This document provides information about pharyngitis (inflammation of the pharynx). It discusses the different causes of pharyngitis including bacterial (e.g. Streptococcus pyogenes), viral (e.g. rhinovirus), and fungal. It provides details on symptoms, diagnosis, treatment, and complications of various types of pharyngitis. It also discusses other conditions that can cause pharyngeal inflammation like diphtheria, tuberculosis, and mononucleosis.
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ACUTE AND CHRONIC CONDITION OF PHARYNX & LARYNX.ppt
1. DR. B. P. SHAH
ASSISTANT PROFESSOR
DEPARTMENTOF ORL and HNS
BPKIHS
2.
3. Definition – inflammation of
the mucous membranes and
submucosal structures of
the pharynx
TYPE:
1. Acute- bacterial, viral,
fungal
2. Chronic nonspecific
3. Chronic specific
4. Bacterial
▪ Group A beta-hemolytic
streptococci (S. pyogenes)*
▪ most common bacterial cause of
pharyngitis
▪ 15-30% of cases in children and
5-10% in adults.
▪ Mycoplasma pneumoniae
▪ Arcanobacterium haemolyticum
▪ Neisseria gonorrhea
▪ Chlamydia pneumoniae
Viral >90%
▪ Rhinovirus , Coronavirus –
common cold
▪ Adenovirus –
pharyngoconjunctival
fever;acute respiratory illness
▪
▪ Parainfluenza virus – common
cold; croup
▪ Coxsackievirus – herpangina
▪ EBV – infectious mononucleosis
▪ HIV
5. Spread by contact with respiratory secretions
Peaks in winter and spring
School age child (5-15 y)
Communicability highest during acute infection
Patient no longer contagious after 24 hours of antibiotics
If hospitalized, droplet precautions needed until no longer
contagious
6. Classic symptoms → Fever,
throat pain, dysphagia
VIRAL → Most likely
concurrent URI symptoms of
rhinorrhea, cough, hoarseness,
conjunctivitis & ulcerative
lesions
STREP → Look for associated
headache, and/or abdominal
pain
Fever and throat pain are usually
acute in onset
7. VIRAL
EBV –White exudate covering
erythematous pharynx and tonsils,
cervical adenopathy,
Subacute/chronic symptoms
(fatigue/myalgias)
transmitted via infected saliva
Adenovirus/Coxsackie –
vesicles/ulcerative lesions present on
pharynx or posterior soft palate
Also look for conjunctivitis
8. Bacterial
GAS – look for whitish exudate covering
pharynx and tonsils
▪ tender anterior cervical adenopathy
▪ palatal/uvular petechiae
▪ scarlatiniform rash covering torso and
upper arms
Spread via respiratory particle droplets
NO school attendance until 24 hours after
initiation of appropriate antibiotic therapy
▪ Absence of viral symptoms (rhinorrhea,
cough, hoarseness)
12. VIRAL –
Supportive care only – Analgesics, Antipyretics,
Fluids
use of oral or intramuscular corticosteroids for pain relief
EBV – infectious mononucleosis
activity restrictions – mortality in these pts most commonly
associated with abdominal trauma and splenic rupture
14. Prevention of ARF if treatment started within
9 days of illness
Reduce symptoms
Prevent local suppurative complications
BUT
Does not prevent the development of the post
streptococcal sequel of acute
glomerulonephritis
15. Clinical diagnosis of scarlet fever
Household contact with documented strep.
Pharyngitis
Past history of ARF
Recent history of ARF in a family member
16. Peritonsillar cellulitis or abscess
Parapharyngeal abscess
IM with severe dysphagia
Severe uncomplicated tonsillitis with dysphagia and dehydration
Sore throat asso with stridor or resp difficulty (absolute)
17. Suppurative
Otitis media
Sinusitis
Peritonsillar and
retropharyngeal
abscesses
Suppurative cervical
adenitis
Nonsuppurative
Acute rheumatic fever
follows only streptococcal
pharyngitis (not group A strep skin
infections)
Acute glomerulonephritis
May follow pharyngitis or
skin infection (pyoderma)
Nephritogenic strains
18. Occurs most commonly in
association with pharyngitis
Strawberry tongue
Rash
▪ Generalized fine, sandpapery
scarlet erythema with
accentuation in skin folds
(Pastia’s lines)
▪ Circumoral pallor
▪ Palms and soles spared
Treatment same as strep
pharyngitis
19. Glandular fever , Kissing disease
IP= 5-7 wks
Acute follicular tonsillitis
Psudomembrane
Tender cervical adenopathy, periorbital
oedema, mono or poly neuropathies
Systemic menifestations
Diagnosis- Paul Bunnell and monospot
tests, IgM ab against EBV viral capsid ag
(gold standard), atypical lymphocytes
21. Etiologic agent: Corynebacterium
diphtheria
Extremely rare, occurs primarily in
unimmunized patients
Gram positive rod
nonspore forming
strains may be toxigenic or
nontoxigenic
▪ exotoxin required for disease
POI-through infected secretions from the nose,
throat, eyes, or skin lesions
22. gray-black pseudomembrane
Bleeds on attempts to remove
"bull-neck”, airway obstruction.
