儿童扁桃体切除术后晚期中央髓鞘溶解症:病例报告

M. Kotb, Menna t-allah Mahmoud El zabet, Walaa El Naggar
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引用次数: 0

摘要

:中央桥脑髓鞘溶解症(CPM)是快速纠正低钠血症的一种众所周知的严重并发症。CPM 是一种非炎症性脱髓鞘病。临床表现为不同程度的协调能力丧失、昏迷、视力模糊、颅神经痛、进行性痉挛、四肢瘫痪、假性球麻痹,直至锁闭综合征、昏迷和死亡。我们报告了一名因全身强直-阵挛发作和败血症而被送入急诊室(ER)的 4.5 岁儿童。他的父母报告说,他在 3 天前接受了扁桃体切除术,手术顺利。扁桃体切除术后两天,他开始发烧。扁桃体切除术后第三天,他在家中抽搐发作,3 小时后才来到急诊室。他又因癫痫发作来到急诊室。通过静脉注射咪达唑仑和左乙拉西坦负荷剂量,他的抽搐得到了控制。他的意识水平在发作后30分钟内仍处于模糊状态。他的格拉斯哥昏迷量表为 12,需要入住儿科重症监护室(PICU)。他的病情因急性肝肾损伤而变得复杂,但在 48 小时内有所好转。入院时,他的血钠水平为 141 毫摩尔/升,住院期间一直没有低于 140 毫摩尔/升。入院后第 7 天,患儿出现左侧内斜视(第 6 颅神经麻痹)和进行性痉挛。磁共振成像显示患儿患有 CPM。尽管血流动力学稳定、没有低钠血症并迅速得到纠正,但该患儿还是出现了孤立的 CPM。该患儿的CPM可能是脓毒症相关脑病的一种孤立表现,也可能是扁桃体切除术后的晚期并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Late Presenting Central Pontine Myelinolysis Post-tonsillectomy in a Child: Case Report
: Central pontine myelinolysis (CPM) is a notorious grave complication of rapid correction of hyponatremia. CPM is a noninflammatory demyelination. It presents clinically with variable degrees of loss of coordination, unconsciousness, blurred vision, cranial nerve affection, progressive spasticity, quadriparesis, pseudo bulbar palsy up to locked in syndrome, coma and death. We report a 4.5-year-old who presented to emergency room (ER) with generalized tonic-clonic seizures, and sepsis. His parents reported that he underwent un-eventful tonsillectomy 3 days earlier. Two days post-tonsillectomy he developed fever. On third day post-tonsillectomy he developed an attack of convulsions at home, 3 hours prior to presenting to ER. He presented to the ER by another attack of seizures. His seizures were controlled on IV midazolam and levetiracetam loading dose. His conscious level was clouded beyond the postictal 30 minutes. His Glasgow Coma scale was 12 which necessitated Pediatric Intensive Care Unit (PICU) admission. His condition was complicated by acute liver and kidney injury that improved within 48 hours. Upon admission his sodium level was 141 mmol/L, and did not drop below 140 mmol/L all through the hospital stay. By the 7 th day after admission the child developed left sided convergent squint (6 th cranial nerve palsy) and progressive spasticity. Magnetic resonance imaging revealed CPM. The isolated CPM in this child developed irrespective of hemodynamic stability, lack of hyponatremia and its rapid correction. CPM in our studied child might be an isolated presentation of sepsis associated encephalopathy, or a late complication post-tonsillectomy.
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