Laryngeal web
 Web formation most commonly in anterior part of larynx
due to arrest of development of larynx most commonly
seen in glottis (between vc)
 C/F
 Since birth
 Small webs – asymptomatic
 Inspiratory stridor
 Dyspnoea or apnoea
 Weak cry
 Hoarseness
 IDL – seen b/w anterior end of vc with concave sharp
posterior margin
 D/D
 From acquired web due to trauma or infection
 Treatment
 Excision by Laser/knife or laryngofissure
Acute epiglottitis
 Supraglottic laryngitis
 PAEDIATRIC
 Marked oedema of epiglottis obstructimg the airway
 Etiology
 H influenza type B
 Age – 2 to 7 years
 Not in newborn as maternal immunity
 Pathology
 Severe cellulitis
 Thick secretions
 C/F
 Rapid progress to respiratory distress within ½ hour
 Abrupt onset and rapid progression
 High grade fever (>40 C)
 Dysphagia and odynophagia
 Drooling of saliva
 Hoarseness
 Muffled (hot potato) voice
 Tripod position- leans forward supporting on upper limb
 Inspiratory stridor which increases in supine position
 Retraction, nasal flaring, cyanosis, septicaemia
 Pharynx is congested
 Diagnosis
 No tongue depressor/IDL
 Examine in OT
 Red and swollen (cherry red) epiglottis – sun rise sign
 Oedema and congestion of supraglottis
 X Ray Neck – swollen epiglottis – thumb sign
 Throat swab
 Blood culture
 Leucocytosis
 Complications
 5-10% mortality
 Reflux laryngospasm
 Cardio-respiratory arrest
 Otitis media
 Pneumonia
 Pericarditis
 Meningitis
 Prevention
 Hib vaccine in children
 Treatment
 Hospitalization in ICU
 Complete bed rest and voice rest
 Intubation/tracheostomy under GA
 Antibiotics- ampicillin, cephalosporins
 IV fluids
 IV steroids
 Oxygen
Adult supraglottitis
 Less severe
 Marked oedema of supraglottis
 Etiology
 H Influenza, streptococci, staphylococci
 C/F
 Sore throat
 Dysphagia
 Pale oedematous supraglottis
 Stridor
 Treatment
 Antibiotics, steroids, anti reflux treatment
 Tracheostomy if needed
Acute laryngotracheobronchitis
 Subglottic croup
 Most common cause of infectious resp obstruction in
children
 Etiology
 Viral – parainfluenza I,II
 Influenza A,B
 Other viruses – myxovirus, adenovirus
 Secondary bacterial infection
 Males>females
 Age group 3 months to 5 years of age
 Involves subglottis (mc), trachea and bronchi
 h/o URTI always
 C/F
 Slow onset
 Starts with URTI
 Low grade fever, cough cold earlier
 Hoarseness
 Brassy or barking cough
 Biphasic stridor
 Signs of airway obstruction – nasal flaring, chest retraction
 Complications
 Middle ear infection, lung infection, tracheitis
 Diagnosis
 Leucocytosis
 X Ray Neck – tapered narrowing of subglottis –
steeple’s sign, wine bottle appearance – bottle sign
 Chest X Ray – pneumonic patches
 Flexible laryngobronchoscopy – subglottic narrowing
 Treatment
 Hospitalization
 Humidification- soften crusts and thick secretions
 Steam inhalation
 Antibiotics
 Oxygen
 IV fluids
 Steroids
 Mucolytics – bromhexine
 Nebulization with racemic adrenaline
 Intubation/tracheostomy – if needed
 Bronchoscopy – to remove secretions
Acute simple/non specific laryngitis
 Acute inflammation of laryngeal mucosa of mild form
 Etiology
 Infections – URTI, tonsillitis, rhinitis or rhinosinusitis
 First viral later bacterial
 GERD
 Allergy
 Voice abuse
 Burns
 Trauma (endotracheal intubation)
 More severe in children as subglottic area is narrower
 Pathology
 Hyperaemia of larynx
 Formation of pseudo membrane
 C/F
 Abrupt onset
 Hoarseness
 Dysphonia
 Pain throat
