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1例罕见的视神经脊髓炎谱系障碍病例,伴有不明原因发热和亚急性认知功能下降,影像学检查正常

A Rare Case of Neuromyelitis Optica Spectrum Disorders With Unknown Fever and Subacute Cognitive Decline With Normal Images.

作者信息

Furuya Kento, Itoh Naoya

机构信息

Department of Emergency, Shizuoka General Hospital, Shizuoka, JPN.

Division of Infectious Diseases, Aichi Cancer Center Hospital, Nagoya, JPN.

出版信息

Cureus. 2022 May 12;14(5):e24950. doi: 10.7759/cureus.24950. eCollection 2022 May.

Abstract

We report the case of a 69-year-old Japanese man who came to our hospital with a chief complaint of fever and cognitive decline for three weeks. There were no neurological abnormalities other than the decreased level of consciousness. He developed urinary retention after admission, so we performed a lumbar puncture, although his head and neck magnetic resonance imaging (MRI) showed no abnormal findings. The cerebrospinal fluid (CSF) examination showed albuminocytologic dissociation and the anti-aquaporin 4 antibody was positive. Thus, we diagnosed him with neuromyelitis optica spectrum disorder (NMOSD). NMOSD is an autoimmune disease that causes demyelination. The clue to diagnosing NMOSD is demyelinating findings on MRI. Therefore, it is difficult to diagnose NMOSD if there are no abnormalities on the images. However, abnormal MRI findings are not necessary for the diagnosis of NMOSD. Thus, NMOSD cannot be ruled out even if MRI findings are normal and the real clue to diagnosing NMOSD is the anti-aquaporin 4 antibody.

摘要

我们报告了一例69岁的日本男性病例,他因发热和认知功能减退三周前来我院就诊。除意识水平下降外,无其他神经学异常。入院后他出现了尿潴留,因此我们进行了腰椎穿刺,尽管他的头部和颈部磁共振成像(MRI)未显示异常。脑脊液(CSF)检查显示蛋白细胞分离,抗水通道蛋白4抗体呈阳性。因此,我们诊断他患有视神经脊髓炎谱系障碍(NMOSD)。NMOSD是一种导致脱髓鞘的自身免疫性疾病。诊断NMOSD的线索是MRI上的脱髓鞘表现。因此,如果图像上没有异常,很难诊断NMOSD。然而,MRI异常表现对于NMOSD的诊断并非必要。因此,即使MRI表现正常,NMOSD也不能排除,而诊断NMOSD的真正线索是抗水通道蛋白4抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bbd/9188466/7dfb9065ff38/cureus-0014-00000024950-i01.jpg

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