Diagnosis of musculoskeletal conditions in children and adolescents
Most musculoskeletal symptoms in children and adolescents are associated with benign, transient, noninflammatory conditions, and are often related to trauma. The challenge for general practitioners is to distinguish these conditions from musculoskeletal pain associated with serious pathology, such as fracture, infection, systemic inflammatory disease or malignancy.
Serious conditions to exclude | Alerting features (‘red flags’) |
---|---|
musculoskeletal injury | |
trauma (eg fracture, dislocation) nonaccidental injury [NB2] |
pain associated with other signs of injury (eg nonweightbearing, swelling, deformity, bruising) |
musculoskeletal infection | |
pain and systemic upset (eg crying, loss of appetite) nonweightbearing fever, tachycardia, hypotension dehydration signs of inflammation (eg acute swelling, erythema, marked reduction in range of motion) monoarticular arthritis [NB3] recent Streptococcus pyogenes (group A streptococcus) pharyngitis or impetigo, and new cardiac murmur or signs of cardiac failure | |
malignancy in childhood | |
leukaemia neuroblastoma benign and malignant bone, cartilage and fibrous-tissue tumours |
bone pain, pain with nocturnal waking, pain out of proportion to examination findings fever weight loss lymphadenopathy hepatosplenomegaly bruising, bleeding |
systemic inflammatory disease | |
juvenile idiopathic arthritis (JIA) systemic lupus erythematosus (SLE) and other inflammatory connective tissue diseases systemic vasculitides including IgA vasculitis and Kawasaki disease |
arthralgia or arthritis constitutional symptoms rash eye symptoms (eg ocular pain, redness, photophobia, visual loss) recurrent fevers |
amplified musculoskeletal pain syndromes (AMPS) | |
localised AMPS (complex regional pain syndrome [CRPS]) diffuse AMPS (paediatric fibromyalgia) |
pain out of proportion to examination findings |
nonrheumatological systemic disease | |
vitamin deficiencies genetic skeletal dysplasias haemoglobinopathies, haemophilia and haemarthroses |
various depending on the condition: arthralgia or arthritis bowel symptoms (eg pain, diarrhoea, rectal bleeding) loss of weight, growth impairment, deformity anaemia, bleeding tendency, bruising, haemarthrosis productive cough |
Note:
NB1: This list is not exhaustive. NB2: If nonaccidental injury (child abuse) is suspected, immediately refer children for paediatric and forensic expert advice. Hospital paediatric services can often provide initial phone advice and directions for follow-up and care. In some jurisdictions, it is mandatory to report nonaccidental injuries in infants and children to state authorities. NB3: Monoarticular arthritis (monoarthritis or monoarthropathy) is acute inflammation involving a single joint. In children and adolescents, the most important diagnosis to exclude is septic arthritis, but it may also be an early single-joint presentation of an oligo-or polyarticular inflammatory process. |
Common noninflammatory musculoskeletal conditions in children and adolescents include:
- mechanical and trauma-related conditions
- benign nocturnal limb pain
- postactivity musculoskeletal pain
- benign hypermobility
- overuse-related trauma
- degenerative changes in growing bone
- amplified pain syndromes (AMPS), including localised AMPS (also known as complex regional pain syndrome CRPS) and diffuse AMPS (also known as paediatric fibromyalgia).
Benign hypermobility (or generalised joint hypermobility) is very common in healthy children and adolescents. It may be associated with diffuse AMPS but rarely requires any investigation or referral to a specialist. See the separate topic Benign hypermobility.
Nonaccidental injury1 (child abuse) must be considered in children and adolescents with multiple musculoskeletal injuries or repeat presentations with injuries. If nonaccidental injury is suspected, immediately refer children for paediatric and forensic expert advice.
Systemic inflammatory conditions in children and adolescents are uncommon. If a general practitioner suspects a child or adolescent may have a systemic inflammatory condition, they should discuss the case early with a specialist.
Specific systemic inflammatory conditions are covered in detail elsewhere; refer to the relevant clinical topic. Important paediatric systemic inflammatory conditions include:
- all types of juvenile idiopathic arthritis (JIA)
- juvenile dermatomyositis
- systemic lupus erythematosus (SLE)
- systemic vasculitides including immunoglobulin A vasculitis and Kawasaki disease
- autoinflammatory periodic fever syndromes
- acute rheumatic fever.