 Fever
 Dry cough worst at night
 Stridor in children
 Erythema and oedema of epiglottis, arytenoids and ventricles with
normal vocal cords earlier with later hyperemia of vc and subglottis
 Pharyngeal and nasal congerstion
 Treatment
 Bed rest
 Voice rest
 Soft bland diet
 Avoid smoking and alcohol
 Steam inhalation with inhalant capsules
 Cough sedatives
 Antibiotics – cephalosporin, amoxy clav
 Steroids
 Anti reflux treatment
 Tracheostomy/intubation if needed in childrens
Laryngeal diptheria
 Etiology
 Corynebacterium diptheriae
 Secondary to faucial diptheria
 Age < 10 years
 Both sexes
 Pesudomembrane formation
 Exotoxins liberated
 C/F
 Gradual onset
 Low grade fever
 Sore throat
 Hoarseness
 Croupy cough
 Inspiratory stridor
 Dyspnoea
 Diptheritic membrane – grey white on tonsil, pharynx,
soft palate, larynx, trachea, on removal leaves a rough
bleeding surface
 Cervical lymphadenopathy – bull neck appearance
 Complications
 Cardiac – myocarditis, circulatory failure
 Neurogenic – paralysis of palate, larynx and pharynx
 Asphyxia and death due to airway obstruction
 Diagnosis
 Clinical
 Throat swab
 Smear and culture
 Treatment
 Diptheria anti toxin – 20000 to 100000 units IV as a
single saline infusion after test dose
 Antibiotics – benzyl pencillin, erythromycin
 Complete bed rest for 2 to 4 weeks
 Oxygen
 Steroids
 IV fluids
 DL Scopy for removal of diptheritic membrane
 Intubation/tracheostomy
Tubercular laryngitis
 Etiology
 Mycobacterium tuberculosis
 95% cases secondary to pulmonary TB, 5% primary
 Route – infected sputum to larynx (mc), lymphatic,
haematogenic
 Males (mc)
 Age gp 20 – 40 years
 Involves posterior part of larynx (mc – interarytenoid
region)
 C/F
 Weak voice
 Hoarseness
 Odynophagia and dysphagia
 Hemoptysis
 Hyperaemia of vc
 Impaired adduction of vc
 Mouse nibbled appearance of vc/ moth eaten appearance
due to ulcers
 Pseudo edema of epiglottis – turban epiglottis
 Bowing of vc
 D/D – malignancy, syphilis, chronic laryngitis
 Diagnosis
 DL Scopy and biopsy
 Mantoux test
 Chest X Ray
 Sputum examination
 Stages
 1 – inflammation
 2- granulomatous (yellowish grey nodule)
 3- ulcerative
 4- cicatrization (healing)
 Treatment
 Multi drug ATT – rifampicin, isoniazid, pyrazinamide,
ethambutol for 6-9 months
 Voice rest
 NSAID
 Anti inflammmatory gargles
 Tracheostomy if stridor
 Laryngeal reconstruction
Chronic non specific laryngitis
 Chronic irritation of larynx
 Types
 1. hyperemic – diffuse inflammation and symmetrical
involvement of larynx (true cords, false cords, inter
arytenoid region and root of epiglottis)
 2. localised – nodules, polyp
 Pathology
 Pseudo stratified columnar epithelium changes into
squamous epithelium
 Keratinization (leukoplakia) of statified squamous
epithelium of vc
 Hyperplasia
 Etiology
 Age >20 years/30-50 years
 Males (8:1 mc)
 Infections – PNS, tonsil, teeth, lungs
 Allergy
 Dust, fumes and other atmospheric pollutants
 Smoking and alcohol
 Spices
 GERD
 Voice abuse
 Mouth breathing
 Chronic throat clearing
 Chronic cough
 Inadequate hydration
 C/F
 Hoarseness – worst in morning due to dryness of mouth
 Constant clearing of throat
 Throat discomfort/ FB sensation
 Dry and irritating cough
 Hyperaemia of larynx, vc dull red
 Viscid secretions at vc and interarytenoid region
 D/D – chronic specific laryngitis
 Diagnosis – X Ray PNS/Chest X Ray, throat swab, flexible
laryngoscopy/biopsy
 Treatment
 Treat infections
