Rheumatology Flashcards

1
Q

Five key areas

A
  • Trauma (accidental and NAI)
  • Infection (septic arthritis, osteomyelitis, reactive arthritis, Reiter’s syndrome, rheumatic fever)
  • Tumour (leukaemia, primary bone tumours, neuroblastoma)
  • Inflammation (JIA, vasculitis - HSP and Kawasaki disease)
  • Normal variants (benign night pains, flat feet, in-toeing, normal growth)

NB - Also remember mechanical, muscule disease and metabolic.

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2
Q

Juvenile idiopathic arthritis (JIA)

A
  • Disease of childhood onset characterised primarily by arthritis persisting for at least 6 weeks and currently having no known cause
  • Chronic inflammatory arthropathy
  • Commonest rheumatic disease in childhood
  • Clinical diagnosis with no diagnostic tests
  • Group of diseases - overlap with adult inflammatory arthropathies
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3
Q

Arthritis in adults vs children

A
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4
Q

Uveitis

A
  • 30% oligoarthritis
  • 10% other JIA
  • 50% extended oligoarthritis

NB - Screening by paediatric ophthalmologist using slitlamp

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5
Q

What is an enthesis?

A
  • Insertion to bone of:
    • Tendon
    • Ligament
    • Joint capsule
    • Fascia
  • Enthesis associated arthritis commonly presents in:
    • Ankylosing spondylitis
    • Reiter’s syndrome
      • Conjunctivitis
      • Urethritis
      • Plantar fasciitis
      • Arthritis
    • IBD arthritis
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6
Q

Seronegative vs seropositive

A
  • Seronegative
    • Asymmetrical
    • Large lower limb joint (AS/ERA/Reiter’s/IBD)
    • Large and small joint (psoriatic)
  • Seropositive
    • Symmetrical
    • Large and small joint arthritis
    • Wrists and MCPs
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7
Q

ALL

A
  • Joint pain (shoulders, elbows, knees) - tender with warm effusions
  • Young children (most common age 2-5)
  • Tiredness and pallor
  • Low Hb and normocytic normochromic anaemia
  • Raised ESR and CRP
  • ANA present in 1 in 40
  • Marrow trephine for diagnosis
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8
Q

Benign night pains

A
  • 6 years of age
  • Pain after physical activity
  • Wake after exercise screaming at night
  • Mum massages legs
  • Maybe a dose of calpol
  • Better next day
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9
Q

Primary bone tumour

A
  • 14 years
  • Deep boring pain in R hip at night
  • Struggles to school, given up paper round etc
  • Limp
  • Daytime pain
  • Weight loss and fever
  • Treatment assumes micrometastases so for Osteosarcoma chemo + surgery and in Ewing’s sarcoma chemo + surgery + autologous SCT + radiotherapy
  • Long term follow-up due to treatment toxicity
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10
Q

Rheumatic fever

A
  • Age 5-17 years
  • Painful migratory polyarthritis
  • Not much to find in joints
  • Fever
  • Rash
  • Loud pansystolic murmur
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11
Q

Septic arthritis

A
  • Painful joint
  • Hot, red and swollen (not always seen in deep joints like the hip)
  • Pseudoparalysis
  • Pyrexia >38.5oC
  • Inability to weight bear
  • Raised ESR (>40mm/h), CRP and WCC (>12x109/l)
  • Commonly staphylococcus aureus, streptococcus pneumoniae and haemophilus influenza
  • Management
    • ABCDE and resuscitation
    • Aspiration with microscopy and gram stain, culture and sensitivity
    • Blood cultures
    • High dose IV antibiotics
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12
Q

Osteomyelitis

A
  • Classic presentation is acutely unwell child, pyrexia, local erythema and tenderness
  • Swollen joint can mean you miss the painful adjacent bone
  • X-ray sgows Brodie’s abscess in metaphysis
  • Most often subacure presentation (limp, night pain, point tenderness)
  • Management
    • Blood cultures
    • Bone aspiration
    • High dose IV antibiotics
    • Splintage of the limb
  • Changes on X-ray occur late so normal does not exclude
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13
Q

Henoch Schonlein Purpura (HSP)

A
  • Most common vasculitis in children
  • 50% under 6 years, 90% under 10 years
  • Rash on extensor surfaces
  • Arthritis is same pattern of joints
  • Blood and protein in the urine
  • HTN - glomerulonephritis
  • Abdominal pain
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14
Q

Kawasaki Disease

A
  • Early features
    • Fever
    • Arthritis
    • CV issues
    • Rash
    • Cervical lyphadenopathy
    • Thrombocytosis
    • Non-purulent conjunctivitis
  • Late signs
    • Aneurysms
    • Peeling skin
    • Cardiac ischaemia
    • MI
  • Treat with IVIG
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15
Q

NAI

A
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16
Q

Changes to the MSK system in normal development

A
  • Proportion of limb lengths to trunk increase with age
  • Children are significantly more flexible and subtle so compare opposite sides for flexibility
  • Children under 2 have flat feet and a broad based gait - an adult pattern of gait isn’t established until nearer the age of 7
17
Q

Benign leg pain vs malignant leg pain

A
18
Q

Reactive arthritis

A
  • Most common cause of joint swelling in children
  • Triggered by infectious agents outside the joint - most commonly unidentified viral infection
  • Short lived self-limiting illness
  • Specific constellations of features overlapping with reactive arthritis include:
    • Rheumatic fever (streptococcal infection)
      • Carditis, arthritis, neirological features and rash
      • Raised ESR, ASO titre and Dnase B
      • Treat with penicillin
    • HLAB27 associated reactive syndrome/Reiter’s (post enteric of GU infection)
      • Usually boys
      • Urethritis, arthritis, conjunctivitis, plantar fasciitis after gram-negative infection or STD
      • Self-limiting once infection treated
    • Transient synovitis of the hip
      • Idiopathic
      • 3-10 years develop gradual onset hip pain
      • US confirms effusion
      • Conservative management
    • Discitis
      • Usually self-limiting
      • Peak onset 1-3 years with child refusing to walk
      • Difficult to diagnose but if in doubt give antibiotics
19
Q

Salter-Harris Classification of Growth Plate Injuries

A
20
Q

Mechanical

A

*

21
Q

Benign or self-limiting conditions of childhood

A
  • Osgood Schlatter’s syndrome
    • Boys aged 11-12 who are physically active
    • Pain over tibial tuberosity with swelling and local tenderness
  • Anterior knee pain
    • Cause unknown
  • Irritable hip
  • Pulled elbow
    • Tofflers radial head partially slips from the enfolding annular ligament
    • Reduction is effected by supination and pronation of the forearm with the elbow flexed
22
Q

Metabolic

A
  • Causes of rickets
    • Vitamin D deficiency
    • Calcium deficiency
    • Hypophosphatemic (vitamin D resistant) impaired parathormone dependent proximal renal tubular resorbtion of phosphate
    • Vitamin D dependedent rickets
    • Hypophosphatasia