Van Putten Willemina K, Hachimi-Idrissi Said, Jansen Anna, Van Gorp Viola, Huyghens Luc
Paediatric Intensive Care Unit, Brussels University Hospital, Laarbeeklaan 101, 1090 Brussels, Belgium.
Case Rep Med. 2012;2012:358520. doi: 10.1155/2012/358520. Epub 2012 Dec 18.
Anti-N-methyl-D-aspartate receptors encephalitis (ANMDARE) is a well-defined, life threatening, but treatable disorder that often occurs as a paraneoplastic manifestation of ovarian teratomas in adult women. We report a child with this disorder who displayed a subacute onset of delirium, seizures, and autonomic instability. Antibodies against NMDA receptor were detectable in the serum and in the cerebrospinal fluid. No teratoma or other tumour was detected. We speculate that the previous viral/mycoplasma infection may be the trigger of this encephalitis. This patient showed a reversal of the neurological symptoms after intravenous immunoglobulin. Prompt recognition of this disorder followed by immunotherapy results in full neurological recovery.
抗 N-甲基-D-天冬氨酸受体脑炎(ANMDARE)是一种明确的、危及生命但可治疗的疾病,在成年女性中常作为卵巢畸胎瘤的副肿瘤表现出现。我们报告了一名患有这种疾病的儿童,其出现了谵妄、癫痫发作和自主神经不稳定的亚急性发作。血清和脑脊液中可检测到抗 NMDA 受体抗体。未检测到畸胎瘤或其他肿瘤。我们推测先前的病毒/支原体感染可能是这种脑炎的触发因素。该患者静脉注射免疫球蛋白后神经症状得到逆转。及时识别这种疾病并进行免疫治疗可使神经功能完全恢复。