2012, Number 2
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Rev Mex Neuroci 2012; 13 (2)
Paroxistic sympathetic hyperactivity: Descritption of two pediatric cases and literature review
Domínguez-Jiménez E, Piña-Ramírez BM, García-Ramírez JL, Lambert-Cerda C, Arellano-De la Hoz JD, Bravo-Oro A
Language: Spanish
References: 35
Page: 98-103
PDF size: 468.08 Kb.
ABSTRACT
Introduction: Paroxysmal sympathetic hyperactivity
occurs in association with several conditions that affect
central nervous system. The main clinical
manifestations are self-limited episodes of hypertension,
tachycardia, tachypnea, hyperhidrosis, alterations in
level of consciousness, excessive salivation, hypertonia
with extensor posture, fever and pupillary dilation.
Recognition is often delayed, which increases the
morbidity and mortality.
Case report: We report two
pediatrics cases that developed sympathetic storm,
one of them after a severe cranial trauma and the
second case associated to hydrocephalus and
hypoxic encephalopathy.
Discussion: The
pathophysiology remains unclear. Limited knowledge
exist about the cerebral area involved or the specific
biochemical abnormalities responsible for the
syndrome. Some of the proposed mechanisms include
heightened activity of the sympathoexcitatory centers
in diencephalon or brainstem, with alterations in
neurotransmitters. The pharmacological management
with first-line drugs like morphine sulfate and betablockers
are considered the most effective although
the level of evidence is low as it is based on some small
case reports. In our cases we use baclofen and
propranolol with good control of the disorder.
Conclusions: Early identification of paroxysmal
sympathetic hyperactivity on high-risk patients is
important to minimize unnecessary diagnostic testing
and therapeutic interventions, as well as to promote
timely and appropriate treatment and minimize
secondary morbidity.
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