 Life style modifications for LPR
 Avoid smoking, alcohol
 Voice therapy/voice rest
 Steam inhalation
 Expectorant
 Treat allergy
 Steroid topic inhalers
 Surgical – MLS, stripping of vc (one vc at a time)
Pachyderma laryngitis
 Chronic lartyngitis affecting posterior part of larynx
 Interarytenoid region, post vc
 Males
 Etiology
 Alcohol, smoking, GERD
 C/F
 Hoarseness, irritation in throat
 Symmetrical red grey granulations or whitish mass on both
vc (post part) and interarytenoid region, ulcer
 Diagnosis – biopsy
 Treatment – removal of granulations, anti reflux, speech
therapy
Atrophic laryngitis
 Laryngitis sicca
 Atrophy of laryngeal mucosa with crust formation associated
with atrophic rhinitis and pharyngitis
 Females
 C/F
 Hoarseness of voice which improves on coughing and removal of
secretions
 Dry irritating cough, dyspnoea
 Atrophic mucosa covered with crusts which bleed on removal
 Treatment – humidification, loosening of secretions (laryngeal
sprays containing glucose in glycerine, expectorants)
Lupus of larynx
 Indolent tubercular infection associated with lupus of nose
and pharynx due to increased host resistance or decreased
bacterial virulence involving anterior parts of larynx
 Epiglottis
 Females
 C/F
 Painless, asymptomatic, no pulmonary TB
 Scattered yellowish pink nodules in epiglottis which can
ulcerate
 Complications – perichondritis, cartilage destruction
 Treatment - ATT
Syphilis of larynx
 Etiology – Treponema Pallidium
 C/F
 Hoarseness, dyspnoea, inspiratory stridor
 Gumma over epiglottis, anterior commissure and
anterior vocal cords
 Diagnosis – biopsy, VDRL
 Complications – laryngeal stenosis, perichondritis
 Treatment
 Procaine pencillin, doxycycline
 Tracheostomy
Leprosy of larynx
 Etiology – M Leprae (Hansen bacilli)
 Associated with leprosy of skin and nose
 Affects epiglottis, aryepiglottic folds and arytenoids
 C/F – hoarseness, muffled voice, no pain
 Dull grey nodules which may ulcerate
 Diagnosis – biopsy
 Complications – laryngeal stenosis, deformity
 Treatment – dapsone, rifampicin, clofazimine for 5 – 10
years
 Steroids
 Tracheostomy
Scleroma of larynx
 Klebsiella Rhinoscleromatis (Frisch bacilli)
 Subglottis
 C/F
 Hoarseness, wheeze, dyspnoea, cough
 Smooth red or pink swelling in subglottic region which can
spread to trachea
 Diagnosis – biopsy
 Complications – subglottic stenosis
 Treatment – streptomycin, doxycycline, tetracycline
 Steroids
 Tracheostomy

Stridor

  • 1.
    Dr Manpreet SinghNanda Associate Professor ENT MMMC&H Solan
  • 2.
    Stridor  Abnormal highpitched noisy respiration due to flow of air through a partially obstructed narrowed lower airway mainly larynx and tracheobronchial tree  Types  Inspiratory – supraglottis, glottis, hypopharynx  Expiratory (wheeze) – thoracic trachea, bronchi, bronchioles  Biphasic – cervical trachea, subglottis  Stertor – snoring low pitched noise due to obstruction in nasopharynx and oropharynx  Rales and crepitations – distal portion of bronchial tree and alveoli
  • 3.
    Etiology  Neonates –laryngomalacia (mc), laryngeal webs, cysts, subglottic stenosis, laryngeal paralysis  Children – laryngotracheobronchitis (croup), acute epiglottis, laryngeal FB  Nose – choanal atresia  Tongue – macroglossia, haemangioma, lymphangioma  Mandible – micrognathia  Pharynx – abscess  Larynx – paralysis, trauma  Trachea – tumours, FB, stenosis, TOF  Oesophagus – FB  Neck – tumours, abscess
  • 4.
