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Two Case Reports of Paroxysmal Sympathetic Hyperactivity Following Craniotomy for Cerebral Hemorrhages Daisuke INOUE 1 , Kenji MIKI 1 , Megumu MORI 1 , Tetsuhisa YAMADA 2 , Yasutoshi KAI 1 , Yoshihiro NATORI 1 1Department of Neurosurgery, Aso Iizuka Hospital 2Department of Emergency Medicine, Aso Iizuka Hospital Keyword: paroxysmal sympathetic hyperactivity , stroke , cerebral hemorrhage pp.79-84
Published Date 2019/1/10
DOI https://doi.org/10.11477/mf.1436203899
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 Paroxysmal sympathetic hyperactivity(PSH)is a clinical condition characterized by abnormal paroxysmal surges in sympathetic nervous system activity. PSH is well known to happen after severe head injury and hypoxic encephalopathy. There are reports of cases of PSH developing after stroke, but PSH is not well recognized in the stroke field in Japan.

 Case 1 is a 79-year-old woman who became unconscious and suffered a large left mixed-type hemorrhage. Emergency craniotomy was performed. Two months postoperatively, she developed a high fever, tachycardia, tachypnea, and decerebrate posture. After taking clonazepam, her symptoms improved, and she was transferred to another hospital. Case 2 is a 67-year-old man with right hemiplegia, a history of thrombectomy for left M1, occlusion and left carotid artery stenting for asymptomatic left severe carotid artery stenosis performed one year previously. Five hours after right corotid artery stenting, he became restless and hemiplegic on his left side. His computed tomography showed extensive cerebral hemorrhage in the right hemisphere necessitating emergency craniotomy. About a month after surgery, he had a high fever, tachypnea, tachycardia, and decerebrate posture. Taking gabapentin improved his symptoms.

 Prolonged PSH may be a factor greatly impairing activities of daily living in stroke patients. It is important to diagnose and treat PSH early.


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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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