Infectious Diseases Flashcards

1
Q

What are the features of scarlet fever?

A

Occurs 24-48 hours after the sore throat

4Ss and 4Ps
S: Sore throat
S: Swollen tonsils
S: Strawberry tongue
S: Sandpaper rash
P: Perioral sparing
P: non-Painful
P: non-Pruritic
P: Peeling

>> Rash 24-48 hours after onset of fever/sore throat/strawberry tongue, occurring in the groin, axilla, neck and antecubital fossa
>> Generalized sandpaper rash with periorbital sparing within 24 hours
>> Look for Pastia’s lines (axillary rash)
>> Rash is nonpruritic and nonpainful, blanchable
>> Fades in 3-4 days
>> May be followed by desquamation

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2
Q

What is the specific management for Scarlet fever?

A

Penicillin for 10 days

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3
Q

What is the specific management for rheumatic fever?

A
  • Penicillin for 10 days
  • Prednisone if carditis is severe
  • Secondary prophylaxis with daily penicillin
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4
Q

What is the Jones criteria for diagnosing rheumatic fever?

A

2 major or 1 major + 2 minor PLUS evidence of preceding streptococcal infection
>> History of scarlet fever
>> Group A streptococcal pharyngitis culture
>> Positive rapid Ag detection test
>> Raised ASOT
>> Raised anti-DNA-ase B

Major criteria:

  • Migratory polyarthritis
  • Carditis/new heart murmur
  • Subcutaneous nodules
  • Erythema marginatum
  • Syndenham’s chorea

Minor criteria (PEACE)

  • PR interval prolonged
  • ESR raised
  • Arthralgias
  • CRP elevated
  • Elevated temperature (fever)
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5
Q

What are the common presenting features of rubella?

A

STAR complex

  • Sore throat
  • Arthritis
  • Rash

+ Low-grade fever and occipital nodes prodrome

Rash:

  • 1-4 days after start of symptoms
  • Starts on the face
  • Spreads to neck and trunk

>> Excellent prognosis in acquired disease
>> Irreversible defects in congenital rubella syndrome

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6
Q

What are the presenting features of EBV?

A

Peak incidence: 15-19 years

Infants and young children: asymptomatic/mild disease

Adolescents:
- 2-3 days prodrome of malaise and anorexia
- Classical triad of:
>> Fever
>> Generalized non-tender lymphadenopathy
>> Exudative pharyngitis/tonsilitis
- Hepatosplenomegaly
- Periorbital edema
- Rash: more common after inappropriate treatment with B-lactam antibiotics due to misdx of strep throat
- Any “-itis”

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7
Q

What are the investigations that will aid the diagnosis of EBV infection?

A
  • Monospot test
    >> 85% sensitive in adults
    >> 50% sensitive in children <4 years
  • EBV titres
  • CBC and differentials: anemia, thrombocytopenia
  • Blood smear: atypical lymphocytes and Downey cells
  • Throat culture to rule out strep throat
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8
Q

What are the complications of EBV infection?

A

Short-term:

  • Splenic rupture
  • Airway obstruction
  • Guillain-Barre syndrome/ADEM
  • Hemophagocytic lymphohistiocytosis

Long-term (can be short-term)

  • Burkitt’s lymphoma
  • Nasopharyngiocarcinoma (NPC)
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9
Q

What is the management for EBV infection?

A

SUPPORTIVE

  • Adequate rest
  • Hydration
  • Saline gargles and analgesics for sore throat

Acyclovir does NOT reduce duration of symptoms or result in earlier return to school or work.

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10
Q

What are the possible causes for fever in children?

A

Infection

  • CNS
  • Ears
  • Eyes
  • Upper and lower respiratory tracts
  • Lung parenchyma
  • Heart
  • GI system
  • Genitourinary systems: esp. UTI
  • Skin - Connective/soft tissue
  • Bones and joints
  • Sepsis

Inflammatory/Autoimmune causes

  • Kawasaki disease
  • SLE
  • JIA
  • IBD

Neoplastic

  • Leukemia
  • Lymphoma
  • Neuroblastoma

Iatrogenic

  • Dehydration
  • Drugs and toxins
  • Post-immunization
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11
Q

What are the questions to ask when evaluating a febrile child?