     Children affectedmore – narrrow airway, softer cartilage collapse easily  Adults  Malignancy of larynx, pharynx, tongue, neck, trachea (mc)  Infections – ludwigs angina  Allergy – angioneurotic oedema  Trauma – fractures, iatrogenic, radiotherapy, caustic agents  Neurogenic - paralysis
  • 5.
    Assessment  Mc physicalsign of larynx  History  Age – at birth (congenital), after few weeks (laryngomalacia)  Onset – sudden (FB)  Progress – rapid (acute epiglottitis), gradual (subglottic haemangioma, malignancy)  h/o fever – infective  h/o cough – aspiration, TOF  h/o hoarseness – vc  h/o apnoea and cyanosis – tracheobronchomalacia  h/o trauma, intubation  h/o FB  Improves in prone position – laryngomalacia, macroglossia, micrognathia  Improves during crying – B/L chonal atresia  Worsens during crying - laryngomalacia
  • 6.
    Examination  Note thetype of stridor  Note the sound of stridor  - musical quality – laryngomalacia  - breathy – vc paralysis  - aspiration – vc paralysis  - barking cough – tracheomalacia  Note associated symptoms  - hoarseness – larynx  - wheeze – bronchi  - dysphagia – hypopharynx  Note the severity  - subcostal, intercostal, suprasternal recession  - cyanosis
  • 7.
     Detailed examinationof oral cavity, nasal cavity, pharynx and larynx (IDL)  INVESTIGATIONS  Oxygen saturation monitoring  - arterial blood gas estimation, pulse oxymetry  Radiographs  - x ray chest, neck  - CT, MRI  pH monitoring
  • 8.
     Endoscopy – - Bronchoscopy  - Oesophagoscopy  - Laryngoscopy  Along with intubation in OT  Flexible endoscopy  Videofluoroscopy – chest movements  USG Neck
  • 9.
    Treatment  Acute condition Admit  Conservative  - oxygen and humidification  - antibiotics  - IV steroids  - Nebulized epinephrine  - mucolytics  - IV fluids  - CPAP (Continued Positive Airway Pressure)
  • 10.
     Intubation  Endotrachealintubation – nasal (secure)  Preferred  Ventilatory bronchoscopy  Endoscopy and FB removal  Not done in acute epiglottitis, impacted FB, trismus, severe subglottic stenosis, mandible fracture, supraglottic tumours
  • 11.
     Tracheostomy  Cricothyroidotomy Chronic  - Anti reflux treatment  - Systemic steroids  - Prophylactic antibiotics  - Treat the cause
  • 12.
    Congenital lesions oflarynx  Laryngomalacia  Subglottic stenosis  Laryngeal web/atresia/cyst  Vocal cord paralysis  Subglottic haemangioma  Laryngocele  Laryngo oesophageal cleft
  • 13.
    Laryngomalacia  Congenital laryngealstridor  Excessive flaccidity of supraglottic larynx which gets sucked in during inspiration producing stridor and sometimes cyanosis  Pathology  Excessive softening of laryngeal skeletal framework -> indrawing of aryepiglottic folds -> narrowing -> stridor
  • 14.
    Clinical features  M:F2:1  Low socio economic group  Intermittent low pitched inspiratory stridor develops during first two weeks of life (rare at birth)  Aggravates on crying, feeding, exertion  Relieved in prone position, rest and sleep  Seen maximum at 9-12 months of age  Completely disappears after 2 years of age (5 years)  Normal cry and voice  In severe cases – feeding difficulty, failure to thrive and cyanosis
  • 15.
    Signs  Awake flexiblelaryngoscopy  Anterior collapse of arytenoid  Posterior collapse of epiglottis  Inward collapse of aryepiglottic folds  Omega shaped/tubular epiglottis  Prominent arytenoids  Normal vocal cords
  • 16.
     Complications –GERD, recurrent URTI, OSA  D/D – laryngeal webs, cysts  Treatment  Conservative (90%)  - Reassurance  - Observation  - Treat the URTI  Tracheostomy  Surgery (10%) – when failure to thrive or cyanosis  - Supraglottoplasty (Aryepiglottoplasty)
  • 17.
