PGALS: Approach to Child with Arthritis. Prof Chris Scott Paediatric Rheumatology

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Transcription:

PGALS: Approach to Child with Arthritis Prof Chris Scott Paediatric Rheumatology

Introduction In a prospective study from The Royal Hospital for Sick Children, Edinburgh, every 58th child presented with an acute atraumatic limp. A survey of adolescents in British Columbia revealed that musculoskeletal complaints were perceived as the 2 nd most common health concern after acne. Juvenile Arthritis is the most common cause of musculoskeletal disability in children. Musculoskeletal pain can be the presenting feature of many different conditions, including life threatening conditions Fischer SU..1999 Foster & Cabral, 2006

Poor training of Paediatricians and GP s in PR Lack of resources Poor training Perception of rarity Underdiagnosis Poor exposure

Case Presentation 14 month girl Presents with toe walking 5 week history

Age appropriate differential diagnoses Any age Age 0-4 yrs Age 4-10 yrs Age 11-16 yrs Trauma Septic arthritis Reactive arthritis Juvenile idiopathic arthritis (JIA) Malignancy Developmental dysplasia of the hip Transient synovitis Non-accidental injury Perthe s Transient synovitis Slipped upper femoral epiphysis (SUFE)

History Onset Pain: Sudden (injury, Septic) vs indolent (JIA) Timing Pain: EMS Nocturnal Pain Bone Pain Intensity Pain: JIA not severe Enthesitis can be Severe septic, malignancy or amplified pain Disability: Severe not common in early JIA Response to Meds: JIA, reactiveand Osteoid Osteoma Malignancy and septic not Family: Psoriaisis, Ank spond, crohns, Lupus? Social, infectious contacts, immunisations, Growth etc

SEPSIS Complete non-weight bearing Any attempt to move the limb causes extreme distress Constant severe pain Night pain and waking Fever Immunocompromised child - due to primary disease or medications JUVENILE IDIOPATHIC ARTHRITIS Joint swelling lasting > 6 weeks Stiffness / slowness in the mornings Joint pain may not be verbalised in the very young child and may manifest as being grumpy, clumsy or avoiding activities Regression of achieved milestones RED FLAGS Leg length discrepancy and muscle wasting suggest chronicity (many months) MALIGNANCY Night pain Severe and non-remitting pain Pallor, bruising, anaemia, thrombocytopenia Lymphadenopathy Hepatosplenomegaly Systemic symptoms - lethargy, weight loss, night sweats, fever Back pain in the unwell child NON ACCIDENTAL INJURY Delay in seeking medical attention Changeable history inconsistent with pattern of injury or developmental stage of the child Repeated presentations Un-witnessed injury Complete non-weight bearing with occult fracture

Case Presentation 14 month girl Presents with toe walking Left side only 5 week history Timing: initially only in morning Cries often when taken out of bed and refuses to walk? pain Now most of the time No weight loss, no fever, no systemic features Previously well Development normal Milestones appropriate, walked normally from 11-13 months.

O/E First full general and systems based on excluding differential Then MSK screen (PGALS) If any abnormality: Full joint exam Look for features specific suspected autoimmune diseases

Specific Features: Skin Psoriasis White scaly plaques Vasculitis: Henoch Schonlein Purpura Kawasaki Disease Bechets Polyarteritis Nodosa SLE sjia Juvenile Dermatomyositis Sarcoidosis/Blau s disease Inflammatory Bowel Disease Scleroderma Palpable purpura on the lower limbs Polymorphous erythematous macules over trunk. Can be variable. Later peeling of the fingers and toes is characteristic. Oral or genital ulcers, papulopustular lesions, erythema nodosum Variable, erythema multiforme, skin nodules, livedo reticularis Malar rash, discoid lupus, vasculitis rash, photosensitivity Salmon patches Heliotrope rash around the eyes, gottrons papules over extensor surfaces, skin ulceration, calcinosis, periungual erythema erythematous/tan coluored maculopapular rash, Panniculitis Erythema nodosum, pyoderma gangernosum Oedema, sclerosis,

Eyes