sore throat Flashcards

1
Q

Case:
Our patient is D.P., a 3yr /M from San Andres, Manila who was
brought to the ER due to fever and drooling.
History of Present Illness
5 days prior to consult, the patient had colds with no associated
fever. No consult was done.
2 days prior to consult, the patient now had fever with Tmax 39,
anorexia and irritability.
1 day prior to consult, the patient’s fever persisted. It was now
associated with sore throat and drooling, prompting consult at the
ER today.
Ancillary History
Past Medical History: No previous hospitalizations or surgery, (-)
no history of asthma
Family Medical History: (-) Family history of bronchial asthma or
malignancy, (-) family history of DM and hypertension
Birth and Maternal History: Born FT to an 29 year old primigravid,
with no fetomaternal complications.
Immunization history: given BCG x 1 dose, OPV x 3 doses,
Hepatitis B x 2 doses, DPT x 3 doses , measles x 1 dose c/o the
local health center. No other immunizations were given.

Nutritional History: breastfed for 5 months , non-picky eater
Developmental History: sits without support at 8 mo, walks with
support and one-word sentences at 1 yr old
Personal and Social History: Lives with extended family in a 2
room apartment
PHYSICAL EXAMINATION
General Survey
Awake, muffled voice , sitting forward, mouth open, neck
extended
Anthropometrics
Weight =14 kg, height =95 cm
Vital signs
BP 90/60 HR 110 bpm RR 40 bpm T 39 C O2 sats (room air) = 100%
Skin
No rash, no jaundice
Head and Neck
Pink conjunctivae, anicteric sclerae, (-) nasal congestion, (+)
cervical lymphadenopathies, (+) pain with turning of the neck, (+)
bulging of posterior pharyngeal wall
Chest and Lungs
Equal chest expansion, (-) retractions, (-)rales, (-) wheezes, (+)
stridor
Cardiac
Adynamic precordium, distinct heart sounds, tachycardic, regular
rhythm, no murmurs
Abdomen
Normoactive bowel sounds, (-) tenderness, (-) guarding or
rebound tenderness, (-) hepatomegaly, intact Traube’s space
Extremities
Full and equal pulses, (-) edema/cyanosis/clubbing, CRT less than
2 sec

LABORATORY RESULT:
CBC
Date Normal
WBC 11 x109/L
RBC 3.1x109/L
Hgb 110 g/L
Hct 0.38%
MCV 85fL
MCH 25 pg
Platelets 350x109/L
Neut% 0.85
Lymph% 0.15
Mono% 0.0
Eo% 0.0
Baso% 0.0
Head CT scan (with contrast): central lucency, ring enhancement
and scalloping of the walls of lymph node
Lateral neck soft tissue xray: increased width in the
retropharyngeal space
Chest xray: N
Laryngoscopy: Abscess formation in deep cervical fascia

A
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2
Q

What are the different causes of sore throat?

A

ID: Pharyngitis, Peritonsillar abscess,
Retropharyngeal abscess, Infectious
mononucleosis, Epiglottitis, herpangina,
COVID, HFMD, Diphtheria
Non-ID: esophagitis (hot food/drinks),
GERD

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3
Q

What is the pathophysiology of acute pharyngitis?

A

secondary to infectious or non-infectious causes
(smoking, air pollutants, hot food)
- Virus: influenza, parainfluenza, adenovirus, rhinovirus,
RSV, coronavirus, enterovirus, EBV, etc
- Bacteria: GABHS, mycoplasma, Chlamydia
pneumoniae, Fusobacterium necrophorum, Chlamydia
trachomatis
- With infectious pharyngitis, bacteria/ viruses may
directly invade the pharyngeal mucosa, causing a local
inflammatory response.
- Rhinovirus and coronavirus can cause irritation of the
pharyngeal mucosa secondary to nasal secretions

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4
Q

what is the most common bacterial pathogen in acute pharyngitis?

A

Group A beta-hemolytic Steptococcus (GABHS/GAS)/Steptococcus
pyogenes

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5
Q

What is the virulence factor?

A

Produce exotoxin A, B, or C. M protein is an important
GAS virulence factor that facilitates resistance to
phagocytosis

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6
Q

What are the clinical manifestations of acute pharyngitis?