myocarditis, neuritis, and acute tubular necrosis
Myocarditis -2 weeks after onset
Peripheral neuritis -3 to 7 weeks later. Motor rather
than sensory nerves. Commonly affects the soft palate
and pharyngeal muscles.
Definitive diagnosis -pseudomembrane to be cultured
in Loeffler's,Tellurite, and blood agar media
Chinese character" appearance –Albert stain
23. Treatment - antitoxin and antibiotics
Booster vaccination should be given during the recovery period and serial
electrocardiograms should be obtained for early detection of cardiac
complications. Disease eradication should be documented by two
negative cultures after completing treatment.
Diphtheria toxoid booster injection - recommended every 10 years in
adults
24. Clinically
Pallor of the mucosa
Typical ulcers
Painful
Superficial
Shallow
Undermined edge
Caseous floor
Etilogy:
Secondary to Pulmonary
Tuberculosis
Inv- sputum Z-N staining, phenol auramine
stain, PCR
Except for Rx for with ATT, no specific Rx
needed for pharyngeal TB
25. Secondary :
-Hyperaemic mucosa
-Mucous patches
-Snail track ulcers
Primary :Chancre, rare in
the pharynx
Tertiary: Gumma
Pinkish rubbery swellings
--►typical ulcer
Single painless
indurated papule
Deep punched
out edge
Necrotic dirty
yellow floor
26. Inflammation of the mucous membranes covering the
larynx with accompanied edema of the vocal cords
Acute [<3wks duration]–Think infectious → most
commonly viral – symptoms most commonly resolve in 7-
10 days
Chronic [>3wks duration]– Inhalation of irritant fumes,
vocal misuse, GERD, smokers
27. A. Acute infection B. Chronic infection
Acute simple laryngitis Chronic laryngitis
Acute epiglottitis Tuberculosis
Viral LTB Scleroma
Bacterial LTB Candidiasis
Spasmodic croup Sarcoidosis
C. Laryngeal edema
D. Laryngo-pharyngeal reflux disease (LPRD)
28. Etiology
Viral infection (common cold)
Vocal abuse
Allergy / smoking / environmental pollution
Gastro esophageal reflux disease
Thermal / chemical burn due to inhalation
Use of asthma inhalers
Laryngeal trauma (endotracheal intubation)
Undue physical or psychological stress
29. History of upper respiratory tract infection
Hoarseness: high pitched husky voice
Dry, paroxysmal cough, mainly at night
Sore throat worsened by talking; fever,
malaise
Laryngoscopy: red, swollen supraglottic
mucosa; mild erythema / swelling of true
vocal cords; inspissated secretions b/w vocal
cords
30. Prevention: avoidance of cold fluids, cold air, smoking,alcohol
consumption
Absolute voice rest
Tincture Benzoin steam inhalation & mucolytics
Anti-tussives: dextromethorphan, codeine
Pantoprazole for GERD; analgesics for pain
Antibiotics: for secondary bacterial infections
Steroid: for laryngeal edema
31.
32. Synonym: Acute Supraglottitis , Supraglottic laryngitis
Definition: Rapidly developing inflammation of epiglottis &
adjacent tissues, due to bacterial infection, may cause life-
threatening airway obstruction
Causative agents: Haemophilus influenzae type b (Hib),
Streptococcus pyogenes, Streptococcus pneumoniae,
Staphylococcus aureus
33. Distress (respiratory)
Dysphagia
Drooling (due to inability to swallow)
Severe sore throat / odynophagia
Muffled voice
Sudden onset & rapid progression in children (in
hours); Indolent course in adults (in days)