    Congenital laryngeal haemangioma Subglottic haemangioma  Benign vascular malformation involving subglottis  C/F  Females mc  Asymptomatic for 3 to 6 months of age  With increase size progressive disease  Inspiratory or mostly biphasic stridor which is progressive  Appears with URTI  Aggravated by crying or agitation  Dyspnoea and cyanosis  Associated with cutaneous haemangioma or mediatinal haemangioma  Rapid growth till 1 year of age then regress
  • 18.
     Diagnosis  XRay Neck – soft tissue seen  CT Scan/MRI with contrast – mass in larynx  DL Scopy – Reddish blue mass in subglottis  Biopsy  Treatment  Observation  Antibiotics and anti inflammatory  Steroids –IV dexamethasone, intra lesional  Intubation/tracheostomy  Resection – Co2 and KTP lasers/laryngofissure
  • 19.
    Congenital subglottic stenosis Abnormal thickening of cricoid cartilage or fibrous tissue below the vc  Here subglottic diameter in full term <3.5 – 4 mm (normal 4.5 – 5.5 mm) and in preterm 3 mm (normal 3.5mm)  C/F  Evident after 1st week of life with URTI  Biphasic stridor  Dyspnoea  Normal cry  Grading I - <50% obstruction, II – 51-70% obstruction, III – 71-99% obstruction, IV – no detectable lumen..
  • 20.
     Diagnosis  XRay Neck, CT/MRI  Bronchoscopy/MLS/DL Scopy  Treatment  Observation – improves as larynx grows  II/III/IV – tracheostomy  Excision – laser (Co2/KTP), Laryngotracheoplasty
  • 21.
    Laryngeal web  Webformation most commonly in anterior part of larynx due to arrest of development of larynx most commonly seen in glottis (between vc)  C/F  Since birth  Small webs – asymptomatic  Inspiratory stridor  Dyspnoea or apnoea  Weak cry  Hoarseness  IDL – seen b/w anterior end of vc with concave sharp posterior margin
  • 22.
     D/D  Fromacquired web due to trauma or infection  Treatment  Excision by Laser/knife or laryngofissure
  • 23.
    Acute epiglottitis  Supraglotticlaryngitis  PAEDIATRIC  Marked oedema of epiglottis obstructimg the airway  Etiology  H influenza type B  Age – 2 to 7 years  Not in newborn as maternal immunity  Pathology  Severe cellulitis  Thick secretions
  • 24.
     C/F  Rapidprogress to respiratory distress within ½ hour  Abrupt onset and rapid progression  High grade fever (>40 C)  Dysphagia and odynophagia  Drooling of saliva  Hoarseness  Muffled (hot potato) voice  Tripod position- leans forward supporting on upper limb  Inspiratory stridor which increases in supine position  Retraction, nasal flaring, cyanosis, septicaemia  Pharynx is congested
  • 25.
     Diagnosis  Notongue depressor/IDL  Examine in OT  Red and swollen (cherry red) epiglottis – sun rise sign  Oedema and congestion of supraglottis  X Ray Neck – swollen epiglottis – thumb sign  Throat swab  Blood culture  Leucocytosis
  • 26.
     Complications  5-10%mortality  Reflux laryngospasm  Cardio-respiratory arrest  Otitis media  Pneumonia  Pericarditis  Meningitis  Prevention  Hib vaccine in children
  • 27.
     Treatment  Hospitalizationin ICU  Complete bed rest and voice rest  Intubation/tracheostomy under GA  Antibiotics- ampicillin, cephalosporins  IV fluids  IV steroids  Oxygen
  • 28.
    Adult supraglottitis  Lesssevere  Marked oedema of supraglottis  Etiology  H Influenza, streptococci, staphylococci  C/F  Sore throat  Dysphagia  Pale oedematous supraglottis  Stridor  Treatment  Antibiotics, steroids, anti reflux treatment  Tracheostomy if needed
  • 29.
    Acute laryngotracheobronchitis  Subglotticcroup  Most common cause of infectious resp obstruction in children  Etiology  Viral – parainfluenza I,II  Influenza A,B  Other viruses – myxovirus, adenovirus  Secondary bacterial infection  Males>females  Age group 3 months to 5 years of age  Involves subglottis (mc), trachea and bronchi  h/o URTI always
  • 30.