A

Viral:
1. Gradual onset
2. Moderate throat pain
3. Sx of viral URTI (conjunctivitis, coryza, cough)
4. Contacts with cold sx
5. Vesicles and ulcers (HSV)
6. Conjunctivitis (adenovirus)
Bacterial (GABHS):
1. Rapid onset significant sore throat
2. Fever >38C
3. Headache
4. Nausea/vomiting, abdominal pain
5. No URTI sx
6. red, enlarged tonsils with exudate, strawberry tongue,
palatal petechiae
7. Cervical LNE – swollen, tender, anterior cervical LN
8. Scarlatiniform rash – fine, red, popular, “sandpaper”
rash of scarlet fever. It begins from the face then
becomes generalized. Cheeks are red and area around
the mouth is more pale (circumoral pallor-like). Rash
blanches with pressure. More intense in the skin
creases, esp antecubital fossae, axillae, inguinal
creases (Pastia’s lines/Pastia’s sign)
§ (+)tourniquet test/ Rumpel-Leeds
phenomenon – capillary fragility can cause
petechiae distal to a tourniquet or
constriction from clothing
- Diarrhea, cough/colds, hoarseness, conjunctivitis are
NOT GAS, likely viral.

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7
Q

What is Pastia’s lines?

A

(+)tourniquet test/ Rumpel-Leeds
phenomenon – capillary fragility can cause
petechiae distal to a tourniquet or
constriction from clothing

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8
Q

How do we diagnose acute pharnyngitis?

A
  • to detect GAS infection
    1. throat C/S – gold standard for GABHS
    2. Rapid antigen detection test (RADT) – for GABHS
  • Not readily available locally
  • > 95% specificity, less sn: (+) no TC/S, (-) do TC/S
    3. Streptozyme (+) - measures 5 Ab including anti-
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9
Q

What is the gold standard in the diagnosis of acute pharyngitis?

A

Throat C/S

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10
Q

What is the treatment for acute pharyngitis?

A

Antipyretic – Paracetamol, Ibuprofen for fever and pain
2. Lozenges, anesthetic sprays
3. Antibiotics (GABHS)
- 1st line: Penicillin V 25-50 mkd po q6 x 10 d:
- 2nd line: Amoxicillin 50mg/kg q6 x 10d
If with penicillin allergy: macrolide
Erythromycin 40mkd po q6h x 10d
Clarithromycin 15mkd q12 x 10d
Azithromycin 12mkd po x 5d
Clindamycin 20-30 mkd po q8h
- Recurrent:
1st line: Penicillin V or Amoxicillin
2nd line: Cefuroxime 20mkd po q12 or Co-amoxiclav 20-
40 mkd q8 x 10d
4. Tonsillectomy
- For recurrent streptococcal pharyngitis
- Paradise criteria:
(+) TCS, severe and frequent
>7 episodes in the previous year
>5 episodes in each of the preceding 2
years
>3 episodes in each of the preceding 3
years

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11
Q

What are the complications of GABHS

A
  1. Rheumatic fever
  2. Post-streptococcal GN
  3. Peritonsillar/retropharyngeal abscess
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12
Q

What is peritonsillar abscess?

A
  • “Quinsy”
  • Most common deep-space head and neck infection in
    adults and children
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13
Q

What is the pathogenesis of peritonsillar abscess?

A

Bacterial invasion through the capsule of the tonsils
- Usually adolescents, >12yo
- GABHS and mixed anaerobes, S.viridans (mixed flora)
- Onset: follows as a complication of acute tonsillitis

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14
Q

What are the clinical manifestations of peritonsillar abscess?

A
  1. Recent hx of ATP that becomes more severe, gradual
    onset
  2. Fever, sore throat, dysphagia, odynophagia, drooling,
    trismus
  3. Asymmetric tonsillar bulge with displaced uvula –
    diagnostic PE finding
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15
Q

what is the diagnostic PE finding in peritonsillar abscess?

A

Asymmetric tonsillar bulge with displaced uvula

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16
Q

How do we diagnose peritonsillar abscess?

