Paediatric Rheumatology / Orthopaedics Flashcards

1
Q

State some differentials for Henoch-Schonlein purpura

A
  • Meningococcal septicaemia
  • Leukaemia
  • DIC / pancytopenia
  • Haemolytic uraemic syndrome
  • Immune thrombocytopenic purpura (ITP)
  • Non-accidental injury
  • Forceful coughing/vomiting
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Henoch-Schonlein purpura - state the following:
- Pathophysiology
- Most common age
- Presentation (including any red flags)
- Investigations
- Management

A

Pathophysiology:
- IgA vasculitis
- Purpuric rash affecting the lower limbs and buttocks
- Inflammation causes IgA deposits in blood vessles, leading to leaking of small blood vessels under the skin

Most common age:
- Children < 10 years

Presentation:
- Purpuric rash affecting the lower limbs and buttocks
- Joint pain
- Abdominal pain
- Renal involvement (IgA nephritis)

Investigations:
Need to exclude other serious pathologies = multiple investigations
- FBC and blood film
- CRP and blood cultures
- U&Es and renal profile
- Serum albumin

Management:
Mainly supportive = analgesia, rest and hydration
- Use of steroids is controversial
*can expect to improve within a few days, however may have recurrence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

State at what age septic arthritis is most common in children

A

Under 4

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

State some differentials for septic arthritis in children

A
  • Juvenile idiopathic arthritis
  • Transient synovitis
  • SUFE (slipped upper femoral epiphyses)
  • Perthes disease
  • Fracture
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Kawasaki disease - state the following:
- Pathophysiology
- Most common age
- Presentation (including any red flags)
- Investigations
- Management

A

Pathophysiology:
- Medium vessel vasculitis
- No clear cause or trigger

Most common age:
- Under 5’s (boys and asian children)

Presentation:
- Persistent high fever (> 5 days)
- Widespread erythematous maculopapular rash
- Desquamation on hands and feet
- Strawberry tongue
- Cracked lips
- Cervical lymphadenopathy
- Bilateral conjuntivitis

Investigations:
- Inflammatory markers (particularly ESR)
- Echo (coronary artery pathology)
- FBC (anaemia, leukocytosis, thrombocytosis)
- LFTs (elevated liver enzymes, hypoalbuminaemia)
- Urinalysis (elevated WCC)

Management:
- IV immunoglobulins (reduce risk coronary artery aneurysms)
- High dose aspirin (reduce risk thrombosis)
- Follow up echocardiograms for coronary artery pathology

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

State some cardinal features of Kawasaki disease

A
  • High fever (not responding to typical antipyretics)
  • Maculopapular rash
  • ‘Strawberry tongue’ mucositis
  • Desquamation of hands and feet
  • Conjunctivitis (non-sticky, sparing limbus)
  • Anterior cervical lymphadenopathy
  • Arthritis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Detail the typical progression of Kawasaki disease

A

Over period of disease = approx. 5-10 weeks

Acute phase (1-2 weeks)
- Worst symptomatically with fever, rash and lymphadenopathy

Subacute phase (2-4 weeks):
- Symptoms improving slightly
- Desquamation and arthralgia
- Risk of coronary artery aneurysm forming

Convalescent phase (2-4 weeks):
- Remaining symptoms settle
- Blood tests return to normal
- Coronary artery aneurysm tends to regress

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

State 2 common triggers of Henoch-Schonlein purpura

A
  • URTI
  • Gastroenteritis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

State the WHO pain ladder management for children

A

Only 2 steps

  1. Simple - Paracetamol or Ibuprofen
  2. Morphine

Codeine and Tramadol aren’t used due to unpredictability with metabolism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

State some differentials for hip pain - try and group in age categories:
- 0-4 years
- 5-10 years
- 10-16 years

A

0-4 years:
- Septic arthritis
- Transient synovitis
- Developmental dysplasia of the hip

5-10 years:
- Septic arthritis
- Transient synovitis
- Perthes disease

10-16 years:
- Septic arthritis
- SUFE
- Juvenile idiopathic arthritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

State some red flags for hip pain

A

Joint related:
- Red hot swollen joint
- Persistent pain
- Stiffness in morning

Systemic:
- Under 3 years old
- Fever
- Waking at night from pain
- B symptoms e.g. night sweats, weight loss
- Fatigue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Transient synovitis ‘irritable hip’ - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
- Temporary irritation and inflammation of the synovial membrane
- Most common cause of hip pain in ages 3-10

Presentation:
Often recent history of viral URTI
- Hip pain
- Inability to weight bear
- Limp
- Mild low grade temperature
Onset can be acute or gradual

Investigations:
- Generally not needed unless unsure of diagnosis or septic arthritis cannot be ruled out (consider joint aspiration)

