Spinal disorders
Pain, onset of deformity, loss of
weight, night sweats, family history, disa-bility, other disorders.
•
Inspection: asymmetry, scapular prominence,
skin lesions (especially midline pits
and haemangiomas), café au lait spots
(associated with neurofibromatosis), foot deformity, leg atrophy.
•
Feel: spinal tenderness.
•
Move: forward flexion, hamstring
tightness.
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General: neurological examination.
•
Investigations: radiographs, CT, MRI, bone scan.
Take it seriously! More likely to
be caused by significant pathology than in adult (e.g. osteoid osteoma,
eosinophilic granuloma). Beware of the following, especially in young
children—several weeks of symptoms; night pain; increasing symptoms; abnormal
neurology; recent onset of scoliosis; night sweats. Pain may be referred from
intra-abdominal or intrathoracic process. Investigate thoroughly, but remember
50% of children experience back pain by 15yrs of age.
Inflammation (probably infection)
of the disc space:
•
Age group: any age (infants and children
rather than adolescents).
•
Symptoms: fever; irritability; unwilling to
walk; back pain, abdominal pain.
Symptoms may be vague.
•
Investigations: bloods (i CRP and ESR); MRI; bone scan.
•
Treatment: antibiotics (according to local
policy), at least until inflammatory
markers return to normal.
•
Outcome: usually do well.
Diastematomyelia:
spinal cord is split by a central cartilaginous/bony
prom-inence.
•
Signs: other abnormalities are common
(e.g. scoliosis, clubfoot, cavus foot);
cutaneous lesions seen in most children; positive neurology seen in 50%.
•
Management: consider resection of spur if
neurology appears/is progressive.
•
Spina
bifida.
See Scheuermann’s
disease
•
Definition: defect of pars interarticularis
(spondylolysis). If bilateral and at
the same level may result in anterior displacement of one vertebra upon another
(spondylolisthesis). Usually due to a stress fracture through a congenitally
dysplastic pars.
•
Incidence: uncommon, associated with spina
bifida, metabolic (e.g. osteopetrosis),
connective tissue (e.g. Marfan’s), hyperextension sports (e.g. gymnastics).
•
Symptoms/signs: sudden/insidious onset of pain
exacerbated by activity. Decreased
forward flexion and straight leg raise.
•
Investigations: X-rays—lateral and oblique spinal views.
Look for ‘Scotty dog’s collar’. Bone
scan/SPECT for occult fractures and evidence of healing.
•
Management: non-operative usually. Rest and
change of activities; consider
short-term bracing, analgesia, hamstring stretches, and core strengthening. Operative
intervention seldom required for stabilization.
•
Definition: hypoplastic/absent sacrum; most
common in infants of diabetic
mothers.
·Signs:
abnormal pelvic ring affecting
lower limbs with associated neurology.
·Management:
tailor towards severity of
agenesis and neurology.
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