A
  1. Does this child really have a fever?
  2. How old is this child?
  3. Are there any risk factors for infections?
  4. How ill is this child?
  5. Is there any rash?
  6. Is there a focus of infection?
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12
Q

What is this lesion? What is the management?

A

Impetigo
- Honey-crust lesion with fluid exudation
- Common organisms
>> Streptococcus pyogenes
>> Staphylococcus aureus

Management

  • Avoid going to school
  • Topical antibiotics: fucidic acid or mupirocin cream
  • Systemic antibiotics if severe: cephalexin, erythromycin
  • Eradicate nasal carriage by nasal antibiotic creams
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13
Q

What is the diagnosis? What are the common organisms? What are the complications?

A

Periorbital cellulitis

Common organisms

  • Staphylococcus aureus
  • Streptococcus pyogenes
  • Hemophilus influenzae type B

Complications

  • Orbital cellulitis
  • Orbital abscess
  • Meningitis
  • Cavernous sinus thrombosis
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14
Q

What is the Centor criteria for Streptococcal A pharyngitis (for adults)?

A
  1. History of fever
  2. Tonsilar exudates
  3. Tender anterior cervical adenopathy
  4. Absence of cough

Age <15y: +1
Age >44y: -1

>> Score -1, 0, 1: antibiotics and throat culture not necessary
>> Score 2, 3: throat culture, and give antibiotics if throat culture positive
>> Score 4, 5: empirical antibiotics with follow-up throat culture

McIsaac Criteria: HOT LACE
HOT: fever >38C, Lymphadenopathy, Age (3-14 years), Cough absent, Exudative tonsils

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15
Q

What are the complications of Group A streptococcal pharyngitis?

A
  • *Preventable by Antibiotics**
  • AOM
  • Mastoiditis
  • Sinusitis
  • Cervical adenitis
  • Retropharyngeal/Peritonsillar abscess
  • Sepsis
  • *Immune-Mediated**
  • Scarlet fever
  • Acute rheumatic fever
  • Post-streptococcal glomerulonephritis
  • Reactive arthritis
  • PANDAS (pediatric autoimmune neuropsychiatric disorder associated with Group A streptococcus)
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16
Q

Which immune-mediated sequelae of strep throat is preventable by antibiotics?

A

Rheumatic fever is preventable if antibiotics (penicillin V x 10 days) are given within 9 days of symptom onset. Post-streptococcal glomerulonephritis is NOT preventable.

>> Rheumatic fever: post-strep throat
>> Post-streptococcal glomerulonephritis: post-strep throat and post-skin infection

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17
Q

What are the complications of rheumatic fever?

A
  • *Acute**
  • Myocarditis
  • Conduction system aberration
  • Valvulitis
  • Pericarditis
  • *Chronic**
  • Valvular heart disease (AR, MR)
  • Infectious endocarditis +/- thromboembolic phenomenon
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18
Q

When does post-streptococcal glomerulonephritis occur?

A

1-3 weeks following the initial skin/throat GAS infecton

>> Peak at 4-8 years
>> Males > Females

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19
Q

How can the diagnosis of post-streptococcal glomerulonephritis be confirmed?

A

History/Presentation
- Asymptomatic
- Microscopic or macroscopic hematuria
- Other signs of nephritic syndrome
>> Proteinuria (<50mg/kg/day)
>> Hematuria
>> Azotemia
>> RBC casts
>> Oliguria
>> Hypertension

  • *Investigations**
  • Elevated ASOT
  • Elevated anti-DNA-ase B levels
  • Low C3 complement
  • Confirm hematuria and proteinuria with urine dipstick
  • Confirm azotemia with RFT
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20
Q

What is the management for post-streptococcal glomerulonephritis?