34. Simply depressing child's
tongue with tongue depressor
or indirect laryngoscopy may
visualize enlarged, cherry red
epiglottis in some situations
These procedures may
precipitate complete airway
obstruction, hence avoided
35. Pt appears anxious
Leans forward with
support of both
forearms
Extends neck in an
attempt to maintain an
open airway
36. 1. Flexible laryngoscopy: carried out only in
ICU or OT with intubation / tracheostomy
set ready
2. Post-intubation direct laryngoscopy
3. Plain x-ray soft tissue of neck lateral view
4. Culture from epiglottis during intubation:
+ve in 15% cases of H. influenzae
5. Blood culture: +ve in 15% cases of H.
influenzae
38. Lateral view taken in erect position only
Enlargement of epiglottis (thumb sign)
Absence of well defined vallecula (Vallecula sign)
Thickening of aryepiglottic folds (cause for stridor)
Circumferential narrowing of subglottic portion of
trachea during inspiration (25% cases)
Ballooning of hypopharynx
42. Hospitalization, careful monitoring & isolation
Hydration + humidification + oxygen tent therapy
Secure airway in acute stridor → Mechanical
ventilation till swelling + inflammation subside
IV Ceftriaxone: 100 mg/kg/d in 2 divided doses
Hydrocortisone: 100 mg IV stat & 25 mg Q8H
Rifampicin prophylaxis for household contacts
43. Endotracheal intubation
Trans-nasal: preferred
Trans-oral
Percutaneous trans-laryngeal ventilation by needle
cricothyrotomy
Tracheostomy: last resort for acute stridor
44. Hib vaccination for all children
Rifampicin prophylaxis (20 mg/kg /day; max. 600 mg) for 4
days should be given to all household contacts if:
a. child in household < 4 years, not received
appropriate doses of Hib vaccine
b. immuno-compromised child, despite vaccination
Children > 2 years with epiglottitis do not need vaccination
as disease provides immune protection
45. Commonest infective cause of stridor in children
Mean age for presentation = 18 months
Causative agents:
Parainfluenza virus type I, II, III
Influenza virus
Respiratory syncytial virus
Rhinovirus
Measles
46. Gradual onset preceeded by URTI of > 48 hrs
Hoarseness
Biphasic stridor, mainly at night
Dry cough (like barking of seal)
Low grade fever (< 102 F)
Child prefers to lie down, but is restless
Dysphagia & drooling absent
47. Plain X-ray soft tissue neck, AP view
a. Church steeple or pencil-point sign: squared
appearance of subglottic area replaced by cone shaped
narrowing just below vocal cords
b. Ballooning of hypopharynx
Flexible laryngoscopy: narrowed subglottic area
48.
49.
50.
51. Hospitalization
Humidification & mucolytic drugs
Hydration with IV fluid
Hydrocortisone: 100 mg IV stat & 25 mg Q8H
Oxygen tent: es bronchospasm & pulm. edema
Antibiotic (IV Ceftriaxone): 100 mg/kg/day
Racemic adrenaline (1:1000) nebulization
Intubation /Tracheostomy for acute stridor
52. Synonym: pseudo-membranous croup
More severe than viral LTB
Causative agent: Staphylococcus aureus
Pathology: sloughing of respiratory epithelium
C/F: Hoarseness, biphasic stridor, dry cough, high grade fever
(> 102F), child supine but restless
X-ray neck, AP view: church steeple sign
Rx: moist air + oxygen + antibiotics
53. Synonym: spasmodic croup
Etiology: unknown (? Influenza virus infection)
causing subglottic mucosal edema
C/F: Child below 3 years with rapid onset of biphasic
stridor + barking cough + low grade fever
(< 102 F). Dysphagia & drooling are absent.
X-ray neck, AP view: church steeple sign
Rx: Moist air + oxygen + supportive treatment. Rarely
endotracheal intubation. Avoid sedatives.
54. Acute
epiglottitis
Viral croup Bacterial
croup
Spasmodic
croup
R.P.
abscess
Age (yr) 3-7 1-3 1-8 1-3 1-3
Voice Normal or
muffled
Hoarse Hoarse Hoarse Hoarse
Cough Absent Barking
seal-like
Barking
seal-like
Barking
seal-like
Absent
Stridor Inspiratory Biphasic Biphasic Biphasic Inspiratory
Dysphagia
+ drooling
Severe Absent Absent Absent Severe
Fever > 102 F < 102 F > 102 F < 102 F > 102 F
Posture Quiet,
sitting
Restless,
supine
Restless,
supine
Restless,
supine
Restless,
sitting
55. Definition: Chronic non-specific inflammation causing
irreversible changes of laryngeal mucosa
Etiology of chronic laryngitis:
Viral infection (common cold)
Vocal abuse
Allergy / smoking / environmental pollution
Gastro esophageal reflux disease
Thermal / chemical burn due to inhalation
Laryngeal trauma (endotracheal intubation)
Undue physical or psychological stress
56. Hoarseness (worse in morning) + dry cough for > 3 wk
Persistent clearing of throat
H/o previous URTI / GERD may be present
Laryngoscopy: hyperemic laryngeal mucosa
with sub-mucosal edema
Treatment:Voice test + medicated steam inhalation +
systemic antibiotic. Avoidance of alcohol & tobacco.