Management:
- Generally symptomatic management with analgesia
Safety netting advice to attend A&E if they develop a fever
Review 2 days after and at 1 week after to check symptoms are resolving
*Recurrence can occur in up to 20% of cases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Perthes disease - state the following:
- Pathophysiology
- Most common age and gender
- Presentation
- Investigations
- Management

A

Pathophysiology:
- Idiopathic temporarily disrupted blood flow to the femoral head, leading to avascular necrosis

Most common age:
- Children aged 5-10 years
- More common in boys

Presentation:
- Hip pain (think also of pain in knee - referred pain)
- Limp
- Restricted hip movements
*No history of trauma

Investigations:
- First line = X-ray (although this can sometimes be normal)
Additional tests
- Inflammatory blood tests (to rule out other differentials)
- Bone scan
- MRI scan

Management:
Conservative if young and not severe
- Crutches
- Bed rest
- Traction
- Analgesia
- Physiotherapy to retain ROM
If severe, may need surgical intervention
Regular x-rays can be used to monitor recovery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Slipped upper femoral epiphysis - state the following:
- Pathophysiology
- Most common age / gender / main risk factor
- Presentation
- Investigations
- Management

A

Pathophysiology:
- Occurs when the head of the femur is displaced, along the growth plate

Most common age:
- 8-15 years (average 12 years)
- More common in boys
- Obesity is the main risk factor

Presentation:
Typically obese boy, undergoing a growth spurt
May have a minor trauma that triggered symptoms
- Hip pain disproportional to severity of trauma
- Restricted ROM
- Painful limp
- Prefer to keep hip in external rotation (limited internal rotation)

Investigations:
- First line = X-ray
Additional tests
- Inflammatory blood tests (to rule out other differentials)
- Bone scan
- MRI scan

Management:
- Surgery is the only management, required to return femoral head to correct position and fix to keep it in place

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Osteosarcoma - state the following:
- Pathophysiology
- Most common age
- Presentation (including any red flags)
- Investigations
- Management

A

Pathophysiology:
- Type of bone cancer
- Femur is most common bone affected, also commonly the tibia and humerus

Most common age:
- Between 10-20 years

Presentation:
- Persistent bone pain (worse at night, often waking from sleep)
- Bone swellings / palpable mass
- Restricted joint movements

Investigations:
- Very urgent x-ray within 48 hours (shows periosteal reaction “sun burst” appearance)
- Blood tests (may show raised ALP)
- May require further tests for staging etc. e.g. MRI, bone biopsy, PET scan

Management:
- Surgical resection of lesion, often resulting in amputation
- Plus adjuvant chemotherapy
- Include MDT approach e.g. physiotherapist, psychologist etc.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Talipes ‘club foot’ - state the following:
- Pathophysiology
- Management

A

Pathophysiology:
- Congenital fixed abnormal ankle position
- Can occur spontaneously or as part of other syndromes
- Often identified at newborn examinations

Management:
- Ponseti method
- May require surgery if Ponseti method is unsuccessful

17
Q

State the 2 types of talipes or “club foot” and briefly describe them

A

Talipes equinovarus:
- Ankle plantar flexed and supinated

Talipes calcaneovalgus:
- Ankle dorsiflexed and pronated

18
Q

Outline the Ponseti method for club foot management

A

Performed by a trained therapist
Often started soon after birth
Repeated until foot is in the correct position

  • Manipulation of feet and cast applied to hold in position
  • At some point, an Achilles tenotomy is performed to release tension in the achilles tendon
  • Then a brace is used to hold feet in correct position when not walking, until about 4 years old “boots and bars”
19
Q

Outline how positional talipes differs from congenital club foot and how management changes

A

In congenital club foot, there is a fixed ankle position which cannot be manipulated into position

However in positional club foot, it occurs when the child is at rest however is able to be manipulated into position and there is no bony abnormality

The Ponseti method is used for congenital club foot, however in positional club foot, a more conservative approach is required with a physiotherapist

20
Q

Developmental dysplasia of the hip - state the following:
- Pathophysiology
- Presentation
- Investigations
- Management

A

Pathophysiology:
- Congenital condition where there are abnormalities of fetal bone development of the hips
- Leads to a tendancy of the hip subluxation or dislocation
- If not treated, can lead to problems in adulthood with recurrent dislocations and degenerative changes

Presentation:
Generally picked up on newborn examinations
- Clunking sensation on Barlow and Ortolani test
Can be picked up later in life with hip asymmetry, different leg lengths or reduced ROM in hips

Investigations:
Screened for at newborn check
- Further tests with ultrasound
- X-rays may be used in older infants

Management:
< 6 months old = Pavlik harness, kept on for around 2 months (hips are flexed and abducted)
> 6 months old or failed harness = Surgery followed by spica cast

21
Q

State 3 risk factors for developmental dysplasia of the hips

A
  • Breech presentation / birth
  • First degree family history DDH
  • Multiple pregnancy