A
  • Fluid and sodium restriction
  • Loop diuretics
    >> Edema
    >> Hypertension
  • Dialysis may be required
  • Penicillin V x 10 days if active GAS infection is present

95% children recover completely within 1-2 weeks

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21
Q

What is the definition of fever of known origin?

A

Daily or intermittent fevers for at least 2 consectuvei weeks of uncertain cause after careful history and physical and initial laboratory assessment

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22
Q

How does one assess a child presenting with fever?

A

History
- Characteristics of the fever
>> Duration
>> Height and pattern of fever
- Associated symptoms: headaches, dizziness, cough, SOB, HOV, rhinorrhea, wheezing/stridor, diarrhea, vomiting, change in stool character, oliguria, foul-smelling urine, change in urine colour and frequency, rash, unwilling to walk etc.
- TOCC: travel, cluster, contact
- Constitutional symptoms: feeding, irritability, ?playful, ?consolable, chills, rigor

  • *Physical Examination**
  • Toxic VS. Non-toxic
  • Alertness and consciousness
  • Vitals: temperature, BP, P, RR, SaO2, U/O — tachycardia, tachypnea, desaturation
  • Growth chart
  • Skin x Rash or foci of infection
  • Systematic review: HEENT, chest, CVS, abdomen, genitalia, neuro, lymph nodes

Investigations
- For young children: full septic workup
>> Blood for CBC, d/c, C/ST, ESR, CRP, RLFT
>> Urine for urinalysis, C/ST
>> Stool for C/ST, microscopy
>> Sputum for C/ST, virology
>> NPA for C/ST, virology
>> CXR

NB: Febrile neonates should be considered high risk regardless of clinical presentation and laboratory findings — septic until proven otherwise

23
Q

What is the disease? What is the causative organism?
Name the clinical features of the disease, the management and common complications.

A

5th Disease/Erythema Infectiosum

  • Parvovirus B19
  • Incubation 4-14 days
  • Mode of transmission: respiratory secretions or infected blood
  • 7-10 days of flu-like illness and fever
  • Rash
    >> Onset 10-17 days after symptoms of flulike illness and fever
    >> May be warm, pruritic and non-painful
    >> Uniform, erythematous, maculopapular, “lacy” rash
    >> “Slapped cheeks” – bilateral cheecks with circumoral pallor
    >> May affect trunk and extremities
  • Glove-and-socks syndrome
  • STAR complex (Sore Throat, Arthritis, Rash)
  • Management is mainly supportive
  • Complications
    >> Aplastic crisis (as in post-viral EBV, HHV-6, HBV, HDV, HEV & HIV infections)
    >> Rash may reappear under sunlight or after exercise months later
24
Q

What is this disease? What is the causative organism? Name the clinical features.

A

Hand, Foot and Mouth Disease

  • Coxsackie A (usually coxsackie A-16) virus
  • Incubation period: 3-5 days
  • Vesicles and pustules on an erythematous base in the hands, foots and mouth
  • Vesicles on the POSTERIOR ORAL CAVITY (pharynx, tongue)

>> Management: supportive
>> Main complication: dehydration

25
Q

This is measles. Describe the clinical features of the disease, and the mode of transmission.

A

Measles: Morbillivirus

  • Incubation: 8-13 days
  • Transmission: Airborne
  • 3Cs Prodrome: Cough, Coryza, Conjunctivitis
  • Koplik spots 1-2 days before rash onset
  • Rash:
    >> Erythematous maculopapular rash that starts from the face down
    >> Spares the palms and soles
  • Desquamation

Definitive diagnosis
- Positive serology for measles IgM

26
Q

What is the management for measles?

A

Symptomatic treatment for the patient

  • Notify Department of Health
  • Respiratory isolation

For close contacts:
- Unimmunized
>> Measles vaccine within 72 hours of exposure
>> IgG within 6 days of exposure

27
Q

What are the complications of measles?

