ILA + lecs-infection + rhem Flashcards

1
Q

Child develops fever, high pitched cry and lethargy over 8 hour period. Progressively less responsive. Then becomes hypotensive with a delayed capillary refill time, and develops tachycardia and a purpuric rash. Diagnosis?

A

meningitis

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2
Q

What is a septic screen, and what does each thing screen for?

A

BUFALO!!
blood culture for bacteria, FBC, CRP, urine sample (common due to UTIs being common, usually do a clean catch)
Check renal function, liver function and clotting function -U+Es, LFT, clotting screen??
Consider: CXR, LP, rapid antigen screen and PCR on CSF/blood/urine
PCR for viruses and meningococcal/pneumococcal
Do LP to identify organism and therefore correct abx and length of time

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3
Q

What is a contraindication to a LP and what indicates this CI?

A

Raised ICP- can see because: HR goes down and BP goes up and Possible focal neuro symptoms
Clotting problems eg APTT Contraindicates LP
If ventilated or on lots of fluid blouses – don’t want to put in position that will cause reap distress

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4
Q

What are possible complications of a LP?

A

Complications of LP can be CSF leak (cause headache), infection at site, bleeding

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5
Q

The microbiologist rings to confirm a CSF white cell count of 500 with no red cells. The cells are predominantly neutrophils. CSF glucose is low and CSF protein raised. Gram film shows gram negative diplococci. What is the likely diagnosis?

A

Meningitis – bacterial caused by N. Meningitisidis – meningococcal septicaemia

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6
Q

What would be the immediate management of a child with meningitis?

A

What would be the immediate management of a child with meningitis?
ABCD
IV abx
IV fluids to raise BP – give bolus, give 0.9 saline (crystalloid) 200 ml as do 20x10

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7
Q

What antibiotics would you prescribe in a child with meningitis?

A

Cefotaxime 100 as first dose

Give amanpicillin/ amoxicillin if less than three month as could have a listeria infection

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8
Q

What is the cause of the purpura in a meningitis rash?

A

Infection causes inflammatory toxins which causes capillary leakage causing DIC and microemboli in vasculature, tissues become necrotic

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9
Q

What measures may be used to stabilise and manage a patient with meningitis, after abx, if they contribute to deteriorate?

A

Ventilate for airway and breathing- reduces the metabolic demand and can be if gcs drops protects their airway
Fluids for circulation
Vasodilator in shock so reduce fluid as capillaries are already leaky
Check urine – catheter
Adrenaline – inotrope- improves heart function
Central access eg femoral or internal jugular line in young child
Broader abx eg merypenin or clindamycin

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10
Q

How is meningitis carried and passed on?

A

Nasopharyngeal carrying – airborne

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11
Q

What first-line treatment is recommended to reduce the risk of meningitis in “close contacts”? Are there any contraindications to this treatment?

A

Give prophylactic rifampicin or ciprofloxacin to eradicate nasopharyngeal carriage in household contacts. If pt has had group c meningitis then contacts should get this vaccine.
If have received rifampicin before may be less effective.
Rifampicin is CI in breast feeding or pregnancy
USUALLY use ciptoflaxacin as less contraindications and only need one dose

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12
Q

What might you warn any people receiving prophylactic medications for meningitis?

A

Red urine SE
Liver toxicity—hepatitis, liver failure in severe cases
Abdominal — nausea, vomiting, abdominal cramps, diarrhea
Flu-like symptoms—chills, fever, headache, arthralgia, and malaise.
Allergic reaction—rashes, itching, swelling of the tongue or throat, severe dizziness, and trouble breathing

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13
Q

How is a “close contact” defined in infectious diseases?

A

people living in the same house; university students sharing a hall of residence ; a boyfriend or girlfriend

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14
Q

Laura, a two year old, presents to her general practitioner with a two month long history of malaise, pallor and reduced appetite. She has occasional febrile episodes, associated with a pink rash, and with a persistent complaint of soreness in her left thigh. Despite walking at the age of 13 months, she is now reluctant to weight bear. Her birth and development history show no concerns and all her immunisations are up to date. On examination, she has a low grade fever (37.7°C) and generalised cervical lymphadenopathy. When made to walk, she limps, but does not seem to be in too much discomfort. She is reluctant to move her left leg. There is a full range of passive movement and no specific site of tenderness. The rest of her examination is essentially normal. What is the differential diagnosis?

