Gross Maximilian, Berger Rafal, Neunhoeffer Felix, Nordmeyer Johannes, Bevot Andrea
Department of Pediatric Cardiology, Pulmonology and Pediatric Intensive Care Medicine, University Children's Hospital Tübingen, Tübingen, Germany.
Department of Thoracic and Cardiovascular Surgery, University Hospital Tübingen, Tübingen, Germany.
Front Pediatr. 2025 Jun 6;13:1610035. doi: 10.3389/fped.2025.1610035. eCollection 2025.
Guillain-Barré syndrome (GBS) is an important cause of flaccid paralysis in children and is mainly associated with antecedent infections. Surgery as an additional trigger for GBS is a well-documented phenomenon in adults, but is significantly less reported in pediatric patients. This case report describes an infant with post-surgical GBS following cardiac surgery, highlighting the diagnostic challenges and differential diagnoses of post-surgical GBS in the pediatric intensive care setting.
A former extremely preterm infant with congenital cytomegalovirus (CMV) infection underwent a second surgery for re-coarctation of the aorta with aortic arch hypoplasia at the chronological age of six months. While requiring extracorporeal membrane oxygenation postoperatively, the girl presented with flaccid paralysis of the lower extremities. Magnetic resonance imaging of the brain, spine, and nerve conduction studies demonstrated findings consistent with acute motor-sensory axonal neuropathy-type GBS. She was treated with intravenous immune globulin and ganciclovir due to CMV reactivation (plasma 14,000 copies/ml). Gradual neurological improvement was noted over the following months, while persistent motor deficits remained, suggesting potential disease transition into chronic inflammatory demyelinating polyneuropathy.
This case report emphasizes the importance of considering post-surgical GBS in critically ill children with postoperative paralysis. Recognition may be delayed due to variable initial presentations and accompanying factors such as sedation and extracorporeal life support.
吉兰 - 巴雷综合征(GBS)是儿童弛缓性麻痹的重要病因,主要与前驱感染有关。手术作为GBS的额外触发因素在成人中是一种有充分文献记载的现象,但在儿科患者中的报道明显较少。本病例报告描述了一名心脏手术后发生手术后脑炎综合征(GBS)的婴儿,突出了儿科重症监护环境中手术后脑炎综合征(GBS)的诊断挑战和鉴别诊断。
一名曾患有先天性巨细胞病毒(CMV)感染的极早产儿在实际年龄为6个月时接受了第二次手术,以修复主动脉缩窄伴主动脉弓发育不全。术后需要体外膜肺氧合支持时,该女孩出现了下肢弛缓性麻痹。脑部、脊柱的磁共振成像以及神经传导研究显示的结果与急性运动感觉轴索性神经病型GBS一致。由于CMV重新激活(血浆中14,000拷贝/毫升),她接受了静脉注射免疫球蛋白和更昔洛韦治疗。在接下来的几个月中,神经功能逐渐改善,但仍存在持续性运动功能缺陷,提示可能已转变为慢性炎症性脱髓鞘性多发性神经病。
本病例报告强调了在术后出现麻痹的危重症儿童中考虑手术后脑炎综合征(GBS)的重要性。由于初始表现多样以及存在诸如镇静和体外生命支持等伴随因素,诊断可能会延迟。