FEVER AND RASH Flashcards

(88 cards)

1
Q

_________: 4 serotypes
•Carried by Aedes aegypti

A

•Dengue virus

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2
Q

____________ is usually associated with secondary dengue infections

A

Dengue hemorrhagic fever

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3
Q
  • Etilogy: RNA virus (Paramyxoviridae Family)
  • Mode of Transmission: by droplet spray during the prodromal period
  • Period of communicability: 4 days before & 4 days after the onset of the rash
A

RUBEOLA (MEASLES)

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4
Q

Pathognomonic Sign:
•Koplik spots
Øgrayish white dots with red border opposite the lower molars
Øappear before the prodrome

A

RUBEOLA/ MEASLES

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5
Q

WHAT ARE THE 3C’s prodrome in rubeola/ measles?

A

•prodrome: high-grade fever + 3 C’s (conjunctivitis, cough, coryza) for 3-5 days

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6
Q
  • @ height of fever: maculopapular rash appears on the hairline or face and spreads cephalocaudally
  • Rash fades downward à branny desquamation and disappears within 7-10 days
A

RUBEOLA/ MEASLES

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7
Q

•Vitamin A:
–single dose
–100,000 IU orally for 6 mo-1 yr
–200,000 IU for > 1 yr old
–Especially indicated for hospitalized patients & with complications (ophthalmologic evidence of vitamin A deficiency & malnourished patients)

A

Rubeola/ measles

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8
Q

Measles: Complications

A
  • Otitis media
  • Pneumonia
  • Encephalitis (Subacute sclerosing panencephalitis)
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9
Q
  • Caused by: altered measles virus harbored intracellularly in CNS
  • Occurs 7-10 years post measles infection
A

Subacute sclerosing panencephalitis

(SSPE)

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10
Q

What happens in the stage 1 of SSPE?

A
  • Stage 1
  • Subtle changes in behavior & deterioration of schoolwork, decreased attention span, temper outbursts
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11
Q

What happens in the stage 2 of SSPE?

A
  • Stage 2
  • Massive, repetitive myoclonic jerks esp. of the axial muscles
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12
Q

What happense in the stage 3 of SSPE?

A
  • Stage 3
  • Choreo-athetosis, rigidity, dystonia, decreased sensorium, dementia, stupor, coma
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13
Q

What happens in stage 4 of SSPE?

A
  • Stage 4
  • loss of central control for breathing, heart rate, blood pressure
  • è death
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14
Q
  • Due to RNA virus of Togaviridae family
  • Spread by oral droplet or transplacentally to the fetus
  • Period of highest communicability: 5 days before & 6 days after the onset of the rash
A

German Measles/ Rubella

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15
Q

Forchheimer spots
Ødiscrete rose spots on the soft palate
Øjust before the onset of rash
20% of patients

A

Rubella: Clinical Manifestations

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16
Q

The Rash

  • can be the first symptom to appear
  • maculopapular rash begins on the face and spreads quickly cephalocaudally
  • Duration: 3 days
  • w/o desquamation

low grade fever for 1-3 days
•retroauricular, posterior cervical & suboccipital lymphadenopathy (begins 24 hrs before the rash and remains for 1 week)
•Polyarthritis esp.in older girls

A

RUBELLA

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17
Q

RNA virus

(Togaviridae Family→ replicates in the respiratory epithelium
•spreads to regional lymph nodes→spreads to regional lymph nodes

A

RUBELLA

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18
Q

Risk for congenital defects & disease is greatest with primary maternal infection during the 1st trimester

A

Congenital Rubella

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19
Q
  • Intrauterine growth retardation
  • Congenital cataracts
  • Microcephaly
  • Structural heart defects like PDA
  • “blueberry muffin” skin lesions
  • Sensorineural Hearing Loss
  • Motor and mental retardation
A

Congenital Rubella

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20
Q
  • Human herpesvirus type 6
  • Aka Exanthem Subitum, Sixth disease
A

ROSEOLA

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21
Q

High grade fever for 3-5 days
•Rash appears coincident with resolution of fever
•Rash: small, evanescent morbilliform, blanching, pink (rose-colored) rash
•Appears on trunk è to face & extremities
lasts for 1-3 days

