Pediatric Intensive Care Unit, Bakirkoy Dr Sadi Konuk Education and Research Hospital, University of the Health Sciences, Istanbul, Turkey.
Pediatric Neurology, Bakirkoy Dr Sadi Konuk Education and Research Hospital, University of the Health Sciences, Istanbul, Turkey.
J Med Virol. 2021 Sep;93(9):5599-5602. doi: 10.1002/jmv.27018. Epub 2021 Apr 23.
The relation between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and demyelinating Guillain-Barre syndrome (GBS) has been defined. We aim to report the clinical features of a child with axonal GBS associated with SARS-CoV-2. A 6-year-old male presented with symmetric ascending paralysis progressed over a 4-day course and 2 days of fever. He had bilateral lower and upper limb flaccid weakness of 1/5 with absent deep tendon reflexes. He had severe respiratory muscle weakness requiring invasive mechanical ventilation. On admission, SARS-CoV-2 returned as positive by real-time polymerase chain reaction on a nasopharyngeal swab. Cerebrospinal fluid analysis showed elevated protein without pleocytosis. He was diagnosed with GBS associated with SARS-CoV-2 infection. The nerve conduction study was suggestive of acute motor axonal neuropathy. Ten consecutive therapeutic plasma exchange sessions with 5% albumin replacement followed by four sessions on alternate days were performed. On Day 12, methylprednisolone (30 mg/kg/day for 5 days) was given. On Day 18, intravenous immunoglobulin (2 g/kg/day) was given and repeated 14 days after due to severe motor weakness. On Day 60, he was discharged from the hospital with weakness of neck flexor and extensor muscles of 3/5 and the upper limbs and the lower limbs of 2/5 on home-ventilation. Our patient is considered to be the youngest patient presenting with a possible para-infectious association between axonal GBS and SARS-CoV-2 infection. The disease course was severe with a rapid progression, an earlier peak, and prolonged duration in weakness as expected in axonal GBS.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染与脱髓鞘性吉兰-巴雷综合征(GBS)之间的关系已经确定。我们旨在报告一例与 SARS-CoV-2 相关的轴索性 GBS 患儿的临床特征。
一名 6 岁男性,表现为对称上升性瘫痪,病程进展 4 天,发热 2 天。他双侧上下肢无力为 1/5,腱反射消失。他存在严重的呼吸肌无力,需要进行有创机械通气。入院时,SARS-CoV-2 通过鼻咽拭子实时聚合酶链反应呈阳性。脑脊液分析显示蛋白升高而无细胞增多。他被诊断为与 SARS-CoV-2 感染相关的 GBS。神经传导研究提示急性运动轴索性神经病。连续进行了 10 次治疗性血浆置换,每次用 5%白蛋白替代,然后隔日进行 4 次。第 12 天,给予甲泼尼龙(30mg/kg/天,连用 5 天)。第 18 天,由于严重的运动无力,给予静脉注射免疫球蛋白(2g/kg/天),14 天后再次给予。第 60 天,他在家中使用呼吸机出院,颈部屈肌和伸肌、上肢和下肢的无力分别为 3/5 和 2/5。
我们的患者被认为是最年轻的患者,表现为轴索性 GBS 与 SARS-CoV-2 感染之间可能存在的副感染相关性。疾病过程严重,进展迅速,如预期的轴索性 GBS 那样,无力的峰值更早,持续时间更长。