[Anti-NF155 antibody positive autoimmune nodopathy presenting as multiple mononeuropathy with predominantly superficial sensory disturbances].

Q4 Medicine
Shuhei Yasuda, Hiroya Kuwahara, Yuki Kobayashi, Yohsuke Yagi, Hidenori Ogata, Yoichiro Nishida
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引用次数: 0

Abstract

Anti-NF155 antibody positive autoimmune nodopathy typically presents with symmetric deep sensory disturbance, muscle weakness and tremor. Here, we report a unique case of anti-NF155 antibody positive autoimmune nodopathy presenting as multiple mononeuropathy with predominantly superficial sensory disturbances. A 35-year-old woman presented with progressive superficial sensory disturbances on the right side of her tongue and lip, the left lower limb, the right toes, and the right forehead over a period of 4 years. There was no deep sensory disturbance, muscle weakness, or tremor. Cerebrospinal fluid protein levels were markedly elevated (423 ‍mg/dl), and nerve conduction studies indicated demyelinating neuropathy. MRI revealed swelling and high signal intensity of both the lumbosacral plexuses and the right lingual nerve on short T1 inversion recovery images. Later, serum anti-NF155 antibody was found out to be positive. Even when the neurological symptoms are not typical as nodopathy, we should explore the possibility of nodopathy in the cases in which cerebrospinal fluid protein levels are markedly high.

[抗nf155抗体阳性自身免疫性结节病表现为多发单神经病变,主要表现为浅表感觉障碍]。
抗nf155抗体阳性的自身免疫性结节病典型表现为对称性深度感觉障碍、肌肉无力和震颤。在这里,我们报告了一例独特的抗nf155抗体阳性自身免疫性结节病,表现为多发性单神经病变,主要表现为浅表感觉障碍。女性,35岁,表现为舌唇右侧、左下肢、右脚趾和右前额进行性浅表感觉障碍,持续4年。没有深度感觉障碍、肌肉无力或震颤。脑脊液蛋白水平明显升高(423‍mg/dl),神经传导检查提示脱髓鞘神经病变。MRI显示腰骶神经丛和右侧舌神经在短T1反转恢复图像上肿胀和高信号强度。随后检测血清抗nf155抗体阳性。即使神经系统症状不是典型的无多巴病,我们也应该在脑脊液蛋白水平明显高的病例中探讨有无多巴病的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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