Chronic Inflammatory Demyelinating Polyneuropathy Following Natural Influenza A Infection in a Pediatric Patient: A Case Report and Literature Review.

IF 0.9 Q4 CLINICAL NEUROLOGY
Case Reports in Neurological Medicine Pub Date : 2025-05-05 eCollection Date: 2025-01-01 DOI:10.1155/crnm/8840308
Emily Grew, Garrett Gianneschi, Janet Elgallab
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引用次数: 0

Abstract

Chronic inflammatory demyelinating polyneuropathy (CIDP) following viral infections and influenza vaccination has been well documented. However, there have been no confirmed natural influenza A infections leading to development of CIDP. Therefore, we present the case of a 6-year-old male who developed CIDP following a confirmed influenza A infection. Initially presenting with typical flu-like symptoms, the patient experienced a gradual onset of gait instability and leg weakness approximately 1 month later. Despite initial improvement with intravenous immunoglobulin therapy following a diagnosis of Guillain-Barré syndrome, his symptoms relapsed, including lower extremity weakness, incontinence, and sensory loss. Electromyography confirmed a demyelinating polyneuropathy, leading to a diagnosis of CIDP.

小儿甲型流感感染后慢性炎症性脱髓鞘性多神经病变:1例报告及文献复习。
慢性炎症性脱髓鞘多神经病变(CIDP)后的病毒感染和流感疫苗接种已得到充分证明。然而,目前还没有证实的自然甲型流感感染导致CIDP的发展。因此,我们提出的情况下,6岁的男性谁开发CIDP后确诊甲型流感感染。患者最初表现为典型的流感样症状,大约1个月后逐渐出现步态不稳定和腿部无力。尽管在诊断为格林-巴-罗综合征后静脉注射免疫球蛋白治疗最初有所改善,但他的症状复发,包括下肢无力、大小便失禁和感觉丧失。肌电图证实脱髓鞘性多神经病变,诊断为CIDP。
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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26
审稿时长
11 weeks
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