A
Septic arthiritis 
Osteomyelitis  
Juvenile arthiritis 
Transient synovitis  
Malignancy eg osteosarcoma  
Reactive arthiritis  
SLE 
Systemic JIA
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15
Q

What is the diagnostic criteria for systematic JIA?

A

arthritis with at least two weeks of daily fever. The fever must be greater than 39ºC and return to less than 37ºC between peaks on at least three days (called a quotidian fever). There must be one or more of:
Rash - evanescent (quickly fading) non-fixed erythematous, salmon pink (classically) with fever
Lymph node enlargement.
Hepatomegaly and/or splenomegaly.
Serositis (pericarditis, pleuritis, peritonitis).
Progression:
Average age of onset before the age of 5 years.
Arthritis is only seen at disease onset in one third of children but commonly develops within a few months. It is usually symmetrical and affects several joints.

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16
Q

What investigations would help in child with limp, rash and fever?

A
XR, POSs Us hip  
Blood culture 
ANA 
FBC 
Synovial fluid culture 
Partial septic screen
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17
Q

The investigations are essentially normal apart from the ESR, which is significantly raised. What is the likely diagnosis?

A

Juvenile arthritis – systemic

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18
Q

What are the different types of juvenile arthiritis?

A

Other types other than systemic includes oligoarticular, polyarticular, enthesitis, psoriatic

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19
Q

What drug treatment might be considered in SJA?

A

1st line: NSAIDs
2nd line: corticosteroids;
Methotrexate, Leflunomideand sulfasazine - DMARDS(need to monitor for BM suppression and abnormal LFTs)
; Biological- tocilizmab, adalumab, Abatacept
tanercept is licensed for those patients with polyarticular JIA for whom methotrexate has been ineffective. It is the only anti-TNF licensed in the UK for JIA
joint injections for oligoarticular

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20
Q

Which professionals should be involved in JIA care?

A
Rheumatology 
Physiotherapy 
Occupational therapy 
Clinical psychology 
Play specialist support 
Ophthalmology  
Pain team
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21
Q

Jirou, a three year old boy presents with a seven day history of high fevers. He has now developed red eyes, a rash and is complaining of a sore mouth and throat. On examination he appears miserable and unwell with a diffuse maculopapular rash mainly on his torso. He has bilateral injected conjunctiva, red cracked lips and a strawberry tongue. He has a unilateral 3cm x 2cm cervical swelling, and swollen reddened palms. What is the differential diagnosis?

A
Kawacaski’s disease 
Scarlett fever  
Meningitis 
Sepsis 
Juvenile arthiritis  
Toxic shock syndrome  
Steven Johnson’s syndrome  
Tonsilitis  
Measles 
Rubella 
Parvovirus  
Enterovirus
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22
Q

How would you manage child with high fever, rash, lympadenopathy and dore throat?

A

full septic screen including a lumbar puncture, and has intravenous antibiotics started.

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23
Q

What may you see on blds for Kawasakis?

A

thrombocytosis and a high ESR.

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24
Q

What criteria are used to make Kawasakis diagnosis?

A

Kawasaki’s - assess in children where fever has lasted over 5 days at 39 degrees plus at least four of:
Acronym My HEART —->
My - mucosal involvement - strawberry tongue, swollen throat
H- hand and feet desquamation (peeling) + red and swollen
Eyes non purulent bilat conjunctivitis
Anopathy cervical unilat 1.5cm lymphadenopathy
Rash - truncal
T-Temperature for 5 days

Also other more generic sx:
Liver toxicity—hepatitis, liver failure in severe cases
Respiratory—SOB
Abdominal —N+V+D
Flu-like symptoms—chills, fever, headache, arthralgia, and malaise.

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25
Q

What is the management of Kawasakis?

A

Treat with IV immunoglobulins, aspirin, steroids, infliximab, cyclosporin, if have aneurysm may need long-term warfarin.

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26
Q

Give two possible complications with the first-line treatments used in Kawasakis.

A

IV immunogloblins- MI, haemolsis, aseptic meningitis, PE

Aspirin- Reye’s syndrome (encephalopathy and liver toxicity) and upper GI bleed

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27
Q

What further investigations are indicated in Kawasakis, and why?

A

urinalysis, FHC, inflamm markers, LFTs may show elevation of the transaminases and bilirubin, ECHO once stable to check for complications – no diagnostic tests
Will need long term cardio follow up if have a cardio issue

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28
Q

What is the long-term prognosis in Kawasakis?