A

ROSEOLA

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22
Q

Nagayama spots: ulcers at uvulopalatoglossal junction
•Mild injection of pharynx, palpebral conjunctivae, or tympanic membranes
•Enlarged suboccipital nodes

Pathophysiology: Unknown

A

ROSEOLA

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23
Q
  • _____________is a neurotropic human herpes virus
  • Chickenpox: primary infection

•Period of communicability: 1-2 days before the rash until all lesions have crusted

A

Varicella zoster virus

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24
Q

•_________ activation of latent sensory ganglion neurons

A

Herpes Zoster (shingles):

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25
* The Rash * Trunk àother parts of the body * Macule/papuleà vesicleà crust * In various stages are of evolution
Varicella
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Pathogenesis: ## Footnote Human herpes virus * Inoculates in mucosa of the upper respiratory tract and tonsilar lymphoid tissue * spreads to reticuloendothelial system * Viremia è Cutaneous lesions
Varicella
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* The Rash * same as varicella with severe pain & tenderness along the posterior nerve roots
Herpes Zoster
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* The Rash * same as varicella with severe pain & tenderness along the posterior nerve roots
herpes zoster
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Human herpes virus * Transported via sensory axons to the dorsal root ganglia (during 10 infection) * Latent infection in neurons and satellite cells * reactivatiionè rash within dermatomal distribution
Herpes Zoster
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What are the secondary complications of Varicella?
* secondary bacterial infection * encephalitis or meningitis * Pneumonia * glomerular nephritis
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* Fetuses infected at 6-12 wks of gestation have maximal interruption of limb development à short & malformed limbs covered with cicatrix – skin lesion with zigzag scarring * Fetuses infected at 16-20 wks of gestation - eye & brain involvement
Congenital Varicella
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* Most common cause: Coxsackievirus A16 * Enterovirus 71: more severe
HAND, FOOT & MOUTH DISEASE (HFMD
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The Rash ØTender maculopapular, Ulcerative intraoral lesions on tongue & buccal mucosa Øvescicular, pustular lesions on hands & feet
HFMD
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What are the complications of HFMD
•Complication: myocarditis, pericarditis, shock
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* **parvovirus B19** * Common in 5-15 years old * Transmission: large droplet spread & blood transfusion
ERYTHEMA INFECTIOSUM
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* Fifth disease * Incubation period: 16-17 days * Infectious stage: low grade fever, malaise, rhinorrhea * post-infectious stage: Rash, joint pains
ERYTHEMA IN**F**ECTIOSUM
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Parvoviris B19 * Viremia * Fever, Malasie, * rhinorrhea Attacks erythroid cell line •Fall in hemoglobin •transient arrest of erythropoiesis
ERYTHEMA INFECTIOSUM: Infectious stage
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ERYTHEMA INFECTIOSUM Fall in Hemoglobin and arrest of eryhtropoiesis is DANGEROUS for:
1. Immunocompromisedà chronic infection (chronic anemia) 2. chronic hemolytic diseaseà transcient aplastic crisis 3. pregnant women (fetus) à fetal anemiaàfetal demise
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Tx for Erythema Infectiosum 1. Immunocompromisedà chronic anemia: \_\_\_\_\_\_\_\_\_\_ 2. chronic hemolytic diseaseà transcient aplastic crisis: \_\_\_\_\_\_\_\_\_\_\_\_ 3. pregnant women (fetus) à fetal anemia: \_\_\_\_\_\_
1. IVIG 2. PRBC transfusion 3. in-utero rbc transfusion
40
ERYTHEMA INFECTIOSUM: Post infectious stage
* Th-1–mediated cellular immune response→ * production of specific immunoglobulin M (IgM) antibodies→ * formation of immune complexes→ * deposition of the immune complexes in the skin, joints Rash, Arthralgia
41
RASH: 3 phases I: **“slapped-cheek”** è macular erythema on trunk & proximal extremities è Central clearing II: **lacy, reticulated appearance** •Fades without desquamation III: **wax & wane in 1-3 weeks**
Erythema Infectiosum
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* **Neisseria meningitidis** * **Groups A, B, C, W135, Y** – more common * 6-12 months age group * Secretions from colonized upper RT of patients & asymptomatic carriers •Mode of transmission: person to person through infected droplets •Period of communicability: until 24 hours after start of antibiotics •Asymptomatic colonization to fulminant sepsis **•**