Reversible within few weeks.
57.
58. Hoarseness (worse in morning) + dry cough for > 3 wk
Persistent clearing of throat
H/o previous URTI / GERD may be present
Laryngoscopy:
▪ Mild congestion of laryngeal mucosa
▪ Patches of epithelial thickening
▪ Broad based polypoid lesions
59. Kleinsasser’s classification:
Grade I: simple squamous cell hyperplasia
or keratosis
Grade II: squamous cell hyperplasia + atypia (mild
to moderate dysplasia)
Grade III: carcinoma in situ with intact basal
membrane
60. Absolute voice rest for 48 hours
Systemic antibiotic
Tincture Benzoin steam inhalation
Analgesics & anti histamine-decongestant
Micro-laryngoscopic excision of lesion & HPE
Grades I & II: no further treatment
Grade III: total excision of lesion / radiotherapy
61. Avoid breathing polluted air
Avoid tobacco in any form (chewing, smoking)
Avoid recreational drugs like marijuana
Avoid alcohol consumption
Avoid talking or shouting at noisy places
Avoid continuous throat clearing
Avoid whispering loudly
62. Commonly associated with pulmonaryTB
Posterior commissure arytenoids, vocal cords, ventricular
bands & epiglottis mainly affected
Method of spread:
Bronchogenic: contact of larynx with sputum
containing tubercular bacilli
Hematogenous
63. 1. Exudation + hyperemia in subepithelial layers
2. Mono-nuclear round cell infiltration of subepithelial layers
causing pseudo-edema
3.Tubercle formation: granuloma with epithelioid cells +
Langhans giant cells + caseation necrosis
4. Ulceration: shallow ulcers with undermined edges involving
arytenoids & epiglottis (moth eaten or mouse nibbled
appearance)
5. Cicatrization: ulcers heal by fibrosis
64. History of pulmonaryTB
Weakness of voice followed by hoarseness
Cough with hemoptysis
Throat pain
Referred earache
Dysphagia & odynophagia due to perichondritis
65. Impairment of vocal cord adduction (first sign)
Areas affected commonly are inter-arytenoid
area, posterior vocal cords + false cords +
epiglottis
Congestion of these areas with surrounding
pallor
Pseudo-edema mamillated appearance of
interarytenoid area + turban-shaped epiglottis
Shallow, undermined ulcers
Vocal cord palsy + perichondritis
66. Diagnosis
Direct laryngoscopy & biopsy
Chest X-ray, P.A. view
Sputum for A.F.B.
Treatment
Anti-tubercular medication for 9 months
67. Drinking lot of fluids - Drink 7-9 glasses of water per day; also good are
herbal tea and chicken soup.
maintaining good general health - Exercise regularly.
Avoiding smoking -They are bad for the heart, lungs and vocal tract.
Eating a balanced diet - Include vegetables, fruits and whole grain
foods.
Avoid dry, artificial interior climates.
Do not eat late at night - may have problems when stomach acid backs
up on the vocal cords.
Use a humidifier to assist with hydration.
68.
69. Infections with acute or chronic lymphadenitis
Tumors
Congenital
Thyroglossal cyst
Epidermoid cyst
Branchial cyst or fistula
Lymphangioma
Haemangioma and arterio-venous malformations
70. Definition:
Congenital epithelial cysts, which arise on the
lateral part of the neck due to failure of
obliteration of the second branchial cleft in
embryonic development.
71. Branchial anomalies result
from improper development
of the branchial apparatus
Branchial apparatus develops
2nd-6th week
Neck is shaped like a hollow tube
with circumferential ridges =
Arches (mesoderm)
Ridges between arches = Clefts
and Pouches
▪ Clefts = outside (ectoderm)
▪ Pouches = inside (endoderm)
▪ “CAP”
72. Many theories
congenital
i. Branchial apparatus theory
ii. Cervical sinus theory
The cervical lymph nodes cystic
transformation ( inclusion
)theories.
73. Solitary, painless mass in the
neck of a child or a young
adult.