A

Prognosis depends upon the degree of cardiac involvement. Most (50-70%) coronary artery aneurysms regress after a period of 1-2 years, although giant aneurysms never resolve entirely and have a worse prognosis.

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29
Q

What is the common causitive agent of:
epiglottitis
whooping cough
croup

A

Haemophilus influenza b
pertussis
Parainfluenza

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30
Q

Is Varicella Zoster (VSZ) serious? How does it present?

A

self-limiting but can result in death if subsequent encephalitis, secondary staph/strep infection, purpura fulminans (vasculitis skin and tissues )

VESICULAR lesions that starts at HEAD and TRUNK and spreads to the peripheries
Become papules then vesicles (fluid filled) with erythema and then pustules (scan over - no longer contagious)
Itching, fever and scratching
If lesions continue beond 10 days suggests poor immunity
dangerous to non-immune pregnant women

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31
Q

How does HSV present?

A

stomatitis, cold sore, occasional encephalitis

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32
Q

What are the phases of presentation of Kawasakis from week 1-3?

A

fever over 5 days, red eyes (NON exudative conjunctivitis), stomatis, raised platelets, cracked red lips, rash, red and oedematous palms and soles, strawberry tongue, cervical lymphadenopathy. In second week get peeling of fingers and toes. Third week onwards get CVS.

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33
Q

What are differentials of a prolonged fever?

A

kawasakis, deep abscess, osteomyelitis, TB, IE, EBV/HIV, malaria, SLE, vasculitis, IBD, sarcoidosis, malignancy, juvenile arthritis

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34
Q

What are the CSF findings for bacterial vs viral meningitis?

A

bacterial: Raised cell count
Raised protein
Low glucose
Bacteria identified in blood or CSF culture or PCR

viral: Raised cell count  
Normal protein 
Normal glucose 
Virus identified in CSF, stool, throat or blood 
commonly HSV encephalitis
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35
Q

What are the causes of meningitis is a:

a) <3 month old
b) >3 month old
c) >6 yr old

A

<3 months: e coli, listeria, GpB strep: give cefotaxime plus amoxicillin
>3 months: N. meningococcus, strep pneumococcus, haemophilus influenza: give just cefotaxime
>6 yrs: N. meningoccocus, strep pneumonia

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36
Q

How is encephalitis treated?

A

give acyclovir and treat as HSV

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37
Q

What are symptoms of meningitis?

A

Older children report: headache, photophobia, neck stiff, kernig’s sign positive
Drowsy/ irritable/ coma/ seizures
Vomit

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38
Q

What is Kernigs sign?

A

Kernigs= child lies supine with hip and knee flexed. Back pain on extension of knee.

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39
Q

What are early vs late signs of raised ICP?

A

Early sign of raised ICP – reduced consciousness, abnormal pupils, abnormal posturing, bradycardia, htn
Full fontanelle, papilledema (late sign raised ICP)

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40
Q

What are complications of meningitis?

A

hearing loss, hydrocephalus, local vasculitis or infarction

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41
Q

What is septicaemia presentation?

A

Red/purple non-blanching rash.
Cold hands and feet.
Tachypnoea.
Flu like symptoms

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42
Q

What is necrotising fasciitis?

A

Typically group A strep
Severe S/c infection
Debridgement required – emergency

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43
Q

What is toxic shock syndrome?

A

Fever, hypotension, erythema/macula rash
Toxin released from S.areus and group A strep
Go into shock, multile organ involvement

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44
Q

What are congenital infections?

A

HIV, Hep B, rubella, HSV, VSV, syphilis, TB, GpB strep, CMV

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45
Q

What is Epstein Barr virus linked to?

A

Burkitt’s lymphoma, nasopharyngeal carcinoma, autoimmune conditions eg MS

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46
Q

How does EBV present and what is the treatment?

A

May present with fever, tonsillitis, lymphadenopathy (known as mono or glandular fever)
Treat symptomatically, steroids in airways comprimised
Amoxicillin and ampicillin should avoided as can cause a rash.

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47
Q

What virus presents similarly to EBV?

A

Cytomegalovirus (CMV)

48
Q

What can CMV lead to?

A

Can lead to neuro and hearing problems

49
Q

How does Erythema infectiosum present?

