Spinal primary central nervous system lymphoma: Case report and literature review

被引:8
|
作者
Feng Li
Chen Dingbang
Zhou Hongyan
Shen Cunzhou
Wang Haiyan
Sun Xunsha
Liang Xiulin
Chen Ling [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Dept Neurol, Natl Key Clin Dept, 58 Zhongshan 2nd Rd, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Key Discipline Neurol, Affiliated Hosp 1, 58 Zhongshan 2nd Rd, Guangzhou 510080, Guangdong, Peoples R China
关键词
PCNSL; Spinal cord; CSF cytology; PRIMARY CNS LYMPHOMA; T-CELL LYMPHOMA; DIAGNOSIS; CORD; FEATURES; BIOPSY; AREA;
D O I
10.1016/j.jocn.2018.01.034
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Primary central nervous system lymphoma (PCNSL) is a very rare tumor of increasing incidence. It is often misdiagnosed due to the unspecific presentation or unavailable biopsy, and results in poor prognosis. PCNSL involved the spinal cord is extremely sparse. Here we report a gentleman presented with oneyear history of progressive tremor in the left limbs and slight dysarthria as well as three-month history of paraparesis, tinnitus and insomnia. MR images disclosed the swollen cerebellum and cauda equine, with contrast enhancement in both meninges and nerve roots. The cerebrospinal fluid (CSF) revealed extremely high protein level. Tubercular meningitis was considered and anti-tuberculosis therapy was given for weeks but without relief. With progressive deterioration, the PCNSL was eventually presumed according to positive CSF cytology and exclusion of systemic involvement. However, the patient passed away within days. We then reviewed the current diagnostic methods of PCNSL The biopsy, as the gold standard for PCNSL diagnosis, is not eligible for all patients suspected PCNSL The presurgical diagnostic algorithm of PCNSL has been fixed by clinicians and we suggest the early and repeated CSF cytology should be included for definitive diagnosis. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:16 / 19
页数:4
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