History of intermittent
swelling and tenderness of the
lesion during upper respiratory
tract infection may exist.
Discharge if associated with a
sinus tract.
May present with locally
compressive symptoms.
+ family history.
74. Primary lesion: Branchial cysts are
smooth, nontender, fluctuant
masses, along the upper one third of
the anteromedial border of the
sternocleidomastoid muscle
between the muscle and the
overlying skin.
Secondary lesion: tender if
secondarily inflamed or infected.
When associated with a sinus tract,
mucoid or purulent discharge onto
the skin or into the pharynx may be
present.
75. Branchiogenic carcinoma
Tuberculous adenitis
Lipoma
Metastatic malignant neoplasms (SCCA from a primary site in the
aerodigestive tract)
Cystic hygroma (lymphangioma)
Carotid body tumors
Lymphomas
Hemangiomas
Thyroid cysts
Ectopic thyroid
Cervical thymic cysts
Thyroglossal duct cyst
Parotid cystic tumors
76. Cyst arising from lateral neck and having lymphoepithelial
characteristics should be regarded as a branchial cyst.
Usually occur in the 2nd or 3rd decade of life.
Most commonly found in the anterior triangle of the neck
anterior to the upper third of the sternomastoid.
A cyst occupying the posterior triangle is extremely rare.
Hence they should be suspected in all the cystic swellings of
the neck except the median ones.
77. • Ultrasound
• Round mass with uniform low
echogenicity and lack of
internal septations
• Advantages: No radiation, no
sedation for children, low
cost
• Not typically ordered alone
78. Well defined, low density
unilocular mass with a thin
uniformly enhancing rim
• More radiation, higher cost,
may require sedation
(children)
79. MRI allows for finer
resolution during
preoperative
planning.The wall
may be enhancing on
gadolinium scans.
80. Antibiotics
Should cover respiratory flora and Staph aureus (broad
spectrum)
Cover 2-4 weeks
Abscess
Consider needle aspiration to drain
▪ May work without causing as much scaring as I&D
I&D if needle aspiration doesn’t work
Once infection cleared, operate
81. Complete surgical excision of tract and cyst is
treatment of choice in most cases
1st cysts
Must identify facial nerve as tract is usually associated
with it
If possible, wait till 2 years of age
▪ Mastoid tip defined
▪ Facial nerve larger and deeper
▪ Controversy: waiting can lead to more infections more scar
more difficult surgery
Lacrimal probes can help locate tract
82.
83. 3rd and 4th cysts
Must identify the recurrent laryngeal nerve as
closely associated (will be deep to tract)
Removal of ipsilateral thyroid lobe is advocated to
ensure complete removal of tract
Perform DL to examine pyriform sinus
▪ Fogarty vascular catheter can be placed through the
sinus tract
84. foramen caecum - site of
the development of the
thyroid at the base of
tongue.
tongue develops, the
thryroid diverticulum
descends in the neck,
maintaining its connection
to the foramen caecum
A cyst can be located
anywhere along the
migratory tract if it fails to
become obliterated.
85. located in the midline at or just
below the hyoid bone.
Due to communication with the
mouth via the foramen caecum
the cyst can become infected.
The cyst is smooth, soft and
non-tender.
Owing to its attachment to the
foramen caecum, the cyst does
move upwards when the tongue
protrudes.
86. May contain thyroid
tissue
▪ Potentially the only
functioning thyroid
Perform U/S or CT to
look for thyroid and to
assess lesion
May contain cancer
▪ 1%
▪ Papillary carcinoma
87. Early surgical excision to avoid the
complications of infection
Surgery entails complete excision of the cyst
and its tract upward to the base of the tongue
(Sistrunk Operation)
88. congenital malformations of lymph tissue
- result from the failure of lymph spaces
to connect to the rest of the lymphatic
system.
present as a soft, smooth, nontender
mass that is compressible and can be
transilluminated.
Depending on the size and location, there
might be respiratory compromise and
difficulty in feeding.
89. Goals: Improvement of cosmetic appearance,
relieve of impaired breathing and eating.
Big lesions causing respiratory embarrassment
might need urgent intubation at birth.
Surgery is difficult because of the infiltrative nature
of these lesions.
Preferred treatment : infiltration with Bleomycin,
alcohol or other sclerosing agents.
90. benign tumors of the
capillary vessels of the skin
occur anywhere, but are
common in the face and
neck
Typical growth, stationary
and involutionary phase
Treatment : conservative
(wait and see); excision or
sclerosation