Iwai Kenji, Amo Kiyoko, Kuki Ichiro, Fukuoka Masataka, Kim Kiyohiro, Yamairi Chiharu, Togawa Masao
Department of Pediatric Emergency Medicine, Osaka City General Hospital, Osaka, Japan.
Department of Pediatric Emergency Medicine, Osaka City General Hospital, Osaka, Japan.
Brain Dev. 2019 Feb;41(2):217-220. doi: 10.1016/j.braindev.2018.08.004. Epub 2018 Aug 28.
Sjögren syndrome (SS) is a systemic inflammatory and autoimmune disease characterized by systemic disorders of the exocrine glands, predominantly the salivary and lacrimal glands. Here, we report a 4-year-old boy who presented with the repetition of generalized tonic-clonic seizures for 1-2 min. Initially, he was diagnosed with idiopathic autoimmune encephalitis and was treated with steroids. He was eventually diagnosed with SS based on the examination results, such as inflammatory cell infiltration into the minor salivary glands and positive serum anti-SSA/Ro antibody. Although central nervous system complications are rare in pediatric SS, this condition should be considered in the differential diagnosis when a patient presents with idiopathic autoimmune encephalitis of unknown cause. Furthermore, SS can occur in relatively young children and can present without imaging abnormalities.
干燥综合征(SS)是一种全身性炎症性自身免疫性疾病,其特征为外分泌腺,主要是唾液腺和泪腺的系统性紊乱。在此,我们报告一名4岁男孩,他出现全身性强直阵挛性癫痫发作,持续1 - 2分钟,并反复发作。最初,他被诊断为特发性自身免疫性脑炎,并接受了类固醇治疗。最终,根据检查结果,如小唾液腺有炎性细胞浸润以及血清抗SSA/Ro抗体阳性,他被诊断为干燥综合征。尽管小儿干燥综合征的中枢神经系统并发症罕见,但当患者出现病因不明的特发性自身免疫性脑炎时,在鉴别诊断中应考虑这种情况。此外,干燥综合征可发生于相对年幼的儿童,且可能不伴有影像学异常表现。