A

aka slapped cheek - caused by parvovirus 19
fever then headache, coryzal and myalgia followed by slapped cheek face rash a week later which spreads to arms and sometimes arthropathy
transmission from mother to the foetus can lead to foetal Hydrops.
remember can cause APLASTIC CRISIS in those with haemolytic anaemias!

50
Q

What are the four types of enteroviruses?

A

polioviruses, Coxsackie A viruses (CA), Coxsackie B viruses (CB), and echoviruses

51
Q

What can Coxsackie A virus and enterovirus 71 cause?

A

hand foot and mouth disease – painful vesicular (ulcers) lesions of hands, feet, mouth and tongue.

52
Q

What can enteroviruses lead to?

A

cause encephalitis, myocarditis and pericarditis

53
Q

How does measles present?

A

1) prodrome: irritable, conjunctivitis, fever, coryzal symptoms, fever
2) Koplik spots white spots (‘grain of salt’) on buccal mucosa
3) rash: red-brown starts head/neck then to whole body, maculopapular / blotchy rash

54
Q

How does mumps present?

A

parotitis (can lead to increased amylase levels), swollen face, orchitis

55
Q

What are the NICE red flag features in a child with a fever?

A
pale/ mottled skin
unresponsive
weak/ continuous cry
grunting
tachypnoea >60 RR
reduced skin turgor
< 3 months
non blanching rash
bulging fontanelle
neck stiff
seizure
focal neuro signs
sevre/mod chest recessions
56
Q

What are the NICE amber flag features in a child with a fever?

A
pallor
decreased activity and responsiveness
nasal flaring
tachypnoea but <60
sats <95
crackles
tachycardia
CRT >3 secs
dry mucus membranes
infant poor feed
reduced UO
ages 3-6 months
fever for over 5 days
rigors
swollen limb/ joint/ not bearing weight
57
Q

What are the NICE green flag features in a child with a fever?

A

normal: colour; response to social cues; content, moist mucus membranes

58
Q

What is the difference between a septic screen for <1 month infant and <3 infants?

A

Under 3 months: FBC, Blood culture, CRP, Urine culture
Under 1 month: as above and Lumbar puncture (LP)
1-3 months LP if: Unwell or WBC <5 or >15

59
Q

When do you give abx to an unwell infant?

A

All infants under 1 months and 1-3 months if unwell or WBC <5 or>15

60
Q

For children over 3 months with red or amber features what is the septic screen?

A

FBC, Blood culture, CRP, Urine culture
LP if clinical features
CXR consider if clinical features

61
Q

For child with NICE green features what do you do?

A

Urine test, observe and reexamine

62
Q

When is a child at its worst stages of immunity?

A

6 months - natural immunity wears off

63
Q

What is Primary immune deficiency:?

A

immunity lower due to genetic or prematre baby - Immunoglobulins worse in preterm babies as crosses the placenta in third trimester

64
Q

How does Primary immune deficiency present?

A

present with recurrent infections, fail to thrive, skin problems, organomegaly. Look at FBC (low WCC), total Ig GAM, response to immunisations, number T and B cells.

65
Q

What is mx for Primary immune deficiency:?

A

Manage with abx, prompt treatment, replace iG, bone marrow transplant

66
Q

Describe what type of vaccines are which?

A

Live attenuated: MMR, BCG, rotavirus
Inactivated: whole cell pertussis
Inactivated toxin: diphtheria, tetanus
Recombinant: acellular pertussis

67
Q

What vaccines are given at 2 months?

A
6 in 1: diphtheria
hepatitis B
Hib (Haemophilus influenzae type b)
polio   
tetanus
pertussis

MenB
Rotavirus

68
Q

What vaccines are given at 3 months?

A
6 in 1: diphtheria
hepatitis B
Hib (Haemophilus influenzae type b)
polio   
tetanus
pertussis

PCV
rotavirus

69
Q

What vaccines are given at 4 months?

A

6 in 1

Men B

70
Q

What vaccines are given at 1 yr?

A
Hib
MenC (1st dose)
MMR (1st dose)
Pneumococcal (PCV) vaccine (2nd dose)
MenB (3rd dose)
71
Q

What vaccines is given at 3-4 yrs?

A
MMR (2nd dose)
4-in-1 pre-school booste: diphtheria 
tetanus 
whooping cough
polio
72
Q

What vaccine is given at 13-14 yrs?

A

HPV vaccine

73
Q

What vaccine is given at 14 yrs?

A

3-in-1 teenage booster: tetanus, diphtheria and polio.

