已发表论文

舞蹈病和利用类固醇治疗患有神经功能缺损和脑脊液淋巴细胞增多症的短暂性头痛综合征患者的有效性:病例报告

 

Authors Zhao L, Wang R, Fang H, Song B, Liang D, Xu Y

Received 11 February 2019

Accepted for publication 24 May 2019

Published 24 July 2019 Volume 2019:12 Pages 2247—2250

DOI https://doi.org/10.2147/JPR.S204869

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Ms Justinn Cochran

Peer reviewer comments 2

Editor who approved publication: Dr Katherine Hanlon

Background: The clinical manifestations of the transient headache and neurologic deficits with cerebrospinal fluid lymphocytosis (HaNDL) syndrome are variable, and involuntary movements have not been reported. The etiology and treatment of the syndrome are not entirely clarified.
Case: A 25-year-old female presented with recurrent transient headache, involuntary movements (left upper extremity chorea) and paralysis. Lumbar punctures showed intracranial hypertension and cerebrospinal fluid pleocytosis. Symptoms and intracranial hypertension were relieved after administration of steroids.
Discussion/conclusion: Chorea may also present in the HaNDL syndrome. Steroids might relieve the symptoms of the HaNDL syndrome, which indicates the possible treatment strategy for HaNDL and supports the infectious or postinfectious autoimmune etiology hypothesis.
Keywords: syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis (HaNDL), involuntary movement, steroids, intracranial hypertension




Figure 1 Cerebral magnetic resonance imaging and angiography.