| Literature DB >> 30170935 |
Kenji Iwai1, Kiyoko Amo2, Ichiro Kuki3, Masataka Fukuoka3, Kiyohiro Kim3, Chiharu Yamairi2, Masao Togawa2.
Abstract
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.Entities:
Keywords: Encephalitis; Epilepsy; Seizure; Sjögren syndrome; Steroid
Mesh:
Year: 2018 PMID: 30170935 DOI: 10.1016/j.braindev.2018.08.004
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961