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pubmed-article:20678162pubmed:abstractTextBACKGROUND:?Hashimoto encephalopathy (HE) is a rare autoimmune disorder. It is defined as a 'corticosteroid-responsive encephalopathy associated with thyroiditis'. CLINICAL OBSERVATION:? We describe a boy who suffered from HE, responded only to intravenous immunoglobulin therapy. This is the first case report of immunoglobulin therapy in paediatric HE. CONCLUSION:?After review of the literature, we recommend that unexplained encephalopathy in children should lead to evaluation of thyroid autoantibody titres. Immunoglobulins should be considered.lld:pubmed
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pubmed-article:20678162pubmed:authorpubmed-author:BergerIIlld:pubmed
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pubmed-article:20678162pubmed:authorpubmed-author:CastielYYlld:pubmed
pubmed-article:20678162pubmed:copyrightInfo© 2010 The Author(s)/Journal Compilation © 2010 Foundation Acta Paediatrica.lld:pubmed
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pubmed-article:20678162pubmed:volume99lld:pubmed
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pubmed-article:20678162pubmed:year2010lld:pubmed
pubmed-article:20678162pubmed:articleTitlePaediatric Hashimoto encephalopathy, refractory epilepsy and immunoglobulin treatment - unusual case report and review of the literature.lld:pubmed
pubmed-article:20678162pubmed:affiliationThe Neuro-Pediatric Unit, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. itberg@hadassah.org.illld:pubmed
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