A
  • *Secondary Bacterial Infections**
  • AOM
  • Sinusitis
  • Pneumonia
  • Encephalitis
  • *Other rare complications**
  • Subacute sclerosing panencephalitis
  • Myocarditis
  • Pericarditis
  • Glomerulonephritis
  • Stevens-Johnson Syndrome
  • Thrombocytopenia
28
Q

This is roseola infantum. What is the causative organism? What are the clinical features and possible complications?

A

HHV-6

  • High-grade fever
  • Rash
    >> Eppears once fever subsides
    >> Blanchable, pink, maculopapular rash
    >> Starts at neck and trunk; spreads to face and extremities (starts from middle!)
  • Irritability
  • Poor feeding
  • Lymphadenopathy
  • Erythematous TM and pharynx
  • Nagayama sign (see picture)
  • *Complications**
  • CNS: febrile seizures, aspetic meningitis
  • Thrombocytopenia
  • Post-viral aplastic anemia
29
Q

What are the possible complications of varicella infection/chickenpox?

A
  • *Skin**
  • Bacterial superinfection (esp. Streptococcus pyogenes >> Scarlet fever)
  • Necrotizing fasciitiis
  • *CNS**
  • Acute encephalitis
  • Cerebellar ataxia

Systemic
- Hepatitis
- DIC
- Congenital varicella syndrome
>> Mental retardation/intellectual disability, microcephaly, hydrocephalus
>> Chorioretinitis, cataract
>> Cutnaeous scarring
>> Limb aplasia
>> Soft tissue calcification

30
Q

What is the diagnosis? Describe the clinical appearance and the management plan.

A

Diaper Dermatitis: Irritant Contact Dermatitis

  • Shiny red macules with NO FLEXURAL INVOLVEMENT >> sparing of skin folds
  • Management
    >> Eliminate direct skin contact with urine and feces
    >> Allow periods of rest without a diaper
    >> Frequent diaper changes
    >> Topical barriers
    :: Perolatum
    :: Zinc oxide
    :: Paste
    >> Short-term low-potency topical corticosteroids in severe cases
31
Q

What is the diagnosis? Describe the clinical features and management.

A

Diaper dermatitis: Candidal dermatitis

  • Erythematous macerated papules/plaques with SHARP MARGINS, scaling and SATELLITE LESIONS
  • Involves the intertriginous areas, i.e. involves skin folds
  • Management
    >> Examine for coexisting oral thrush
    >> Topical antifungal agents: NYSTATIN
32
Q

What is the diagnosis? Describe the lesion and possible management plan.

A

Infantile seborrheic dermatitis

  • Yellow, greasy macules/plaques on erythema with scaling
  • Cradle cap: yellow or white greasy scales on the forehead/face
  • Starts from 2-3 weeks of life and usually clears in a few weeks
  • Usually never occur
  • Can occur in adults
  • Management
    >> Usually self-limiting
    >> Short-term topical low-potency corticosteroids
33
Q

What is the diagnosis? Describe the lesion and other common clinical features.

A

Atopic dermatitis

  • Erythematous papules with crusting, oozing, excoriation and lichenification
  • Location
    >> Facial and extensor involvement during infancy
    >> Flexural involvement in late childhood
    >> Usually spares the diaper area
  • Chronic relapsing course with a personal or family history of atopy
    >> Atopic dermatitis
    >> Allergic rhinitis
    >> Asthma
  • Prone to impetigo and are at risk for generalized cutaneous infection of HSV
34
Q

Delineate the typical management plan for eczema.

A

Affects 10-20% of children

  • *Non-medical Treatment**
  • Non-soap cleansers and moisturizing soaps
  • Fragrance-free and dye-free laundry detergent
  • Food/Allergen avoidance
  • Traditional Chinese Medicine

Enhance barrier function of the skin
- Regular application of moisturizers
- Emollients
>> Fragrance-free and dye-free
>> To hydrate skin
>> To reduce pruritis
>> Twice daily application is recommended even in the absence of symptoms
>> Apply especially after swimming or bathing
>> E.g. petrolium jelly, cetaphil cream

