Paroxysmal sympathetic hyperactivity represents an uncommon and potentially
life-threatening complication of severe brain injuries, which are most commonly
traumatic. This syndrome is a clinical diagnosis based on the recurrent
occurrence of tachycardia, hypertension, diaphoresis, tachypnea, and
occasionally high fever and dystonic postures. The episodes may be induced by
stimulation or may occur spontaneously. Underdiagnosis is common, and delayed
recognition may increase morbidity and long-term disability. Trigger avoidance
and pharmacological therapy can be very successful in controlling this
complication. Fat embolism syndrome is a rare but serious complication of long
bone fractures. Neurologic signs, petechial hemorrhages and acute respiratory
failure constitute the characteristic presenting triad. The term cerebral fat
embolism is used when the neurological involvement predominates. The diagnosis
is clinical, but specific neuroimaging findings can be supportive. The
neurologic manifestations include different degrees of alteration of
consciousness, focal deficits or seizures. Management is supportive, but good
outcomes are possible even in cases with very severe presentation. We report two
cases of paroxysmal sympathetic hyperactivity after cerebral fat embolism, which
is a very uncommon association.