Acar Türkan, Acar Bilgehan Atılgan, Karabacak Mustafa, Aras Yeşim Güzey
Sakarya University, Faculty of Medicine, Neurology Department, Sakarya, Turkey.
Noro Psikiyatr Ars. 2018 Sep 17;57(4):340-342. doi: 10.29399/npa.23233. eCollection 2020 Dec.
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.
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。