Anti-inflammatory therapy
- Topical steroids
>> Intermittent use to treat active, inflamed, palpable plaques
>> Discontinue once the areas are smooth
>> Side effects
:: Skin atrophy
:: Purpura
:: Striae
:: Steroid acne
:: Glaucoma when used around the eyes
- Topical immunomodulators
>> Calcineurin inhibitors: Tacrolimus, pimecrolimus
>> Side effects: skin burning, transient irritation
>> NOT indicated in children younger than 2 years
>> Pros over topical steroids
:: No skin atrophy
:: Safe for face and neck
:: Rapid sustained effect in controlling pruritis
- Systemic immunomodulators
>> Cyclosporin, azathioprine, tacrolimus and mycophenolate mofetil
- Phototherapy
- Antihistamines for pruritis
- Treat concomittant Staphylococcus infection: ?cloxacillin PO x 10 days

35
Q

What is the diagnosis? What is the management plan?

A

Eczema Herpeticum
(Eczema + herpes infection)
>> THIS IS PAINFUL

  • Admission
  • Consult ophthalmologist
  • Systemic antivirals (?acyclovir)
36
Q

What is the diagnosis? Describe the lesion and management plan.

A

Molluscum Contagiosum

  • Caused by poxviruses
  • Spread by direct skin-to-skin contact
  • Smooth, skin-coloured, 2-6mm, DOMED papules with CENTRAL UMBILICATION
  • Predilection for skin folds (axillae and groin)

>> Warts tend to have a more jagged surface
>> Herpes simplex lesions are fluid-filled vesicles
>> Milia tend to be whiter in colour and more concentrated on hte face

Management

  • Cantharidin (off-label but effective - extract from blister beetle)
  • Cryotherapy
  • Laser therapy
  • Imiquimod 5% cream
37
Q

What is the diagnosis? Describe the lesion and provide a typical management plan.

A

Tinea (corporis)

  • Round erythematous plaques with CENTRAL CLEARING and a SCALY BORDER

Management
- Topical anti-fungal for skin (usually 1-6 weeks)
>> Terbinafine 1% cream
>> Clotrimazole 1% cream
>> Luliconazole 1% cream
- Systemic anti-fungal for nails/head (onychomycosis or tinea capitis)
>> Terbinafine
>> Itraconazole
>> Griseofulvin: reserved for severe cases
- Tinea pedis
>> Avoid humidity
>> Anti-fungal for at least 3 weeks

38
Q

What is this lesion? Describe the clinical features and a possible management plan.

A

Scabies

(Sarcoptes scabies var. hominis)

  • HIGHLY CONTAGIOUS AND PRURITIC
  • Polymorphic lesions in web spaces/folds
  • Diagnosis: clinical, skin scraping

Management
- Permethrin 5% cream for patient AND FAMILY
>> 2 applications, 1 week apart
>> Apply below the neck in older children and adults
>> Apply to the whole body for toddlers and infants
- Other insecticides
>> Lindane
>> Sulphur
>> Benzyl benzoate

39
Q

What are the side effects of topical steroids?

A
  • Skin atrophy
  • Purpura
  • Striae
  • Steroid acne
  • Glaucoma if used around the eye
40
Q

What is the diagnosis? Describe the lesion and the common associations.

A

Erythema multiforme

  • TARGET (classically bull’s-eye) lesions with damaged skin in the CENTRAL ZONE
  • All lesions appear within 72 hours
  • Fixed by at least 7 days
  • Severe forms: Stevens-Johnson Syndrome (toxic epidermal necrolysis)
  • *Common associations**
  • Virus: HSV, Orf virus
  • Bacteria: Mycoplasma
  • Parasite: Histioplasma
  • Drugs: NSAIDs, carbamazepine (1502), other anticonvulsants, allopurinol (5801), sulfonamides and penicillins
41
Q

What kills in Stevens-Johnson syndrome?

A

Dehydration and infections

Morbidity:

  • Ocular sequalae
  • Scarring of skin
  • Esophageal stricture
42
Q

What is the diagnosis? Name the clinical features/diagnostic criteria and the possible management plan.

