Hiperactividad simpática paroxística: una entidad subdiagnosticada. Caso clínico
Author
dc.contributor.author
Roa Cáceres, Cristian
Author
dc.contributor.author
Rosas Orrego, Camila
Admission date
dc.date.accessioned
2021-04-08T15:47:20Z
Available date
dc.date.available
2021-04-08T15:47:20Z
Publication date
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2020
Cita de ítem
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Rev Med Chile 2020; 148: 1034-1038
es_ES
Identifier
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0034-9887
Identifier
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https://repositorio.uchile.cl/handle/2250/179024
Abstract
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Paroxysmal sympathetic hyperactivity may appear after brain injury. Its clinical manifestations are sporadic and self-limited crisis of arterial hypertension, hyperthermia, tachycardia, hyperhidrosis, muscle tension, sialorrhea and mydriasis. These subside with the administration of morphine and beta-blockers. It may be caused by a dysautonomia leading to increased levels of catecholamines due to the lack of brain regulation. We report a 19 years-old man with a history of illicit drug and alcohol consumption, with a secondary axonal injury due to a cranioencephalic trauma. During hospitalization, he had recurrent, self-limited episodes of dysautonomia. An infectious cause was discarded. When morphine was administrated suspecting the presence of pain, the crisis subsided, which helped to establish the diagnosis of paroxysmal sympathetic hyperactivity.