MenACWY

74
Q

What is the difference between allergy hypersensitivity and atopy?

A

Allergy is defined as a hypersensitive reaction initiated by immunological mechanisms
Hypersensitivity is stereotypical responses to a specific stimulus at a dose that is normally tolerated by most ppl
Atopy is a tendency to produce IgE in response to specific stimuli tolerated by most people

75
Q

What is the difference between food IgE and non IgE related allergy presentation?

A

Non IgE food allergy involves GI tract normally
IgE food allergy can present as urticaria, itching, facial swelling, anaphylaxis- wheeze, stridor, abdo pain, shock, collapse

76
Q

How are allergies diagnosed?

A

history, skin prick test and IgE specific antibodies in blood

77
Q

What is reactive arthiritis?

A

Reactive arthritis – follows STI/ gastroenteritis eg salmonella or shigella
(remember: cant see, wee or climb tree)

78
Q

What is juvenile idiopathic arthiritis?

A

onset before 16th with persisting joint swelling lasting for at least 6 weeks

79
Q

How does the arthirtis present in JIA?

A

persistent swellings, joint swelling in morning, loss of ROM, pain, joint deformity, warm, colour change, stiff after periods of rest, thickening of the synovium

80
Q

ix for JIA?

A

blds (FBC, CRP, ESR, RF, HLA B27, ANA)

XR to exclude differentials

81
Q

What are complications of JIA?

A

uveitis, growth failure, OP

82
Q

What is oligoarticular JIA?

A

less than 4 joints involved in first 6 months (may become extended oligoarticular if >4 become involved after 6m)

83
Q

What are the clinical features of oligoarticular JIA?

A

Most commonly involved joints in descending order: KNEE, ankle, wrisgt, elbow, small joints hand/feet
ANA
Chronic anterior uveitis is associated
Asymmetrical

84
Q

What is polyarticular JIA?

A

More than 4 joints involved in first 6 months

85
Q

What are the clinical features of polyarticular JIA?

A

Rheumatoid factor positive (often fingers involved and systemic sx) and negative (spine and temporomandibular may be involved)
Symmetrical

86
Q

What is psoriatic JIA?

A

Nail pitting and dactylitis
Asymmetry
Psoriasis in a first-degree relative.

87
Q

What is enthesitis JIA?

A

ERA affects enthuses – inflamed tendon/ligaments when inserts into bone eg achilles
ERA causes sacroiliitis later
Lower limb and larger joints intitally
HLA 27

88
Q

How does sytemix JIA present?

A

sJIA often presents with a specific fever pattern
Typical rash – salmon pink and macular
Lymphadenopathy.
Hepatosplenomegaly.
Serositis – inflammation of serous tissue eg pericarditis, peritonitis
Have arthralgia/ myalgia but not arthritis INITIALLY

89
Q

What may be seen on blds for sJIA?

A

On Ix anaemia, raised neutrophils and platelets, raised ESR

90
Q

what may be found in a pGALS examination?

A

Bow legs – genu varum – rickets , oesteogenesis imperfecta

Knock knees – genu valgum – seen often in young children and will resolve itself, JIA

Flat feet – pes planus – usually have flat feet when first learning to walk, marked flat feet are common in hypermobility

Toe walking – muscular dystrophy, JIA, spastic diplegia (CP)

Club foot – talipes equinovarus – entire foot is inverted and supinated, cannot be passively corrected ie not positional from just being in utero, associated DDH. Treat with plaster casting – ponsetti method

Pes cavus – high arched foot – friedrichs ataxia

Scoliosis – lateral curvature in the frontal plane of the spine, caused by idiopathic, spina bifida, CP, marfans, neurofibroma

91
Q

How does rubella present?

A

prodrome of fever, lymphadenopathy, conjunctivitis and coryzal sx
The rash then develops (it may be absent, especially in young children) - initially, pink discrete macules that coalesce, starting behind the ears and on the face, spreading to the trunk and then the extremities.

92
Q

What are key findings to differentiate between rubella, measles and scarlet fever?

A

Rubella (look for suboccipital lymphadenopathy).
Measles (look for Koplik’s spots on buccal mucosa).
Scarlet fever (look for strawberry tongue).

93
Q

1 yr old child, has had a high fever for 2 days, now a rash has appeared on their chest which has spread to their limbs and has been experiencingnconvulsions - what is it?