A
  • Dx is mainly clinical
    1. Throat C/S
    2. Blood C/S
    3. Tests to detect GABHS: RADT, steptozyme, ASO
    4. CT scan with contrast – shows abscess
    § rim-enhancing fluid collection adjacent
17
Q

What is the management of peritonsillar abscess?

A

I&D or needle aspiration
2. Antibiotics – Penicillin, Clindamycin, Cephalosporins,
Metronidazole
DOC: Penicillin G-benzathine 1.2M U/dose IM x 1
Clindamycin 25-30 mkd q6-8h IV/IM
Ceftriaxone 50-75 mkd IV q12-24h
Metronidazole 30mkd IV/po q6
- NAGCOM:
1st line: Ampicillin-Sulbactam 100mkd q6h then step
down to Co-amoxiclav 40mkd q8 x 10d
2nd line: Ceftriaxone 50-75 mkd q12-24h +
Metronidazole 30mkd q6 IV
Allergy: Clindamycin 40mkd q6-8
3. Tonsillectomy – for:
a. failure to improve w/in 24 h of ABX and I&D
b. hx of recurrent tonsillitis
c. complications from abscess – aspiration
pneumonitis

18
Q

What is the pathophysiology of retropharyngeal abscess?

A

The retropharyngeal abscess is between the pharynx
and cervical vertebrae & extending down to the
superior mediastinum
- Usually with infection of retropharyngeal nodes due to
extension of a localized infection of the oropharynx
- Lymphatic spread of infection. May be due to
penetrating trauma to the oropharynx, dental
infection, vertebral osteomyelitis
- Stages: cellulitis –> phlegmon –> abscess

19
Q

Etiology of retropharyngeal abscess?

A

GABHS, Anaerobes, Staphylococcus aureus, Klebsiella,
heamophilus influenza (mixed flora, polymicrobial)

20
Q

Clinical manifestations of retropharyngeal abscess?

A

2/3s have hx of recent ear, nose, or throat infection
2. Fever, irritability, decreased oral intake, drooling
3. Neck stiffness or refusal to move the neck
4. Limitation of neck extension, bulging of the posterior
pharyngeal wall, muffled voice
5. stridor, respiratory distress

21
Q

How do we diagnose retropharyngeal abscess?

A

Dx:
1. C/S – I&D and C/S of abscessed node for definitive dx
2. CT scan with contrast – ID abscess formation
a. Central lucency
b. Ring enhancement
c. Scalloping of LN walls
3. Lateral neck Soft tissue XR – increased width or airfluid
level in the retropharyngeal space
4. Laryngoscopy: Abscess formation in deep cervical
fascia

22
Q

Management of retropharyngeal abscess?

A
  1. ABX – 3rd gen cephalosporin + ampicillinsulbactam/
    clindamycin (mixed patho coverage)
    Ceftriaxone 50-75 mkd IV q12-24h +
    Ampicillin-sulbactam 100 mkd IV q6h
    Clindamycin 25-40 mkd q6-8h
    - NAGCOM:
    1st line: Ampicillin-sulbactam then step down to Coamoxiclav
    40mkd po q8/ Cefuroxime 100-150 mkd IV
    q8
    Step down to Cefuroxime 20 mkd po q12 +
    Metronidazole 30mkd IV x 7d
    Step down to Metronidazole q8 po
    2nd line: Ceftriaxone + Metronidazole x 7d
  2. I&D – if w/ respiratory distress or failure to improve
    with abx
  3. Anticipatory care –WOF complications:
    a. Significant upper airway obstruction
    b. Rupture leading to aspiration pneumonia
    c. Extension to mediastinum
    d. Thrombophlebitis
    e. Lemierre disease – infection of
    parapharyngeal space from oropharynx by
    septic thrombophlebitis of the internal
    jugular vein and embolic lung abscess.
    § Fusobacterium necrophorum
    § CXR: multiple cavitary nodules, bilat. with
    pleural effusion
    § Penicillin or cefoxitin, drainage
    Penicillin G-benzathine 1.2M U/dose IM x 1
    Cefoxitin 100-160 mkd q4-6h IV
23
Q

What is the cause of Infectious mononucleosis?

