Persistent Autonomic Hyperfunction Following Hypertensive Intracerebral Hemorrhage
Journal of Korean Neurosurgical Society
;
: 636-638, 2004.
Article
Dans Anglais
| WPRIM
| ID: wpr-65191
ABSTRACT
Persistent autonomic hyperfunction is not well-recognized disease entity. Recently the authors experienced one case following hypertensive intracerebral hemorrhage in the basal ganglia. It was manifested as storms of hypertension, tachycardia, hyperthermia, severe diaphoresis, hyperventilation and decerebrate posture. Extensive investigations on infection, pheochromocytoma or status epilepticus revealed no abnormalities. Medications including antibiotics, antipyretics and antiepileptic agents were administered, but in vain. However, intravenous morphine infusion managed to stabilize his conditions. To our knowledge, the present case is the first one to be thermographed, and is the second case next to Rossitch's report of autonomic dysfunction following intracerebral hemorrhage.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Phéochromocytome
/
Posture
/
État de mal épileptique
/
Tachycardie
/
Noyaux gris centraux
/
Hémorragie cérébrale
/
Hémorragie intracrânienne hypertensive
/
Antipyrétiques
/
Fièvre
/
Hypertension artérielle
langue:
Anglais
Texte intégral:
Journal of Korean Neurosurgical Society
Année:
2004
Type:
Article
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