以意识模糊为表现的偏瘫性偏头痛样综合征：1例罕见病例报告
HaNDL Syndrome Presenting With Confusion: A Rare Case Report.
作者信息
Acar Türkan, Acar Bilgehan Atılgan, Karabacak Mustafa, Aras Yeşim Güzey
机构信息
Sakarya University, Faculty of Medicine, Neurology Department, Sakarya, Turkey.
出版信息
Noro Psikiyatr Ars. 2018 Sep 17;57(4):340-342. doi: 10.29399/npa.23233. eCollection 2020 Dec.
Abstract
HaNDL syndrome characterized by sudden onset headache, transient neurological deficits, and cerebrospinal fluid (CSF) lymphocytosis, is a self-limited clinical entity that is rarely seen. In this article, we present a case with HaNDL syndrome in a 28-year-old male patient who presented with confusion and agitation after sudden onset of headache, right hemiparesis, and lymphocytosis pleocytosis.
摘要
短暂性头痛、神经功能缺损和淋巴细胞增多综合征（HaNDL综合征）以突发头痛、短暂性神经功能缺损和脑脊液淋巴细胞增多为特征，是一种临床自限性疾病，较为罕见。在本文中，我们报告了一例28岁男性HaNDL综合征患者，该患者在突发头痛、右侧偏瘫和淋巴细胞增多性脑脊液细胞增多后出现意识模糊和躁动。
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