Acute Bulbar Palsy-Plus Variant of Guillain-Barré Syndrome in a 3-Year-Old Girl.

Child neurology open Pub Date : 2022-08-01 eCollection Date: 2022-01-01 DOI:10.1177/2329048X221115476
Saihari S Dukkipati, Daniel J Zhou, Andria M Powers, Ezequiel A Piccione, Sookyong Koh
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引用次数: 2

Abstract

We present a case of a 3-year-old girl who rapidly developed bilateral facial palsy, dysphagia, dysphonia, areflexia, and ataxia soon after receiving an influenza vaccine. Brain and spine Magnetic resonance imaging (MRI) scans with and without contrast showed enhancement of cranial nerves III, V, VII, and X, as well as the anterior and posterior cervical spinal and cauda equina roots. cerebrospinal fluid (CSF) studies showed white blood cell count of 19 cells/cm2, glucose 81 mg/dL, and protein 116 mg/dL, with negative infectious and autoimmune labs. Serum IgM and IgG antibodies against GM1, GD1a, GD1b, GM2, GT1A, GQ1b were negative. The patient was treated with intravenous immunoglobulin, which led to a full recovery. Upon three-month follow-up, her neurologic examination demonstrated normal cranial nerves, reflexes, and gait. Her presentation was most consistent with the acute bulbar palsy plus (ABPp) variant of Guillain-Barré syndrome (GBS), a rare and challenging diagnosis especially in her age group.

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1例3岁女童急性球性麻痹加格林-巴勒综合征变异型。
我们报告一个3岁的女孩,她在接种流感疫苗后迅速发展为双侧面瘫、吞咽困难、发音困难、反射性松弛和共济失调。脑和脊柱磁共振成像(MRI)扫描显示颅神经III、V、VII和X,以及颈椎前后根和马尾根增强。脑脊液(CSF)检查显示白细胞计数19个/cm2,葡萄糖81 mg/dL,蛋白质116 mg/dL,感染和自身免疫实验室阴性。血清抗GM1、GD1a、GD1b、GM2、GT1A、GQ1b的IgM和IgG抗体均为阴性。病人接受静脉注射免疫球蛋白治疗,完全康复。随访3个月,神经系统检查显示脑神经、反射和步态正常。她的表现与急性球性麻痹加格林-巴- 综合征(GBS)最一致,这是一种罕见且具有挑战性的诊断,特别是在她的年龄组。
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