**MENINGOCOCCEMIA** •Mode of transmission: person to person through infected droplets •Period of communicability: until 24 hours after start of antibiotics •Asymptomatic colonization to fulminant sepsis •
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•Clinical Manifestations •**Abrupt** onset of fever, chills, headache, vomiting •**Rapid worsening of symptoms within hours** •Diffuse adrenal hemorrhage, DIC, coma and death à **Waterhouse-Friderichsen syndrome** • •
MENINGOCOCCEMIA
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Menigococcemia
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N. meningitis
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Rocky Mountain Spotted Fever (RMSF) causative agent is\_\_\_\_\_\_\_\_ –intracellular bacteria •Ticks: natural host, reservoir, vectors
Rickettsia rickettsii
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Rocky Mountain Spotted Fever Clinical features •What is the Triad: \_\_\_\_\_\_\_\_\_\_\_\_ •**Calf muscle** pain and tenderness •GIT: nausea, vomiting, diarrhea, abdominal pain
Fever, headache, rash
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RMSF
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The rash –Discrete, pale, rose-red blanching maculopapules on ankles, wrist, lower limbs, spread to trunk – petechiael or hemorrhagic – **echymoses, necrotic (in severe cases)**
RMSF
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Rocky Mountain Spotted Fever Treatment \_\_\_\_\_\_\_\_\_\_\_\_\_ (drug of choice)
51
\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ RITTER DISEASE •Common in **less than 5 yrs old** •Most common cause: **phage group 2 staphylococci**, particularly **strains 71 and 55**
Staphylococcal Scalded Skin Syndrome (SSSS)
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: Clinical Manifestations •Rash may be preceded by **malaise, fever, irritability, and exquisite tenderness of the skin** •**Scarlatiniform erythema** develops diffusely and is accentuated in flexural and periorificial areas •The conjunctivas are inflamed and occasionally become purulent
SSSS
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The Rash •**Brightly erythematous ski**n  wrinkled appearance  blisters and erosions •Circumoral erythema, radial crusting and fissuring around the eyes, mouth, and nose
SSSS
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**Nikolsky sign** = areas of epidermis may separate in response to gentle shear force •Large sheets of epidermis may peel away  moist, glistening, denuded areas  secondary cutaneous infection •Desquamative phase begins after 2–5 days of cutaneous erythema •Healing occurs without scarring in 10–14 days
SSSS
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SSSS: Treatment
* Antibiotics: Oxacillin * Clindamycin may be added to inhibit bacterial protein (toxin) synthesis * The skin should be gently moistened and cleansed * Application of an emollient provides lubrication and decreases discomfort
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* Menstruating women 15-25 yo * Use of tampons * Non-menstrual TSS: nasal packing, wound infection, sinusitis, tracheitis, pneumonia, emphysema, abscess, osteomyelitis, burns
Staphylococcal Toxic Shock Syndrome
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Staphylococcal Toxic Shock Syndrome: Diagnostic Criteria
Major Criteria (all required) Acute Fever \>38.8C Hypotension Rash (erythroderma w/ convalescent desquamation)
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Staphylococcal Toxic Shock Syndrome: Diagnostic Criteria
Minor Criteria (3 or more) Mucous membrane inflammation Vomiting, diarrhea Renal abnormalities Liver abnormalities Muscle abnormalities CNS abnormalities Thrombocytopenia (\<100,000/mm3)
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Staphylococcal Toxic Shock Syndrome: Diagnostic Criteria Exclusionary Criteria
Absence of another explanation Negative blood culture (except for Staph.aureus)
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SSSS
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pathogenesis Scarlet and SSSS
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\_\_\_\_\_\_\_\_\_\_\_\_: Clinical Manifestations •The Rash –**begins around the neck and spreads over the trunk and extremities** –papular, erythematous rash that blanches on pressure **and feels rough (sandpapery)** –lasts 3–4 days fades desquamation
Scarlet Fever
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\_\_\_\_\_\_\_\_\_\_: Clinical Manifestations **•Fever •Pharyngitis *•Strawberry tongue***
Scarlet Fever