A

roseola - pink/red rash, lymphadenoapthy, D+V usually

6-24 months may get High fever, maculopapular rash + convulsions

94
Q

How does scarlet fever present?

A

Erythematous ‘pinhead’ Sandpaper rash , spares the face, on neck and chest first, desquaminates around the fingers and toes + ‘Strawberry tongue’
Fever, Malaise, headache, nausea..

95
Q

What is stevens johnson syndrome?

A

differential for chickenpox

- more severe, mouth ulcers, conjuctivitis

96
Q

What is erythema multiforme?

A

skin condition considered to be a hypersensitivity reaction to drugs, associated with herpes
Widespread, itchy rash with characteristic “target lesions” that look like bullseye targets, upper limbs are more commonly affected.

97
Q

How does Infectious Mononucleosis present aka glandular fever?

A

fever, coryzal sx, Sore throat; tonsillar enlargement is common, classically exudative and may be massive; palatal petechiae and uvular oedema, Fine macular non-pruritic rash, which rapidly disappears, lymphadenopathy

98
Q

What is impetigo?

A

Staph/strep skin infection

More common if they have pre-existing eczema or other skin conditions

Erythema’s macules that become vesicular/pustular - GOLDEN CRUST over - non-bullous type, which is more common

99
Q

What is the mx of impetigo?

A

fusidic acid be used first-line in localised infections, three times a day for seven days
Oral abx are only needed when infection is extensive or resistant to topical treatment, or causing systemic symptoms. Flucloxacillin is 1st line

100
Q

How does staph scalded skin present?

A

Nikolsky’s sign – separation of the skin on gentle pressure.
Skin looks thin and wrinkled followed by the formation of fluid filled blisters
(bullae) that burst and look like severe burns.

101
Q

How does shingles present?

A

infection of underlying nerve
acute, unilateral, painful blistering rash caused by reactivation of Varicella
Zoster Virus (VZV). Rash will no cross the mid-line.
mx with acyclovir

102
Q

How is candida treated?

A

1st line: miconazole PO and topical a topical imidazole (eg clotrimazole, econazole, miconazole, or ketoconazole)

103
Q

How do you differentiate candida from nappy rash?

A

Candida can cause a more inflamed rash which is a brighter or darker red, it
will also have satellite lesions and oral lesions.

104
Q

What causes roseola?

A

Human Herpes virus 6 (hence it is sometimes called sixth disease)

105
Q

4 year old child, presents with a rough rash on the torso which is sparing the face and generally unwell. What is it

A

scarlet fever

106
Q

2 Year old presents with general malaise, fever and an itchy generalised vesicular rash. WHat is it?

A

chicken pox

107
Q

A 3 year old presents with a fever of 39 degrees, mum and dad have given paracetamol but it has not gone down, the child now has bilateral red eyes
and cracked lips.

A

kawasakis disease

108
Q

A 5 year old child has been unwell with an non-specific illness, he now has purpuric non-blanching rash on his buttocks and legs, we also complains of abdo pain and joint pain.

A

Henoch-Schonlein purpura

109
Q

What is the mx of scarlet fever?

A

1st line:PO penicillin V four times a day for 10 days

110
Q

How is SSSS mx? (staph scolded skin)

A

IV antibiotics (Flucoxacillin)
Topical therapy fusidic acid
Fluid and electrolyte management (consider burns unit)
Analgesia with paracetmol

111
Q

What are the complications of measles?

A

Otitis media: the most common complication
Pneumonia: the most common cause of death
Encephalitis occurs 1 – 2 weeks following the illness
Sub acute sclerosing panencephalitis - 5 – 10 yrs later.
Febrile convultions
Myocarditis

112
Q

What is Molluscum contagiosum?

A

This is a viral skin infection caused by the molluscum contagiosum virus, which is a type of poxvirus.
flesh coloured papules (raised individual bumps on the skin) that characteristically have a central dimple.
very contagious
treat like a wart

113
Q

How does scabies typically present?

A

Incredibly itchy (type IV hypersensitivity reaction), as small red spots, the classical location of the rash is between the fingerwebs, then spreads to the whole body.

114
Q

mx of scabies?

A

Wash everything!!

Cover them in cream for 8 hours then wash it off. 5% permethrin cream, to whole body except the head, then repeat in a week.

manage close contacts

115
Q

mx of whooping cough?

A

Whooping cough - azithromycin or clarithromycin if the onset of cough is within the previous 21 days