     C/F  Slowonset  Starts with URTI  Low grade fever, cough cold earlier  Hoarseness  Brassy or barking cough  Biphasic stridor  Signs of airway obstruction – nasal flaring, chest retraction  Complications  Middle ear infection, lung infection, tracheitis
  • 31.
     Diagnosis  Leucocytosis X Ray Neck – tapered narrowing of subglottis – steeple’s sign, wine bottle appearance – bottle sign  Chest X Ray – pneumonic patches  Flexible laryngobronchoscopy – subglottic narrowing
  • 32.
     Treatment  Hospitalization Humidification- soften crusts and thick secretions  Steam inhalation  Antibiotics  Oxygen  IV fluids  Steroids  Mucolytics – bromhexine  Nebulization with racemic adrenaline  Intubation/tracheostomy – if needed  Bronchoscopy – to remove secretions
  • 33.
    Acute simple/non specificlaryngitis  Acute inflammation of laryngeal mucosa of mild form  Etiology  Infections – URTI, tonsillitis, rhinitis or rhinosinusitis  First viral later bacterial  GERD  Allergy  Voice abuse  Burns  Trauma (endotracheal intubation)  More severe in children as subglottic area is narrower
  • 34.
     Pathology  Hyperaemiaof larynx  Formation of pseudo membrane  C/F  Abrupt onset  Hoarseness  Dysphonia  Pain throat  Fever  Dry cough worst at night  Stridor in children  Erythema and oedema of epiglottis, arytenoids and ventricles with normal vocal cords earlier with later hyperemia of vc and subglottis  Pharyngeal and nasal congerstion
  • 35.
     Treatment  Bedrest  Voice rest  Soft bland diet  Avoid smoking and alcohol  Steam inhalation with inhalant capsules  Cough sedatives  Antibiotics – cephalosporin, amoxy clav  Steroids  Anti reflux treatment  Tracheostomy/intubation if needed in childrens
  • 36.
    Laryngeal diptheria  Etiology Corynebacterium diptheriae  Secondary to faucial diptheria  Age < 10 years  Both sexes  Pesudomembrane formation  Exotoxins liberated
  • 37.
     C/F  Gradualonset  Low grade fever  Sore throat  Hoarseness  Croupy cough  Inspiratory stridor  Dyspnoea  Diptheritic membrane – grey white on tonsil, pharynx, soft palate, larynx, trachea, on removal leaves a rough bleeding surface  Cervical lymphadenopathy – bull neck appearance
  • 38.
     Complications  Cardiac– myocarditis, circulatory failure  Neurogenic – paralysis of palate, larynx and pharynx  Asphyxia and death due to airway obstruction  Diagnosis  Clinical  Throat swab  Smear and culture
  • 39.
     Treatment  Diptheriaanti toxin – 20000 to 100000 units IV as a single saline infusion after test dose  Antibiotics – benzyl pencillin, erythromycin  Complete bed rest for 2 to 4 weeks  Oxygen  Steroids  IV fluids  DL Scopy for removal of diptheritic membrane  Intubation/tracheostomy
  • 40.
    Tubercular laryngitis  Etiology Mycobacterium tuberculosis  95% cases secondary to pulmonary TB, 5% primary  Route – infected sputum to larynx (mc), lymphatic, haematogenic  Males (mc)  Age gp 20 – 40 years  Involves posterior part of larynx (mc – interarytenoid region)
  • 41.
     C/F  Weakvoice  Hoarseness  Odynophagia and dysphagia  Hemoptysis  Hyperaemia of vc  Impaired adduction of vc  Mouse nibbled appearance of vc/ moth eaten appearance due to ulcers  Pseudo edema of epiglottis – turban epiglottis  Bowing of vc
  • 42.
     D/D –malignancy, syphilis, chronic laryngitis  Diagnosis  DL Scopy and biopsy  Mantoux test  Chest X Ray  Sputum examination  Stages  1 – inflammation  2- granulomatous (yellowish grey nodule)  3- ulcerative  4- cicatrization (healing)
  • 43.