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Scarlet Fever: Strawberry tongue
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\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ •Fever, rash •Shock •Multiorgan system failure
Streptococcal Toxic Shock Syndrome
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Streptococcal Toxic Shock Syndrome: Cinical Criteria •Hypotension + 2 or more of the ff:
Renal impairment Coagulopathy Hepatic impairment Acute Respiratory Distress Syndrome Generalized erythematous macular rash Soft tissue necrosis
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\_\_\_\_\_\_\_\_\_\_\_\_\_ Definition: \_\_\_\_\_\_\_\_\_\_\_ is an autoimmune disease affecting the **heart and extra- cardiac sites (joints, brain, skin and others)** •Develops **2-3 weeks after an acute episode of pharyngitis** Group A Strep (GAS)
Rheumatic Fever (RF)
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Jone's Criteria f What are the major classification?
* Carditis (friction rub, murmur, cardiomegaly, CHF) * Arthritis (migratory polyarthritis, swollen, red, tender) * Chorea * Subcutaneous nodules * Erythema marginatum
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Jone's Criteria What are the minor classification?
* Fever * Arthralgia * Acute phase reactants (ESR, C-reactive protein, leukocytosis) * Prolonged P-R interval on ECG
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\_\_\_\_\_\_\_\_\_\_\_ •2 Major Criteria •OR •1 Major + 2 Minor Criteria + supporting evidence of antecedent Group A streptococcal infection
Jones Criteria
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\_\_\_\_\_\_\_\_\_\_ characterized by the development of **Aschoff’s Bodies** within the **myocardium** Gross features: •**Aschoff bodies are multiple tiny nodules (1-2 mm in diameter)**
Carditis:
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Microscopic features: 1. Fibrinoid necrosis ( destroyed fragmented collagen) 2. Surrounded by lymphocytes and histiocytes & 3. Aschoff cells (large mononuclear or multinuclear macrophages)
Aschoff’s body
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Rheumatic Mitral Valve
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Erythema Marginatum
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secondary prevention RF
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\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_ •Acute febrile vasculitis •Affects medium-sized artery w/ striking predilection for the coronary arteries •20% of untreated cases develop coronary artery aneurysm •Unknown cause
KAWASAKI DISEASE
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KAWASAKI Fever x 5 days + 4 of the ff:
CONJUNCTIVA –bilateral, non-exudative RASH - ADENOPATHY – unilateral, cervical, \>1.5cm STRAWBERRY TONGUE, erythema of oropharyngeal mucosa, dry cracked lips HANDS & FEET EDEMA CRASH & BURN
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\_\_\_\_\_\_\_\_\_\_\_\_\_ •The Rash –Maculopapular –Erythema multiforme or –Scarlatiniform
KAWASAKI DISEASE
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\_\_\_\_\_\_\_\_\_\_ •Conjunctivitis •Strawberry tongue •Perineal desquamation
KAWASAKI DISEASE
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Periungual desquamation
Kawasaki Disease
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KAWASAKI DISEASE Clinical Phases Phase Symptoms Timing ACUTE Febrile
•CRASH & BURN •Perineal desquamation •Myocarditis 1st-2nd week of illness
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What is the SUBACUTE phase of Kawasaki?
* Fever has resolved * Irritability, conjunctivitis,anorexia * Periungual desquamation of fingers and toes * Arthritis * CORONARY ARTERY ANEURYSM
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What is the CONVALESCEN phase of Kawasaki?
CONVALESCENT •Clinical signs and symptoms have abated •ESR and CRP still elevated Until 6-8 weeks after onset
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* Main symptom: Arthritis * Systemic-onset JRA: fever and rash * Other types: oligoarthritis and polyarthritis
Juvenile Rheumatoid Arthritis (JRA)
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Systemic-onset _____________ Clinical Features •Fever •Rash •Arthritis •Visceral involvement •Hepatosplenomegaly, lymphadenopathy, serositis **•(+)Koebner phenomenon**
JRA
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Systemic-onset JRA Clinical Features •The rash –**Transient/Evanescent (\<1hr)** –Faint, erythematous, salmon-colored, macular, linear or circular on trunk and proximal extremities **–Non-pruritic**
JRA
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Systemic-onset JRA Clinical Features
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