Rhabdomyolysis results from muscular fibre lysis with release of cellu
lar contents (myoglobin, enzymes, electrolytes) into the plasma. Traum
atic (crush syndrome) and non-traumatic rhabdomyolysis have been mostl
y reported in adults. Traumatic rhabdomyolysis are mostly due to ische
mic and reperfusion injuries. Non-traumatic rhabdomyolysis include sev
eral factors: muscular compression (comas) cytotoxic injury (infection
s and poisonings), ischemia (shock, cardiorespiratory arrest) or exces
sive muscular activity (seizures, strenuous exercise). The main etiolo
gies reported in children are: anoxic-ischemic encephalopathy (includi
ng sudden infant death and life threatening events); electrolyte disor
ders; severe hyperthermia; poisonings; hereditary myopathies Non-traum
atic rhabdomyolysis must be suspected in these circumstances requiring
blood creatinine phosphokinase measurements. Indeed, clinical signs a
re inconstant and non-specific, and functional signs are difficult to
appreciate in children. During the initial phase, the main risk is arr
hythmias secondary to hyperkalemia. The two main complications are the
compartmental syndrome leading to irreversible vasculo-nervous injuri
es and acute renal failure. Treatment of traumatic and nontraumatic rh
abdomyolysis includes correction of hyperkalemia, active fluid loading
in order to prevent acute renal failure and alkalinisation. Prognosis
of rhabdomyolysis relates to the aetiology and the presence of acute
renal failure. (C) 1998, Elsevier, Paris.