     Treatment  Multidrug ATT – rifampicin, isoniazid, pyrazinamide, ethambutol for 6-9 months  Voice rest  NSAID  Anti inflammmatory gargles  Tracheostomy if stridor  Laryngeal reconstruction
  • 44.
    Chronic non specificlaryngitis  Chronic irritation of larynx  Types  1. hyperemic – diffuse inflammation and symmetrical involvement of larynx (true cords, false cords, inter arytenoid region and root of epiglottis)  2. localised – nodules, polyp  Pathology  Pseudo stratified columnar epithelium changes into squamous epithelium  Keratinization (leukoplakia) of statified squamous epithelium of vc  Hyperplasia
  • 45.
     Etiology  Age>20 years/30-50 years  Males (8:1 mc)  Infections – PNS, tonsil, teeth, lungs  Allergy  Dust, fumes and other atmospheric pollutants  Smoking and alcohol  Spices  GERD  Voice abuse  Mouth breathing  Chronic throat clearing  Chronic cough  Inadequate hydration
  • 46.
     C/F  Hoarseness– worst in morning due to dryness of mouth  Constant clearing of throat  Throat discomfort/ FB sensation  Dry and irritating cough  Hyperaemia of larynx, vc dull red  Viscid secretions at vc and interarytenoid region  D/D – chronic specific laryngitis  Diagnosis – X Ray PNS/Chest X Ray, throat swab, flexible laryngoscopy/biopsy
  • 47.
     Treatment  Treatinfections  Life style modifications for LPR  Avoid smoking, alcohol  Voice therapy/voice rest  Steam inhalation  Expectorant  Treat allergy  Steroid topic inhalers  Surgical – MLS, stripping of vc (one vc at a time)
  • 48.
    Pachyderma laryngitis  Chroniclartyngitis affecting posterior part of larynx  Interarytenoid region, post vc  Males  Etiology  Alcohol, smoking, GERD  C/F  Hoarseness, irritation in throat  Symmetrical red grey granulations or whitish mass on both vc (post part) and interarytenoid region, ulcer  Diagnosis – biopsy  Treatment – removal of granulations, anti reflux, speech therapy
  • 49.
    Atrophic laryngitis  Laryngitissicca  Atrophy of laryngeal mucosa with crust formation associated with atrophic rhinitis and pharyngitis  Females  C/F  Hoarseness of voice which improves on coughing and removal of secretions  Dry irritating cough, dyspnoea  Atrophic mucosa covered with crusts which bleed on removal  Treatment – humidification, loosening of secretions (laryngeal sprays containing glucose in glycerine, expectorants)
  • 50.
    Lupus of larynx Indolent tubercular infection associated with lupus of nose and pharynx due to increased host resistance or decreased bacterial virulence involving anterior parts of larynx  Epiglottis  Females  C/F  Painless, asymptomatic, no pulmonary TB  Scattered yellowish pink nodules in epiglottis which can ulcerate  Complications – perichondritis, cartilage destruction  Treatment - ATT
  • 51.
    Syphilis of larynx Etiology – Treponema Pallidium  C/F  Hoarseness, dyspnoea, inspiratory stridor  Gumma over epiglottis, anterior commissure and anterior vocal cords  Diagnosis – biopsy, VDRL  Complications – laryngeal stenosis, perichondritis  Treatment  Procaine pencillin, doxycycline  Tracheostomy
  • 52.
    Leprosy of larynx Etiology – M Leprae (Hansen bacilli)  Associated with leprosy of skin and nose  Affects epiglottis, aryepiglottic folds and arytenoids  C/F – hoarseness, muffled voice, no pain  Dull grey nodules which may ulcerate  Diagnosis – biopsy  Complications – laryngeal stenosis, deformity  Treatment – dapsone, rifampicin, clofazimine for 5 – 10 years  Steroids  Tracheostomy
  • 53.
    Scleroma of larynx Klebsiella Rhinoscleromatis (Frisch bacilli)  Subglottis  C/F  Hoarseness, wheeze, dyspnoea, cough  Smooth red or pink swelling in subglottic region which can spread to trachea  Diagnosis – biopsy  Complications – subglottic stenosis  Treatment – streptomycin, doxycycline, tetracycline  Steroids  Tracheostomy