A

Epstein Barr virus (EBV)

24
Q

What is the pathophysiology of infectious mononucleosis?

A

After acquisition in the oral cavity, EBV initially infects
crypt epithelial cells causing pharyngitis. Virus spreads
to contiguous structures (salivary glands) with viremia
and infection of B lymphocytes in the blood and RES
(liver, spleen)
- CD8 T lymphocytes - atypical lymphocytes
characteristic of infectious mononucleosis

25
Q

mode of transmission of IM?

A

oral secretions

26
Q

what is the triad of infectious mononucleosis?

A

b. Pharyngitis + exudates
c. Generalized LNE – anterior and posterior
cervical, submandibular > axillary, inguinal
§ Epitrochlear LNE is particularly suggestive
of Mono

27
Q

What are the clinical manifestations of infectious mononucleosis?

A
  1. Classic triad:
    a. Fatigue
    b. Pharyngitis + exudates
    c. Generalized LNE – anterior and posterior
    cervical, submandibular > axillary, inguinal
    § Epitrochlear LNE is particularly suggestive
    of Mono.
  2. Prolonged fever (>1 wk)
  3. Headache, myalgia
  4. Abdominal pain
  5. Hepatosplenomegaly
  6. Ampicillin rash – after tx with ampicillin, amoxicillin.
    - Morbilliform, vasculitic rash probably immune
    mediated and resolves spontaneously
  7. Gianotti-Crosti syndrome – symmetric rash on the
    cheeks with multiple erythematous papules, which
    may coalesce into plaques for 15-50 days. Appears as
    atopic dermatitis, also on the extremities and buttocks.
28
Q

What do you call the rash found in patients with Infectious mononucleosis?

A

Gianotti-Crosti syndrome – symmetric rash on the
cheeks with multiple erythematous papules, which
may coalesce into plaques for 15-50 days. Appears as
atopic dermatitis, also on the extremities and buttocks.

29
Q

How do we diagnose Infectious mononucleosis?

A

Dx:
- Usually clinical
1. PBS – atypical lymphocytosis
2. EBV Ab test – confirmatory
3. EBV C/S (transformation assay) – tedious, takes 4-6w:
proliferation and rapid growth, mitotic figures, large
vacuoles, granular morphology, and cell aggregation.
4. CBC – elev WBC (10-200K, lymphocytosis), mild
thrombocytopenia
5. Mild elev of ALT, AST
6. Heterophile Ab test – Paul-Bunnell Ab detected by
Paul-Bunnell-Davidsohn test for sheep red cell
agglutination. Titers >1:28 or >1:40. (+) in 75% of cases
in 1st week and 90-95% of cases in 2nd week

30
Q

What is the management of infectious mononucleosis?

A
  1. Rest, adequate food, nutrition
  2. NSAIDs, Paracetamol
  3. Avoid contact sports for 2-3 weeks
    a. Inc. risk of splenic rupture
  4. CS (<2 wks): Prednisone 1mkd po x7d then taper fo 7d:
    a. Airway obstruction
    b. Dec plt
    c. Hemorrhage
    d. Anemia
    e. Seizures
    f. Meningitis
31
Q

Give the complications of infectious mononucleosis

A

Complications
1. Subcapsular splenic hemorrhage/ splenic rupture –
most feared complication. Occurs most freq during the
2nd wk. commonly related to trauma, usually mild.
2. Airway obstruction from swelling of tonsils and
oropharyngeal lymphoid tissue. Mgt:
tonsilloadenoidectomy, ET intubation x 12-24h
3. Alice-in-Wonderland syndrome/ metamorphopsia –
perceptual distortions of sizes, shapes, and spatial
relationships
4. Meningitis – mononuclear cells in CSF, facial nerve
palsy, encephalitis
5. Guillain-Barre syndrome, Reye syndrome
6. Hemolytic anemia – (+) Coombs test, (+) cold
agglutinins for red cell Ag i
7. Aplastic anemia – rare. Presents at 3-4 wks, recover
within 4-8d. Mgt: BM transplant
8. Myocarditis, interstitial PN, pancreatitis, parotitis,
orchitis

Prognosis: Good prognosis. Recovery complete in 2 months.