A

Stevens-Johnson Syndrome

  • Variable skin rash and at least 2 mucosal lesions
  • Usually preceded by a respiratory prodrome
  • Mucosal lesions include:
    >> Purulent conjunctivitis
    >> Hemorrhagic erosions or necrosis over lips, peri-anus and urethral opening

Associations
- Drugs: NSAIDS, sulfonamides, penicillins, tetracyclines, anticonvulsants etc.
- Infections: HSV, Mycoplasma, Orf virus, EBV, TB, histioplasmosis etc.
>> Usually milder erythema multiforme (VS. drugs – SJS)

Management

  • Hospitalization: burns unit or PICU where standard burn protocols are followed
  • Fluid replacement
  • Nutritional support
  • Increased environmental temperature (28-30C)
  • Regular culture of skin, blood and urine for infection
  • Ophthalmology follow-up regularly
  • Treat with acyclovir if HSV suspected
43
Q

What is the diagnosis? What is the management?

A

Urticaria

  • Can be very florid but usually disappears within 24 hours
  • Skin is normal-looking after the rash recedes
  • Second most common type of drug reaction
  • Results from a release of histamine from mast cells in the dermis

Management
- Antihistmaines
- IV hydrocortisone for any accompanying angioedema
- IM adrenaline
>> 1:1000 = 1mg/mL
>> Adrenaline 0.05-0.5mL

44
Q

Describe fixed drug eruptions.

A

Sharply demarcated erythematous oval patches on the skin or mucous membranes that reoccurs in the SAME location upon subsequent exposure to the drug – FIXED LOCATION – and thus the name “fixed drug eruptions”

Common drugs

  • Antimicrobials: tetracycline, sulfonamides
  • Anti-inflammatories
  • Barbiturates
  • Phenophthalein
45
Q

What are the common drug reactions?

A
  1. Exanthematous eruptions
  2. Urticaria
  3. Fixed Drug Eruptions
  4. Erythema multiforme >> Stevens-Johnson Syndrome >> Toxic Epidermal Necrolysis
46
Q

What is the diagnosis? How would you manage this patient?

A

Meningococcemia

  • *Investigations**
  • Blood culture
  • Blood: CBC, clotting, RLFT, ESR, CRP
  • CSF culture
  • Skin lesion culture
  • Urinalysis and C/ST
  • *Treatment**
  • Resuscitation
  • Fluids
  • Antibiotics
47
Q

What are the differential diagnosis of a rash following a viral infection?

A
  • Idiothrombocytopenic purpura
  • Henoch-Scholein Purpura (HSP) — see picture
    >> Vasculitis with RBC extravasation
    >> Usually benign and self-limiting
    >> Palpable purpura on buttocks and legs
    >> Abdominal pain
    >> Athralgia
    >> Fever

    >> Transient microscopic hematuria
48
Q

How does one manage a case of diphtheria?

A
  1. Throat swab and culture to confirm
  2. Treatment is based on clinical suspicion
    >> Diphtheria antitoxin
    >> Penicillin G or erythromycin to halt further toxin production and prevent carrier
49
Q

What are the possible complications of diphtheria?

A

5-10% mortality

  • Airway obstruction
  • Recurrent nerve palsy
  • Diphtheritic peripheral neuritis
  • Diphtheritic myocarditis
50
Q

In whom does pertussis have the greatest incidence?

A

Children <1year (not fully immunized)
Adolescents (waning immunity)

51
Q

What are the common causative organisms of preorbital and orbital cellulitis?

A
  • *- Staphylococcus aureus
  • Streptococcus pyogenes
  • Streptococcus pneumoniae
  • Moraxella catarrhalis**
  • Hemophilus influenzae type B
52
Q

ORBITAL CELLULITIS IS AN OCULAR AND MEDICAL EMERGENCY.

A
53
Q

What are the cardinal signs of orbital involvement?

A
  1. Decreased visual acuity
  2. Ophthalmoplegia/diplopia
  3. Pain with extraocular eye movement
  4. Googly eyes