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突发听力损失作为日本多发性硬化症和血清学阳性视神经脊髓炎谱系障碍患者的首发症状。

Sudden hearing loss as the initial symptom in Japanese patients with multiple sclerosis and seropositive neuromyelitis optica spectrum disorders.

作者信息

Tanaka Masami, Tanaka Keiko

机构信息

Multiple Sclerosis Center, Utano National Hospital, 8 Ondoyama, Narutaki, Ukyo-ku, Kyoto, 616-8255, Japan; Department of Neurology, Kaikoukai Josai Hospital, Nagoya 453-0815, Japan; Department of Neurology, Fujita Health University, School of Medicine, Toyoake, Aichi 470-1192, Japan.

Department of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata 951-8585, Japan.

出版信息

J Neuroimmunol. 2016 Sep 15;298:16-8. doi: 10.1016/j.jneuroim.2016.06.004. Epub 2016 Jun 15.

Abstract

Sudden hearing loss may occur in rare cases of relapsing-remitting multiple sclerosis (RRMS). There have also been reports of idiopathic sudden sensorineural hearing loss (SNHL) in patients with neuromyelitis optica spectrum disorders (NMOSD), but the frequency of such cases is unclear. We conducted a retrospective analysis of the medical records of 173 consecutive patients with multiple sclerosis (MS) and 101 consecutive patients with NMOSD who tested positive for anti-aquaporin-4 antibodies in addition to 37 consecutive patients with clinically isolated syndromes (CIS) to investigate the frequency and onset timing of SNHL. SNHL was observed in six (3.5%) of the RRMS cases, one (1.0%) of the seropositive NMOSD cases, and three (8.1%) of the CIS cases. SNHL occurred ahead of onset in 4/6 MS patients and in all of 3 CIS patients. Patient with NMOSD exhibited SNHL 6years after the onset of NMOSD. Although SNHL is rare, these results suggest the risk of developing demyelinating lesions in the central nervous system and further conversion to MS in the future.

摘要

突发听力损失可能在复发缓解型多发性硬化症(RRMS)的罕见病例中出现。也有视神经脊髓炎谱系障碍(NMOSD)患者发生特发性突发性感音神经性听力损失(SNHL)的报道,但此类病例的发生率尚不清楚。我们对173例连续性多发性硬化症(MS)患者、101例连续性抗水通道蛋白4抗体检测呈阳性的NMOSD患者以及37例连续性临床孤立综合征(CIS)患者的病历进行了回顾性分析,以研究SNHL的发生率和发病时间。在RRMS病例中有6例(3.5%)、血清学阳性的NMOSD病例中有1例(1.0%)以及CIS病例中有3例(8.1%)观察到SNHL。4/6例MS患者和所有3例CIS患者的SNHL发生在疾病发作之前。NMOSD患者在NMOSD发病6年后出现SNHL。虽然SNHL很罕见,但这些结果提示了未来发生中枢神经系统脱髓鞘病变并进一步转化为MS的风险。

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