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一名幼儿的抗N-甲基-D-天冬氨酸受体脑炎:诊断难题。

Anti-NMDA receptor encephalitis in a toddler: A diagnostic challenge.

作者信息

Khundakji Yasmin, Masri Amira, Khuri-Bulos Najwa

机构信息

Faculty of Medicine, The University of Jordan, Amman, Jordan.

Department of Pediatrics, Division of Child Neurology, Faculty of Medicine -The University of Jordan, Amman, Jordan.

出版信息

Int J Pediatr Adolesc Med. 2018 Jun;5(2):75-77. doi: 10.1016/j.ijpam.2018.03.001. Epub 2018 Apr 30.

Abstract

Anti N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune disorder and is considered to be one of the most common causes of encephalitis in children. Despite the fact that around half of all reported cases are of children, the number of studies that report infants and toddlers is very small. Furthermore, reports on children from the Middle East particularly are extremely rare. We report a 21-month-old Jordanian female toddler with NMDAR encephalitis, who initially presented with behavioral changes and some autistic features. She presented a diagnostic challenge due to a concurrent urinary tract infection and gastroenteritis. Multiple investigations were conducted and she was treated with methylprednisolone and intravenous immunoglobulin (IVIg) empirically as well as plasma exchange and rituximab once the diagnosis was confirmed. Her condition improved gradually. We discuss her clinical picture and the diagnostic challenges within this age group; we also review the current related literature.

摘要

抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种自身免疫性疾病,被认为是儿童脑炎最常见的病因之一。尽管所有报告病例中约有一半是儿童,但报告婴幼儿病例的研究数量非常少。此外,特别是来自中东地区儿童的报告极为罕见。我们报告一例21个月大的约旦女童患有NMDAR脑炎,她最初表现为行为改变和一些自闭症特征。由于并发尿路感染和肠胃炎,她的诊断面临挑战。进行了多项检查,确诊后经验性地给予她甲基强的松龙和静脉注射免疫球蛋白(IVIg)治疗,以及血浆置换和利妥昔单抗治疗。她的病情逐渐好转。我们讨论了她的临床表现以及该年龄组内的诊断挑战;我们还回顾了当前的相关文献。

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