Anti-contactin-associated protein 1 antibody-positive nodopathy presenting with central nervous system symptoms

IF 2.9 4区 医学 Q3 IMMUNOLOGY Journal of neuroimmunology Pub Date : 2024-07-27 DOI:10.1016/j.jneuroim.2024.578420
Yasuko Mori , Nobuaki Yoshikura , Yuki Fukami , Akira Takekoshi , Akio Kimura , Masahisa Katsuno , Takayoshi Shimohata
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Abstract

Contactin-associated protein 1 (Caspr1) is widespread in both the peripheral and central nervous systems (CNS). However, anti-Caspr1 antibody-positive nodopathy associated with CNS symptoms has not previously been reported. In this case, a 69-year-old man presented with polyneuropathy and memory loss. The patient had negative myoclonus, positive myoclonus, and pseudoathetosis in the upper limbs, and we detected anti-Caspr1 antibodies in the serum and cerebrospinal fluid. Therefore, anti-Caspr1 nodopathy was diagnosed. After rituximab treatment, all symptoms of polyneuropathy, involuntary movements, and memory impairment improved. In conclusion, anti-Caspr1 antibodies might also affect the CNS; therefore, CNS symptoms of anti-Caspr1 nodopathy require attention.

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出现中枢神经系统症状的抗接触素相关蛋白 1 抗体阳性结节病
接触素相关蛋白 1(Caspr1)广泛存在于外周和中枢神经系统(CNS)中。然而,与中枢神经系统症状相关的抗Caspr1抗体阳性结节病以前从未报道过。在本病例中,一名 69 岁的男子出现多发性神经病变和记忆力减退。患者有阴性肌阵挛、阳性肌阵挛和上肢假性瘫痪,我们在血清和脑脊液中检测到了抗 Caspr1 抗体。因此,抗 Caspr1 结节病被确诊。在接受利妥昔单抗治疗后,多发性神经病、不自主运动和记忆障碍等症状均有所改善。总之,抗 Caspr1 抗体也可能影响中枢神经系统,因此需要关注抗 Caspr1 结节病的中枢神经系统症状。
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来源期刊
Journal of neuroimmunology
Journal of neuroimmunology 医学-免疫学
CiteScore
6.10
自引率
3.00%
发文量
154
审稿时长
37 days
期刊介绍: The Journal of Neuroimmunology affords a forum for the publication of works applying immunologic methodology to the furtherance of the neurological sciences. Studies on all branches of the neurosciences, particularly fundamental and applied neurobiology, neurology, neuropathology, neurochemistry, neurovirology, neuroendocrinology, neuromuscular research, neuropharmacology and psychology, which involve either immunologic methodology (e.g. immunocytochemistry) or fundamental immunology (e.g. antibody and lymphocyte assays), are considered for publication.
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